Anesthesia Management in a case of Patent Ductus Arteriosus with Eisenmengerisation undergoing a Caesarean Section

摘要

Eisenmengers Syndrome consists of pulmonary hypertension and a right-to-left or bidirectional shunt with peripheral cyanosis. The shunt may be atrial, ventricular, or aortopulmonary. It is commonly found with left to right shunt reversal during end stages of PDA, VSD, and ASD. The presence of Eisenmengers syndrome places the pregnant patient at a high risk for maternal and neonatal mortality. The associated high pulmonary artery pressure with fixed vascular resistance are not reversed surgically. The prognosis of the same being dependent on the pulmonary hypertension. We discuss a case management of a primigravida with PDA and Eisenmengerisation in 28 weeks of gestation presenting with breathlessness. Introduction In 1897 Victor Eisenmenger coined the term Eisenmenger complex which included large VSD and pulmonary hypertension. 1 Wood redefined this in 1958 as pulmonary hypertension with reversed or bidirectional shunt, associated with septal defects or patent ductus arteriosus. Eisenmenger's syndrome is associated with high maternal mortality (30-36%) and high foetal wastage. 2 We describe successful management of a patient with this syndrome undergoing caesarean section. Case Report A 20 year old primigravida weighing 45kg in 27weeks of gestation presented with complaints of dyspnea on exertion. She had been hospitalized in the past for breathlessness and URTI at 8 years of age and was diagnosed case of Non cyanotic heart disease with PDA with left to right shunt. She was treated with Digoxin, Lasix and syrup Kesol. Now she was a registered ANC patient with regular check ups and Inj. Penidura prophylaxis taken. She was apparently alright for the first 20 weeks of pregnancy when she started feeling breathlessness and easy fatigability. Gradually the dyspnoea had progressed from Grade 1 to Grade 3 with bluish discolouration of toes. On examination, she had differential cyanosis and Grade 2 clubbing. There were no signs of raised JVP or pedal oedema. Auscultation of the chest revealed a Loud P2 and ejection systolic murmur at pulmonary area. Systolic murmur in tricuspid area. ECG revealed right axis deviation and right ventricular hypertrophy. The two dimensional echocardiography was called for and showed a large PDA measuring 7 mm and 10mm ampulla. Systolic Right to Left flow and minimal diastolic Left to Right flow with moderate to severe pulmonary hypertension and a bi-directional shunt. Pulmonary arterial systolic pressure (PASP)-120 mm Hg. Grade II-III TR. Mild RA ,RV dilatation, normal biventricular function. USG abdomen revealed IUGR. Patient was advised bed rest, oxygen therapy by ventimask and given digoxin O.25 mg and T.lasix 40Mg OD. The patient progressively worsened as her pregnancy advanced and became dyspnoeic at rest.An elective caesarean section was therefore planned at 28 weeks.Her haemoglobin was 14.6 gm% and haematocrit was 39.1% . Bleeding time (BT) 1min 15secs. Clotting time(CT) 3mins. Biochemistry was within normal limits. Arterial blood gas on room air revealed pH 7.45, PaO2 65mmHg, PaCO2 30 mmHg, SaO2 88%. She was premedicated with ranitidine 50 mg and metoclopromide 10 mg intravenously. Prophylactic antibiotics were given. On being taken to the OT, routine monitoring initiated included 3 lead ECG, SaO2, non-invasive blood pressureand hourly urine output. Under local anaesthesia, left radial artery and right cubital vein for CVP monitoring were cannulated ; peripheral venous access with 18 G cannula taken on the left hand dorsum . Her baseline BP was 110/76, heart rate was 86/ min & CVP was 8 mmHg. Initial oxygen saturation on room air 88% improved to 96% with oxygen at 8 L/min through a facemask with partial rebreathing reservoir bag. Under all aseptic precautions, after local infiltration, an epidural catheter was passed at L2-L3 level by loss of resistance technique and was fixed at 10cms. After a test dose, 8 cc of 0.5% bupivacaine, 7 cc of 2% Lignocaine and 25 micrograms Fentanyl was given slowly.