dr.k.venkatesan md ii year

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Dr.K.VENKATESAN MD II YEAR

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Dr.K.VENKATESAN MD II YEAR. SYNERGISTIC EFFECT OF MAGNESIUM SULPHATE AND FENTANY ADDED TO INTRATHECAL BUPIVACAINE FOR MILD PREECLAMSIA. GUIDE. PROF&HOD.DR.P.S.SHANMUGAM MD,DA. DEPARTMENT OF ANESTHESIA KILPAUK MEDICAL COLLEGE & HOSPITAL CHENNAI. aim of the study. - PowerPoint PPT Presentation

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Page 1: Dr.K.VENKATESAN MD II YEAR

Dr.K.VENKATESAN MD II YEAR

Page 2: Dr.K.VENKATESAN MD II YEAR

PROF&HOD.DR.P.S.SHANMUGAM MD,DA. DEPARTMENT OF ANESTHESIA KILPAUK MEDICAL COLLEGE & HOSPITAL CHENNAI

Page 3: Dr.K.VENKATESAN MD II YEAR

To study and compare the effect of added fentanyl 25(mic gm) & Mgso4 0.1cc 50%(50mg) to 0.5% 2cc(10mg)bupivacaine in spinal anesthesia

Patients undergoing elective LSCS With mild gestational hypertension(PIH)

Page 4: Dr.K.VENKATESAN MD II YEAR

Adequate analgesia following caesarian section decreases morbidity , improves patient ambulation &outcomes ,facilitate care of the new born.

Intrathecal MgSO4 , NMDA antagonist has been shown to prolong analgesia without significant side effects in healthy parturients

Correlation was found between serum & CSF Mg concentration in patients with preeclampsia

Page 5: Dr.K.VENKATESAN MD II YEAR

Ethical committee approval Informed patient consent Randomised double blind controlled

study Statistical significance is ‘p’ value less

than 0.05 SAB performed

With pt in right lateral position25G quincke needle

Page 6: Dr.K.VENKATESAN MD II YEAR

60 patient ASA risk I &II undergoing elective caesarian section with mild PIH .

IV line secured with 18G venflon, and preloaded with RL 10-12ml /kg

All pts received 5L of O2 / min through face mask throughout procedure

Pts treated with titrated doses of Inj.ephedrine 6mgI.V if BP<90mmhg Inj.Atropine 0.6mg if HR<60/min

After delivery of baby Inj. Syntocin 10 IU in drip and 10 IU IM given

Page 7: Dr.K.VENKATESAN MD II YEAR

Mild PIH is defined as SBP 140 – 160 and DBP 90 – 110mm Hg with or without proteinuria after 20 wk. gestation

60 pts with average age of 18 – 35 undergoing elective LSCS under SA were randomized into three groups of 20 each

Minimal fasting period is 8hrs All pts received premedication with Inj.

Ranitidine 50mg IV and Inj. Metoclopramide 10 mg IV, 15 min before surgery

Page 8: Dr.K.VENKATESAN MD II YEAR

INCLUSION EXCLUSION

Age between 18-35 years

Elective LSCS under spinal

anesthesia Mild PIH

(BP<160/110mmhg)

ASA I/II

Contraindication to regional anesthesia

Heart disease Fetal distress Seizure disorder Severe eclampsia Pts with

coagulation defect Allergy to LA

Page 9: Dr.K.VENKATESAN MD II YEAR

Group C: control group,(N=20) patients 0.5%

2cc(10mg)bupivacaine + 0.6cc normal saline .

Group F: Fentanyl(N= 20) patients received 0.5% 2cc

bupivacaine +0.5cc( 25mic gm )fentanyl +0.1cc NS.

Group M:Mgso4 group (N=20),0.5% 2cc bupivacaine

+0.5cc fentanyl +0.1cc 50%(50mg) Mgso4 .

Page 10: Dr.K.VENKATESAN MD II YEAR

Variables were analysed by ANOVA Variables analysed and interperted by

post Hoc test Statistical significance is ‘p’ <0.05

Page 11: Dr.K.VENKATESAN MD II YEAR

NIBP PULSEOXIMETER ECG RESPIRATORY RATE URINE OUTPUT

Page 12: Dr.K.VENKATESAN MD II YEAR

GRADE RESPONSE DEGREE OF BLOCK

0 NO MOTOR BLOCK NIL(0%)

1 UNABLE TO STRAIGHT LEG RAISE

PARTIAL(33%)

2 UNABLE TO FLEX KNEE AGAINST RESISTANCE

ALMOST COMPLETE(66%)

3 UNABLE TO FLEX ANKLE

COMPLETE

Page 13: Dr.K.VENKATESAN MD II YEAR

SCORE RESPONSE

1 ANXIOUS OR RESTLESS OR BOTH

2 COPERATIVE, ORIENTED & TRANQUIL

3 RESPONDS TO COMMANDS

4 BRISK RESPONSE TO STIMULUS

5 SLUGGISH RESPONSE TO STIMULUS

6 NO RESPONSE TO STIMULUS

Page 14: Dr.K.VENKATESAN MD II YEAR

SCORE RESPONSE

0 NORMAL SENSATION

1 ANALGESIA (LOSS OF PIN PRICK SENSATION)

2 ANAESTHESIA (LOSS OF TOUCH SENSATION)

Page 15: Dr.K.VENKATESAN MD II YEAR

Block onset timeDuration of sensory blockadeHigher level of sensory blockTime to reach highest blockTwo segment regression timeDuration of postop analgesiaHemodynamic parameters

Page 16: Dr.K.VENKATESAN MD II YEAR

SENSORY BLOCK ONSET TIME Time interval between end of anesthetic injection

and appearance of cutaneous analgesia in dermatomes T-12,T-10,T-8,T-6

DURATION OF MOTOR BLOCK Administration of anesthetic and attainment of

grade 0 in Bromage motor scale DURATION OF ANALGESIA

Administration of anesthetic and disappearance of cutaneous level of sensation at each dermatomal level

POST-OP ANALGESIA DURATION Administration of anesthetic and time of

analgesic requirement in PACU

Page 17: Dr.K.VENKATESAN MD II YEAR

The onset of both sensory and motor block was delayed in the group M ,when compared to both C&F group(p<0.001)

Motor block and analgesic duration was prolonged in the Group M , level of significance (p<0.05)

Two segment regression time increased in M group (P<0.001)

Group M is hemodynamicaly stable when compared to other groups (p<0.019)

Attainment highest level sensory block varies from T1-T6 , delayed in group M with significance level (p<0.08)

Intensity of motor block is more with group M, but with less significance (p<0.291)

Page 18: Dr.K.VENKATESAN MD II YEAR

Occurrence of other complications like Bradycardia , nausea ,shivering were comparable in all groups

Two Patient in group F complained of itching Usage of vasopressors is more in group C

when compared to other groups Fetal outcome assessed by first min and fifth

min APGAR was similar between groups (p>0.3)

Height and weight are similar between groups(p<0.586)

Investigations were similar between groups (p<0.32)

Page 19: Dr.K.VENKATESAN MD II YEAR

Duration of post-op analgesia is prolonged in M group when compared to other groups (p<0.001)

Use of vasopressors is reduced in group M(p<0.03)

Page 20: Dr.K.VENKATESAN MD II YEAR

SENSORY BLOCK ONSET TIME

F M C

Page 21: Dr.K.VENKATESAN MD II YEAR

F M C

Page 22: Dr.K.VENKATESAN MD II YEAR

F M C

Page 23: Dr.K.VENKATESAN MD II YEAR

ANALGESIC & MOTOR BLOCK DURATION

F M C

Page 24: Dr.K.VENKATESAN MD II YEAR

MOTOR BLOCK ONSET TIME

F M C

Page 25: Dr.K.VENKATESAN MD II YEAR

POST-OP ANALGESIA DURATION

F M C

Page 26: Dr.K.VENKATESAN MD II YEAR

Magnesium is the second most abundant intracellular cation

Involved in the regulation of many ion channels and enzymatic reaction

Has application in anesthesia because of its action as a non competitive NMDA receptor antagonist with anti-nociceptive effect

Page 27: Dr.K.VENKATESAN MD II YEAR

Mgso4 has been shown to have anti-nociceptive effects , because of its antagonistic action on the NMDA receptor

Passage of magnesium across BBB is limited

It can potentiate opioid analgesia by both central and peripheral mechanism

MgSO4 causes 1.vasodilation by ca2+ block

2.analgesic effect3.inhibition of catecholamine release

Page 28: Dr.K.VENKATESAN MD II YEAR

Mg inhibit calcium entry into the cell via a non-competitive NMDA receptor blockade

Mg is also a physiological calcium antagonist at different voltage gated calcium channel, it may be important for anti-nociception

Mg decreases incidence of post operative shivering

Response to NMDA receptor is greatly enhanced when ECF Mg concentration below physiological level.

Page 29: Dr.K.VENKATESAN MD II YEAR

Decrease in pain intensity is not due to direct analgesic effect of Mg

But due to prevention of subsequent NMDA activation

Baseline CSF Mg level in pt with preeclamsia differ from normal patients which suggest base line alteration in BBB

Normal CSF Mg level was 2.2meq+/- 0.9, plasma 1.6Meq, CSF:plasma ratio 1.39

Mg is neuroprotective in ischemic as well as excitotoxic brain injury

Page 30: Dr.K.VENKATESAN MD II YEAR

Mg may dilate cerebral blood vessel and thus responsible for relieving vasospasm in pt with preeclampsia

Clinical relevant dose of Mg has no significant effect on V MCA, autoregulation and cerebral reactivity CO2

Mg produce central desensitisation Mg can potentiate NM junction Spinal NMDA receptor antagonist is the

reason for potentiation of LA and prolongation of post operative analgesia

Page 31: Dr.K.VENKATESAN MD II YEAR

It is a synthetic opioids Phenylpiperidine derivatives Directly inhibit the NMDA receptor Action of opioids in the bulbospinal

pathways are critical for analgesic efficacy

Distribution of opioids receptors in descending pain control circuits indicates substantial overlap between µ & Κ receptors

µ receptors produce analgesia within descending pain control circuits.

Page 32: Dr.K.VENKATESAN MD II YEAR
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In parturients with mild PIH undergoing LSCS the addition of Mgso4 50mg to the intrathecal combination of bupivacaine & fentanyl prolongs the duration of analgesia Prolongs motor block durationDelayed onset of sensory blockProlongs post op analgesia

Ref.pubmed,intl.journal of obstetric anesthesia ,SOAP.

Page 35: Dr.K.VENKATESAN MD II YEAR

THANK U