Retrospective study on the usefulness of pulse oximetry for the identification of young children with severe illnesses and severe pneumonia in a rural outpatient clinic of Papua New Guinea.
Ambulatory Care
/ methods
Child, Preschool
Community Health Centers
/ organization & administration
Feasibility Studies
Female
Health Plan Implementation
/ organization & administration
Humans
Hypoxia
/ diagnosis
Infant
Male
Oximetry
Papua New Guinea
Pneumonia
/ complications
Randomized Controlled Trials as Topic
Retrospective Studies
Rural Health Services
/ organization & administration
Severity of Illness Index
Journal
PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081
Informations de publication
Date de publication:
2019
2019
Historique:
received:
16
12
2018
accepted:
04
03
2019
entrez:
16
4
2019
pubmed:
16
4
2019
medline:
1
1
2020
Statut:
epublish
Résumé
This secondary analysis of data of a randomized controlled trial (RCT) retrospectively investigated the performance of pulse oximetry in identifying children with severe illnesses, with and without respiratory signs/symptoms, in a cohort of children followed for morbid episodes in an intervention trial assessing the efficacy of Intermittent Preventive Treatment for malaria in infants (IPTi) in Papua New Guinea (PNG) from June 2006 to May 2010. The IPTi study was conducted in a paediatric population visiting two health centres on the north coast of PNG in the Mugil area of the Sumkar District. A total of 669 children visited the clinic and a total of 1921 illness episodes were recorded. Inclusion criteria were: age between 3 and 27 months, full clinical record (signs/symptoms) and pulse oximetry used systematically to assess sick children at all visits. Children were excluded if they visited the clinic in the previous 14 days. The outcome measures were severe illness, severe pneumonia, pneumonia, defined by the Integrated Management of Childhood Illness (IMCI) definitions, and hospitalization. Out of 1921 illness episodes, 1663 fulfilled the inclusion criteria. A total of 139 severe illnesses were identified, of which 93 were severe pneumonia. The ROC curves of pulse oximetry (continuous variable) showed an AUC of 0.63, 0.68 and 0.65 for prediction of severe illness, severe pneumonia and hospitalization, respectively. Pulse oximetry allowed better discrimination between severe and non-severe illness, severe and non-severe pneumonia, admitted and non-admitted patients, in children ≤12-months of age relative to older patients. For the threshold of peripheral arterial oxygen saturation ≤ 94% measured by pulse oximetry (SpO2), unadjusted odds ratios for severe illness, severe pneumonia and hospitalization were 6.1 (95% Confidence Interval (CI) 3.9-9.8), 8.5 (4.9-14.6) and 5.9 (3.4-10.3), respectively. Pulse oximetry was helpful in identifying children with severe illness in outpatient facilities in PNG. A SpO2 of 94% seems the most discriminative threshold. Considering its affordability and ease of use, pulse oximetry could be a valuable additional tool assisting the decision to admit for treatment.
Identifiants
pubmed: 30986206
doi: 10.1371/journal.pone.0213937
pii: PONE-D-18-35884
pmc: PMC6464326
doi:
Types de publication
Journal Article
Multicenter Study
Observational Study
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
e0213937Déclaration de conflit d'intérêts
The authors declared that no competing interests exist.
Références
PLoS One. 2014 Mar 13;9(3):e90990
pubmed: 24626194
Int J Tuberc Lung Dis. 2011 Mar;15(3):317-25
pubmed: 21333097
Bull World Health Organ. 2016 Dec 1;94(12):893-902
pubmed: 27994282
Thorax. 2011 Oct;66 Suppl 2:ii1-23
pubmed: 21903691
BMJ Open. 2016 Aug 17;6(8):e011094
pubmed: 27534987
Bull World Health Organ. 2009 Apr;87(4):263-70
pubmed: 19551234
PLoS One. 2015 Sep 15;10(9):e0136166
pubmed: 26372640
Ann Trop Paediatr. 2005 Mar;25(1):23-7
pubmed: 15814045
Paediatr Int Child Health. 2015 Feb;35(1):65-8
pubmed: 25547179
Arch Pediatr Adolesc Med. 1995 Nov;149(11):1259-63
pubmed: 7581759
Arch Dis Child. 2016 Aug;101(8):694-700
pubmed: 26699537
BMJ. 1999 Jan 9;318(7176):86-91
pubmed: 9880280
PLoS One. 2015 Nov 18;10(11):e0143213
pubmed: 26580403
BMJ. 1993 Mar 6;306(6878):612-5
pubmed: 8369033
World J Pediatr. 2012 Aug;8(3):247-51
pubmed: 22886198
Radiology. 1982 Apr;143(1):29-36
pubmed: 7063747
Lancet Infect Dis. 2017 Nov;17(11):1133-1161
pubmed: 28843578
Arch Dis Child. 2002 Feb;86(2):108-12
pubmed: 11827904
Lancet Infect Dis. 2015 Apr;15(4):439-50
pubmed: 25769269
J Trop Pediatr. 2017 Oct 1;63(5):402-413
pubmed: 28158795
J Trop Pediatr. 2006 Oct;52(5):307-10
pubmed: 16943216
Lancet Infect Dis. 2009 Apr;9(4):219-27
pubmed: 19324294
PLoS Med. 2012;9(3):e1001195
pubmed: 22479155