Dr. Minnu Panditrao's Dexmedetomidine for intraoperative sedation & analgesia

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Dexmedetomidi ne For Intraoperative Sedation & Analgesia

description

Prof. Minnu Panditrao shares her own ideas about the use dexmedetomidine for various indications i.e. for sedation, intra and post operative analgesia.

Transcript of Dr. Minnu Panditrao's Dexmedetomidine for intraoperative sedation & analgesia

Page 1: Dr. Minnu Panditrao's Dexmedetomidine for intraoperative sedation & analgesia

DexmedetomidineFor

IntraoperativeSedation

& Analgesia

Page 2: Dr. Minnu Panditrao's Dexmedetomidine for intraoperative sedation & analgesia

Dr. Mrs. Minnu M. Panditrao

CONSULTANTDEPARTMENT OF ANESTHESIOLOGY &

INTENSIVE CAREPublic Hospital Authority’s RAND MEMORIAL HOSPITALFREEPORT, GRAND BAHAMA

COMMONWEALTH OF THE BAHAMAS

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FORMERLY:

ProfessorDepartment of Anaesthesiology

and Critical CareDr. D Y Patil Medical College

Pimpri, Pune, India

Page 4: Dr. Minnu Panditrao's Dexmedetomidine for intraoperative sedation & analgesia

alpha 2 Adrenergic Receptor Agonists

• Imidazole class of drugs• Older drugs : xylazine detomidine medetomidine in veterinary medicine!• Clonidine : first agent ( in humans)

•Clarke KW, Hall LW. “Xylazine” a new sedative for horse and cattle. Vet rec1969; 85: 512-517•Tamsent A, Gordh T. Epidural clonidine produces analgesia, Lancet1984; 2:231-232

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alpha 2 Adrenergic Receptor Agonists

Dexmedetomidine

What is so special about it?

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Dexmedetomidine

• a D – enantiomer of medetomidine• New Entrant in this class• approved in 1999 by FDA for clinical

application in humans• Structure:

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Actions• Central Sedation, anxiolysis and analgesia

Bradycardia and hypotension

• Peripheral Decreased GI secretions, inclusive of saliva Decreased GI motility Inhibition of rennin-Angiotensin (RA) system

and decreased release of rennin Increased Glomerular Filtration Rate (GFR), Increased excretion of Na, water and thus

diuresis Decreased intra-ocular pressure Decreased insulin release

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MECHANISM CLINICAL (CNS) EFFECTS

• neither the nerve/ terminal is allowed to get stimulated, nor it can transmit/ propagate the signal forwards.

• at supra-spinal level as well as at spinal level Supra-spinal: Locus coeruleus:

– Brainstem center - modulates wakefulness– Major site for hypnotic actions (sedation,

anxiolysis)– Mediated via various efferent pathways:

• Thalamus and subthalamus cortex• Nociceptive transmission via descending spinal tracts• Vasomotor center and reticular formation

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MECHANISM CLINICAL (CNS) EFFECTS

• Spinal: Spinal cord Binding to 2 receptors analgesia

At Substantia gelatinosa (Lamina II),

closing the gate at the dorsal horn to stimuli coming from Aδ and C fibers

Inhibit release of nociceptive humoral transmitters like Substance P release of substance P

•Kuraishi Y, Hirota N, Sato Y, et al Noradrenergic inhibition of the release of Substance P from the primary afferents in the rabbit spinal cord dorsal horn. Brain res.1985; 309: 177- 182

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CNS ACTIONS

Dexmedetomidine

• Sedation – central, G-proteins (inhibition)• Analgesia – spinal cord, Substance P

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CELLULAR MECHANISM

Ca++

Ca++

Ca++

– +

Decrease in influx of Ca++

Decrease in actionpotential due to

hyperpolarization

a2A

a2AR

Go Gk K+

K+

K+

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CNS ACTIONS• Sedation, resembles the physiologic

sleep with less prominent respiratory depression

• Action is supposed to be mediated through α2A subset of receptors and is very specific for dexmedetomidine as compared to clonidine

• Are easily arousable and additional sedative/ adjuvant is not needed to maintain the sedation•Hunter JC, Fontana DJ, Hedley LR et al. Assessment of the role of alpha 2 adrenoceptor subtypes in anti nociceptive , sedative and

hypothermic action of dexmedetomidine in transgenic mice Br J Pharmacol1997; 122: 1339-1344

•Venn RM, Bradshaw CJ, Spencer R et al. Preliminary UK experience of dexmedetomidine, a novel agent for post operative sedation in intensive care unit. Anaesthesia 199; 54: 1136-1142

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Actions on Cardio-Vascular system

• Totally devoid of any direct effects on myocardium

• Transient increase in BP : attributable to peripheral vasoconstriction due to stimulation of α2B adrenoreceptors in peripheral vascular smooth muscles.

• Significant bradycardia & Hypotension

secondary to central inhibitory α2A

agonist effect• All these effects can be offset or overcome

with use of atropine, ephedrine or volume loading

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Clinical Uses of Dexmedetomidine

• Craniotomy: aneurysm, AVM

• Cervical spine surgery

• Conventional CABG

• Off-pump CABG• Vascular surgery• Thoracic

surgery

• Bariatric surgery• Back surgery, evoked potentials• Head injury• Burn• Trauma• Awake intubation

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Clinical Uses of Dexmedetomidine

Sedation in CT and MRI imaging studiesMason K, Ped Anesth 2008Koroglu A, Anesth Analg 2006

Outpatient third molar surgeryUstin Y, J Oral Maxilfac Surg 2006Cheung C, Anaesthesia 2007

Cataract surgeryAlhashemi J, Br J Anaest 2006

Cardiac catheterizationTosun Z, J Card Vasc Anesth 2006Mester R, Am J Therap 2008

GI ProceduresDemiraran Y, Can J Gastroenter 2007Dex may be a good alternative to midazolam for upper endoscopy

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Dex: Use in Coronary Artery Surgery

Coronary Artery Surgery Patients

Dexmedetomidine : Herr study, n=300: Dex vs. controls [propofol]• Faster time to extub in dex gp - by 1 hr• 70% did not require morphine vs. 34% controls• Dex pts had less Afib (7 vs 12 pts)

Herr DL: Crit Care Med 2000;28:M248. Washington Hospital

CABG and Lung Disease

• RCT, n= 20. Dex started at end of surgery, 0.2 to 0.7 ug/kg/hr, + continued 6 hr after extubation vs. controls (propofol)

Dexmedetomidine• Faster time to extub: 7.8 + 4.6 h v. 16.5 + 11.8 h• No difference in PaCO2 between gps 30 min after extub: 37.9 v.

34.9 mmHgSumping ST: CCM 2000;28:M249. Duke

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Dex: Use in Thoracotomy + Thoracoscopy Thoracotomy + thoracoscopy patients

• COPD, pleural effusion, marginal pulmonary function, pCO2 + pO2 with opioids

• Thoracic epidural: mainly for thoracotomy, Dex: mainly for thoracoscopy

Dexmedetomidine• Patients are arousable, but sedated• Does not ventilatory drive• Greatly need for opioids• Alternative to thoracic epidural • Continue after extubation

Vascular surgery

• Usually at risk for CAD, ischemia, HTN, tachycardia• Dex attenuates periop stress response• Dex attenuates BP w AXC, especially thoracic aorta

Dexmedetomidine: RCT, n=41. Dex continued 48 hr postop• HR in dex gp at emergence- 73 + 11 v. 83 + 20 bpm• Better control of HR, Plasma NE levels in dex group

Talke et al: Anesth Analg 2000;90:834. Multicenter

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Dex: Use in Other Surgical Procedures

Abdominal surgery

• Dexmedetomidine provides analgesia without respiratory depression• Especially useful in elderly undergoing colon resections, TAH, + other

stressful procedures

Bariatric surgery

• Dexmedetomidine Improves Postop Pain Mgt after Bariatric Surgery• Morphine use in dex gp• Pain score better in dex gp: 1.8 vs 3.4 , % time pain free in PACU in dex

gp: 44% vs 0 • Better control of HR in dex gp

Neck + back surgery

• Dex causes minimal effect on SSEP monitoring• Smooth emergence, especially cervical spine• Easy to evaluate neuro function prior to + after extubation

Ramsay MA, et al: Anesthesiology, 2002: A-910 and A-165. Baylor

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Dex: Use in Other Surgical Procedures

Burns patients

•2 agonist effect assists in the management of burn patients; blunts catecholamine surge•Use in intubated and non-intubated burn patients•Outpatient dressing changes instead of ketamine

Trauma and Alcohol withdrawal patients

•Benzodiazepines typically used- Intubation and ventilation often required if extreme agitation•Dexmedetomidine is an alternative to BZD- Spontaneous breathing, Hemodynamic stability, Adequate sedation, Prevention of autonomic effects of withdrawal, Pain control

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Dex: Use in Neuro anesthesia

Effect of Dexmedetomidine on Cerebral Blood Flow• Animal models

– Dex causes a reduction in CBF up to 45%– Dex has no effect on the CMRO2

– Dex produces the concentration-dependent constriction of pial arteries and veins

– Dex limits hypercapnea- and hypoxia-induced cerebral vasodilationZornow MH et al, Anesth Analg; 1990

Fale A et al, Anesth Analg; 1994Karlsson et al, Anesth Analg; 1991

• Human study (TCD)– Mean CBF velocity decreased with an increase in plasma

concentration of Dex– Pulsatility index increased at higher level of Dex (indicates an

increase in CVR) Zornow MH et al, J Cereb Blood Flow Metab; 1993

Cognitive Function• There is strong evidence that a2 – agonists improve prefrontal cortical

function (PFC)Arnstein et el. Arch Gen Psychiatry 1996

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Dex: Use in Neuro anesthesia

Effect on ICP

• Animal model– ICP was unchanged despite an increase in systemic blood

pressure in rabbits– ICP was decreased in the presence of intracranial

hypertension Zornow MH et al, Anesth Analg 1992

• Human study– Dex has no effect on lumbar CSF pressure in patients

undergoing transphenoidal pituitary tumor resectionTalke P et al. Anesth Analg 1997

Effect on SSEPs and AEP

• There is a lack of effect on cortical AEP• Dex does not affect cortical (P25-N35) response• Dex depresses median nerve P15-N20 amplitudes

Thornton C et al. Br J Anaesth 1999

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Dex: Use in Neuro anesthesia

Antinociception· a2 – Agonists attenuate hemodynamic responses to laryngoscopy and intubation

Lawrence CJ et al Anaesthesia 1997

· a2 – Agonists decrease peri operative oxygen consumption Taittonen MT Br J Anaesth 1997

• Dex reduces NE level during emergence from anesthesia (2 to 3 times lower than placebo)

Talke P et al. Anesth Analg 2000

Effect on BIS• BIS values after Dex infusion for 1 hour were: 65 at 0.2 mg/kg/hr, 60 at 0.6

mg/kg/hr• Volunteers readily awakened from hypnosis by talking ; BIS returned to awake

levelBIS before and after subjects were asked to perform various tasks

Hall JE et al. Anesth Analg 2000

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Dex: Use in Neuro anesthesia- Neuro protective effects

• Inhibition of ischemia induced NE release may be associated with neuroprotection

• Dex prevents delayed neuronal death after focal ischemia

• Dex decreased total ischemic volume by 40% compared to placebo

Jolkkonen J et al. Euro J Pharm 1999Hoffman WE et al Anesthesiology 1991

• Dex enhances glutamine disposal by oxidative metabolism in astrocytes

Huang R et al. J Cereb Blood Metab 2000

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Dexmedetomidine: Use in Craniotomy

Craniotomy for Aneurysm / AVM

Anesthesia considerations• Smooth induction + emergence, Prevent rupture• Avoid cerebral ischemia, Hypothermia (33 oC) CMRO2, CBF, CBV, CSF,

ICP

Dexmedetomodine• sympathetic stimulation• or no change in ICP• shivering w/o respiratory depression• Preserved cognitive function- reliable serial neuro exams

Doufas AG et al: Stroke 2003;34. Louisville, KY

Craniotomy• Postoperative infusion of Dex in patients recovering from transphenoidal

hypophysectomy reduced plasma catecholamines by 70%Talke P et al Anesth Analg 1997

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Dex Use in Neuro: Clinical Experience

Spinal Fusion

• Intraoperative switching from a propofol infusion to Dex in patients undergoing cervical fusion resulted in:

– A neurological examination that was successfully performed in the OR on an intubated patient

– Clinically insignificant hemodynamic changes during and after the switchover

Bloom M et al J Neurosurg Anesth 2001

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Dex Use in Neuro: Clinical Experience

Carotid Endartrectomy • A combination of superficial and deep cervical plexus blocks is the most

common regional anesthetic technique in the NYU medical center• Sedation with dexmedetomidine (0.2-0.4 mcg/kg/hr) offers a comfortable

and cooperative patient during the operation• Less agitation and respiratory depression than with a continuous infusion

of propofol or repeated doses of fentanyl and/or midazolam

Functional Neurosurgery

• Dex infusion at 0.1 – 0.2 mcg/kg/hr allowed us to achieve a tranquil state sufficient to complete neuropsychiatric testing required for mapping of the cortical speech area, as well as to perform an awake tumor resection

• A lack of respiratory depression offers an advantage over other techniqueBekker A et al. Anesth Analg 2001

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Dex Use in Ophthalmology:Effect of dexmedetomidine premedication on the intraocular pressure changes after succinylcholine and intubation: BJABritish Journal of Anaesthesia 100 (4): 485–9 (2008)

February 19, 2008

Details - 40 patients with no pre-existing eye disease undergoing GA, Random premedication with Dex 0.6 mcg/kg or saline, HR, MAP, and IOP measured

• IOP- Succinylcholine and intubation increased IOP in both groups. However, in the Dex group, the IOP rise was not different from the baseline value and was significantly lower than in the saline group .

• MAP- After intubation, the MAP in the control group was higher than that in the dex group and exceeded the baseline value

• HR- HR also showed less fluctuation in the dex group than in the saline group

Result:• Premedication with a dose dex 0.6 mg/kg over 10 min blunted the

↑IOP caused by succinylcholine & intubation• Attenuated the hemodynamic response to laryngoscopy & intubation.

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Dex Use in Ophthalmology: Conclusion

of IOP with succinylcholine & endotracheal intubation can be blunted with i.v. dexmedetomidine premedication.

Hemodynamic stability is an additional advantage

Dex could be a beneficial premedication in open globe injuries

Single i.v. dose of dexmedetomidine 0.6 mcg/kg IOP by 34%

The present study (0.6 mcg/kg) was based on a previous clinical study, where the selected dose resulted in a significant IOP and prevented IOP response to intubation

Dexmedetomidine attenuates sympathoadrenal responses to tracheal intubation. Br J Anaesth 1992; 68: 126–31

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PROCEDURAL SEDATION• Koroglu A, Br J Anaesth 2005;94:821

– Dex vs midazolam for MRI sedation– 80 patients, 1-7 yrs– Dex: 1ug/kg bolus, then 0.5 ug/kg/hr– Midazolam: 0.2 mg/kg, then 0.36 mg/kg/hr– Efficacy: 32/40 (dex) vs 8/40 (midazolam)– Onset: 19 min (dex) vs 35 min (midazolam)– Similar CV effects - nothing significant

• Concl: dex > efficacy vs midazolam• Problem – midaz rarely sole agent for

MRI

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PROCEDURAL SEDATION

• Koroglu A, Anesth Analg 2006;103:63– Dex vs propofol for MRI sedation– 60 patients aged 1-7 yrs– Dex: 1ug/kg bolus, then 0.5 ug/kg/hr– Propofol: 3 mg/kg bolus, then 6 mg/kg/min– Efficacy similar: 83% (dex) vs 90% (propofol)– Onset – 11 min (dex) vs 4 min (propofol)– rec time with dex (27 vs 18 min)– hypoxia with dex (0% vs 13%)

• Concl: Consider as alternative to propofol

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Dex Use in MRI• 80 children aged 1-7 years • Randomly assigned to either

dexmedetomidine or midazolam

– 10-minute loading doses: 1 mcg/kg dexmedetomidine, 0.2 mg/kg midazolam

– Infusions: 0.5 mcg/kg/h dexmedetomidine, 6 mcg/kg/h midazolam1

• The quality of MRI was significantly better (P<.001) and the rate of adequate sedation was significantly higher (P<.001) with dexmedetomidine

Quality of MRI

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Clinical Administration

• Onset of 30 minutes as compared to that of midazolam 3-5 minutes and that of propofol 30-50 seconds

can be decreased by infusion of standard loading dose of 1µg/kg, over 10 minutes

• Offset of sedative action in 5 minutes, while midazolam has about 2 to 6 hours and propofol has 3-8 minutes.

• Duration of analgesic action of about 4 hours as compared to that of Fentanyl up to 60-80 minutes

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Indications & Dosage

• A pre-anaesthetic medication and as a psychosedation in short outpatient surgical procedures

• initial loading dose of intra venous infusion of dexmedetomidine 1- 6 µg / kg for 10 minutes till 3 on Mackenzie’s Sedation assessment score (till the patient showed awakening responses to calling in spite of closed eyes) and maintained on

0.4 µg/kg/hr•Taniyama K, Oda H, Okawa K et al. Psychosedation with dexmedetomidine hydrochloride during minor oral surgery. Anesth Prog 2009; 56:n75-80

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Indications & Dosage

• In the dose of 0.2 to 0.7 µg/kg/hr, found to attenuate the stress induced sympatho adrenal responses to laryngoscopy, endotracheal intubation, surgical stimulation and provide overall increased hemodynamic stability & as an adjuvant to other anaesthetic agents, including inhalational agents like isofluraneBhatia P. Dexmedetomidine: a New agent in Anaesthesia & Critical care Practice.

http://dexmedtomidine.com

Aanta R, Jaakola ML, Kallio A, Kanto J. Reduction of minimum alveolar concentration of isoflurane by dexmedetomidine .Anesthesiology 1997;80 : 1055-1060

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Indications & Dosage

• Can be used to obtund the autonomic pressor response due to laryngoscopy and endotracheal intubation

• In the dose of 1 µg / kg diluted in 100ml of saline solution, infused over 15 minutes

• After a stabilization period of 5 minutes• Suitably induced, relaxed & trachea

intubated

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Indications & Dosage

• an intra-operative analgesic in GA as an alternative to opioids

• Infusion of standard loading dose of 1µg/kg, over 10 minutes followed by maintenance of 0.2- 0.7 µg/kg/hr. diluted in 0.9 % normal saline

Scheinin B, Lindgren L, Bandel T, Scheinin H, Scheinin M. Dexmedomidine attenuates sympatho adrenal responses to tracheal intubation and reduces need for thiopentone and peri-operative fentanyl Br J Anaesth 1992; 68: 126-131

Menda F, Koner O, Sayin M, Ture H et al. Dexmedetomidine as an adjunct to anaesthetic induction to attenuate hemodynamic response to endotracheal intubation in patients undergoing fast track CABG. Ann Can J Anaesth 2010’ 13: 16-21

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Indications & Dosage

• It has been found to provide neuro-protective effect by decreasing cerebral blood flow without increasing either with cerebral metabolic rate (CMRO2) or intra cranial pressure (ICP)

• sole sedating agent with local anesthetic agents in a high risk patient

• used as anti-shivering and for thermoregulation

•Zornov MH, Maze M, Dyek JB. Shafer SL. Dexmedetomidine decreases cerebral blood flow velocity in humans J Cereb Blood Flow Metab 1993; 13: 350-352•Rich JM. Dexmedetomidine as a sole sedating agent with local anesthesia in a high risk patient for axillo-femoral bypass graft: a case report. AANA Journal2005; 73:357-360

Page 40: Dr. Minnu Panditrao's Dexmedetomidine for intraoperative sedation & analgesia

alpha 2 Adrenergic Receptor Antagonist

Atipamezole• Effectively reverses Psychomotor

side-effects• Reverses Sedation &

Sympatholysis• Reverses Analgesia• t ½ is 1 ½ - 2 hours.

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To compare the efficacy of

Dexmedetomidine vs

Fentanyl

as sedative & analgesic in

short general anaesthesia in

day care obstetric &

gynaecological surgeries

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AIMS AND OBJECTIVES

• To compare the time required for onset and offset of sedation, quality of intra-operative & post-operative analgesia and the time required for post-operative recovery using Inj. Dexmedetomidine and Inj. Fentanyl

• To evaluate cardio-respiratory and any other systemic side effects at equal doses

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METHODOLOGY

• Age group 18 - 65 years of ASA-I & II •Randomized into two equal groups of 20 each by computer generated model

•Pre-medicated with Inj. Glycopyrrolate 0.2mg i.v.

• Group A: patients received Inj. Dexmedetomidine 1μg/kg i.v. 10 min. prior to induction by infusion

• Group B: patients received Inj. Fentanyl 1μg/kg i.v. 10 min. prior to induction by infusion

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• Induction done with Inj. Propofol i.v in titrated doses

• Maintained with 66% N2O, 33% Oxygen & Isoflurane ( titrated concentration) with the patient breathing spontaneously on Magill circuit

• Time to eye opening at the conclusion of surgery was recorded

• In post anaesthesia care unit patients were evaluated periodically for

- vitals - sedation using Ramsay sedation scale

- visual analog scale - time of rescue analgesia (when VAS >5) - Standard Aldrete score for post anaesthesia

recovery

METHODOLOGY

Page 45: Dr. Minnu Panditrao's Dexmedetomidine for intraoperative sedation & analgesia

RESULTS

• Demographic profile for Age, Sex and ASA grade had no statistical significance & hence were comparable

• The requirement of Propofol was significantly reduced in Dex Group

• Comparison of pulse rate in Dexmedetomidine Group showed significant fall immediately after pre medication , without any intervention it returned to baseline, & remained equivalent to that in Fentanyl Group throughout surgery

Line diagram showing comparision of pulse rate in study groups

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RESULTS

• No significant change in blood pressure seen in Dex. group whereas continuous fluctuation of systolic BP seen in fent.group

• No significant change in diastolic BP & Respiratory rate seen in any of the groups

• significant fall in saturation was observed with Fentanyl group

• The time of eye opening is highly significantly early in Dex. group (p<0.001) and delayed eye opening seen with fentanyl group

Line diagram showing comparision of systolic blood pressure in study groups

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Line diagram showing comparision of SPO2 in study groups

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RESULTS

• The post operative analgesia duration was more in Dex. group (approx. 4-6 hrs.), whereas in Fentanyl group patients required rescue analgesia within 1 – 1.5 hrs of surgery

• The sedation was highly significantly profound in fentanyl group according to Ramsay sedation score (p < 0.001) after 15 min of surgery

• The quality of recovery was highly significantly better (Aldrete score = 9+)was observed in most of the patients after 30 min in Dex.group & Similar results were seen only after 1.5 – 2 hrs. in Fentanyl Group

Line diagram showing comparision of VAS score in study groups

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Line diagram showing comparision of Ramsay sedation in post operative in study groups

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P < 0.001 at 1.5 hrs.

P < 0.001 at 15 min.Line diagram showing comparision of standard aldrete score in post operative in study

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TO EVALUATE THE EFFECT OF ADDITION OF DEXMEDETOMIDINE TO 0.5% HYPERBARIC BUPIVACAINE

INTRATHECALLY

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AIMS & OBJECTIVES• To study the onset and duration of analgesia with

the addition of 10 µg Dexmedetomidine to 0.5% heavy Bupivacaine in sub-arachnoid block

 • To evaluate the quality of block and post

operative analgesia as compared to control i.e. 0.5% heavy Bupivacaine

• To observe any side effects of intrathecal administration of Dexmedetomidine with 0.5% Bupivacaine intra operatively and post operatively

Page 50: Dr. Minnu Panditrao's Dexmedetomidine for intraoperative sedation & analgesia

METHODOLOGY• Patients of ASA I,II and age group 18-65 years

were randomized into two equal groups of 20 each by a computer generated model

• Group A (Dexmedetomidine Group) were given 3ml of 0.5% heavy Bupivacaine + 0.5ml (10 µg) of Dexmedetomidine

• Group B (Control Group) were given 3ml of 0.5% heavy Bupivacaine + 0.5ml of Water for injection

• Patients will be preloaded with Ringer Lactate solution 10 ml/kg body

• Spinal anaesthesia was given using a 26G Quincke’s needle in sitting position through a midline approach

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METHODOLOGY• Sensory block was tested by pinprick method till T6

sensory level • Degree of motor blockade was assessed by modified

Bromage scale• Intraoperative vitals were monitored• Hypotension: SBP < 90 mm Hg or a decrease of

>20% from baseline. Hypotension was treated with a bolus administration of 250 ml Ringer lactate and 6 mg of i.v. Mephentermine if required

• Bradycardia was defined as HR < 50 bpm and was treated with 0.6 mg of i.v. Atropine

• Postoperatively, 2 segment sensory regression, motor regression and time to rescue analgesia were monitored

Page 52: Dr. Minnu Panditrao's Dexmedetomidine for intraoperative sedation & analgesia

• No statistically significant difference for age, height , weight, Sex wise and ASA distribution in both groups

RESULTS

Page 53: Dr. Minnu Panditrao's Dexmedetomidine for intraoperative sedation & analgesia

• Difference in sensory onset not statistically significant

• Motor onset significantly shorter in Dexmedetomidine Group (t value-2.54,

p value < 0.05) • Difference in peak

sensory insignificant

• Peak motor significantly longer in Dex Group(t value-4.59, p value<0.0001)

RESULTS

0

1

2

3

4

5

6

7

8

Av

era

ge

Time of Peak sensory (T3) Time of Peak motor(T4)

After spinal anesthesia

Multiple bar diagram showing comparison of time of sensory and motor Peak after spinal anesthesia in study groups

Group A

Group B

Page 54: Dr. Minnu Panditrao's Dexmedetomidine for intraoperative sedation & analgesia

• 2 segment sensory regression

• motor regression and

• time of rescue analgesia significantly longer in Dex. Group

RESULTS Parameters Group A Group B t

ValueP

ValueMean SD (n=20)

Mean SD (n=20)

2 segment sensory regression (T5)

190.3 34.80 98.65 14.95

10.81 <0.0001

Motor regression (T6)

265.05 57.50 138.7 14.76

9.51 <0.0001

Time of rescue analgesia (T7)

342.75 76.94 189 20.71 8.62 <0.0001

0

50

100

150

200

250

300

350

Ave

rag

e

2 segment sensoryregression (T5)

Motor regression(T6)

Time of rescueanalgesia (vas > 7)

(T7)

Level of sensory blockade

Multiple bar diagram showing comparison of level of sensory blockade in study groups

Group A

Group B

Page 55: Dr. Minnu Panditrao's Dexmedetomidine for intraoperative sedation & analgesia

• Both groups with manageable Bradycardia & Hypotension0

1

2

3

4

No

. o

f cases

Bradycardia Hypotension

Side effect

Multiple bar diagram showing side effect wise distribution of cases in study groups

Group A

Group B

Line diagram showing comparision of heart rate in study groups

0

10

20

30

40

50

60

70

80

90

100

HR (min)

Avera

ge

Group A

Group B

Line diagram showing comparision of systolic blood pressure in study groups

0

20

40

60

80

100

120

140

SBP (mm Hg)

Avera

ge

Group A

Group B

Line diagram showing comparision of diastolic blood pressure in study groups

0

10

20

30

40

50

60

70

80

90

Pre – op At 3 min At 10min

At 15min

At 30min

At 45min

At 60min

End ofSurgery

Post -op

DBP (mm Hg)

Avera

ge

Group A

Group B

Page 56: Dr. Minnu Panditrao's Dexmedetomidine for intraoperative sedation & analgesia

Indications: Future plans

• Use of dexmedetomidine as an adjuvant to Local Anaesthetic Mixture, in peri- bulbar block

Page 57: Dr. Minnu Panditrao's Dexmedetomidine for intraoperative sedation & analgesia

Summarizing• Quest for an ‘Ideal’ peri-operative

sedative- analgesic goes on… &… on…&….on!!

• α2 agonists are unique class of drugs, with many desirable properties!!

• Clonidine and now dexmedetomidine, are versatile, multi-faceted and potent drugs!!!

• It has been successfully employed in Cardiac, Neuro-surgical, abdominal, Head & Neck Surgeries and Procedural sedation !!!!

Page 58: Dr. Minnu Panditrao's Dexmedetomidine for intraoperative sedation & analgesia

Conclusion!• Dexmedetomidine can be considered a

suitable agent for providing pre-operative sedation & pre-anaesthetic anxiolysis

• Useful in the day care procedures like conscious sedation and procedural sedation

• changing our viewpoint of providing intra & post operative analgesia, without any potential and significant side-effects of existing agents employed for this purpose.

Page 59: Dr. Minnu Panditrao's Dexmedetomidine for intraoperative sedation & analgesia