Transfusion Associated
Malaria
Dr Prakash. I
NICU
Maternal history
 B/O ABC, 2nd of triplets
 32 yrs. old, P0+0,Booked,PH national
 HIV, HBsAg-Neg, VDRL-Non reactive, Rubella-
Immune
 Blood gr - O +ve
 Non consanguineous
Maternal history
GDM-Controlled by diet
MSU-no growth, HVS-E. Coli
h/o PPROM-24 hrs, treated
Betamethasone given- 2 doses
ANSS- 3 independent sacs, 1st triplets with
oligohydramnious
Birth history
 Emergency LSCS
 Apgar score: 1’-6 and 5’-8
 Cried after birth
 Intubated in view of weak respiratory effort
Parameters in NICU
 Birth weight- 930 gm (50th centile)
 HC-24.5 cm (10th centile)
 Temp-36.4’C ,HR-150/min
 RR-45/min with nasal flaring and recession
 BP-47/18, MAP-29 mmHg
Examination
 Pink, good perfusion
 Respiratory: B/L equal air entry, recessions
present
 CVS:S1,S2 normal, No murmur
 Abdomen: soft, normal female genitalia
 CNS: anterior fontanels at level, no abnormal
movements
In NICU
 Respiratory support-24 days + 15 days
(invasive/non invasive)
 Chest X ray – RDS
 Surfactant- 2 doses
 IV antibiotics : 7 days (clinical grounds)
 CVS- ?PDA
 ECHO: moderate size PDA, no volume overload,
Mild pulmonary hypertension
 CNS- Normal for age
 Clinical jaundice: phototherapy (4days)
 Feeding: stared on day 2 →day 25. Intermittent
feed intolerance
 Day 11: packed RBC (as per the NICU guideline)
On day 39
 The baby was on full oral feeds
 On neoblend with low parameters
 Setback:
 Frequent apnea
 temperature instability
 bradycardia and desaturations
 Respiratory support- 12 days (invasive /non invasive)
 Chest X ray: para hilar and upper zonal haziness noted
 Septic screening : ↑ CRP (>100)  WBC,  platelets  Hb
Management
 PRBC and FFP
 PRBC: D11, D15, D39, D40, D42 =5
Platelet transfusion: D39, D40, D41 (total – 6)
 IV antibiotics -10 days.
 Blood smear (D 39) : positive for malaria parasite
 P. vivax ring form, gametocytes, schizonts and trophozoites
 Oral chloroquine and primaquin was given
 Repeat blood smear done after 7 days was negative
for malarial parasite.
 Retrospectively maternal history was reviewed
in detail (The history was non-significant ):
 Non-Endemic region
 No H/O of Blood product transfusion
 No H/O fever or malaria
 Blood bank was informed
Incident report
 Transfusion history for the last 2 mo of the patient
 Both donors were tested for malaria in the pre-transfusion screening and both
showed negative for malaria Ag
 Both donors was called for a repeat sample but both are unavailable
Transfusion
date
Donor Tested for
malaria Ag
Result
14/01/15 A Yes Neg
18/01/15 B Yes Neg
11/02/15 C Yes Neg
14/02/15 D Yes Neg
 Transient cholestasis (D39)
 USG abdomen showed
Normal size and echotexture
No intra or extra hepatic cholestasis
GB collapsed
On discharge: Baby is well, on full oral feeds,
stable and gaining weight

Morbidity (1)

  • 1.
  • 2.
    Maternal history  B/OABC, 2nd of triplets  32 yrs. old, P0+0,Booked,PH national  HIV, HBsAg-Neg, VDRL-Non reactive, Rubella- Immune  Blood gr - O +ve  Non consanguineous
  • 3.
    Maternal history GDM-Controlled bydiet MSU-no growth, HVS-E. Coli h/o PPROM-24 hrs, treated Betamethasone given- 2 doses ANSS- 3 independent sacs, 1st triplets with oligohydramnious
  • 4.
    Birth history  EmergencyLSCS  Apgar score: 1’-6 and 5’-8  Cried after birth  Intubated in view of weak respiratory effort
  • 5.
    Parameters in NICU Birth weight- 930 gm (50th centile)  HC-24.5 cm (10th centile)  Temp-36.4’C ,HR-150/min  RR-45/min with nasal flaring and recession  BP-47/18, MAP-29 mmHg
  • 6.
    Examination  Pink, goodperfusion  Respiratory: B/L equal air entry, recessions present  CVS:S1,S2 normal, No murmur  Abdomen: soft, normal female genitalia  CNS: anterior fontanels at level, no abnormal movements
  • 7.
    In NICU  Respiratorysupport-24 days + 15 days (invasive/non invasive)  Chest X ray – RDS  Surfactant- 2 doses  IV antibiotics : 7 days (clinical grounds)  CVS- ?PDA  ECHO: moderate size PDA, no volume overload, Mild pulmonary hypertension
  • 8.
     CNS- Normalfor age  Clinical jaundice: phototherapy (4days)  Feeding: stared on day 2 →day 25. Intermittent feed intolerance  Day 11: packed RBC (as per the NICU guideline)
  • 9.
    On day 39 The baby was on full oral feeds  On neoblend with low parameters  Setback:  Frequent apnea  temperature instability  bradycardia and desaturations  Respiratory support- 12 days (invasive /non invasive)  Chest X ray: para hilar and upper zonal haziness noted  Septic screening : ↑ CRP (>100)  WBC,  platelets  Hb
  • 10.
    Management  PRBC andFFP  PRBC: D11, D15, D39, D40, D42 =5 Platelet transfusion: D39, D40, D41 (total – 6)  IV antibiotics -10 days.  Blood smear (D 39) : positive for malaria parasite  P. vivax ring form, gametocytes, schizonts and trophozoites  Oral chloroquine and primaquin was given  Repeat blood smear done after 7 days was negative for malarial parasite.
  • 11.
     Retrospectively maternalhistory was reviewed in detail (The history was non-significant ):  Non-Endemic region  No H/O of Blood product transfusion  No H/O fever or malaria  Blood bank was informed
  • 12.
    Incident report  Transfusionhistory for the last 2 mo of the patient  Both donors were tested for malaria in the pre-transfusion screening and both showed negative for malaria Ag  Both donors was called for a repeat sample but both are unavailable Transfusion date Donor Tested for malaria Ag Result 14/01/15 A Yes Neg 18/01/15 B Yes Neg 11/02/15 C Yes Neg 14/02/15 D Yes Neg
  • 13.
     Transient cholestasis(D39)  USG abdomen showed Normal size and echotexture No intra or extra hepatic cholestasis GB collapsed On discharge: Baby is well, on full oral feeds, stable and gaining weight