An 18 yr old nulliparous women was admitted at 41 weeks gestation
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POST CAESAREAN SECTION ARREST:A DIAGNOSTIC DILEMMA Tony Thomas StR 3 Wishaw General Hospital An 18 yr old nulliparous woman was admitted at 41 weeks gestation in an otherwise uneventful pregnancy in spontaneous labour. Post admission BP was elevated[systolic 180-142/diastolic 86-102] with a maternal tachycardia of 100-146.Urine dipstick showed 4+ proteinuria and investigations were normal except for a urate level of 4.3mg/dL.She received a one off dose of 10mg nifedepine[used as patient was asthmatic] for the raised blood pressure. Labour was augmented with amniotomy and syntocinon after an epidural. The persistent tachycardia was attributed to nifedepine /epidural although the possibility of venous thromboembolism was considered. An ECG done showed only sinus tachycardia and arterial blood gasses were normal. We proceeded to an emergency caesarean section in view of poor progress[cervical dilatation arrested at 5 cms for 7hours in spite of syntocinon],persistent maternal tachycardia and pre-ecclampsia, initially under an epidural block which was converted to a general anaesthetic post skin incision as the patient had complained of pain. Patient had a normal recovery post reversal of GA[54 minutes from induction] after an uneventful C/S. However 17 minutes post reversal patient was unresponsive ,with decerebrate posturing and a brady arrest. She was resuscitated, intubated and shifted to critical care. Supportive management was initiated with ventilatory assistance for 22 days.She did not require blood products or inotropes. CTPA done was supportive of amniotic fluid embolism while CT brain done on the day of arrest and repeated on day 2 were normal. A 2D echo raised suspicion of an ASD but a trans oesophageal echo showed only a prominent chian network[which is associated with a patent foramen ovale].An MRI done on day3 showed evidence of scattered infarction involving mainly the corpus callosum, frontal lobes and water shed areas of the brain. Clinical picture showed steady improvement progressing from quadriparesis and weak speech on day 25 to almost full recovery by day 60 with residual defects at time of report being short term memory loss and 3-4/5 power in lower limbs Discussion Brady arrest with cerebrovascular insult in the immediate post caesarean section period is rare. This case presents an acute diagnostic dilemma as none of the classic features of the differential diagnosis considered [AFE,PTE,Paradoxical embolism, atypical presentation of ecclampsia] were present. A detailed history revealed that the patient was born prematurely at 26 weeks gestation and suffered from chlamydial pneumonia,severe bronchopulmonary dysplasia ,patent ductus arteriosus and intraventricular haemorrhage. Whether these events could have contributed to opening of an intracardiac communication between the arterial and venous circulations is a matter of debate[Kozelj et al.1999].The presence of only mild coagulopathy was another interesting observation.[PT 17.2(N),PTT 44.7 N range(25.5 -38.5),platelet count 164] and could point to the relatively small size of the embolus[Nagar etal.2005].Inspite of absence of a clear diagnosis treatment available is only supportive with anticoagulation and ventilatory/rehabilitation support. The near complete recovery that the patient had supports the widely held view that primary determinant of outcome will be number of emboli reaching cerebral ,coronary and pulmonary vascular beds regardless of how aggressive therapy may be .[Noble and St-Amand1993] References Kozelj M. Novak-Antolic Z. Grad A. Peternel P. Patent foramen ovale as a potential cause of paradoxical embolism in the postpartum period. European Journal of Obstetrics, Gynecology, & Reproductive Biology. 84(1):55-7, 1999 May M. Nagar, A. Gratrix, H. O’Beirne, S. Enright Survival following amniotic fluid embolism and cardiac arrest complicated by sub-capsular liver haematoma. International Journal of Obstetric Anesthesia, Volume 14, Issue 1, Pages 62-65 ,2005 Jan Noble WH. St-Amand J. Amniotic fluid embolus. [Review] [53 refs] [Case Reports. Journal Article. Review] Canadian Journal of Anaesthesia. 40(10):971-80, 1993 Oct
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