High Frequency of Blackwater Fever Among Children Presenting to Hospital With Severe Febrile Illnesses in Eastern Uganda

Clin Infect Dis. 2017 Apr 1;64(7):939-946. doi: 10.1093/cid/cix003.

Abstract

Background: In the Fluid Expansion as a Supportive Treatment (FEAST) trial, an unexpectedly high proportion of participants from eastern Uganda presented with blackwater fever (BWF).

Methods: We describe the prevalence and outcome of BWF among trial participants and compare the prevalence of 3 malaria-protective red blood cell polymorphisms in BWF cases vs both trial (non-BWF) and population controls.

Results: Of 3170 trial participants, 394 (12.4%) had BWF. The majority (318 [81.0%]) presented in eastern Uganda and were the subjects of further analysis. BWF cases typically presented with both clinical jaundice (254/318 [80%]) and severe anemia (hemoglobin level <5 g/dL) (238/310 [77%]). Plasmodium falciparum parasitemia was less frequent than in non-BWF controls, but a higher proportion were positive for P. falciparum histidine rich protein 2 (192/246 [78.0%]) vs 811/1154 [70.3%]; P = .014), suggesting recent antimalarial treatment. Overall, 282 of 318 (88.7%) received transfusions, with 94 of 282 (33.3%) and 9 of 282 (3.4%) receiving 2 or 3 transfusions, respectively. By day 28, 39 of 318 (12.3%) BWF cases and 154 of 1554 (9.9%) non-BWF controls had died (P = .21), and 7 of 255 (3.0%) vs 13/1212 (1%), respectively, had severe anemia (P = .036). We found no association with G6PD deficiency. The prevalence of both the sickle cell trait (10/218 [4.6%]) and homozygous α+thalassemia (8/216 [3.7%]) were significantly lower among cases than among population controls (334/2123 [15.7%] and 141/2114 [6.6%], respectively), providing further support for the role of malaria.

Conclusions: We report the emergence of BWF in eastern Uganda, a condition that, according to local investigators, was rare until the last 7 years. We speculate that this might relate to the introduction of artemisinin-based combination therapies. Further studies investigating this possibility are urgently required.

Keywords: African child; blackwater fever; haemoglobinopathies; hemoglobinuria; malaria.

MeSH terms

  • Age Factors
  • Biomarkers
  • Blackwater Fever / complications
  • Blackwater Fever / diagnosis*
  • Blackwater Fever / epidemiology*
  • Blackwater Fever / parasitology
  • Child, Preschool
  • Erythrocytes / metabolism
  • Erythrocytes / parasitology
  • Female
  • Glucosephosphate Dehydrogenase / genetics
  • Hemoglobinopathies / complications
  • Hemoglobinopathies / genetics
  • Humans
  • Infant
  • Male
  • Mutation
  • Patient Outcome Assessment
  • Phenotype
  • Polymorphism, Genetic
  • Prevalence
  • Severity of Illness Index
  • Symptom Assessment
  • Uganda / epidemiology
  • Urinalysis

Substances

  • Biomarkers
  • Glucosephosphate Dehydrogenase