MANAGEMENT OF PERINATAL ASPHYXIA

 

DR.RHISHIKESH THAKRE.

DM (Neonatology), MD, DNB (Ped), DcH, FCPS.

 

Perinatal asphyxia is one of the leading causes on neonatal morbidity and mortality in our country. A scientific and rationale approach to its management is therefore necessary to have any impact on the outcome.

A good history and relevant clinical examination is mandatory for optimum care.

History should specifically look at the intra partum events like malpresentation,prolonged labor,difficult labor,meconium passage,antepartum haemorrhage,non reassuring fetal heart rate patterns on intrapartum monitoring,and obstetric accidents.In some conditions asphyxia would set in inspite of no identifiable risk factors and then conditions like cord compression,cord prolapse,neuromuscular disorders,maternal medications,congenital malformations  and maternal hypothyroidism should be looked for specifically.

 Clinical examination by itself can give clue to the aetiology of asphyxia like - Meconium staining (MAS) ,large baby (difficult labor),evidence of caput (prolonged second stage),SGA (intrauterine asphyxia),depressed baby (drugs,neuromuscular disorder),bruises(difficult / traumatic labor),anemia(antepartum haemorrhage),polycythemia (SGA,precipitate labor)and dysmorphism

(occult anomalies).

 

BASIC CARE :

Should be a daily routine in the management of all these babies -

1.Strict asepsis.

2,Ensure neutral thermal environment.

3.Monitor vital parameters – HR,RR,BP,and Pulse Oximetry.

4.Urine output.

5.Daily weight.

6.Nutrition.

           

ANTICIPATION IS THE KEY TO THE MANAGEMENT.

 

TIMETABLE OF COMPLICATIONS IN ASPHYXIA:

 

1.Seizures – First 48 hours.Severe the asphyxial insult early is the onset and refractory are the seizures.

2.Oliguria – Eight hours and after, on maintenance IV fluids.Severe the insult and prolonged the insult longer is the renal damage.

3.Hypoglycemia – Nadir of blood glucose physiologically takes place by 2 hours postnatally and in conditions like asphyxia the onset is likely to be early .The best predictor of its occurrence would be therefore cord blood glucose .A  high value is a predictor of early  rebound hypoglycemia in the neonate.

4.Hypocalcemia – After 72 hours unless complicated by associated conditions like maternal diabetes,maternal hyperparathyroidism etc.

5.Shock –Timing  depends on the aetiology.Hypovolumic shock is seen in labor room due to obstetric accidents,cardiogenic shock usually after  6 hours but more so by the underlying severtity of the asphyxial insult , septic shock usually after first 6 hours depending upon the infection severity, and rarely neurogenic shock after 72 hours in stage 3 HIE.

6.Hematological complications – Intra partum asphyxia ,meconium passage,preeclampsia cause neutropenia which is self limitng and lasts for not more than 24 hours thus mimicking sepsis.Anemia and polycythemia usually is determined by the obstetric events.Thrombo

cytopenia sets in by 24 hours and is usually associated with bone marrow depression. DIC occurs  as a terminal event in the course of asphyxia.

7.Electrolyte imbalance – Hyponatremia is usually due to SIADH and manifests by 24 hrs.Hyperkalemia is due to renal impairment and usually seen by 36 hrs.Critical evaluation of fluid administered is therefore important.

8.HIE – Occurrence is determined by timing of asphyxia,its severity, and its duration.If 48 hours have passed and no neurological signs have appeared its unlikely to occur thereafter.

 

 

 

 

 

Manangement of seizures –

 

1.Need for intubation,cardiac massage,and administration of drugs in labor room are the singlemost markers to predict early occurrence of seizures.Persistent low apgar scores at 5 mts or more,cord blood ph < 7 are good objective markers .

2.Basic evaluation should include review of maternal drugs,blood glucose, serum calcium and serum electrolytes. Further evaluation is based on clinical suspicion.

3.Seizures in asphyxia usually die down or burn themselves by 48 hours. Not all seizures require treatment. Onlylif seizures are more than 3 in a hour or lasting for 3 mts  or more they warrant anticonvulant.There is no role of prophylactic anticonvulant therapy in asphyxia.Phenobarbitone,Phenytoin,initially by loading dose followed by maintenance dose are the first line drugs.Concomitant evaluation and correction for treatable causes like hypoglycemia,hypocalcemia,hypomagnesemia,and pyridoxine deficiency is required.

4.Radiological evaluation is required only in intractable seizures where metabolic workup is negative.

5.In refractory seizures use of drip of midazolam,lorazepam or diazepam may be required. Role of sodium valproate is occasional. Use of newer anticonvulants like lamotrigene,clobazam,gabapentin etc is not well known in neonates.

 

 

Management of renal failure.

 

1.Urine output is by itself not a reliable marker of renal insufficiency hence renal parameters need to be monitored.

2.Fluid restriction is required once intrinsic renal failure sets in. A careful evaluation of electrolytes would direct the fluid management.

3.Daily monitoring of urine output, urine specific gravity, and body weight are adjuvant to basic care.

4.Rarely peritoneal dialysis is required in case of persistent oliguria.

 

Management of metabolic derangement –

 

1.Hypoglycemia needs to be corrected by 10 % D.Only if it is  symptomatic it warrants a bolus otherwise in asymptomatic cases maintenance infusion is all that is required.Ensure drip infusion rate preferably by infusion pump.

2.Only symptomatic hypocalcemia needs correction.Evaluate for hypomagnesemia in case of persistent hypocalcemia.

3.Hyponatremia should be anticipated and prevented by restricted fluid  administration.

 

Management of shock –

 

1.Hypovolumic shock needs  replacement with fluids, plasma, or blood.Isolated diastolic shock is the earliest marker of impending shock.Unexplained tachycardia is a good bedside clue.

2.Cardiogenic shock warrants use of pressors like dopamine

and / or dobutamine. In case of refractory shock inspite of use of pressors of 20 microgram/kg/mt steroids may be tried.

3.Role of CVP to determine the cause of shock is not routinely done or advocated,

4.Septic shock should be suspected based on intrapartum risk factors for sepsis, core axillary mismatch and results of sepsis screen.

 

 

 Clinical predictors of poor outcome –

1.Refractory seizures.

2.Neurological defecit at the end of first week.

3.HIE stage 3 at the time of discharge.

 

KEY POINTS :

1.Anticipation is the key in prevention and management of asphyxia.

2.The manifestations are determined by the timing,severity and duration of asphyxia.