Travel time and perinatal mortality after emergency caesarean sections: an evaluation of the 2-hour proximity indicator in Sierra Leone.


Journal

BMJ global health
ISSN: 2059-7908
Titre abrégé: BMJ Glob Health
Pays: England
ID NLM: 101685275

Informations de publication

Date de publication:
12 2020
Historique:
received: 09 09 2020
revised: 22 11 2020
accepted: 24 11 2020
entrez: 23 12 2020
pubmed: 24 12 2020
medline: 25 6 2021
Statut: ppublish

Résumé

Longer travel times are associated with increased adverse maternal and perinatal outcomes. Geospatial modelling has been increasingly used to estimate geographic proximity in emergency obstetric care. In this study, we aimed to assess the correlation between modelled and patient-reported travel times and to evaluate its clinical relevance. Women who delivered by caesarean section in nine hospitals were followed up with home visits at 1 month and 1 year. Travel times between the location before the delivery and the facility where caesarean section was performed were estimated, based on two models (model I Ouma The median reported travel time was 60 min, compared with 13 and 34 min estimated by the two models, respectively. The 2-hour access threshold correlated with a patient-reported travel time of 5.7 hours for model I and 1.8 hours for model II. Longer travel times were associated with transport by boat and ambulance, visiting one or two facilities before reaching the final facility, lower education and poverty. Lower perinatal mortality was found both in the group with a reported travel time of 2 hours or less (193 vs 308 per 1000 births, p<0.001) and a modelled travel time of 2 hours or less (model I: 209 vs 344 per 1000 births, p=0.003; model II: 181 vs 319 per 1000 births, p<0.001). The standard model, used to estimate geographical proximity, consistently underestimated the travel time. However, the conservative travel time model corresponded better to patient-reported travel times. The 2-hour threshold as determined by the Lancet Commission on Global Surgery, is clinically relevant with respect to reducing perinatal death, not a clear cut-off.

Identifiants

pubmed: 33355267
pii: bmjgh-2020-003943
doi: 10.1136/bmjgh-2020-003943
pmc: PMC7754652
pii:
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Commentaires et corrections

Type : ErratumIn

Informations de copyright

© Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: None declared.

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Auteurs

Alex J van Duinen (AJ)

Institute of Clinical and Molecular Medicine, Norwegian University of Science and Technology, Trondheim, Norway aalke.j.v.duinen@ntnu.no.
Department of Surgery, St Olav's Hospital, Trondheim University Hospital, Trondheim, Norway.

Håvard A Adde (HA)

Institute of Clinical and Molecular Medicine, Norwegian University of Science and Technology, Trondheim, Norway.

Ola Fredin (O)

Geological Survey of Norway, Trondheim, Norway.
Department of Geography, Norwegian University of Science and Technology, Trondheim, Norway.

Hampus Holmer (H)

Department of Global Public Health, Karolinska Institutet, Stockholm, Sweden.

Lars Hagander (L)

Centre for Surgery and Public Health, Clinical Sciences Lund, Skåne University Hospital, Lund University, Lund, Sweden.

Alimamy P Koroma (AP)

Ministry of Health and Sanitation, Freetown, Sierra Leone.
Department of Obstetrics and Gynaecology, Princess Christian Maternity Hospital (PCMH), University Teaching Hospitals Complex, University of Sierra Leone, Freetown, Sierra Leone.

Michael M Koroma (MM)

Ministry of Health and Sanitation, Freetown, Sierra Leone.
Department of Obstetrics and Gynaecology, Princess Christian Maternity Hospital (PCMH), University Teaching Hospitals Complex, University of Sierra Leone, Freetown, Sierra Leone.

Andrew Jm Leather (AJ)

King's Centre for Global Health & Health Partnerships, King's College London, London, UK.

Arne Wibe (A)

Institute of Clinical and Molecular Medicine, Norwegian University of Science and Technology, Trondheim, Norway.
Department of Surgery, St Olav's Hospital, Trondheim University Hospital, Trondheim, Norway.

Håkon A Bolkan (HA)

Institute of Clinical and Molecular Medicine, Norwegian University of Science and Technology, Trondheim, Norway.
Department of Surgery, St Olav's Hospital, Trondheim University Hospital, Trondheim, Norway.

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