Background Necropsy studies from Africa have shown that Pneumocystis carini
i pneumonia (PCP) is common in infants with HIV infection. We aimed to desc
ribe the rate, clinical presentation, and outcome of PCP in young Malawian
children with acute severe pneumonia.
Methods Children aged between 2 months and 5 years who were in hospital wit
h a diagnosis of severe pneumonia were admitted to a study ward for clinica
l monitoring. We carried out blood culture, immunofluorescence on nasophary
ngeal aspirate samples to test for PCP, polymerase chain reaction to detect
HIV, and chest radiography.
Findings 16 cases of PCP were identified among 150 children With radiologic
ally confirmed severe pneumonia. All were HIV-positive and younger than 6 m
onths. 21 children had bacterial pneumonia (including one who was also PCP
positive) and 114 were not confirmed. The most common bacterial pathogens a
mong children without PCP were Streptococcus pneumoniae (eight) and non-typ
hoidal salmonellae (seven). On admission, children with confirmed PCP had a
lower mean age, body temperature, and oxygen saturation than children with
bacterial pneumonia and were less likely to have a focal abnormality on au
scultation. Oxygen requirements were much greater in children with PCP than
those with bacterial pneumonias (96 of 105 hospital days vs 15 of 94, p<0.
0001). Ten of 16 children with PCP and six of 21 with bacterial pneumonia d
ied (relative risk 2.19 [95%. CI 1.0-4.7]). The overall case-fatality rate
of severe pneumonia was 22%, In addition to a strong association with PCP,
a fatal outcome was significantly and independently associated with HIV inf
ection (2.98 [1.1-7.9]) and with age under 6 months (2.76 [1.0-5.2]).
Interpretation PCP is common and contributes to the high mortality from pne
umonia in Malawian infants, Clinical features are helpful in diagnosis. The
study highlights the impact of HIV infection and difficult issues of manag
ement in countries with few resources.