“EFFECTS OF INTRAVENOUS LIGNOCAINE 2% AND LIGNOCAINE SPRAY 10% FOR INTUBATION RESPONSE IN PATIENTS WITH EJECTION FRACTION <50% - COMPARATIVE STUDY"
INTRODUCTION
Laryngoscopy
and tracheal intubation is one of the commonest procedures done by all
anesthesiologists on daily basis. Direct laryngoscopy and intubation leads to
reflex release of catecholamines resulting in hemodynamic response meaning
transient increase in heart rate, systolic blood pressure, diastolic blood
pressure[1,2] and occasionally cardiac arrhythmias[3] .
Laryngoscopy
and endotracheal intubation is an essential part of general anaesthesia in
cardiac surgery. Direct laryngoscopy and intubation through the larynx is a
noxious stimulus, which can provoke unwanted response in the cardiovascular,
respiratory and other physiological systems[4] .
Lignocaine is the most frequently used local
anesthetic, available in multiple concentrations. It is also routinely used by
various techniques for local, peripheral and epidural anesthesia. One of the
uses of lignocaine is to anaesthetize airway. Intravenous lignocaine acts by
inhibiting sympathetic response associated with intubation by increasing
threshold for stimulation of airway and central inhibition of sympathetic
transmission, dose which used for this action is 1.5mg/kg IV bolus which has 30%
depressive effect on CVS [5,6,7].
Lignocaine has been evaluated in numerous
trials as a spray or gel to suppress response associated with laryngoscopy[8,9,10].
It has also been used to reduce the incidence of postoperative sore throat,
cough, and hoarseness of voic1[11,12,13,14]. This anesthetic has
also been given via nebulizer for awake intubation in difficult airway patients[15,16].
More commonly, lignocaine inhalation has been utilized to reduce the frequency
of chronic cough in patients with asthma and chronic obstructive lung disease
(COPD)[17,18]. This route of administration appears to produce low
serum levels and a reduced frequency of adverse effects compared to gel or
spray formulations.
We plan to compare lignocaine spray
(10%) and intravenous lignocaine(2%, 1.5mg/kg) to attenuate the sympathoadrenal
response along with standard drugs used for premedication and induction. This
study has been designed to assess the effects on hemodynamic parameters due to
laryngoscopy and endotracheal intubation in patient undergoing CABG with
ejection fraction less than or equal to 50%.
AIMS & OBJECTIVES
Aim
of this comparative study is to assess effects of lignocaine spray and
Intravenous Lignocaine
on
the following:
1)
Hemodynamic response to laryngoscopy on:
1.
Heart rate
2.
Systolic and Diastolic blood pressure
3.
Mean Arterial Pressure
4.
Central Venous Pressure
5.
ECG for Arrhythmias
2)
Post-operative sore throat.
MATERIALS AND METHOD
This Prospective Randomized study was conducted in
Department of Anaesthesiology, D Y
Patil University School of Medicine & Hospital, Nerul, Navi Mumbai.
STUDY DESIGN:
Prospective
Comparative study
STUDY DURATION:
October
2017 to June 2019
Eligibility Criteria:
INCLUSION
CRITERIA
1. Patient
with Ejection Fraction(EF) <50% undergoing Coronary Artery Bypass Graft
(CABG) under general anaesthesia
2. Adult
patients in the age group of 30 to 75 yrs.
3. American
Society of Anesthesia (ASA) status II or III for patients undergoing elective surgeries
4.
Patients with all laboratory
investigations within normal limits and
hemodynamically stable patient.
EXCLUSION
CRITERIA
1.
Those unwilling to participate.
2. Patients
with difficult airway (MPC III / IV)
3.
Patients with ASA status IV.
4. Patients
undergoing emergency surgery.
5.
Patients known or suspected to have an
allergy to lignocaine.
SAMPLE SIZE AND SUBJECT:
Approval of
Institutional Ethics Committee was obtained before start of the study in October
2017. A valid informed written consent was obtained prior to enrolling the
subject in the study.
A prospective, randomized, comparative study was
conducted in 60 patients of ASA grade II or III between the age group 30-75
years posted for CABG with ejection fraction less than or equal to 50%
requiring general anesthesia to compare the effect of intravenous lignocaine
and lignocaine spray on hemodynamic response to laryngoscopy and endotracheal
intubation.
MATERIAL USED:
Following materials were available for our study:
a)
Lignocaine
(preservative free) – 2%
b)
Lignocaine
(topical) - 10% spray
c)
10 ml
syringe
d)
Normal
saline for dilution
PREPARATION OF DRUGS:
1)
1.5mg/kg of
study drug 2% lignocaine was diluted till 10ml with normal saline for
intravenous injection.
2)
Lignocaine 10%
spray attached with spraying
nozzle.
STUDY
PROCEDURE/ DATA COLLECTION METHOD:
Pre
anaesthesia assessment:
Prior to surgery, preoperative visit were made
and a detailed history of the patient was taken. Informed consent was taken
from all the patients included in the study.
Following
informed consent along with proper preoperative evaluation and relevant
investigations as per the case record form the patient was randomly allocated
to either of the two groups.
Randomization was done using random number
table generated from computer software.
The
patients were randomly divided into 2 groups:
Ø
Group
1 (n=30):
Intravenous 2% lignocaine (preservative free)
1.5mg/kg
Ø
Group
2 (n=30):
lignocaine spray 10%
Ø
After
obtaining written consent, initial pre-operative counseling was done to gain
confidence of patient, thereby minimizing the emotional component of stress.
All
the patients were given intradermal test dose of 0.2ml 2 % lignocaine on
ventral aspect of left forearm.
The
nature of the procedure was explained to the patients. Baseline reading which
included heart rate (beats/min), systolic blood pressure (mmHg), diastolic
blood pressure (mmHg) and mean arterial pressure (mmHg), central venous
pressure (CVP) and electrocardiogram (ECG) for all cases were noted pre
operatively.
Procedures
for study drug administration and for anesthetic induction were rigorously
standardized.
· GROUP 1: After
standard induction, this group of patients received intravenous 2% Lignocaine
(preservative free) 3 minutes prior to laryngoscopy .
· GROUP 2:
Patients vocal cords were sprayed with 10% lignocaine spray as soon as the
vocal cords are visualized by direct laryngoscopy.
Patient
taken to the operation theatre, where automated recordings (Data scope) of
heart rate (HR) and systolic (SBP), diastolic (DBP), and mean (MBP) blood
pressures were recorded at 0 min, 1 min, 3min and repeated at 5-minute interval
till 20 mins from induction. After 3 minutes of pre-oxygenation, premedication
with Inj. Glycopyrrolate (4ug/kg), Inj. Midazolam (0.03mg/kg), Inj. buprenorphine
(1mcg/kg) was given. This was followed by induction of General Anaesthesia with
Inj. Thiopentone (5 mg/kg) followed by Inj. Vecuronium (0.1mg/kg) and the
patient was intubated.
Group
1 received intravenous 2% lignocaine (preservative free) 1.5 mg/kg 180 sec just
before laryngoscopy.
Laryngoscopy
was done at 3 minutes after dose of Vecuronium for passage of the endotracheal tube followed
by mechanical ventilation with 1.2% Isoflurane
in 60% Air/ 40%
O2 at
2 L/min and adequate tidal volume. The patient was left undisturbed for an additional 20 minutes
of hemodynamic recordings, at which point the study was terminated.
The
standard monitors were used on all patients to eliminate variability in
determining blood pressure or heart rate and recording data. Our induction
technique was parallel the drug dosages and sequence frequently used in the
anesthesia department.
Method
for Statistical Analysis:
The
quantitative data was represented as their Mean ± SD. Categorical
and nominal data were expressed in percentage. The t-test was used for
analyzing quantitative data, or else non parametric data, was analysed by
Mann-Whitney test. Categorical data was analysed by using chi-square test. The
significance threshold of p value was set at < 0.05. All analysis was
carried out by using SPSS software version 21.
AIRWAY ANATOMY [19, 20]
The
relevant anatomy of the posterior surface of the tongue, the soft palate,
epiglottis, larynx and trachea, with their nerve supply is explained briefly to
understand the physiological effects of endotracheal intubation.
TONGUE:
It
is a soft mobile organ which is present in floor of the mouth. The posterior
part of the tongue forms the anterior wall of the oropharynx. The dorsum of the
tongue is long and extends from the tip to the base of the epiglottis and with
it forms the glosso-epiglottic fold. It is separated into palatine and pharyngeal
parts by a V shaped sulcus terminalis. The thick mucous membrane covering the
tongue is posteriorly continuous with that on the anterior surface of
epiglottis over the median and lateral glosso-epiglottic folds and the
valleculae of the epiglottis between them.
EPIGLOTTIS:
Epiglottis
is a leaf like structure. Its lower tapering end is attach to the back of the
thyroid cartilage with the help of thyro-epiglottic ligament
LARYNX:
The anaesthesiologist should be thorough with knowledge of the anatomy of the
larynx. The larynx is located within the anterior aspect of the neck, anterior
to the inferior portion of the pharynx and superior to the trachea. Its primary
function is to protect the lower airway by closing abruptly upon mechanical
stimulation, thereby halting respiration and preventing the entry of foreign
matter in to the airway. Other function of larynx includes phonation, coughing,
the Valsalva maneuver and control of ventilation, and acting as sensory organ. Structurally,
the larynx composed of 3 large unpaired cartilages (cricoid, thyroid,
epiglottis); 3 paired cartilages which are small (arytenoids, corniculate,
cuneiform); and a number of intrinsic muscles. The hyoid bone, while
technically not a part of larynx, provides muscular attachments from above that
aid in laryngeal motion. Larynx extends from C4-C6 cervical vertebra.
Figure
1. Entrance to larynx (posterior view)
The
laryngeal inlet has large oblique shaped opening bounded by epiglottis antero-posteriorly.
Bounded on each side by the aryepiglottic fold of mucous membrane and
postero-inferiorly by the inter-arytenoid fold of mucous membrane. Each
aryepiglottic fold is a narrow and deep fold that extends postero-inferiorly
from the margin of the epiglottis to the arytenoid cartilage. It contains the aryepiglottic muscle and
near its inferior end two small pieces of cartilage which form the cuneiform
and corniculate tubercules in its free edge. The interarytenoid fold of mucous
membrane passes between them forms the inferior boundary of inlet and encloses
the muscle which passes between the posterior surfaces of the arytenoid cartilages.
Vocal
cords are two folds of mucous membrane stretching antero-posteriorly from the
vocal processes of the arytenoid cartilage to the posterior surface of the
thyroid cartilage and enclosed within each of them is a band of fibroelastic
tissue known as the vocal ligament. The opening between the two folds forms the
glottis which is the narrowest portion of the airways in the adult.
Figure 2. Laryngoscopic view of vocal cord
To view the larynx at direct laryngoscopy and then to pass a tracheal
tube depends on getting the mouth, the oropharynx and the larynx into one
plane. Flexion of the neck brings the axes of the oropharynx and the larynx in
line but the axis of the mouth still remains at right angles to the others;
their alignment is achieved by full extension of the head at the atlanto-occipital
joint. This is the position, with the nose craning forwards and upwards.
On
laryngoscopy, first views the base of the tongue, the valleculae and the
anterior surface of the epiglottis. The laryngeal aditus then comes into view
bounded in front by the posterior aspect of the epiglottis, with its prominent
epiglottic tubercle. The aryepiglottic folds are seen on either side running
postero - medially from the lateral aspects of the epiglottis; they are thin in
front but become thicker as they pass backwards where they contain the cuneiform
and corniculate cartilages.
The vocal cords appear as pale, glistening ribbons that extend from the angle
of the thyroid cartilage backwards to the vocal processes of the arytenoids.
Between the cords is the triangular (apex forward) opening of the rima
glottidis, through which can be seen the upper two or three rings of the trachea.
TRACHEA:
Trachea
is a wide tube with 13-15 mm diameter and 11- 14 cm in length. It begins at the
larynx and terminates at the level of the fourth thoracic vertebra, where it bifurcates
into the two main bronchi. The tracheal architecture consists of C shaped
cartilages which are joined posteriorly by the trachealis muscle. Vertically
these cartilages are joined to each other by fibroelastic tissue.
NERVE SUPPLY:
Glossopharyngeal
nerve:
This cranial nerve is a mixed type of nerve. Motor fibers of this
nerve supply the stylopharyngeus
muscle. Parasympathetic fibers supplies the parotid gland.
The
pharyngeal branch consists of:
1.
One or two branches which supply the
mucous membrane of the pharynx, posterior one third of the tongue, anterior
surface of the epiglottis, glosso-epiglottic folds, valleculae and pyriform
fossa are also supplied by this nerve.
Figure 3. Nerve Supply of the Airway
2.
The larger branch accompanies the
pharyngeal branches of the vagus to the pharyngeal plexus. One of its branches
joins a branch of superior laryngeal nerve to form the carotid sinus nerve
which supplies the carotid sinus and the carotid body.
Vagus nerve:
Vagus
is a mixed type of cranial nerve. In the neck it is found with the internal jugular vein and the internal
carotid artery above and the common carotid artery below. All three structures
are enclosed in the carotid sheath. It gives off multiple branches, among all
three of which supply those areas of the pharynx and larynx stimulated by the
endotracheal intubation.
1. Pharyngeal branch
2. Superior laryngeal nerve:
This branch divides into external and internal laryngeal nerves. The external
branch descends on the anterior aspect of the thyroid cartilage to the cricothyroid
muscle to which it supplies. The internal branch, Supplies sensory branches to
the larynx above the level of the glottis.
3.
Laryngeal
nerve: The recurrent laryngeal nerves provide the motor supply to the
intrinsic muscles of the larynx apart from cricothyroid, as well as the sensory
supply to the laryngeal mucosa inferior to the vocal cords.
PHYSIOLOGY OF PRESSOR RESPONSES[21,22]
Direct laryngoscopy and endotracheal intubation following induction of
anaesthesia is almost always associated with hemodynamic changes due to reflex
sympathetic discharge caused by epipharyngeal and laryngopharyngeal
stimulation. Here in with have explained briefly the physiology and effects of
laryngoscopy and intubation to understand the haemodynamic changes.
SYMPATHETIC NERVOUS SYSTEM.
The
sympathetic efferent nerve fibres originate from nerve cells in the lateral
grey column of the spinal cord between the first thoracic and second lumbar
segments (the thoracic outflow). Preganglionic fibres are myelinated. Ganglia
are located either in the paravertebral sympathetic trunk or in prevertebral
ganglia, such as the celiac ganglion. The sympathetic part of postganglionic
fibres are long, non-myelinated sympathetic part of the system has a wide
spread action on the body as the resulting preganglionic fibres synapsing on
many postganglionic neurons and the suprarenal medulla releasing the
sympathetic transmitters epinephrine and nor epinephrine. The sympathetic
nervous system prepares the body for emergencies and severe muscular activity.
There is no sympathetic out flow from cervical part of the cord nor from the
lower lumbar and sacral parts. Those preganglionic fibres which are destined to
synapse with cell bodies whose fibres are going to run with cervical nerves
must ascend in the sympathetic trunk and those of lower lumbar and sacral
nerves must descend in the trunk to lumbar and sacral ganglia.
Figure 4.
Sympathetic supply to heart
Afferent sympathetic fibres
All the afferent fibres have their cell bodies in the posterior root
ganglia of spinal nerves. The afferent fibres reach the spinal nerve in the
white ramus communicants. Central processes enter the spinal cord by posterior
nerve root. From there they ascend through the cord to brain stem.
THE CARDIOVASCULAR REFLEXES
The
cardiovascular responses to noxious airway manipulation are initiated by
proprioceptors responding to tissue irritation in the supraglottic region and
trachea. It is located in close proximity to the airway mucosa. The superficial
location of the proprioceptors and their nerves is the reason that topical
local anaesthesia of the airway is such an effective means of blunting
cardiovascular responses to airway interventions. The glossopharyngeal and
vagal afferent nerves transmit these impulses to the brain stem, which, in
turn, causes autonomic activation through both the sympathetic and
parasympathetic nervous systems.
In
adults and adolescents, the more common response to airway manipulation is
hypertension and tachycardia, mediated by the cardio accelerator nerves and
sympathetic chain ganglia. This response includes widespread release of
norepinephrine from adrenergic nerve terminals and secretion of epinephrine
from the adrenal medulla.
In
addition to activation of the autonomic nervous system, laryngoscopy and
endotracheal intubation result in stimulation of the central nervous system
(CNS), as evidenced by increases in electroencephalographic activity, cerebral
metabolic rate, and cerebral blood flow (CBF).
PHARMACOLOGY
OF LIGNOCAINE23,24,25
Lignocaine
was synthesised in 1943 in Sweden by Lofgren, it was introduced into clinical
practice by Gordh in the year 1948. It is most commonly used local anesthetic
agent.
PHARMACOLOGY
Clinically lignocaine is an amino-amide of xylidine-de-ethyl amino 2:6
dimethyl acetanilidine.
STRUCTURAL FORMULA:
PHYSICAL
PROPERTIES:
It
consists of lipophilic aromatic group, hydrophilic tertiary amine and
intermediate amide bond. It is a stable, colorless crystalline solid whose
hydrochloride salt is readily soluble in water, not decomposed by boiling,
acids or alkalies and withstands repeated autoclaving. It should be stored at
room temperature.
The
pKa of lignocaine is 7.72. At the normal tissue pH of 7.4 approximately 65% of
lignocaine exists in the charged cationic form, whereas 35% exists in the
uncharged base form.
Lipid solubility:
Determination of partition co-efficient by means of n-heptane/pH 7.4 buffer
system has given a value of 2.9.
Plasma protein binding: At a
concentration of 2mcg/ml approximately 65% is bound to plasma proteins.
Lignocaine is a local anaesthetic of moderate potency and duration, with good
penetrative powers and has rapid onset
of action. It is effective by all routes of administration. Lignocaine
sometimes causes vasodilation, Adrenaline may be used as adjuvant.
prolongs
the duration of lignocaine as it reduces the rate of systemic absorption. With
repeated injections, tachyphylaxis often occurs. The hydrochloride salt in
water has a pH of 6.5. Hepatic extraction ratio 65-70%. Plasma half life of 1.6
hrs. Volume of distribution – 1.3 L/hr.
PREPARATIONS OF LIGNOCAINE
1.
Topical forms:
Topical spray 4% and 10% solution
Gel: 2% or 2.5%
Solution: 2% or 4% or 5%
2.
Parenteral
forms: 0.5%, 1% .2%, or 4% as lignocaine hydrochloride.
Lignocaine is stored at temperature < 25ºC protected from light.
Lignocaine is also available along with adrenaline in 1: 1 lakh or 1: 2 lakh concentrations.
Figurer 5. Lignocaine 2%
Each ml contains:
Lignocaine Hydrochloride I.P. 21.3 mg
Sodium Chloride I.P. 6.0 mg
Water for injection 1.P. q.s.
Figure 6. lignocaine spray 10%
Each
ml contains:
Lidocaine USP 100mg
Ethanol
I.P. 30.4% v/v
Flavoured Base q.s.
PHARMACODYNAMICS
Local
effects:
Lignocaine
blocks the conduction of impulses in the nerve fibres at the site of injection
by closing sodium channels.
Sensory
and motor fibres are inherently equally sensitive to lignocaine.
Smaller
fibres and nonmyelinated nerve fibres are blocked more easily than longer and
myelinated fibres.
Autonomic
fibres are more susceptible than somatic fibres. Among somatic fibres order of
blockade are pain-temperature-touch-deep pressure sense.
Addition
of vasoconstrictor like Adrenaline (1:50,000 to 1:2 lakh) cap
Prolong
the duration of action of lignocaine by decreasing the rate of removal from the
local site of injection in to the circulation
Reduces
the systemic toxicity; of lignocaine by decreasing the rate of absorption and
keeping the plasma concentration lower.
It
is very effective surface analgesic causing rapid absorption from mucosal
surface. The peak blood concentration is achieved within 4 to 15 minutes
after instillation. Given intravenously,
peak blood levels are achieved immediately.
Systemic
effects:
Cardiovascular
system
Heart:
Lignocaine is placed under classification of class 1- B anti-arrhythmic drugs
classification.
It
suppresses the automaticity in ectopic foci by antagonizing phase IV
depolarization in Purkinje fibres and ventricular muscles by blocking sodium
channels.
It
does not depress SA node automaticity.
The
rate of phase-0 depolarization is not decreased except in presence of
hyperkalaemia.
Lignocaine
markedly decreases the action potential duration and effective refractory
period in Purkinje fibres and ventricular muscles.
Conduction
velocity is not decreased.
It
has practically no effect on action potential duration and effective refractory
period of atrial fibres. Atrial re-entry is not affected.
It
can suppress the re-entrant ventricular arrhythmias either by abolishing one
way block or by producing two way blocks. At therapeutic plasma concentration
of 3- 5mcg/ml, it causes little depression of cardiac contractility. There are
no significant autonomic actions. All cardiac effects are direct actions.
Lignocaine
is widely used in the management of ventricular dysrhythmias in a dose of 1 to
2 mg/kg bolus intravenously and 2.4 mg/min as infusion. It acts by its membrane
stabilizing effect and depression of automaticity at atrio-ventricular node. It
has been used effectively in the management of ventricular arrhythmias
following myocardial infarction and cardiac surgery.
Vascular
smooth muscle.
Lignocaine
exists in two isomers, and the ability to produce vasoconstriction appears
vested in one of the isomers. Hence lignocaine produces vasoconstriction with
low doses and vasodilation at higher doses, very large doses cause circulatory
collapse as a result of medullary depression and direct vasodilation.
At
doses > 75mcg/kg/min with plasma concentration of > 10-20mcg/ml
lignocaine causes asystole and cardiovascular collapse.
Central
nervous system
It
readily crosses blood brain barrier causing central nervous system stimulation
followed by depression with higher doses. The severity of the central nervous
system effect correlates with plasma concentration. Central nervous system is
more susceptible to toxic effects than the cardiovascular system. Mild toxic
effects may cause drowsiness and sedation. Objective signs of central nervous
system toxicity are usually excitatory in nature and may cause shivering,
muscular tithing and convulsions. It has been shown to possess analgesic
properties when given intravenously. Reduction of MAC of inhalational
anaesthetic agents is used as an index of its central analgesic property.
Higher serum levels produce a central stimulant effect, and this is due to
initial blockade of inhibitory pathway at limbic or higher centres in the
cerebral cortex.
Neuromuscular
junction:
It
can affect transmission at the neuromuscular junction and hence potentiate the
effect of the depolarizing and non-depolarizing muscle relaxants.
Metabolism:
Lignocaine
gets metabolized by the liver microsomal enzymes, oxidases and amidases. The
main pathway in man appears to be due to oxidative de-ethylation of lignocaine
to monoethyl glycinexuylidide followed by subsequent hydrolysis of monoethyl
glycinexylidide to xylidine. Lignocaine is excreted by kidneys.
Dosage:
The
factors on which the dosage of lignocaine depends are the weight of the
patients and the different absorption rates from various sites and injections.
The maximum safe dose of lignocaine is 4.5 mg/kg without epinephrine and 7
mg/kg with epinephrine.
A
concentration of 0.25-5% of lignocaine hydrochloride is used for infiltration.
If extensive block is required, then 0.5% with epinephrine is used. 0.5%
lignocaine without adrenaline is used for intravenous regional anaesthesia. 1%
lignocaine is usually sufficient for most nerve blocks. In dentistry, 2% lignocaine
with adrenaline 12.5 mcg/ml (1:80,000) is useful. A concentration of 1.5-2%
solution of lignocaine is used for epidural analgesia and sometimes with the
addition of adrenaline 5 mcg/ml 1:200,000). For surface application, lignocaine
solution in a concentration of (4%) for spraying or for application using wool
pledgets.
It
is used in a concentration of 2% as a lubricating gel in urethral surgery and
for lubricating endotracheal tubes. In the management of cardiac dysrhythmias,
it is used in the dose of 1-2 mg/kg iv as a bolus dose followed by 2-4 mg/min
(20-60 mcg/kg/min) as infusion and then the dose is reduced. Caution must be
exercised in the presence of low cardiac output and after cardiac surgery and a
slow infusion rate must be maintained.
Toxicity:
The
appearance of toxic symptoms is due to two factors. The toxicity of the drug
and its serum levels.
Toxic
symptoms may occur at plasma levels of 5mcg/ml in an awake patient, while
levels of 10mcg/ml are toxic in the anaesthetised patient. Plasma levels depend
on the speed with which lignocaine enters the circulation, which in turn
depends on the dosage and rate of absorption of the drug from various sites.
Peak blood levels are attained in 1 minute after intravenous administration and
start decreasing by 3-4 minutes. Following laryngotracheal administration, peak
blood levels are attained in 9-15 minutes. Alveolar absorption occurs at a
faster rate than absorption from bronchial and bronchiolar mucosa. It is
thought that, mucosal absorption simulate intravenous administration. However,
systemic absorption of lignocaine may be slowed through larynx and tracheal
mucosa as it is diluted with secretions lining the upper airway, impeding
systemic absorption. Hence laryngotracheal administration is associated with
delayed peak levels that are lower but more sustained. The peak blood levels
after epidural injection follow a similar pattern to those seen after
intra-muscular injection (average 18 minutes for plain lignocaine and after 23
minutes for lignocaine with adrenaline)
Side
effects
Commonest
side effects are nausea, drowsiness, and dizziness. At a higher level
shivering, muscular twitching, tremors and convulsions, bradycardia, decreased
respiration with hypoxia can occur. Circulatory collapse may occur with very
high dosage.
Hypersensitivity
This
is due to an antigen-antibody reaction. Hypersensitivity to local anaesthetics
is more common with ester-linked drugs than with amide group of drugs. This is
more commonly seen in atopic individuals and can manifest as local oedema,
urticaria, or angioneurotic oedema. Dermatitis may be encountered as a result
of skin application. Anaphylaxis occurs less commonly. Although amide agents
appear to be relatsively free from allergic type reactions, solution may
contain preservatives like paraben and methylparaben whose chemical structure
is similar to that of para-aminobenzoic acid.
REVIEW OF LITERATURE
Ul
Islam M, Ahmad
I, Shah
AA, Islam
A;Attenuation of haemodynamic response to
laryngoscopy and oral endotracheal intubation in coronary artery bypass surgery
patients: intravenous morphine and lidocaine versus intravenous morphine and
lidocaine spray. J
Ayub Med Coll Abbottabad. 2014
Jul-Sep;26(3):275-8[26].
In 2014, there was
randomized control trial conducted with 60 patients who were schedules for
elective CABG. There were two groups i.e group A (IV morphine 0.1mg/kg & IV
lignocaine 1.5mg/kg) and group B (IV morphine 0.1mg/kg & lignocaine spray
1.5mg/kg). Demographic data was comparable in both groups.
With this study they
concluded that lignocaine spray in addition to IV morphine had no better effect
on attenuation of hemodynamic changes to laryngoscopy and intubation compared
to intravenous lignocaine and morphine in CABG surgery patients.
Abou-Madi
MN, Keszler
H, Yacoub
JM;Cardiovascular
reactions to laryngoscopy and tracheal intubation following small and large
intravenous doses of lidocaine. Can Anaesth Soc J. 1977 Jan;24(1):12-9[27].
In
1977, Abou-Mandi MN et al, studied hemodynamics changes to laryngoscopy and
endotracheal intubation after giving small and large intravenous doses of
lignocaine (0.75mg/kg & 1.5mg/kg).
With
this study they came to a conclusion that 1.5mg/kg dose of lignocaine had
complete protection against cardiac arrythmias of all types. Small dose of
lignocaine (0.75mg/kg) was ineffective in this respect. While the larger dose
also had borderline protection against hypertention and tachycardia, the small
dose prevented only the rise in systolic blood pressure. Possible mechanisms
for theses observations are direct myocardial depressant effect, a central
stimulant effect, a peripheral vasodilation effect and finally an effect on
synaptic transmission.
This study was carried out at the tertiary
level hospital in India. After Approval
from the Institutional Ethics Committee, written informed consent
was obtained from close relatives
of the patients. A total f 60 patients with LVEF>
35%, between30 and 75 years
of age, undergoing elective cardiac
surgery requiring laryngoscopy and intubation were enrolled
for this prospective randomized double blind
study. There were two groups;
Group
A received Lignocaine 1.5mg/kg
i.v and group
B received an
additional dose of
injection Fentanyl 3
mcg/kg i.v. 3
min prior to laryngoscopy. During induction various
hemodynamic parameters was recorded during induction and 10 min intervals after
tracheal intubation.
In
conclusion, given 3 minutes prior to intubation, lignocaine (1.5
mg/kg) and fentanyl
(3μg/kg) both attenuated the
rise in HR, .
We
conclude that both
lignocaine and fentanyl
can be safely used for attenuation of stress
response during laryngoscopy and TI in
patients with cardiac
disease undergoing elective cardiac surgery.
This study was carried out in the department
of Anaesthesiology at the M.R. Medical College’s Basaveshwar Hospital, Govt
General Hospital Gulbarga during the period of two years. Seventy five Patients
of either sex, aged between 20 and 60 Years.
Group-I Received Fentanyl 4µg /kg body weight.
Group-II Received Lignocaine(xylocaine) 1.5 mg
/kg body weight
Group-III Received normal saline.
After intubation, incidence of tachycardia
(HR>100/min) was significantly greater in placebo and lignocaine group than
in fentanyl group (p<0.05). Rise in systolic blood pressure (SBP) and
diastolic blood pressure (DBP) were also statistically significant in placebo
and lignocaine group than in fentanyl group (p<0.05) as compared with
baseline value.
In the present study, Attenuation of pressor
response was seen both with lignocaine and fentanyl. Of the 2 drugs fentanyl
4µg/kg bolus provides a consistent, reliable and effective attenuation of
haemodynamic response to laryngoscopy and endotracheal intubation as compared
to lignocaine 1.5mg/kg iv. bolus.
Fifty
controlled hypertensive ASA grade II patients of either sex aged between 35 and
65 years undergoing routine elective surgical procedures under general
anaesthesia participated in this prospective randomized study. Ethical
committee approval was received and informed consent was obtained from all
patients.
Patients
were randomly assigned one of 2 groups each comprising 25 patients. Group I
received lignocaine 10% (LOX Topical spray, Neon Labs) spray 2 minutes before
induction of anaesthesia. Group II received normal saline spray prior to
induction of anaesthesia and served as control.
There
was a statistically significant (p< 0.05) increase in heart rate, systolic
,diastolic and mean arterial pressure in group II when compared to group I and
also when compared to baseline values. It was concluded that topical lignocaine
10% when sprayed prior to induction of anaesthesia attenuated the pressor
response to laryngoscopy and intubation, but did not abolish it completely.
Mostafa SM1, Murthy
BV, Barrett PJ, McHugh P;Comparison of the effects of topical lignocaine spray
applied before or after induction of anaesthesia on the pressor response to
direct laryngoscopy and intubation. Eur J Anaesthesiol. 1999 Jan;16(1):7-10[9].
In an attempt to attenuate the cardiovascular
pressor response to laryngoscopy and intubation, 30 patients presenting for
routine ophthalmic surgery were studied and were randomly allocated into two
groups: group A (n = 15) received direct laryngeal/tracheal lignocaine spray
immediately before intubation; and group B (n = 15) received orolaryngeal
lignocaine spray before the induction of anaesthesia.
Laryngoscopy and endotracheal intubation
caused a significant increase in heart rate, by 28% in group A and 23% in group
B (P < 0.05 in both), and in diastolic blood pressure, by 28% in group A and
24% in group B (P < 0.05 in both). In group A, the systolic blood pressure
also increased significantly (by 18%) after intubation, but there was no
significant change in group B.
It was concluded that topical lignocaine
administration as an orolaryngeal spray before the induction of anaesthesia is
effective in reducing but not abolishing the pressor response to laryngoscopy
and endotracheal intubation.
Patients were randomly divided into two
groups, 30 in each group.
Group I
received 50 mg of esmolol
group
II received lignocaine 2 mg/kg.
Haemodynamic parameters like pulse, systolic
blood pressure, diastolic blood pressure and mean arterial pressure were
measured before induction of anaesthesia, immediately after intubation then at
intervals of one minute, three minutes, five minutes, seven minutes and 10 1minutes.
There was no significant difference in
demographic or base line vital signs between two groups (Table 1). The mean
systolic blood pressure (SBP) increased on laryngoscopy and tracheal intubation
by 15 mmHg in the group I whereas in group II it was 17.4 mmHg.
There was a significant rise in diastolic
blood pressure (DBP) in both the groups, but the rise was lesser in group II
than in group I.
Both esmolol and lignocaine were not effective
in attenuating hemodynamic stress response to laryngoscopy and tracheal
intubation; however esmolol was superior to lignocaine in blunting the stress
response.
Dr. V. Madhuri
Gopal;Comparative Study of Pressor Response to Laryngoscopy and Intubation with
Oral Spray of Nitroglycerine and Oropharyngeal Spray of Lignocaine;
Sch. J. App. Med.
Sci., 2017; 5(4D):1463-1469[32].
A
clinical prospective comparative randomized study of attenuation of sympathetic
response to laryngoscopy and intubation was done in 60 patients posted for
elective surgeries. The study was conducted after an approval from the hospital
ethics committee.
Group
L - Lignocaine group (n=30) - received oropharyngeal Lignocaine 10% spray 100
mg 3 minutes before induction.
Group
N - Nitroglycerin group (n=30) - received oral nitroglycerin spray 0.8mg 30
seconds before induction.
Heart
rate, systolic and diastolic blood pressure were recorded at baseline, at
induction, 1, 3, 5 and 10 minute intervals after laryngoscopy
From
the present study it can be concluded that
· In Lignocaine
spray group patients who received 10 puffs ( 100 mg) oropharyngeally , 3
minutes before induction , there was a significant rise in the mean heart rate
(HR), systolic blood pressure (SBP), diastolic blood pressure (DBP) , mean
arterial pressure (MAP) occurred one minute following laryngoscopy and
intubation .
·
In Nitroglycerine spray group, who received 2 puffs (0.8 mg) orally 30 seconds
before induction, effectively attenuated arterial pressure response to
laryngoscopy and intubation. Hence, it is concluded that Nitroglycerine oral
spray in the dose of 0.8 mg, given 30 seconds before induction can be a better
alternative in attenuating the haemodynamic responses to laryngoscopy and
intubation without adverse side effects.
Stoelting,
Robert K; Blood pressure and heart rate changes during short-duration
laryngoscopy for tracheal intubation: influence of viscous or intravenous
lidocaine. Anesth Analg 1978; 7:19734[33].
In
1978, Stoelting, Robert K studied blood pressure and heart rate changes during short-duration
laryngoscopy for tracheal intubation. Influence of viscous or intravenous
lignocaine and concluded that the best way to prevent laryngoscopic response
was to minimize the duration of laryngoscopy and intubation to 15 seconds.
He
also suggested that, intravenous lignocaine given in the doses of 1.5 mg/kg 3
mins before laryngoscopy and intubation, sufficiently attenuates the
laryngoscopic reactions. The advantage of intravenous lignocaine claimed by
this author was, it depresses the autonomic nervous system and in addition has
anti arrhythmic properties.
HAMILL
J. F.; BEDFORD, R. F.; WEAVER, D. C.; COLOHAN, A. R. (1981); Lidocaine before
endotracheal intubation: Intravenous or laryngotracheal? Anesthesiology 55,
578-581[34].
Hamill,
bedfore, Weva and Colohan (1981)
compared the effects of intravenous lignocaine verses laryngotracheal topical
lignocaine in attenuation of intubation response. They were interested in
identifying preferred route for the administration of lignocaine prior to
endotracheal intubation. In addition to measuring heart rate and blood
pressure, these authors measured intracranial pressure (ICP) to see if either
route was preferable in preventing a rise in ICP. The patients were randomly
assigned to each group. Each subject received the same induction protocols,
thiopentone 3 mg/kg and succinylcholine 1.5 mg/kg. 1 min after laryngoscopy and
endotracheal intubation 50% nitrous oxide and 50% oxygen was administered.
Using a Mackintosh laryngoscope blade 3, 11 patient received laryngotracheal 4%
lignocaine, via “laryngotracheal anaesthesia” (LTA) set. The other eleven
patients received lignocaine 1.5 mg/kg IV. 2 mins after induction, laryngoscopy
was performed with a Mackintosh blade. Endotracheal intubation was accomplished
in 20 sacs. There was no difference between groups with regards to age, heart
rate, base line blood pressure prior intubation. The group which received
laryngotracheal lignocaine showed significant rise in heart rate, blood
pressure and ICP which remained elevated for 2 mins. The group which received
IV lignocaine showed significant rise in heart rate and blood pressure. However
this rise was limited to 1 min, after which cardiovascular values returned to
base line. ICP in the group which received IV lignocaine did not significantly
increase after endotracheal intubation.
This
data suggested that IV administration of lignocaine is the preferred technique
for administering lignocaine prior to endotracheal intubation.
BENJAMIN
DRENGER AND JACOB Peter; Attenuation of ocular and systemic responses to
tracheal intubation by intravenous lignocaine; British Journal of
Ophthalmology, 1987, 71, 546-54838[35].
This
study was undertaken to determine whether intravenous lignocaine could mitigate
or prevent the ocular reactions and especially the acute increase in
intraocular pressure associated with laryngoscopy and tracheal intubation. Two
groups of children undergoing minor eye surgery under nitrous
oxide-oxygen-halothane anaesthesia were examined. The experimental group (n=
17) received 2 mg/kg lignocaine and the controls (n=18) an equivalent volume of
saline. The incidence of local laryngeal and ocular reflexes was much lower in
the lignocaine group. Pulse acceleration was significantly lower in the lignocaine
group (p<0.025), and the maximal mean intraocular pressure was significantly
less than in the control group (p<0.025). Other ocular reactions were
recorded, and all were attenuated after lignocaine administration. The
beneficial effects of lignocaine, a suppressant of autonomic reflexes, suggest
that intraocular pressure, like the heart rate, rises after intubation as a
result of autonomic stimulation. The use of intravenous lignocaine is thus
recommended for children at risk, such as those needing an urgent operation
because of lacerated eye injury under rapid sequence induction of anaesthesia.
Laurito
CE1, Baughman
VL, Becker
GL, Polek
WV, Riegler
FX, VadeBoncouer
TR;
Effects of aerosolized and/or intravenous lidocaine on hemodynamic responses to
laryngoscopy and intubation in outpatients; Anesth Analg. 1988 Apr;67(4):389-92[36].
A
randomized, double-blind study was carried out on 40 unpremedicated, ASA I-II
adult surgical outpatients to assess the effects of aerosolized lidocaine,
intravenous lidocaine, both, or neither, on circulatory responses to
laryngoscopy and intubation. Lidocaine (4 mg/kg) or saline was given by
nebulizer in the holding area beginning at −15 minutes. The patient underwent a
standarized induction of anesthesia that included IV curare (3 mg)
and O2 by facemask at minute 2, followed by IV thiopental (5 mg/kg) and
succinylcholine (1.5 mg/kg) at minute 5. Lidocaine (2 mg/kg) or saline was
given by IV push at minute 4. Laryngoscopy was begun at 5 minutes and continued
for 45 seconds before intubation. Heart rate and systolic, diastolic, and mean
blood pressures were automatically recorded at 1-minute intervals from 0 to 11
minutes. The four treatment groups included: group 1, aerosolized and IV
saline; group 2, aerosolized saline, IV lidocaine; group 3, aerosolized
lidocaine, IV saline; and group 4, aerosolized and IV lidocaine. There were no
differences among the four treatment groups (n = ten per group) in any of the
four hemodynamic variables before laryngoscopy and intubation. Within each
group, after intubation all four hemodynamic variables increased significantly
over the corresponding baseline values for that group. However, the maximum
values attained after intubation did not differ significantly among the four
treatment groups for any of the four hemodynamic variables, whether those
maxima were expressed as absolute values or as a percentage of baseline. Having
found no difference in the effects of aerosolized and/or intravenous lidocaine
and saline placebo on hemodynamic response to laryngoscopy and intubation in
adult surgical outpatients using a rigidly standardized protocol, it is
recommended that such usage of lidocaine be abandoned.
The
results obtained was that, there was significant rise in all four parameters in
all 4 groups. But the absolute values from each group after laryngoscopy and
intubation had no significant difference with use of aerosolized and
intravenous lignocaine and both or none.
The
pressor response is known to be exaggerated in patients with pregnancy-induced
hypertension, which can result in increased morbidity and mortality in both
mother and newborn. Various pharmacological agents have been used before
induction in an attempt to attenuate the adrenergic response but with varying
degree of success. Esmolol, an ultra short-acting cardioselective β-blocker
with rapid onset and short elimination half-life, is an attractive choice for
attenuating the adrenergic response in pregnant patients. In a prospective,
randomised double blind study we evaluated the efficacy of two bolus doses of
esmolol with or without lidocaine, in patients with pregnancy-induced
hypertension. Eighty such patients undergoing lower segmental caesarean section
were randomly divided into four groups and received the following study drugs
before intubation: group I, esmolol 1 mg·kg−1; group II, esmolol 2 mg·kg−1;
group III, esmolol 1 mg·kg−1 and lidocaine 1.5 mg·kg−1; and group IV, esmolol 2
mg·kg−1 and lidocaine 1.5 mg·kg−1. In groups II, III and IV, the changes in
maternal heart rate, systolic blood pressure and mean arterial pressure in
response to laryngoscopy and intubation were attenuated to a comparable degree
(P>0.05). No adverse effects were noticed in mother or baby. We conclude
that esmolol 1 mg·kg−1 with lidocaine 1.5 mg·kg−1 is effective in attenuating
the adrenergic responses to laryngoscopy and intubation in patients with pregnancy-induced
hypertension.
The
conclude that Esmolol 1 mg/kg with lignocaine 1.5 mg/kg was effective in
attenuating the adrenergic responses to laryngoscopy and intubation in cases of
PIH for LSCS.
The
aim of this study was to investigate the efficacy of lidocaine solution in the
cuff of the endotracheal tube in reducing mucosal damage following tracheal
intubation.
This
was a randomized controlled trial study undertaken in the intensive care unit
patients. Participants, who met all eligibility criteria, were randomly
assigned to one of two groups of patients, according to whether lidocaine or
air was used to fill the tracheal tube cuff. The tracheal mucosa at the site of
cuff inflation was inspected by fiberoptic bronchoscopy and scored at the 24 h
and 48 h after intubation.
In
all, 51 patients (26 patients in the lidocaine group and 25 patients in the
control group) completed the study. After 24 h, erythema and/or edema of
tracheal mucosa were seen in 2 patients (7.7%) of lidocaine group and 6
patients (24%) of air group (P = 0.109). Binary logistic regression analysis
showed that lidocaine has a significant protective effect against mucosal
damage (odds ratio = 0.72, confidence interval = 0.60-0.87).
The
inflation of the tracheal tube cuff with lidocaine was superior to air in
decreasing the incidence of mucosal damage in the 24 h and 48 h post
intubation.
40
patients of ASA grade I and II aged 20-50 years were selected for elective
surgery requiring general anaesthesia for endotracheal intubation.
They
were divided into 2 groups
Group-1:
Lignocaine hydrochloride group. Here patients received inj. Lignocaine
hydrochloride 1.5 mg/ kg i.v. bolus 3 min prior to induction.
Group-2:
Fentanyl citrate group. Here patients received injection Fentanyl citrate 2
mcg/kg i.v. bolus 3 min prior to induction.
All
patients were pre-oxygenated with 100% O2 for 3 min before induction. Induction
was achieved with injection Thiopentone sodium 5 mg/kg i.v. and injection
succinylcholine 2 mg/kg was given i.v. IPPV given with 100% O2 and after
adequate relaxation laryngoscopy and intubation was done. Anaesthesia was
maintained with O2(33%), N2O(67%), Isoflurane(0.5-1.0%) and injection
Vecuronium omide. Peri-operative vitals and complications were recorded.
Reversal was achieved with injection Neostigmine 0.05 mg/kg i.v. and injection
glycopyrollate 0.004 mg/kg i.v.
This
study concluded that Changes in mean pulse rate and MAP was significant after
intubation and intraoperatively with mean pulse rate, MAP being higher in
group-1 than group-2. Thus Fentanyl citrate provides better haemodynamic
stability by increasing sedation, analgesia and depth of anaesthesia. Fentanyl
citrate is safer and more effective in attenuation of haemodynamic response to
laryngoscopy and intubation.
In
Kidwai Memorial Institute Oncology, Banglore, they studied effects of
lignocaine (15 mg/kg) on pressor response during laryngoscopy and intubation in
50 patient of age 20-60 years. They monitored heart rate systolic blood
pressure and rate pressure product
immediately after intubation followed by 2 minutes and 5 minutes.
The
result shows that heart changed from pre induction 81.80 ± 6.74 bpm to 102.20 ±
7.11 bpm immediately after intubation i.e 25% rise. While SBP and MAP changed
from 121.20 ± 8.72 to 153.92 ± 10.25 and 90.59 ± 5.74 to 107.47 ±6.36
immediately after intubation respectively. RPP changed from 9921.60 ± 1148.51
to 9921.60 ± 1148.51 after intubation.
Thus
concluded that intravenous lignocaine is less effective to attenuate the
pressor response and a better alternative should be used after further
comparative studies.
A prospective randomized cross over study was
conducted in Lokmanya Tilak Municipal Medical College and Government Hospital,
Sion, Mumbai, India during the period of January 2012 to September 2013. Sixty
patients requiring tracheal suction through an endotracheal tube received 1.5
mg/kg of lignocaine in the nebulized form or as an intravenous injection on two
different occasions. Heart rate (HR), mean arterial pressure (MAP), systolic
and diastolic blood pressure (SBP and DBP) and peripheral capillary oxygen
saturation (SPO2) were recorded at baseline, after the administration of
lignocaine, after two successive suctions and once in two minutes for the next
16 minutes
In the present study, SPO2 decreased in response to
ETT suctioning in both the study groups as compared to the pre-suctioning
value. However the changes in the SPO2 were not significant when compared
between the groups. Changes in HR, SBP, DBP and MAP were not significantly
different between the two routes of lignocaine administration.
From the present study, we can conclude that the
abolition of haemodynamic response to tracheal suction is similar with both
intravenous and nebulized lignocaine. But the return of MAP towards baseline
value was observed to be earlier with nebulized lignocaine than with
intravenous lignocaine which favours use of nebulized lignocaine over
intravenous lignocaine.
Laryngoscopy and tracheal intubation causes
sympathoadrenal stimulation and cause transient rise in pulse rate and blood
pressure. We evaluated the efficacy of Esmolol and Lignocaine in attenuating
the pressor response during laryngoscopy and inutbation as compared to placebo.
60 patients of ASA I & II between the age group of 20-60 were
randomized to receive either Esmolol 1.5 mg/Kg, Lignocaine 1.5mg/Kg or 5ml normal
saline just prior to induction of anaesthesia. Heart rate (HR), systolic blood
pressure (SBP) and diastolic blood pressure (DBP) were recorded before
induction (baseline) and at regular intervals of 1, 3, 5, 7 and 10 minutes
after induction. Statistical analysis was done using Student’s t test and
chi-square test and p values obtained.
There is an increase in HR, SBP and DBP in the control
group which is maximum at 3 mins after induction (i.e. during laryngoscopy and
tracheal intubation). Whereas in the study groups there was no significant
variation in these parameters from baseline which is found to be more effective
with Esmolol (p-value < 0.001) than Lignocaine.
Esmolol 1.5mg/Kg was found to be more effective in
attenuating pressor response to laryngoscopy and intubation when compared to
Lignocaine.
The
study aimed to evaluate the effects of lignocaine spray on hemodynamic response
of endotracheal intubation patients.
This
study is a randomized clinical trial on a study population comprising patients
admitted to the ICU.
The
patients were divided into three groups using a permuted block randomization.
Group
1, inhaled nebulized lignocaine 4% (75.0 mg/kg). In
Group
2, intravenous (IV) lignocaine 2% (75.0/mg/kg) was injected.
No lignocaine was prescribed for or
administered to the control group. One and four minutes after intubation, the
patients' hemodynamic and vital signs were measured.
Although
the mean arterial blood pressure (MAP) of Group 1 (inhaled nebulized
lignocaine) was smaller than that of Group 2 (IV lignocaine), there was no
significant difference between the two groups. Both groups' MAPs were
significantly different from that of the control group. As for the average
number of pulses, a significant difference was observed between the inhaled and
IV lignocaine groups; hence, the average number of pulses in Group 1
(inhalation) was lower than that of Group 2 (IV injection). This concluded
that:
As
blood pressure is considered to be normal under 140/90 and may not entail any
hemodynamic complications, it can be concluded that inhaled nebulized
lignocaine can control the hemodynamic changes of intubation more effectively
than IV lignocaine.
The aim of this
study was to compare of intravenous and
oropharyngeal spray of lidocaine and high dose of fentanyl on systolic and
diastolic blood pressures and heart rate of patients over
65 years during tracheal intubation.
In this clinical trial, 160 patients over
65 yrs who were randomly divided into five groups of 32 patients. For group one lidocaine spray 10%, group two intravenous lidocaine 1.5 mg/kg, group three lidocaine spray along
with intravenous lidocaine 0.75
mg/kg, and for group four fentanyl 5μg/kg were administered and group
five patients were controls which were
given 1 mg of midazolam along with 2 μg/kg fentanyl. Systolic and diastolic
blood pressures and heart rate were measured before and after anesthesia
and intubation. ANOVA, Scheffe's and Repeated
measure tests were used for data comparison and P<0.05 was considered
significant.
This study concluded that all methods were effective for
efficient blood pressor control during laryngoscopy and tracheal intubation.
Sixty patients with a
cerebral aneurysm were randomly divided into three groups by lidocaine
administration methods before endotracheal intubation: Group 1 (Control, 2%
lidocaine 1.5 mg/kg, intravenous injection); Group 2 (10% lidocaine 1 mg/kg,
intralaryngotracheal spray); Group 3 (10% lidocaine 1.5 mg/kg,
intralaryngotracheal spray). Anesthesia was induced intravenously with
midazolam (0.02 mg/kg) and thiopental sodium (2 - 3 mg/kg), and then maintained
with 50% nitrous oxide in oxygen and 1.0 vol% isoflurane. Blood pressure and
heart rate were measured preinduction, before laryngoscopy, immediately after
epiglottis elevation, immediately after intubation and 3 minutes after
intubation. Data were compared and analyzed within and between groups.
Immediately after
intubation, the increase in blood pressure and heart rate were blunted
significantly in the groups 2 and 3 compared to the intravenous lidocaine
injection group (P < 0.01). However, there were no significant hemodynamic
changes between groups 2 and 3.this study concluded that;
The elevation of blood
pressure and heart rate after endotracheal intubation can be prevented by
intralaryngotracheal spray of 1 mg/kg of 10% lidocaine 3 minutes before
endotracheal intubation.
OBSERVATION
AND RESULT
Table 1. Age of the
participants in the two study groups
|
Age
in years |
Group 1 (2% intravenous lignocaine) |
Group 2 (10% lignocaine spray) |
P-value |
|
Mean (SD) |
64.4 (8.2) |
61.3 (8.8) |
0.12 |
Group
1 (2% intravenous lignocaine); Group 2 (10% lignocaine spray)
The
mean (SD) age of the participants was 64.4 (8.2) years in the group receiving
2% intravenous lignocaine (group 1). In the group receiving 10% lignocaine
spray, the mean (SD) age was 61.3 (8.8) years. The differences in mean age
across the two groups was not statistically significant (P=0.12). Figure 1
presents the diagrammatic representation of the distribution of mean age of the
study subjects according to the two groups.
Figure 1. Age of the participants
in the two study groups
Table 2. Sex distribution
of the participants in the two study groups
|
Sex of the participants |
Group 1 |
Group 2 |
P-value |
|
N (%) |
N (%) |
||
|
Male |
24 (80.0) |
23 (76.7) |
0.75 |
|
Female |
6 (20.0) |
7 (23.3) |
Group
1 (2% intravenous lignocaine); Group 2 (10% lignocaine spray)
In
the group receiving 2% intravenous lignocaine (group 1), the proportion of
subjects who were males was 80% whereas in the group receiving 10% lignocaine
spray, 76.7% were males. The proportion of study subjects according to their
sex among the two groups was not statistically significant (P=0.75). Figure 2
presents the sex distribution of the participants in the two groups.
Figure 2. Sex
distribution of the participants in the two study groups
Table 3. Weight
distribution of the participants in the two study groups
|
|
Group 1 |
Group 2 |
P-value |
|
Mean
weight (Kg) |
62.7 (9.0) |
59.6 (10.5) |
0.23 |
Group
1 (2% intravenous lignocaine); Group 2 (10% lignocaine spray)
The
mean (SD) weight participants was 62.7 (9.0) Kg in the group receiving 2%
intravenous lignocaine (group 1). In the group receiving 10% lignocaine spray,
the mean (SD) weight was 59.6 (10.5) Kg. The differences in mean weight across
the two groups was not statistically significant (P=0.23). Figure 3 presents
the diagrammatic representation of the distribution of mean weight of the study
subjects according to the two groups.
Figure 3. Mean weight of
the participants in the two study groups
Table 4. Diabetics or
Non-diabetics in the participants in the two study groups
|
Group 1 |
Group 2 |
|
|
N (%) |
N (%) |
|
|
Diabetics |
12 (40.0) |
14 (46.6) |
|
Non-diabetics |
18 (60.0) |
16 (53.3) |
Group
1 (2% intravenous lignocaine); Group 2 (10% lignocaine spray)
In
the group receiving 2% intravenous lignocaine (group 1), the proportion of
subjects who were diabetics were 40% whereas in the group receiving 10%
lignocaine spray (group 2), 46.6% were diabetics. Figure 4 presents the
distribution of the diabetics and non-diabetics in the participants in the two
groups.
Figure 4. Diabetics or
Non-diabetics in the participants in the two study groups
Table 5. Mean Left
ventricular ejection fraction (LVEF) of the participants in the two study
groups
|
|
Group 1 |
Group 2 |
P-value |
|
Mean (SD) LVEF (%) |
46.5 (4.7) |
47.3 (3.6) |
0.45 |
Group
1 (2% intravenous lignocaine); Group 2 (10% lignocaine spray)
The
mean (SD) left ventricular ejection fraction (%) of the participants was 46.5
(4.7) in the group receiving 2% intravenous lignocaine (group 1). In the group
receiving 10% lignocaine spray, the mean (SD) LVEF (%) was 47.3 (3.6). The
differences in mean LVEF across the two groups was not statistically
significant (P=0.45). Figure 5 presents the diagrammatic representation of the
distribution of mean LVEF of the study subjects according to the two groups.
Figure 5. Mean Left
ventricular ejection fraction (LVEF) of the participants in the two study
groups
Table 6. Distribution of
the participants in the two study groups by presence of arrythmia
|
Arrythmia |
Group 1 |
Group 2 |
P-value |
|
N (%) |
N (%) |
||
|
Present |
0 (0.0) |
4 (13.3) |
0.04* |
|
Absent |
30 (100.0) |
26 (86.7) |
Group
1 (2% intravenous lignocaine); Group 2 (10% lignocaine spray); *statistically
significant
In
the group receiving 2% intravenous lignocaine (group 1), none of the subjects
developed arrythmia whereas in the group receiving 10% lignocaine spray, 13.3%
developed arrythmia. The proportion of study subjects developing arrythmia
among the two groups was statistically significant (P=0.04). Figure 6 presents
the distribution of the participants in the two groups by presence and absence
of arrythmia.
Figure 6. Distribution of
the participants in the two study groups by presence of arrythmia
Table 7. Distribution of
the participants in the two study groups by presence of sore throat
|
Sore
throat |
Group 1 |
Group 2 |
P-value |
|
N (%) |
N (%) |
||
|
Present |
14 (46.7) |
7 (23.3) |
0.02* |
|
Absent |
16 (53.3) |
23 (76.7) |
Group
1 (2% intravenous lignocaine); Group 2 (10% lignocaine spray); * Statistically
significant
In
the group receiving 2% intravenous lignocaine (group 1), 46.7% of the subjects
developed sore throat whereas in the group receiving 10% lignocaine spray,
23.3% of the subject developed sore throat which is lower than that of group 1.
The proportion of study subjects developing sore throat among the two groups
was statistically significant (P=0.02). Figure 7 presents the distribution of
the participants in the two groups by presence and absence of sore throat.
Figure 7. Distribution of
the participants in the two study groups by presence of sore throat
Table 8. Pre-intubation
hemodynamic parameters in the study subjects in the two study groups
|
|
|
HR |
SBP |
DBP |
MAP |
CVP (mm Hg) |
|
|
|
Beats/minute |
MmHg |
MmHg |
mmHg |
|
|
Pre-intubation |
Group
1 |
85.3 (9.8) |
120.8 (14.1) |
78.1 (9.8) |
92.2 (9.9) |
5.9 (1.7) |
|
|
Group
2 |
86.9 (11.2) |
123.2 (10.8) |
78.8 (7.8) |
93.6 (8.1) |
6.3 (2.1) |
Group
1 (2% intravenous lignocaine); Group 2 (10% lignocaine spray)
Table
8. shows the pre-intubation hemodynamic parameters among the study participants
in the two groups. The parameters assessed were heart rate, systolic and
diastolic blood pressure, mean arterial pressure and central venous pressure.
The findings show that there were no statistically significant differences in
these hemodynamic parameters. Figure 8 shows the diagrammatic representation of
the pre-intubation hemodynamic parameters in the study subjects across the two
groups.
Figure 8. Pre-intubation
hemodynamic parameters in the study subjects in the two study groups
Table 9. Hemodynamic
parameters, immediately post intubation, in the study subjects in the two study
groups
Group
1 (2% intravenous lignocaine); Group 2 (10% lignocaine spray); * Statistically
significant
Table
9. shows the immediate post-intubation hemodynamic parameters among the study
participants in the two groups. The findings show that, except for central
venous pressure, there were statistically significant differences in all other
hemodynamic parameters. Mean heart rate, systolic blood pressure, diastolic
blood pressure and mean arterial pressure were higher in group 2 (10%
lignocaine spray), compared to group 1 (2% intravenous lignocaine). Figure 9 shows
the diagrammatic representation of the hemodynamic parameters in the study
subjects across the two groups, immediately post-intubation.
Figure 9. Hemodynamic
parameters, immediately post intubation, in the study subjects in the two study
groups
Table 10. Hemodynamic
parameters, 1-minute post intubation, in the study subjects in the two study
groups
|
|
|
HR |
SBP |
DBP |
MAP |
CVP (mm Hg) |
|
|
|
Beats/minute |
MmHg |
MmHg |
mmHg |
|
|
1
minute post-intubation |
Group 1 |
102.5 (12.6) * |
140.1 (17.5) * |
89.5 (14.4) * |
106.4 (14.7) * |
5.7 (1.6) |
|
|
Group 2 |
109.7 (15.3) * |
149.4 (17.3) * |
97.3 (12.2) * |
114.7 (12.8) * |
6.1 (1.4) |
Group
1 (2% intravenous lignocaine); Group 2 (10% lignocaine spray); * Statistically
significant
Table
10 shows the 1 minute post-intubation hemodynamic parameters among the study
participants in the two groups. The findings show that, except for central
venous pressure, there were statistically significant differences in all other
hemodynamic parameters. Mean heart rate, systolic blood pressure, diastolic
blood pressure and mean arterial pressure were higher in group 2 (10%
lignocaine spray), compared to group 1 (2% intravenous lignocaine). Figure 10
shows the diagrammatic representation of the hemodynamic parameters in the
study subjects across the two groups, 1-minute post-intubation.
Figure 10. Hemodynamic
parameters, 1-minute post intubation, in the study subjects in the two study
groups
Table 11. Hemodynamic parameters, 3 minutes post
intubation, in the study subjects in the two study groups
|
|
|
HR |
SBP |
DBP |
MAP |
CVP (mm Hg) |
|
|
|
Beats/minute |
MmHg |
MmHg |
mmHg |
|
|
3
minutes post-intubation |
Group
1 |
100.9 (13.6) |
129.7 (19.2) |
85.7 (13.3) |
100.8 (14.0) |
5.9 (2.0) |
|
|
Group
2 |
106.4 (15.5) |
136.4 (18.6) |
89.6 (10.6) |
105.8 (12.4) |
6.7 (1.5) |
Group
1 (2% intravenous lignocaine); Group 2 (10% lignocaine spray)
Table
11 shows the 3 minutes’ post-intubation hemodynamic parameters among the study
participants in the two groups. The findings show that there were no
statistically significant differences in these hemodynamic parameters. Figure
11 shows the diagrammatic representation of the 3 minutes post-intubation
hemodynamic parameters in the study subjects across the two groups.
Figure 11. Hemodynamic parameters, 3 minutes post
intubation, in the study subjects in the two study groups
Table 12. Hemodynamic parameters, 5 minutes post
intubation, in the study subjects in the two study groups
|
|
|
HR |
SBP |
DBP |
MAP |
CVP (mm Hg) |
|
|
|
Beats/minute |
MmHg |
MmHg |
mmHg |
|
|
5
minutes post-intubation |
Group
1 |
93.7 (13.2) |
126.3 (21.1) |
81.7 (14.8) |
96.7 (16.1) |
5.9 (1.2) |
|
|
Group
2 |
100.9 (14.9) |
133.0 (19.6) |
85.2 (11.7) |
101.1 (13.7) |
6.6 (1.6) |
Group
1 (2% intravenous lignocaine); Group 2 (10% lignocaine spray)
Table
12 shows the 5 minutes post-intubation hemodynamic parameters among the study
participants in the two groups. The findings show that there were no
statistically significant differences in these hemodynamic parameters. Figure
12 shows the diagrammatic representation of the 5 minutes’ post-intubation
hemodynamic parameters in the study subjects across the two groups.
Figure 12. Hemodynamic parameters, 5 minutes post
intubation, in the study subjects in the two study groups
Table 13. Hemodynamic parameters, 7 minutes post
intubation, in the study subjects in the two study groups
|
|
|
HR |
SBP |
DBP |
MAP |
CVP (mm Hg) |
|
|
|
Beats/minute |
MmHg |
MmHg |
mmHg |
|
|
7
minutes post-intubation |
Group
1 |
93.6 (11.8) |
126.3 (19.1) |
79.7 (11.9) |
95.2 (13.3) |
6.0 (1.4) |
|
|
Group
2 |
95.9 (14.8) |
129.6 (15.6) |
83.4 (12.0) |
98.9 (12.4) |
6.3 (1.5) |
Group
1 (2% intravenous lignocaine); Group 2 (10% lignocaine spray)
Table
13 shows the 7 minutes post-intubation hemodynamic parameters among the study
participants in the two groups. The findings show that there were no
statistically significant differences in these hemodynamic parameters. Figure
13 shows the diagrammatic representation of the 7 minutes post-intubation
hemodynamic parameters in the study subjects across the two groups.
Figure 13. Hemodynamic parameters, 7 minutes’ post
intubation, in the study subjects in the two study groups
Table 14. Hemodynamic parameters, 10 minutes post
intubation, in the study subjects in the two study groups
|
|
|
HR |
SBP |
DBP |
MAP |
CVP (mm Hg) |
|
|
|
Beats/minute |
MmHg |
MmHg |
mmHg |
|
|
10
minutes post-intubation |
Group
1 |
89.5 (10.1) |
127.3 (15.3) |
82.9 (12.6) |
97.7 (12.5) |
7.3 (1.6) |
|
|
Group
2 |
91.7 (15.9) |
127.5 (13.6) |
83.3 (10.2) |
98.0 (10.4) |
6.9 (1.3) |
Group
1 (2% intravenous lignocaine); Group 2 (10% lignocaine spray)
Table
14 shows the 10 minutes post-intubation hemodynamic parameters among the study
participants in the two groups. The findings show that there were no
statistically significant differences in these hemodynamic parameters. Figure
14 shows the diagrammatic representation of the 10 minutes post-intubation
hemodynamic parameters in the study subjects across the two groups.
Figure 14. Hemodynamic parameters, 10 minutes post
intubation, in the study subjects in the two study groups
Table 15. Hemodynamic parameters, 15 minutes post
intubation, in the study subjects in the two study groups
|
|
|
HR |
SBP |
DBP |
MAP |
CVP (mm Hg) |
|
|
|
Beats/minute |
MmHg |
MmHg |
mmHg |
|
|
15
minutes post-intubation |
Group
1 |
87.0 (7.7) |
123.2 (12.5) |
81.0 (11.4) |
95.5 (10.2) |
6.7 (1.4) |
|
|
Group
2 |
91.5 (10.4) |
127.9 (12.4) |
84.8 (11.0) |
99.2 (10.5) |
6.6 (1.7) |
Group
1 (2% intravenous lignocaine); Group 2 (10% lignocaine spray)
Table
15 shows the 15 minutes post-intubation hemodynamic parameters among the study
participants in the two groups. The findings show that there were no
statistically significant differences in these hemodynamic parameters. Figure
15 shows the diagrammatic representation of the 15 minutes post-intubation
hemodynamic parameters in the study subjects across the two groups.
Figure15. Hemodynamic parameters, 15 minutes post
intubation, in the study subjects in the two study groups
Table 16. Hemodynamic parameters, 20 minutes post
intubation, in the study subjects in the two study groups
|
|
|
HR |
SBP |
DBP |
MAP |
CVP (mm Hg) |
|
|
|
Beats/minute |
MmHg |
MmHg |
mmHg |
|
|
20
minutes post-intubation |
Group
1 |
87.3 (12.4) |
125.6 (10.9) |
82.4 (8.2) |
96.7 (7.5) |
6.2 (1.4) |
|
|
Group
2 |
88.3 (12.5) |
125.4 (10.5) |
82.7 (7.6) |
96.9 (7.9) |
6.6 (1.3) |
Group
1 (2% intravenous lignocaine); Group 2 (10% lignocaine spray)
Table
16 shows the 20 minutes’ post-intubation hemodynamic parameters among the study
participants in the two groups. The findings show that there were no
statistically significant differences in these hemodynamic parameters. Figure
16 shows the diagrammatic representation of the 20 minutes post-intubation
hemodynamic parameters in the study subjects across the two groups.
Figure 16. Hemodynamic parameters, 20 minutes post
intubation, in the study subjects in the two study groups
DISCUSSION
Rationale
for conducting the study
Laryngoscopy
and tracheal intubation are one of the commonest procedures done by
anaesthesiologists. Tracheal intubation following laryngoscopy is a potent
stimulus that increases heart rate and blood pressure. Various measures like
heavy premedication, high-dose narcotics, deep inhalational anesthesia and
potent vasoactive drugs have been used so as to mask these hemodynamic
responses of laryngoscopy and intubation. These measures have potential
cardiovascular side-effects and may also prolong recovery, hence are not
suitable for short procedures. Lignocaine is the most frequently used local
anesthetic. It is also routinely used for local, peripheral and epidural
anesthesia. Lignocaine has been evaluated in numerous trials as a spray or gel
to suppress response associated with laryngoscopy. It has also been used to
reduce the incidence of postoperative sore throat, cough, and hoarseness of
voice. More commonly, lignocaine inhalation has been utilized to reduce the
frequency of chronic cough in patients with asthma and chronic obstructive lung
disease (COPD). Similarly, lignocaine has been used intravenously to modulate
the physiological response following laryngoscopy and tracheal intubation.
Currently, there is limited literature on comparison between lignocaine spray
and intravenous lignocaine in alleviation of cardiovascular response following
tracheal intubation. Therefore, this study was conducted among patients with
ejection fraction <50% and undergoing CABG, to compare the efficacy of
lignocaine spray (10%) and intravenous (2%, 1.5mg/kg) route in attenuating the
sympathoadrenal response on hemodynamic parameters due to laryngoscopy and
endotracheal intubation. The study looked at hemodynamic response such as heart
rate, systolic and diastolic blood pressure, mean arterial pressure and central
venous pressure. Additionally, data on arrhythmias and post-operative sore
throat was also collected.
The administration of anesthesia in patients with cardiac disease,
especially those undergoing CABG, demands an absolutely steady haemodynamics
during induction of general endotracheal anesthesia [46]. Any hemodynamic
perturbation during this phase of presurgery medical management by the
anesthesiologist is very poorly tolerated. This requires a great deal of
experience, training, and understanding of individual cardiac lesions and their
response to various anesthetic drug regime and interventions [46]. Many of
these patients also have fixed cardiac output (CO) and their compensatory
mechanisms are not fully functional [46,47]. Therefore, any increase or
decrease in systemic vascular resistance (SVR) and heart rate, which occurs
during laryngoscopy and tracheal intubation due to sympathetic activation, can
adversely affect the hemodynamics [47]. The cardiopulmonary interactions
resulting from the underlying pathophysiology pose additional challenges for
safe airway management. Patients with poor cardiopulmonary reserve have the
potential to desaturate during induction [47]. This can be attributed to
insufficient apnea time in this subset of patients as opposed to normal healthy
individuals. Thus, it is important to ensure an adequate preoxygenation in
these patients before obtunding their respiratory efforts [47,48]. The current
guidelines for difficult airway (DA) management recognize this problem and
recommends the use of supplemental oxygenation (para-oxygenation) during airway
procedures [48]. While the anatomic DA is one in which obtaining a good
glottic view or passing an endotracheal tube (ETT) is challenging, the
physiologic DA is one where physiological derangements subject the patient to a
higher risk of cardiovascular collapse with intubation and positive pressure
ventilation (IPPV) [46-48]. These physiologic abnormalities should be taken
into consideration while planning for intubation even if no anatomic airway
difficulty is anticipated.
Congenital cardiac and valvular lesions with
increased pulmonary blood flow and consequent pulmonary arterial hypertension,
right ventricular dysfunction/failure leading to preexisting
ventilation-perfusion (V/Q) mismatch present physiologic hindrances to
ventilation [49]. It is not rare to encounter a combined anatomical and
physiological difficulty, and any mismanagement of the airway is poorly
tolerated and can even be fatal. The preexisting risk gets exaggerated when
intubation requires multiple attempts with difficult intubation being an
independent predictor of death [49,50]. Essentially, there are four physiologic
difficulties encountered in cardiac patients while securing airway before
mechanical ventilation. These are hypoxemia, severe acidosis, hypotension
and right ventricular failure [50].
Lignocaine stabilizes the neuronal membrane by inhibiting the
ionic fluxes required for the initiation and conduction of impulses, thereby
effecting local anesthetic action [51]. The onset of action is rapid. Lidocaine
may be absorbed following topical administration to mucous membranes, its rate
and extent of absorption depending upon concentration and total dose
administered, the specific site of application, and duration of exposure [51].
In general, the rate of absorption of local anesthetic agents following topical
application occurs most rapidly after intratracheal administration [51].
Lidocaine is also well-absorbed from the gastrointestinal tract, but little
intact drug appears in the circulation because of biotransformation in the
liver. Lidocaine is metabolized rapidly by the liver, and metabolites and
unchanged drug are excreted by the kidneys [51]. Approximately 90% of lidocaine
administered is excreted in the form of various metabolites, and less than 10%
is excreted unchanged. Studies have shown that peak blood levels of lidocaine
may occur as early as 5 and as late as 30 minutes after endotracheal
administration of a 4% lidocaine HCI solution [51]. Studies of lidocaine
metabolism following intravenous bolus injections have shown that the
elimination half-life of this agent is typically 1.5 to 2 hours [51]. The
half-life may be prolonged two-fold or more in patients with liver dysfunction.
Diabetes is associated with an increased risk of CVD, which is
exaggerated with coexistent hypertension [52]. Many of the underlying molecular
mechanisms, including oxidative stress, inflammation, and fibrosis causing
microvascular and macrovascular complications of diabetes, also cause vascular
remodelling and dysfunction in hypertension [52,53]. Moreover, patients
with hypertension often exhibit insulin resistance and are at greater risk of
diabetes developing than are normotensive individuals [52,53]. Diabetes and
hypertension are closely interlinked because of similar risk factors, such as
endothelial dysfunction, vascular inflammation, arterial remodelling,
atherosclerosis, dyslipidemia, and obesity, thereby, leading to cardiac
diseases [54, 55]. Reports from Framingham and from other studies have
established diabetes mellitus (DM) and hypertensions as a strong risk factor
for cardiovascular morbidity and mortality [52-54]. In addition, several
studies suggest that DM and hypertension have direct adverse effects on the
heart, independent of obstructive coronary artery disease. Specifically,
the Framingham Heart Study identified an association between DM/hypertension
and increased left ventricular (LV) wall thickness [52-54]. These
observations may be important in view of the strong relation between LV
hypertrophy and adverse cardiovascular outcomes.
Key
findings of the study
The
study did not find any baseline differences between the study groups in terms
of age, sex, weight , mean left ventricular ejection fraction and presence or
absence of diabetes. In the group receiving 2% intravenous lignocaine, none of
the subjects developed arrythmia whereas in the group receiving 10% lignocaine
spray, 13.3% developed arrythmia and this difference was statistically
significant (P=0.04), reason group 1(2% lignocaine) didn’t develop arrythmia
because these subjects received anti-arrythmic dose of 2% lignocaine i.e
1.5mg/kg. Subjects who developed arrythmia in group 2, among all 3 subject
developed atrial fibrillation and one developed ventricular tahycardia. Further, in the group receiving 2%
intravenous lignocaine, 46.7% of the subjects developed sore throat whereas in
the group receiving 10% lignocaine spray, a lower proportion i.e. 23.3%
developed sore throat (P=0.02), group 2 subjects experienced sore throat lesser
than group 1 due to the topical action of 10% lignocaine spray which was given
to group 2 subjects . The pre-intubation
hemodynamic parameters were similar across the two groups. However, immediately
upon intubation the heart rate (mean 103.7 vs.111.8), systolic blood pressure
(mean 140.8 vs.155.4 mm Hg), diastolic blood pressure (mean 91.9 vs. 103.7 mm
Hg) and mean arterial pressure (mean 108.1 vs. 120.9 mm Hg) were higher in the group receiving 10% lignocaine spray,
compared to the group that received 2% intravenous lignocaine. Similarly, at 1
minute after intubation, the heart rate
(mean 102.5 vs.109.7), systolic blood pressure (mean 140.1 vs.149.4 mm Hg),
diastolic blood pressure (mean 89.5 vs. 97.3 mm Hg) and mean arterial pressure
(mean 106.4 vs. 114.7 mm Hg) were higher in
the group receiving 10% lignocaine spray, compared to the group that
received 2% intravenous lignocaine. Thereafter, these differences remained
non-significant at 3 min, 7 min, 10 min, 15 min and 20 min post-intubation. 10
minutes post-intubation all vital parameters came to base line values in group
1 and 15 minutes post intubation all vital parameters came to its baseline
values in group 2.
These findings indicate that intravenous
lignocaine is more efficacious in preventing immediate sympathoadrenal response
to laryngoscopy and tracheal intubation than lignocaine spray and is associated
with comparatively lesser incidence of arrythmia but the incidence of
post-operative sore throat was lesser with lignocaine spray.
Comparison of the findings with previous studies
Jokar A et al (2018) conducted a study aimed to evaluate the effects
of lignocaine spray on hemodynamic response of endotracheal intubation
patients. This was a randomized clinical trial on a study population
comprising patients admitted to the ICU. The patients were divided into
three groups. In Group 1, inhaled nebulized lignocaine 4% (75.0 mg/kg) was
sprayed around the patients' epiglottis and larynx. In Group 2, intravenous
(IV) lignocaine 2% (75.0/mg/kg) was injected. No lignocaine was prescribed for or
administered to the control group. One and four minutes after intubation, the
patients' hemodynamic and vital signs were measured. Although the mean arterial
blood pressure (MAP) of Group 1 (inhaled nebulized lignocaine) was smaller than
that of Group 2 (IV lignocaine), there was no significant difference between
the two groups. In terms of the average number of pulses, a significant
difference was observed between the inhaled and IV lignocaine groups. The
average number of pulses in Group 1 (inhalation) was lower than that of Group 2
(IV injection). The study investigators concluded that inhaled nebulized
lignocaine can control the hemodynamic changes of intubation more effectively
than IV lignocaine. This is very much similar to the findings and observations
of the current study.
UI
Islam M et al (2014) conducted a randomized control trial
involving 60 patients scheduled for elective CABG. The study had two groups-
group A (IV morphine 0.1mg/kg & IV lignocaine 1.5mg/kg) and group B (IV
morphine 0.1mg/kg & lignocaine spray 1.5mg/kg). There were no baseline
differences in the study participant characteristics among the two groups. The
authors found that lignocaine spray was as efficacious as intravenous
lignocaine on attenuation of hemodynamic changes to laryngoscopy and
intubation. This is similar to the findings of our study where lignocaine spray
had similar efficacy, compared to intravenous lignocaine and moreover, led to
reduced incidence of arrythmia and post-operative sore throat.
Agrawal A et al (2016)
conducted a prospective randomized cross over study. Sixty patients requiring
tracheal suction through an endotracheal tube received 1.5 mg/kg of lignocaine
in the nebulized form or as an intravenous injection on two different
occasions. Heart rate (HR), mean arterial pressure (MAP), systolic and
diastolic blood pressure (SBP and DBP) and peripheral capillary oxygen
saturation (SPO2) were recorded at baseline, after the administration of
lignocaine, after two successive suctions and once in two minutes for the next
16 minutes. The study found that the changes in the SPO2 were not significant
when compared between the groups. Similarly, the changes in HR, SBP, DBP and
MAP were not significantly different between the two routes of lignocaine
administration. These findings are again similar to the
findings of our study where lignocaine spray had similar efficacy, compared to
intravenous lignocaine, in providing hemodynamic stability during and
post-intubation.
Jalali A et al (2017) performed a study to compare of
intravenous and oropharyngeal spray of lidocaine and high dose of fentanyl on
systolic and diastolic blood pressures and heart rate of patients over 65 years
during tracheal intubation. In this clinical trial, 160 patients were randomly
divided into five groups of 32 patients. For group one, lidocaine spray 10%;
group two, intravenous lidocaine 1.5 mg/kg; group three, lidocaine spray along
with intravenous lidocaine 0.75 mg/kg; and for group four fentanyl 5μg/kg were
administered and group five patients were controls which were given 1 mg of
midazolam along with 2 μg/kg fentanyl. Study results showed no significant
difference between groups in terms of systolic and diastolic blood pressures
and heart rate among groups. The authors concluded that all methods were effective for efficient blood pressure control during
laryngoscopy and tracheal intubation.
Kim SY et al (2002) conducted a study to evaluate the effects of
intralaryngotracheal 10% lidocaine spray on hemodynamic responses to
endotracheal intubation for patients with a cerebral aneurysm. Sixty patients with a cerebral
aneurysm were randomly divided into three groups by lidocaine administration
methods before endotracheal intubation: Group 1 (Control, 2% lidocaine 1.5 mg/kg,
intravenous injection); Group 2 (10% lidocaine 1 mg/kg, intralaryngotracheal
spray); Group 3 (10% lidocaine 1.5 mg/kg, intralaryngotracheal spray). Blood
pressure and heart rate were measured preinduction, before laryngoscopy,
immediately after epiglottis elevation, immediately after intubation and 3
minutes after intubation. Immediately after intubation, the increase in blood
pressure and heart rate were blunted significantly in the groups 2 and 3
compared to the intravenous lidocaine injection group (P < 0.01). The
authors concluded that the elevation of
blood pressure and heart rate after endotracheal intubation can be prevented by
intralaryngotracheal spray of 1 mg/kg of 10% lidocaine 3 minutes before
endotracheal intubation. But in my study that suggest intravenous lignocaine to
be more efficacious than lignocaine spray in attenuation of immediate
sympathoadrenal response of laryngoscopy and endotracheal intubation.
Limitations of the study
1.
The sample
size was limited to only 60 subjects and therefore, the study was not
adequately powered to detect small differences in the hemodynamic variables
that might have been present in the two groups
2.
The
findings of the study are applicable to patients undergoing CABG. We do not
fully understand the expected differences between lignocaine spray and
intravenous lignocaine in different sets of patients undergoing surgery for
other indications
3.
The study
did not test the effects of different doses of lignocaine, both in spray and
intravenous forms.
SUMMARY
Following ethical committee approval, a prospective,
randomized and comparative study was conducted to compare hemodynamic response
such as heart rate, systolic and diastolic blood pressure, mean arterial
pressure and central venous pressure during laryngoscopy and tracheal
intubation between patients receiving lignocaine spray (10%) and intravenous
(2%, 1.5mg/kg) lignocaine. Additional comparisons were done on incidence of
arrhythmias and post-operative sore throat. 60 patients of aged between 30-75
years, of either gender, with ejection fraction of <50% and undergoing CABG
under general anaesthesia were selected for the study. The patients were
randomly allocated into two groups:
GROUP 1: After standard induction, this group of
patients received intravenous 2% Lignocaine (preservative free) 3 minutes prior
to laryngoscopy.
GROUP 2: Patients vocal cords were sprayed with 10%
lignocaine spray as soon as the vocal cords were visualized by direct
laryngoscopy.
Automated recordings (Datascope) of heart rate (HR) and
systolic (SBP), diastolic (DBP), and mean (MBP) blood pressures were recorded
at 0 min, 1 min, 3 min, 7 min, 10 min, 15 min and 20 min from induction. The
standard monitors were used to eliminate variability in recording data.
The key study findings are as follows:
·
The study did not find any baseline
differences between the study groups in terms of age (P=0.12), sex (P=0.75),
weight (P=0.23) and mean left ventricular ejection fraction (P=0.45).
·
In the group receiving 2% intravenous
lignocaine, none of the subjects developed arrythmia whereas in the group
receiving 10% lignocaine spray, 13.3% developed arrythmia. These differences
were statistically significant (P=0.04).
·
In the group receiving 2% intravenous
lignocaine, 23.3% of the subjects developed sore throat whereas in the group
receiving 10% lignocaine spray, a higher proportion i.e. 46.7% developed sore
throat. The proportion of study subjects developing sore throat among the two
groups was statistically significant (P=0.02).
·
The pre-intubation hemodynamic parameters
were similar across the two groups.
·
However, immediately upon intubation the
heart rate (mean 103.7 vs.111.8), systolic blood pressure (mean 140.8 vs.155.4
mm Hg), diastolic blood pressure (mean 91.9 vs. 103.7 mm Hg) and mean arterial
pressure (mean 108.1 vs. 120.9 mm Hg) were higher in the group receiving 10% lignocaine spray,
compared to the group that received 2% intravenous lignocaine.
·
Similarly, at 1 minute after
intubation, the heart rate (mean 102.5
vs.109.7), systolic blood pressure (mean 140.1 vs.149.4 mm Hg), diastolic blood
pressure (mean 89.5 vs. 97.3 mm Hg) and mean arterial pressure (mean 106.4 vs.
114.7 mm Hg) were higher in the group
receiving 10% lignocaine spray, compared to the group that received 2%
intravenous lignocaine.
·
Thereafter, these differences remained
non-significant at 3 min, 7 min, 10 min, 15 min and 20 min post-intubation.
These
findings indicate that intravenous lignocaine is more efficacious in preventing
immediate sympathoadrenal response to laryngoscopy and endotracheal intubation
than lignocaine spray and is associated with comparatively lesser incidence of
arrythmia and post-operative sore throat.
CONCLUSION
Considering the increase in Heart rate, SBP, DBP
and MAP immediately upon intubation in those receiving lignocaine spray
compared to those receiving intravenous lignocaine spray, it seems that
intravenous lignocaine is actually more efficient and should be used to prevent
sympathoadrenal stimulation and hemodynamic changes caused during intubation.
Intravenous lignocaine seems to be an effective
and practical method that can be used for critical elderly patients with
reduced ejection fraction who are at a greater risk of hemodynamic
perturbations. This method is also efficient in preventing cardiac arrythmia
during intubation but shows more incidence of post-intubation sore throat.
REFERENCES
1. Russell
WJ, Morris RG, Frewin DB, et al. Changesin plasma catecholamine Concentration
during endotracheal intubation. Br J Anaesth 1981; 53: 837-9.
2. Derbyshire
DC, Chemielewski A, Fell D, et al. Plasma catecholamine responses to tracheal
intubation.Br J Anasth 1983; 55: 855-
3. Gibbs
JM. The effects of endotracheal intubation on cardiac rate and rhythm. N Z Med
J 1967; 66: 465.
4. Henderson
J. Airway management in the adult. In: Miller RD, editor. Miller's Anaesthesia.
7th ed. Philadelphia: Churchill Livingstone; 2010.p. 1573–1610.
5. Denlinger
JK, Ellison N, Ominsky AJ;Effects of intratracheal lidocaine on circulatory
responses to tracheal intubation.Anesthesiology. 1974 Oct;41(4):409-12.
6. Bidwai
AV, Bidwai VA, Rogers CR, Stanley TH;;Blood-pressure and pulse-rate responses
to endotracheal extubation with and without prior injection of lidocaine;
Anesthesiology. 1979 Aug;51(2):171-3
7. Tam
S, Chung F, Campbell M. Intravenous lidocaine: optimal time of injection before
tracheal intubation;Anesth Analg. 1987 Oct;66(10):1036-8.
8. F.E.
Amadasun. Study of effectiveness intravenous lignocaine in obtunding the
circulatory response to intubation; Niger J Clin Pract;june
2001:4(1);5-7.
9. Mostafa
SM1, Murthy BV, Barrett PJ, McHugh P;Comparison of the effects of topical
lignocaine spray applied before or after induction of anaesthesia on the
pressor response to direct laryngoscopy and intubation. Eur J Anaesthesiol.
1999 Jan;16(1):7-10.
10. Sklar
BZ1, Lurie S, Ezri T, Krichelli D, Savir I, Soroker D;Lidocaine inhalation
attenuates the circulatory response to laryngoscopy and endotracheal
intubation;J Clin Anesth. 1992 Sep-Oct;4(5):382-5
11. Tanaka Y, Nakayama T, Nishimori M, Tsujimura
Y, Kawaguchi M, Sato Y; Lidocaine for preventing postoperative sore throat;
Cochrane Database Syst Rev. 2015 Jul 14;(7):CD004081.
12. Ahmed
A, Abbasi S, Ghafoor HB, Ishaq M.; Postoperative sore throat after elective
surgical procedures; J Ayub Med Coll Abbottabad. 2007 Apr-Jun;19(2):12-4.
13. Lam
F, Lin YC, Tsai HC, Chen TL, Tam KW, Chen CY.; Effect of Intracuff Lidocaine on
Postoperative Sore Throat and the Emergence Phenomenon: A Systematic Review and
Meta-Analysis of Randomized Controlled Trials; PLoS One. 2015 Aug
19;10(8):e0136184. doi: 10.1371/journal.pone.0136184. eCollection 2015.
14. Herlevsen
P, Bredahl C, Hindsholm K, Kruhøffer PK.; Prophylactic laryngo-tracheal
aerosolized lidocaine against postoperative sore throat; Acta Anaesthesiol
Scand. 1992 Aug;36(6):505-7.
15. Hamaya
Y., Dohi S.; Differences in cardiovascular response to airway stimulation at
different sites and blockade of the responses by lidocaine; Anesthesiology.
2000 Jul;93(1):95-103.
16. Babita
Gupta, Santvana Kohli, Kamran Farooque, Gopal Jalwal, Deepak Gupta, Sumit
Sinha, Chandralekha; Topical airway anesthesia for awake fiberoptic intubation:
Comparison between airway nerve blocks and nebulized lignocaine by ultrasonic
nebulizer; Saudi J Anaesth. 2014 | Volume : 8 | Issue :
5 | Page : 15-19.
17. Chong
CF, Chen CC, Ma HP, Wu YC, Chen YC, Wang TL.; Comparison of lidocaine and
bronchodilator inhalation treatments for cough suppression in patients with
chronic obstructive pulmonary disease; Emerg Med J. 2005 Jun;22(6):429-32.
18. Zamora
Lozano J, Cruz Villaseñor JA, Rodríguez Reyes J, Sánchez Rodríguez JP, Briones
Corona G, Gallardo Alonso LA.; Comparison of topical, intravenous, and
intracuff lidocaine for reducing coughing after extubation during emergence
from general anesthesia; Rev Esp Anestesiol Reanim. 2007
Dec;54(10):596-601.
19. William,
Warnick. Gray’s Anatomy. 36th ed.
Edinburg: Churchill livingstone;1984.
20. Carin
A. Hagberg. Basic clinical science considerations. In : Benumof’s Airway
Management- Principle and Practice.
2nd ed. Philadelphia ; Mosby
21. Robert
K. Stoelting, Simon C. Hillier. Pharmacology and Physiology in Anesthetic
Practice. 4th ed. Philadelphia: Lippincott Williams & Wikkings; 2006.
22. Charles
B. Berde, Gary R. Strichartz. Local anaesthetics. In: Ronald D Miller, editors.
Miller’s Anesthesia. 7th ed. Philadelphia: Churchill Livingstone Elsevier;
2005. P.913 – 940
23. Collins
VJ. Local Anesthetics. In: Principles of Anesthesiology – General and Regional
Anesthesia. 3rd ed. Philadelphia: Lea and Febiger; 1993.
24. Reid
LC and Brace DE. Initiation of respiratory tract reflexes and its effects on
heart. Surgy. Gynae. Obstretrics. 1940; 70: 157.
25. King
BD, Harris IC Jr., Freifenstein FE, Elder JD and Dripps RD. Reflex circulating
responses to direct laryngoscopy and tracheal intubation performed during
general anaesthesia. Anesthesiology. 1951; 12: 556-566.
26. Ul
Islam M, Ahmad
I, Shah
AA, Islam
A;Attenuation
of haemodynamic response to laryngoscopy and oral endotracheal intubation in
coronary artery bypass surgery patients: intravenous morphine and lidocaine
versus intravenous morphine and lidocaine spray. J
Ayub Med Coll Abbottabad. 2014 Jul-Sep;26(3):275-8.
27. Abou-Madi
MN, Keszler
H, Yacoub
JM;Cardiovascular
reactions to laryngoscopy and tracheal intubation following small and large
intravenous doses of lidocaine. Can Anaesth Soc J. 1977
Jan;24(1):12-9.
28. Ritesh
Sharma et al ; Comparison of lignocaine and fentanyl for attenuation of
cardiovascular response during laryngoscopy and tracheal intubation in cardiac
surgery patients; International Journal of Biomedical Research 2018; 09(10):
342-345.
29. Gurulingappa,AleemMA,
AwatiMN, AdarshS. Attenuation of Cardiovascular Responses
to Direct Laryngoscopy and
Intubation-A Comparative Study Between iv
Bolus Fentanyl, Lignocaine and Placebo(NS). JClin Diagn Res.2012; 6:
1749-1752.
30. M
Jain, S Gurcoo, A Shora, M Qazi, B Dar, V Buchh, S Ahmad. Efficacy Of Topical
Lignocaine Spray (10%) Applied Before The Induction Of Anaesthesia In
Attenuating The Pressor Response To Direct Laryngoscopy And Endotracheal
Intubation In Controlled Hypertensive Patients. The Internet Journal of
Anesthesiology. 2008 Volume 20 Number 2
31. Rajbhandari
PK1;Lignocaine and Esmolol on Stress Response to Laryngoscopy and
Intubation;JNMA J Nepal Med Assoc. 2014 Apr-Jun;52(194):775-9.
32. Dr.
V. Madhuri Gopal;Comparative Study of Pressor Response to Laryngoscopy and
Intubation with Oral Spray of Nitroglycerine and Oropharyngeal Spray of
Lignocaine; Sch. J. App. Med. Sci., 2017; 5(4D):1463-1469.
33. Stoelting,
Robert K; Blood pressure and heart rate changes during short-duration
laryngoscopy for tracheal intubation: influence of viscous or intravenous
lidocaine. Anesth Analg 1978; 7:19734.
34. HAMILL
J. F.; BEDFORD, R. F.; WEAVER, D. C.; COLOHAN, A. R. (1981); Lidocaine before
endotracheal intubation: Intravenous or laryngotracheal? Anesthesiology 55,
578-581.
35. BENJAMIN
DRENGER AND JACOB Peter; Attenuation of ocular and systemic responses to
tracheal intubation by intravenous lignocaine; British Journal of
Ophthalmology, 1987, 71, 546-54838.
36. Laurito
CE1, Baughman
VL, Becker
GL, Polek
WV, Riegler
FX, VadeBoncouer
TR;
Effects of aerosolized and/or intravenous lidocaine on hemodynamic responses to
laryngoscopy and intubation in outpatients; Anesth Analg. 1988
Apr;67(4):389-92.
37. Bansal
S, Pawar M; Haemodynamic responses to laryngoscopy and intubation in patients
with pregnancy-induced hypertension: effect of intravenous esmolol with or
without lidocaine; Int J Obstet Anesth. 2002 Jan;11(1):4-8.
38. Saeed
Abbasi, Hosein Mahjobipoor, Parviz Kashefi, Gholamreza Massumi, Omid
Aghadavoudi, Ziba Farajzadegan, and Parvin Sajedi; The effect of lidocaine on
reducing the tracheal mucosal damage following tracheal intubation; J Res Med
Sci. 2013 Sep; 18(9): 733–738.
39. Dr
Rupal B. Shah, Dr Gargi M. Bhavsar, Dr Happy R. Ghetia, Dr Manisha V. Thakkar,
Dr Sumegh N. Prajapati; Comparison of Fentanyl and Lignocaine for Attenuation
of Cardiovascular Stress Response to Laryngoscopy and Endotracheal Intubation;
Internal journal of scientific research (IJSR) Volume: 3| Issue: 1| January
2014.
40. M
A Kaleem Siddiqui and Kiran N; Analytical study of effects of intravenous
lignocaine on pressor response during laryngoscopy and intubation;
International Journal of Biomedical Research 2015; 6(02): 104-10747.
41. Akhilesh
Agrawal, Smita S. Lele, Bharati A. Tendolkar; A comparative study of nebulized
versus intravenous lignocaine to suppress the haemodynamic response to
endotracheal suction in patients on mechanical ventilation; Int J Res Med
Science 2016 Aug; 4(8):3224-3228.
42. Dr
Suma R, Dr Linette J Morris, Dr Ceena Panicker; Attenuation of Pressor Response
during Laryngoscopy and Tracheal Intubation by Placebo, Lignocaine and Esmolol
– A Comparative Clinical Study; jmscr | 156 volume | 06-issue |
11-november-2018.
43. Jokar
A, Babaei M, Pourmatin S, Taheri M, Almasi-Hashiani A, Yazdanbakhsh A; Effects
of Intravenous and Inhaled Nebulized Lignocaine on the Hemodynamic Response of
Endotracheal Intubation Patients: A Randomized Clinical Trial..Anesth Essays
Res. 2018 Jan-Mar;12(1):159-164. doi: 10.4103/aer.AER_75_17.
44. Jalali
A, Nasiri E, Khoramian M, Saghafinia M, Siamian H.Hemodynamic Responses to
Tracheal Intubation in Elderly Patients: Intravenous or Spray of Lidocaine
versus Fentanyl;Med Arch. 2017 Dec;71(6):424-429. doi:
10.5455/medarh.2017.71.424-429.
45. Sae
Yeon Kim, Yong Hwan Lee; Effect of Intralaryngotracheal 10% Lidocaine Spray on
Blood Pressure and Heart Rate Changes during Endotracheal Intubation for
Patients with a Cerebral Aneurysm;Korean Journal of Anesthesiology
2002;42(3):298-305.
46. Perbet
S, De Jong A, Delmas J, Futier E, Pereira B, Jaber S, et
al. Incidence of and risk factors for severe cardiovascular collapse after
endotracheal intubation in the ICU: A multicenter observational study. Crit
Care 2015;19:257
47. Heffner
AC, Swords DS, Neale MN, Jones AE. Incidence and factors associated with
cardiac arrest complicating emergency airway management. Resuscitation
2013;84:1500-4.
48. American
Society of Anesthesiologists Task Force on Management of the Difficult Airway.
Practice guidelines for management of the difficult airway: An updated report
by the American Society of Anesthesiologists Task Force on Management of the
Difficult Airway. Anesthesiology 2003;98:1269-77
49. Cook
TM, Woodall N, Frerk C. Royal College of Anaesthetists. 4 th National
Audit Project: Major Complications of Airway Management in the UK. London:
Royal College of Anaesthetists; 2011. p. 62-70.
50. Heinrich
S, Ackermann A, Prottengeier J, Castellanos I, Schmidt J, Schüttler J.
Increased rate of poor laryngoscopic views in patients scheduled for cardiac
surgery versus patients scheduled for general surgery: A propensity score-based
analysis of 21,561 cases. J Cardiothorac Vasc Anesth 2015;29:1537-43
51. Weinberg
L, Peake B, Tan C, Nikfarjam M. Pharmacokinetics and pharmacodynamics of
lignocaine: A review. World J Anesthesiol 2015;4(2):17-29
52. Galderisi
M, Anderson KM, Wilson PWF, et al. Echocardiographic evidence for the existence
of a distinct diabetic cardiomyopathy: the Framingham Heart Study. Am J
Cardiol.1991; 68:85–89.
53. Kleinman
JC, Donahue RP, Harris MI, et al. Mortality among diabetics in a national
sample. Am J Epidemiol.1988; 128:389–40
54. Haffner
S.M., Lehto S., Ronnemaa T., Pyorala K., Laakso M. Mortality from coronary
heart disease in subjects with type 2 diabetes and in nondiabetic subjects with
and without prior myocardial infarction. N Engl J
Med. 1998;339:229–234
55. Su
Y., Liu X.M., Sun Y.M. Endothelial dysfunction in impaired fasting glycemia,
impaired glucose tolerance, and type 2 diabetes mellitus. Am J
Cardiol. 2008;102:497–498
PROFORMA
Name
of the participant:
Age:
Gender:
Date
of surgery:
Diagnosis:
Name
of Surgery:
Airway
Examination:
MPC:
TM
Distance:
Neck
Movement:
ASA Grade:
Randomization
into: ‘GROUP A’ or ‘GROUP B’
Parameters
recorded:
|
Variables |
Pre induction |
0 min |
1 min |
3 Mins |
5 mins |
7 mins |
10 mins |
15 mins |
20 mins |
|
Heart
rate |
|
|
|
|
|
|
|
|
|
|
Systolic
BP |
|
|
|
|
|
|
|
|
|
|
Diastolic
BP |
|
|
|
|
|
|
|
|
|
|
Mean
arterial pressure |
|
|
|
|
|
|
|
|
|
|
CVP |
|
|
|
|
|
|
|
|
|
|
ECG for arrhythmias |
|
|
|
|
|
|
|
|
|
Sore throat: Present / Absent
PATIENT
CONSENT FORM
“EFFECTS OF INTRAVENOUS LIGNOCAINE 2%
AND LIGNOCAINE SPRAY 10% FOR INTUBATION RESPONSE IN PATIENTS WITH EJECTION
FRACTION <50%-
COMPARATIVE
STUDY.”
Name of the Institution: Dr DY Patil
University, School Of Medicine, Nerul, New Mumbai
I have read the information in this
form (or it has been read to me). I was
free to ask any questions and they have
been answered. I am over 18 years of age and, exercising my free power of
choice, hereby give my consent to include me as a participant in “EFFECTS OF INTRAVENOUS LIGNOCAINE 2% AND
LIGNOCAINE SPRAY 10% FOR INTUBATION RESPONSE IN PATIENTS WITH EJECTION FRACTION
<50%- COMPARATIVE STUDY.”
I have read and understood this consent
form and the information provided to me.
(1) I
have had the consent document explained to me.
(2) I
have been explained about the nature of the
study.
(3) My
rights and responsibilities have been explained to me by the investigator.
(4) I
agree not to restrict the use of any data or results that arise from this study
provided such a use is only for scientific purpose.
(5)
I agree to cooperate with the investigator
and I will inform him immediately if I or my patient suffers unusual symptoms.
(6)
I am aware of the fact that I myself/ my
patient can opt out of the study at any time without having to give any reason
and this will not affect me or my patient’s
future treatment in the hospital.
(7)
I am also aware that the investigators may
terminate my patients or my participation
in the study at any time, for any reason, without my consent.
(8)
I hereby give permission to the
investigators to release the information obtained from me as result of
participation in this study to the ethics committee. I understand that they may
inspect my original records.
(9) My
identity will be kept confidential if my data are publicly presented.
(10) I
have had my questions answered to my satisfaction.
(11) I
have decided to include myself or my patient in the research study.
I
am aware, that if I have any questions during this study, I should contact at
one of the addresses listed above. By signing this consent from, I attest that
the information given in this document. I will be given a copy of this consent
document.
Participant’s
initials:
Name and signature / thumb impression
of the participant (or legal representative if participant incompetent):
(Name)
(Signature)
Date:
Time:
Name and signature of impartial
witness (required for illiterate patients):
(Name)
(Signature)
Date:
Time:
Address
and contact number of the impartial witness:
Name and signature of the
Investigator or his representative obtaining consent:
(Name)
(Signature)
Date: Time: ________
पेटंट
कॉन्सेन्ट फॉर्म
“उद्घाटनाच्या भागासह पेटंट्स मधील
प्रवेशाच्या प्रतिसादासाठी इंट्रावेनस लिग्नोकाइन 2% आणि लिग्नोकाइन
स्प्रे 10% - एकत्र अभ्यास. ”
सहभागीचे नावः प्रधान अन्वेषकांचे नाव: पूनम गुप्ता
संस्थेचे नाव: डॉ डी वाय
पाटील विद्यापीठ, स्कूल ऑफ मेडिसिन, नेरूळ,
नवी मुंबई
मी या फॉर्ममधील माहिती वाचली आहे (किंवा ती मला वाचली गेली आहे). मी होतो
कोणतेही प्रश्न विचारण्यास मोकळे आणि त्यांना उत्तर
दिले गेले. माझे वय १ 18 वर्षांहून
अधिक आहे आणि मी माझ्या निवडीच्या विनामूल्य शक्तीचा उपयोग करीत आहे, याद्वारे मला यात सहभागी होण्यासाठी मला संमती देईल
"इंटरेव्हनस लिग्नोकाइनचे परिणाम
2% आणि एज्युकेशन रेस्पॉन्स इन एज्युकेशन रेस्पॉन्स इन एज्युकेशन फ्रॅक्शन
<50% - एकत्रित अभ्यासासह 10% लिग्नोकाइन स्प्रे."
हा संमती फॉर्म आणि मला प्रदान केलेली माहिती मी
वाचली आणि समजली आहे.
(१) मला संमती
दस्तऐवज मला समजावून सांगितले.
(२) मला अभ्यासाचे
स्वरूप कसे आहे याबद्दल स्पष्ट केले आहे.
()) माझे अधिकार व जबाबदार्या मला अन्वेषकांद्वारे स्पष्ट केल्या आहेत.
()) या अभ्यासामुळे उद्भवलेल्या कोणत्याही
डेटाचा किंवा परिणामाचा वापर मर्यादित न ठेवण्यासाठी मी सहमत आहे परंतु अशा प्रकारच्या
वापराचा उपयोग केवळ वैज्ञानिक हेतूसाठी केला जाईल.
()) मी अन्वेषकांना सहकार्य करण्यास
सहमती देतो आणि मला किंवा माझ्या रूग्णात असामान्य लक्षणे आढळल्यास मी त्याला ताबडतोब
सूचित करीन.
()) मला हे माहित आहे की मी
/ माझे रुग्ण कोणत्याही कारणाशिवाय कोणतेही कारण न सांगता अभ्यासाची
निवड करू शकतो आणि याचा मला किंवा माझ्या रूग्णालयाच्या भविष्यातील उपचारांवर परिणाम
होणार नाही.
()) मला हे देखील माहित आहे की तपासकर्ता
माझ्या रूग्णांना किंवा माझ्या अभ्यासामध्ये माझा सहभाग कोणत्याही कारणास्तव,
कोणत्याही संमतीने माझ्या संमतीविना समाप्त करू शकतात.
()) या अभ्यासात भाग घेतल्यामुळे माझ्याकडून
मिळालेली माहिती नीतिशास्त्र समितीला सोडण्यासाठी मी याद्वारे तपास यंत्रणांना परवानगी
देतो. मला समजले आहे की ते माझ्या मूळ नोंदींची तपासणी करू शकतात.
()) माझा डेटा सार्वजनिकपणे सादर केल्यास
माझी ओळख गोपनीय ठेवली जाईल.
(१०) माझ्या
प्रश्नांची उत्तरे मी समाधानाला दिली आहेत.
(११) मी स्वत:
ला किंवा माझ्या रुग्णाला संशोधन अभ्यासामध्ये समाविष्ट करण्याचा निर्णय
घेतला आहे.
मला माहिती आहे की या अभ्यासादरम्यान मला काही प्रश्न
असल्यास,
मी वर सूचीबद्ध केलेल्या एका पत्त्यावर संपर्क साधावा. कडून या संमतीवर स्वाक्षरी करून, मी या दस्तऐवजात दिलेल्या
माहितीची खातरजमा करतो. मला या संमती दस्तऐवजाची एक प्रत दिली
जाईल.
सहभागीचे आद्याक्षरे:
सहभागीचे नाव आणि स्वाक्षरी / अंगठा ठसा (किंवा सहभागी असमर्थ असल्यास कायदेशीर प्रतिनिधी):
_______________ (नाव)
____________ (स्वाक्षरी)
तारीख वेळ: __________________
नाव आणि निःपक्ष साक्षीची सही (निरक्षर रुग्णांसाठी आवश्यक):
______________ (नाव)
________________ (स्वाक्षरी)
तारीख वेळ: ___________
निष्पक्ष साक्षीचा पत्ता आणि संपर्क क्रमांकः
अन्वेषक किंवा त्याच्या प्रतिनिधीची संमती प्राप्त
करणारे यांचे नाव आणि स्वाक्षरी:
___________ (नाव)
________________(स्वाक्षरी)
तारीख: _________ वेळ:
________
रोगी सहमति फार्म
"इंटर्नव्यूस लोनकॉइन के प्रभाव
2% और लेजोनकाइन स्पैनी 10% के साथ संयोजन के परिणामों
में संचरित फलन के लिए <50% - तुलनात्मक अध्ययन।"
प्रतिभागी का नाम: प्रधान
अन्वेषक का नाम: डॉ। पोनम गुप्ता
संस्था का नाम: डॉ डी वाई
पाटिल विश्वविद्यालय, स्कूल ऑफ मेडिसिन, नेरुल, नई मुंबई
मैंने जानकारी को इस रूप में पढ़ा है (या यह मुझे पढ़ा गया है)। मैं था
किसी भी सवाल पूछने के लिए स्वतंत्र हैं और वे जवाब
दिया गया है। मेरी आयु 18 वर्ष से अधिक है, और अपनी पसंद की मुफ्त शक्ति का प्रयोग करते हुए, इसमें
मुझे एक प्रतिभागी के रूप में शामिल करने के लिए अपनी सहमति देते हैं
"इंट्रावेनस लूसोकेन का प्रभाव
2% और लेजोनकाइन स्पैनी 10% है, जो इजेक्शन फ्रैक्शन के साथ मरीजों में इंट्यूशन रिस्पॉन्स के लिए है
<50% - कॉम्पिटिटिव स्टडी।"
मैंने इस सहमति फॉर्म को और मुझे प्रदान की गई जानकारी
को पढ़ और समझ लिया है।
(१) मेरे पास
सहमति पत्र मुझे समझाया गया है।
(२) मुझे अध्ययन
की प्रकृति के बारे में समझाया गया है।
(३) अन्वेषक
द्वारा मुझे मेरे अधिकारों और जिम्मेदारियों को समझाया गया है।
(4) मैं इस अध्ययन से उत्पन्न किसी
भी डेटा या परिणामों के उपयोग को प्रतिबंधित नहीं करने के लिए सहमत हूं, बशर्ते ऐसा उपयोग केवल वैज्ञानिक उद्देश्य के लिए हो।
(५) मैं अन्वेषक
के साथ सहयोग करने के लिए सहमत हूं और यदि मैं या मेरा मरीज असामान्य लक्षणों से पीड़ित
है तो मैं उसे तुरंत सूचित करूंगा।
(६) मुझे इस
तथ्य की जानकारी है कि मैं स्वयं / मेरा रोगी बिना किसी कारण
के किसी भी समय अध्ययन से बाहर हो सकता है और इससे अस्पताल में मेरे या मेरे रोगी के
भविष्य के उपचार पर कोई प्रभाव नहीं पड़ेगा।
(() मुझे यह भी पता है कि जांचकर्ता
मेरी सहमति के बिना, किसी भी समय, किसी
भी समय, मेरे रोगियों या अध्ययन में मेरी भागीदारी को समाप्त
कर सकते हैं।
(() मैं जाँचकर्ताओं को इस अध्ययन
में भागीदारी के परिणामस्वरूप प्राप्त जानकारी को नैतिकता समिति को जारी करने की अनुमति
देता हूँ। मैं समझता हूं कि वे मेरे मूल अभिलेखों का निरीक्षण कर सकते हैं।
(9) यदि मेरा डेटा सार्वजनिक रूप से
प्रस्तुत किया जाता है तो मेरी पहचान गोपनीय रखी जाएगी।
(१०) मेरी संतुष्टि
के लिए मेरे सवालों का जवाब दिया है।
(११) मैंने शोध
अध्ययन में खुद को या अपने मरीज को शामिल करने का फैसला किया है।
मुझे पता है, कि यदि इस अध्ययन
के दौरान मेरे कोई प्रश्न हैं, तो मुझे ऊपर सूचीबद्ध एक पते पर
संपर्क करना चाहिए। से इस सहमति पर हस्ताक्षर करके, मैं इस दस्तावेज़
में दी गई जानकारी की पुष्टि करता हूं। मुझे इस सहमति दस्तावेज की एक प्रति दी जाएगी।
प्रतिभागी के शुरुआती:
प्रतिभागी का नाम और हस्ताक्षर / अंगूठे का निशान (या कानूनी प्रतिनिधि यदि भागीदार अक्षम
हो):
______ (नाम) ______(हस्ताक्षर)
दिनांक: ________________ समय: __________________
निष्पक्ष गवाह का नाम और हस्ताक्षर (अनपढ़ रोगियों के लिए आवश्यक):
_____________ (नाम)
____________(हस्ताक्षर)
दिनांक समय: ___________
निष्पक्ष गवाह का पता और संपर्क नंबर:
अन्वेषक या उसके प्रतिनिधि का नाम और हस्ताक्षर सहमति
प्राप्त करना:
_______________ (नाम)
___________ (हस्ताक्षर)
दिनांक: __________________________ समय: ________
PATIENT INFORMATION SHEET
“EFFECTS OF INTRAVENOUS LIGNOCAINE 2% AND LIGNOCAINE SPRAY
10% FOR INTUBATION RESPONSE IN PATIENTS WITH EJECTION FRACTION <50%- COMPARATIVE STUDY.”
Name of Participant:
You are invited to take part in this research
study. The information in this document is meant to help you decide whether or
not to take part in this study. Please feel free to ask if you have any queries
or concerns.
You
are being asked to participate in this study being conducted in D.Y. Patil
Hospital because you satisfy the eligibility criteria to participate in this
study. You will be one of the subjects we plan to recruit in this study.
What
is the purpose of research?
You have been posted for surgery which needs
administration of general anaesthesia. General anaesthesia involves
laryngoscopy (looking into ones oral cavity and upper respiratory tract using
an instrument called laryngoscope) and endotracheal intubation (insertion of a
tube into trachea for assisted ventilation during anaesthesia). This procedures
at times induces increased heart rate, increase in blood pressure as a reflex
reaction. We will be using lignocaine (either spray or intravenous route) to
suppress the above side effects of laryngoscopy and endotracheal intubation.
The purpose of the study
is to assess the effects of lignocaine spray on hemodynamic parameters due to
laryngoscopy and endotracheal intubation and to compare with that of
intravenous lignocaine in patients with ejection fraction <50%.
Study Procedures
All the patients with EF <50% posted for elective
surgery under general anaesthesia will be given eithe lignocaine spray or
intravenous lignocaine before laryngoscopy and endotracheal intubation. The
efficacy of this drug in reducing the vasopressive effects of laryngoscopy and
endotracheal intubation is to be evaluated by this study.
Possible
risks to you
There
is no risk involved in this study.
Possible
benefits to you
Clinical trials in healthy adults undergoing surgery
under general anaesthesia have proved
that prior use of lignocaine has reduced the vasopressor effects of
laryngoscopy and endotracheal intubation has improved the safety and overall outcome
Possible
benefits to other people
The results of the research may provide benefits to
the society in terms of advancement of medical knowledge and/or therapeutic
benefit to future patients.
Cost
to the participant
The tests will be performed free of cost to you. The
tests will be performed at Dr. DY Patil Hospital.
Confidentiality
of the information obtained from you
You have the right to confidentiality regarding the
privacy of your medical information (personal details, results of physical
examinations, investigations, and your medical history). By signing this
document, you will be allowing the treating physician, other study personnel,
hospital ethics committee to view your data, if required. The results of
clinical tests and therapy performed as part of this research may be included
in your medical record. The information from this study, if published in
scientific journals or presented at scientific meetings, will not reveal your identity.
How will your decision to not
participate in the study affect you?
Your decision not to participate in this research
study will not affect your medical care or your relationship with the treating
physician or the institution. Your doctor will still take care of you and you
will not lose any benefits to which you are entitled.
Right
to new information
If the research team gets any new information during
this research study that may affect your decision to continue participating in
the study, or may raise some doubts, you will be told about that information.
Contact
persons
In
case of conflicts, you can contact the chairperson (convener) of our hospital
ethics Committee at the following address:
Dr.
Chairperson,
Institutional Ethics Committee,
D
Y Patil University and School of Medicine, Nerul, Navi Mumbai.
रुग्ण
माहिती पत्रक
“उद्घाटनाच्या भागासह पेटंट्स मधील
प्रवेशाच्या प्रतिसादासाठी इंट्रावेनस लिग्नोकाइन 2% आणि लिग्नोकाइन
स्प्रे 10% -
एकत्र अभ्यास. ”
सहभागीचे नाव:
आपल्याला या संशोधन अभ्यासामध्ये भाग घेण्यासाठी
आमंत्रित केले आहे. या अभ्यासात भाग घ्यावा की नाही
हे ठरविण्यास मदत करण्यासाठी या दस्तऐवजात माहिती आहे. कृपया
आपल्याकडे काही शंका किंवा शंका असल्यास विचारू मोकळ्या मनाने.
आपल्याला डीवाय मध्ये घेत असलेल्या या अभ्यासामध्ये
भाग घेण्यासाठी सांगितले जाते. पाटील रुग्णालय कारण आपण या
अभ्यासात भाग घेण्यासाठी पात्रता निकष पूर्ण करता. आम्ही या अभ्यासात
भरती करण्याची आमची योजना असलेल्या विषयांपैकी एक असेल.
संशोधनाचा हेतू काय आहे?
आपल्याला शस्त्रक्रियेसाठी पोस्ट केले गेले आहे ज्यास
सामान्य भूल देण्यास आवश्यक आहे. सामान्य भूल मध्ये लॅरिन्गोस्कोपी
(तोंडी पोकळी आणि लॅरीन्गोस्कोप नावाच्या उपकरणाचा वापर करून वरच्या
श्वसनमार्गाकडे लक्ष देणे) आणि एंडोट्राशियल इनट्यूबेशन
(एनेस्थेसिया दरम्यान सहाय्यक वेंटिलेशनसाठी श्वासनलिकेत एक ट्यूब समाविष्ट
करणे) समाविष्ट असते. या प्रक्रियेमुळे
कधीकधी हृदय गती वाढते, रक्तदाब वाढीस प्रतिक्षेप प्रतिक्रिया
म्हणून प्रवृत्त करते. लॅरिन्गोस्कोपी आणि एंडोट्रासीअल इनट्यूबेशनचे
वरील साइड इफेक्ट्स दाबण्यासाठी आम्ही लिग्नोकेन (एकतर स्प्रे
किंवा इंट्राव्हेनस मार्ग) वापरणार आहोत.
अभ्यासाचा उद्देश म्हणजे लॅरिन्कोस्कोपी आणि एंडोट्रासीयल
इनट्यूबेशनमुळे हेमोडायनामिक पॅरामीटर्सवरील लिग्नोकेन स्प्रेच्या प्रभावांचे मूल्यांकन
करणे आणि इजेक्शन फ्रॅक्शन <50% असलेल्या रूग्णांमध्ये इंट्रावेन्स
लिग्नोकेनच्या तुलनेत तुलना करणे.
अभ्यास प्रक्रिया
सर्वसाधारण भूल अंतर्गत निवडक शस्त्रक्रियेसाठी पोस्ट
केलेले ईएफ <%०% असलेल्या सर्व रूग्णांना
लॅरींगोस्कोपी आणि एंडोट्रॅशियल इनट्यूबेशनच्या आधी लिथोकेन स्प्रे किंवा इंट्राव्हेनस
लिग्नोकेन दिले जाईल. लॅरीन्गोस्कोपी आणि एंडोट्रॅसियल इनट्यूबेशनचे
वासोप्रिव्ह प्रभाव कमी करण्यासाठी या औषधाची कार्यक्षमता या अभ्यासाद्वारे मूल्यांकन
केली जावी.
आपल्यासाठी संभाव्य जोखीम
या अभ्यासामध्ये कोणताही धोका नाही.
आपल्याला संभाव्य फायदे
सामान्य भूल देऊन शस्त्रक्रिया करत असलेल्या निरोगी
प्रौढांमधील क्लिनिकल चाचण्यांमुळे हे सिद्ध झाले आहे की लिग्नोकेनच्या पूर्वीच्या
वापरामुळे लॅरिन्गोस्कोपीचे व्हॅसोप्रेसर प्रभाव कमी झाला आहे आणि एंडोट्रॅसियल इनट्यूबेशनमुळे
सुरक्षा आणि एकूणच परिणाम सुधारला आहे.
इतर लोकांना संभाव्य फायदे
संशोधनाच्या परिणामामुळे भविष्यातील रूग्णांना वैद्यकीय
ज्ञानाची प्रगती आणि / किंवा उपचारात्मक फायद्याच्या दृष्टीने
समाजात फायदा होऊ शकेल.
सहभागीची किंमत
या चाचण्या तुम्हाला विनामूल्य दिल्या जातील. डॉ. डी वाय पाटील रुग्णालयात या चाचण्या घेण्यात येतील.
आपल्याकडून प्राप्त माहितीची गोपनीयता
आपल्याला आपल्या वैद्यकीय माहितीच्या गोपनीयतेसंदर्भात
गोपनीयतेचा हक्क आहे (वैयक्तिक तपशील, शारीरिक तपासणीचा निकाल, तपासणी आणि आपला वैद्यकीय इतिहास).
या दस्तऐवजावर स्वाक्षरी करून, आवश्यक असल्यास
आपण उपचार करणार्या डॉक्टर, इतर अभ्यास
कर्मचारी, रुग्णालयातील नीतिशास्त्र समितीला आपला डेटा पाहण्याची
परवानगी देत आहात. या संशोधनाचा एक भाग म्हणून केल्या गेलेल्या क्लिनिकल चाचण्या आणि थेरपीचे
परिणाम आपल्या वैद्यकीय नोंदीमध्ये समाविष्ट केले जाऊ शकतात. या अभ्यासाची माहिती, जर वैज्ञानिक नियतकालिकांमध्ये
प्रकाशित झाली असेल किंवा वैज्ञानिक बैठकींमध्ये सादर केली गेली असेल तर ती आपली ओळख
उघड करणार नाही.
अभ्यासात भाग न घेण्याच्या तुमच्या निर्णयाचा तुमच्यावर
कसा परिणाम होईल?
या संशोधन अभ्यासामध्ये भाग न घेण्याच्या आपल्या
निर्णयाचा आपल्या वैद्यकीय सेवेवर किंवा उपचार करणार्या डॉक्टरांशी किंवा संस्थेशी असलेला संबंध प्रभावित होणार नाही. तुमचा डॉक्टर अद्याप तुमची काळजी घेईल आणि तुम्हाला हक्क असणारे कोणतेही फायदे
गमावणार नाहीत.
नवीन माहितीचा अधिकार
या अभ्यासाच्या अभ्यासानुसार जर संशोधन कार्यसंघाला
कोणतीही नवीन माहिती मिळाली ज्यामुळे या अभ्यासामध्ये भाग घेण्याच्या आपल्या निर्णयावर
परिणाम होऊ शकेल किंवा काही शंका निर्माण होऊ शकतात तर त्या माहितीबद्दल आपल्याला सांगितले
जाईल.
संपर्क व्यक्ती
मतभेद झाल्यास आपण आमच्या रुग्णालयाच्या नीतिशास्त्र
समितीचे अध्यक्ष (संयोजक) यांच्याशी
पुढील पत्त्यावर संपर्क साधू शकता:
ज्ञानेश बेलेकर डॉ
अध्यक्ष, संस्थात्मक नीतिशास्त्र
समिती,
डी वाय पाटील विद्यापीठ व स्कूल ऑफ मेडिसीन, नेरूळ, नवी मुंबई.
पेटेंट की सूचना पत्र
"इंटर्नव्यूस लोनकॉइन के प्रभाव
2% और लेजोनकाइन स्पैनी 10% के साथ संयोजन के परिणामों
में संचरित फलन के लिए <50% - तुलनात्मक अध्ययन।"
प्रतिभागी का नाम:
आपको इस शोध अध्ययन में भाग लेने के लिए आमंत्रित
किया गया है। इस दस्तावेज़ की जानकारी इस अध्ययन में भाग लेने या न लेने में आपकी मदद
करने के लिए है। कृपया बेझिझक पूछें कि क्या आपके पास कोई प्रश्न या चिंता है।
आपको डी। वाई में आयोजित किए जा रहे इस अध्ययन में
भाग लेने के लिए कहा जा रहा है। पाटिल अस्पताल क्योंकि आप इस अध्ययन में भाग लेने के
लिए पात्रता मानदंडों को पूरा करते हैं। आप इस अध्ययन में भर्ती होने की योजना बनाने
वाले विषयों में से एक होंगे।
अनुसंधान का उद्देश्य क्या है?
आपको सर्जरी के लिए तैनात किया गया है जिसे सामान्य
संज्ञाहरण के प्रशासन की आवश्यकता है। सामान्य संज्ञाहरण में लैरींगोस्कोपी (लोगों में मौखिक गुहा और ऊपरी श्वास पथ में लेरिंजोस्कोप नामक एक उपकरण का
उपयोग करके) और एंडोट्रैचियल इंटुबैशन (एनेस्थेसिया के दौरान सहायक वेंटिलेशन के लिए ट्रेकिआ में एक ट्यूब का सम्मिलन)
शामिल है। यह प्रक्रिया कई बार दिल की धड़कन को बढ़ा देती है,
रिफ्लेक्स प्रतिक्रिया के रूप में रक्तचाप में वृद्धि होती है। लॅरिन्गोस्कोपी
और एंडोट्रासीअल इंटुबैषेण के उपरोक्त दुष्प्रभावों को दबाने के लिए हम लिग्नोकाइन
(या तो स्प्रे या अंतःशिरा मार्ग) का उपयोग करेंगे।
अध्ययन का उद्देश्य लैरींगोस्कोपी और एंडोट्रैचियल
इंटुबैषेण के कारण हेमोडायनामिक मापदंडों पर लिग्नोकेन स्प्रे के प्रभावों का आकलन
करना है और इसकी तुलना में फ्रॅक्शन 50% के साथ रोगियों
में अंतःशिरा लिग्नोकाइन की तुलना करना है।
अध्ययन की प्रक्रियाएं
सामान्य एनेस्थीसिया के तहत ऐच्छिक सर्जरी के लिए
तैनात ईएफ <50% वाले सभी रोगियों को लेरिंजोस्कोपी और
एंडोट्रैचियल इंटुबैषेण से पहले ईथ लिग्नोकाइन स्प्रे या अंतःशिरा लिग्नोकाइन दिया
जाएगा। लैरींगोस्कोपी और एंडोट्रैचियल इंटुबैषेण के वासोप्रेसिव प्रभावों को कम करने
में इस दवा की प्रभावकारिता का इस अध्ययन द्वारा मूल्यांकन किया जाना है।
आपके लिए संभावित जोखिम
इस अध्ययन में कोई जोखिम शामिल नहीं है।
आपको संभावित लाभ
सामान्य संज्ञाहरण के तहत सर्जरी करने वाले स्वस्थ
वयस्कों में नैदानिक परीक्षणों ने साबित कर दिया है
कि लिग्नोकेन के पूर्व उपयोग से लैरींगोस्कोपी और एंडोट्रैचियल इंटुबैशन के वैसोप्रेसोर
प्रभाव को कम कर दिया है और सुरक्षा और समग्र परिणाम में सुधार हुआ है।
अन्य लोगों को संभावित लाभ
अनुसंधान के परिणाम भविष्य के रोगियों को चिकित्सा
ज्ञान और
/ या चिकित्सीय लाभ की उन्नति के रूप में समाज को लाभ प्रदान कर सकते
हैं।
प्रतिभागी को लागत
परीक्षण आपके लिए नि: शुल्क किए जाएंगे। परीक्षण डॉ। डी वाई पाटिल अस्पताल में किए जाएंगे।
आपसे प्राप्त जानकारी की गोपनीयता
आपको अपनी मेडिकल जानकारी की गोपनीयता (व्यक्तिगत विवरण, शारीरिक परीक्षाओं के परिणाम,
जांच, और आपके मोबाइल डेटा) की गोपनीयता के बारे में अधिकार है। इस दस्तावेज़ पर हस्ताक्षर करने से,
यदि आवश्यक हो, तो आप इलाज करने वाले चिकित्सक,
अन्य अध्ययन कर्मियों, अस्पताल की नैतिकता समिति
को अपने डेटा को देखने की अनुमति देंगे। इस शोध के भाग के रूप में किए गए नैदानिक परीक्षणों
और चिकित्सा के परिणामों को आपके मेडिकल रिकॉर्ड में शामिल किया जा सकता है। इस अध्ययन
की जानकारी, अगर वैज्ञानिक पत्रिकाओं में प्रकाशित की जाती
है या वैज्ञानिक बैठकों में प्रस्तुत की जाती है, तो इससे आपकी
पहचान उजागर नहीं होगी।
अध्ययन में भाग नहीं लेने का आपका निर्णय आपको कैसे
प्रभावित करेगा?
इस शोध अध्ययन में भाग नहीं लेने का आपका निर्णय
आपकी चिकित्सा देखभाल या उपचार करने वाले चिकित्सक या संस्थान के साथ आपके संबंधों
को प्रभावित नहीं करेगा। आपका डॉक्टर अभी भी आपकी देखभाल करेगा और आप किसी भी लाभ को
नहीं खोएंगे जिसके आप हकदार हैं।
नई जानकारी का अधिकार
यदि इस शोध अध्ययन के दौरान अनुसंधान टीम को कोई
नई जानकारी मिलती है जो अध्ययन में भाग लेने को जारी रखने के आपके निर्णय को प्रभावित
कर सकती है, या कुछ संदेह पैदा कर सकती है, तो आपको उस जानकारी के बारे में बताया जाएगा।
संपर्क करें
अधिक जानकारी / प्रश्नों
के लिए, आप हमें निम्नलिखित पते पर संपर्क कर सकते हैं:
प्रधान अन्वेषक:
संघर्ष के मामले में, आप निम्नलिखित पते पर हमारी अस्पताल आचार समिति के अध्यक्ष (संयोजक) से संपर्क कर सकते हैं:
डॉ। ज्ञानेश बेलेकर
अध्यक्ष, संस्थागत आचार
समिति,
डी वाई पाटिल यूनिवर्सिटी और स्कूल ऑफ मेडिसिन, नेरुल, नवी मुंबई।
medical thesis sample pdf,
medical thesis topics,
medical thesis online full text india,
thesis for medical students,
how to write medical thesis,
proforma for medical thesis,
medical thesis guide,
how to write medical thesis protocol,
medical thesis india,
medical thesis sample pdf,
medical thesis online full text india,
medical dissertation pdf,
thesis topics in medicine free download,
aiims general medicine thesis topics,
md thesis,
medical dissertation examples,
how to write medical thesis 2021,
No comments:
Post a Comment