TY - JOUR
T1 - Clinical pneumonia in the hospitalised child in Malawi in the post-pneumococcal conjugate vaccine era
T2 - A prospective hospital-based observational study
AU - Iroh Tam, Pui Ying
AU - Chirombo, James
AU - Henrion, Marc
AU - Newberry, Laura
AU - Mambule, Ivan
AU - Everett, Dean
AU - Mwansambo, Charles
AU - Cunliffe, Nigel
AU - French, Neil
AU - Heyderman, Robert S.
AU - Bar-Zeev, Naor
N1 - Funding Information:
Competing interests PI has received investigator-initiated research grant support from Bill & Melinda Gates Foundation outside the scope of this work; NC has received research grant support and honoraria for participation in rotavirus vaccine advisory board meetings from GlaxoSmithKline Biologicals and from Takeda Pharmaceuticals outside the scope of this work; NF has received investigator-initiated research grant support from GlaxoSmithKline Biologicals and from Takeda Pharmaceuticals outside the scope of this work. NBZ has received investigator-initiated research grant support from GlaxoSmithKline Biologicals, Takeda Pharmaceuticals, Merck-Sharpe-Dohme and the Serum Institute of India, all outside the scope of this work. All other authors declare that they have no financial disclosures or competing interests.
Funding Information:
Funding This work was supported by the CDC through a cooperative agreement (grant 5U01CK000146-04), Wellcome Trust Programme Grant (Grant number 091909/Z/10/Z) and the MLW Programme Core Award (Grant 206454) from the Wellcome Trust.
Publisher Copyright:
© 2022 BMJ Publishing Group. All rights reserved.
PY - 2022/2/8
Y1 - 2022/2/8
N2 - Objective Assess characteristics of clinical pneumonia after introduction of pneumococcal conjugate vaccine (PCV), by HIV exposure status, in children hospitalised in a governmental hospital in Malawi. Methods and findings We evaluated 1139 children ≤5 years old hospitalised with clinical pneumonia: 101 HIV-exposed, uninfected (HEU) and 1038 HIV-unexposed, uninfected (HUU). Median age was 11 months (IQR 6-20), 59% were male, median mid-upper arm circumference (MUAC) was 14 cm (IQR 13-15) and mean weight-for-height z score was -0.7 (±2.5). The highest Respiratory Index of Severity in Children (RISC) scores were allocated to 10.4% of the overall cohort. Only 45.7% had fever, and 37.2% had at least one danger sign at presentation. The most common clinical features were crackles (54.7%), nasal flaring (53.5%) and lower chest wall indrawing (53.2%). Compared with HUU, HEU children were significantly younger (9 months vs 11 months), with lower mean birth weight (2.8 kg vs 3.0 kg) and MUAC (13.6 cm vs 14.0 cm), had higher prevalence of vomiting (32.7% vs 22.0%), tachypnoea (68.4% vs 49.8%) and highest RISC scores (20.0% vs 9.4%). Five children died (0.4%). However, clinical outcomes were similar for both groups. Conclusions In this post-PCV setting where prevalence of HIV and malnutrition is high, children hospitalised fulfilling the WHO Integrated Management of Childhood Illness criteria for clinical pneumonia present with heterogeneous features. These vary by HIV exposure status but this does not influence either the frequency of danger signs or mortality. The poor performance of available severity scores in this population and the absence of more specific diagnostics hinder appropriate antimicrobial stewardship and the rational application of other interventions.
AB - Objective Assess characteristics of clinical pneumonia after introduction of pneumococcal conjugate vaccine (PCV), by HIV exposure status, in children hospitalised in a governmental hospital in Malawi. Methods and findings We evaluated 1139 children ≤5 years old hospitalised with clinical pneumonia: 101 HIV-exposed, uninfected (HEU) and 1038 HIV-unexposed, uninfected (HUU). Median age was 11 months (IQR 6-20), 59% were male, median mid-upper arm circumference (MUAC) was 14 cm (IQR 13-15) and mean weight-for-height z score was -0.7 (±2.5). The highest Respiratory Index of Severity in Children (RISC) scores were allocated to 10.4% of the overall cohort. Only 45.7% had fever, and 37.2% had at least one danger sign at presentation. The most common clinical features were crackles (54.7%), nasal flaring (53.5%) and lower chest wall indrawing (53.2%). Compared with HUU, HEU children were significantly younger (9 months vs 11 months), with lower mean birth weight (2.8 kg vs 3.0 kg) and MUAC (13.6 cm vs 14.0 cm), had higher prevalence of vomiting (32.7% vs 22.0%), tachypnoea (68.4% vs 49.8%) and highest RISC scores (20.0% vs 9.4%). Five children died (0.4%). However, clinical outcomes were similar for both groups. Conclusions In this post-PCV setting where prevalence of HIV and malnutrition is high, children hospitalised fulfilling the WHO Integrated Management of Childhood Illness criteria for clinical pneumonia present with heterogeneous features. These vary by HIV exposure status but this does not influence either the frequency of danger signs or mortality. The poor performance of available severity scores in this population and the absence of more specific diagnostics hinder appropriate antimicrobial stewardship and the rational application of other interventions.
KW - epidemiology
KW - paediatric infectious disease & immunisation
KW - respiratory infections
UR - http://www.scopus.com/inward/record.url?scp=85124262989&partnerID=8YFLogxK
U2 - 10.1136/bmjopen-2021-050188
DO - 10.1136/bmjopen-2021-050188
M3 - Article
C2 - 35135765
AN - SCOPUS:85124262989
SN - 2044-6055
VL - 12
JO - BMJ Open
JF - BMJ Open
IS - 2
M1 - e050188
ER -