TY - JOUR
T1 - Inpatient versus outpatient management of young infants with a single low-mortality-risk sign of possible serious bacterial infection in sub-Saharan Africa and south Asia
T2 - an open-label, multicentre, two-arm, randomised controlled trial
AU - PSBI Study Group
AU - Baqui, Abdullah H.
AU - Shahidullah, Mohammod
AU - Ahmed, Salahuddin
AU - Roy, Arunangshu Dutta
AU - Khanam, Rasheda
AU - Chowdhury, Nabidul Haque
AU - Lipi, Sabina Ashrafee
AU - Islam, Md Jahurul
AU - Ali, Manajjir
AU - Mekasha, Amha
AU - Estifanos, Abiy Seifu
AU - Muhe, Lulu
AU - Hailemariam, Damen
AU - Keraga, Dorka Woldesenbet
AU - Azeze, Tabot Keskis
AU - Worku, Bogale
AU - Jebessa, Solome
AU - Rongsen-Chandola, Temsunaro
AU - Goyal, Nidhi
AU - Kumar, Amit
AU - Bhandari, Nita
AU - Natchu, Uma Chandra Mouli
AU - Gupta, Manisha
AU - Guha, Aritra
AU - Kaushik, Shayam
AU - Kumar, Surjeet
AU - Jain, Amitabh
AU - Sood, Mangla
AU - Sharma, Rakesh
AU - Dalal, Jagjit Singh
AU - Mittal, Kundan
AU - Kaushal, G. P.
AU - Wadhwa, Vineeta
AU - Seth, Anju
AU - Singh, Varinder
AU - Pemde, Harish
AU - Kumar, Praveen
AU - Chhapola, Viswas
AU - Rao, Yashwant Kumar
AU - Arya, Arun Kumar
AU - Dokania, Krishna Kumar
AU - Prakash, Ved
AU - Singh, Shakal Narayan
AU - Kumar, Neeraj
AU - Kumar, Shiv
AU - Singh, Vinay Pratap
AU - Singh, Pramod Kumar
AU - Jehan, Fyezah
AU - Nisar, Imran
AU - Baloch, Benazir
N1 - Publisher Copyright:
© 2025 The Author(s). Published by Elsevier Ltd. This is an open access article under the CC BY license. http://creativecommons.org/licenses/by/4.0/
PY - 2025/11
Y1 - 2025/11
N2 - Background: Research has shown low mortality in young infants with a single low-mortality-risk possible serious bacterial infection (PSBI) sign. Outpatient treatment of young infants (age <2 months) with a single low-mortality-risk PSBI sign might be as effective and safe as hospitalisation. Outpatient treatment overcomes the challenges of hospitalisation and improves access in low-resource settings. Our aim was to assess clinical outcomes in patients with one low-mortality-risk PSBI sign treated as outpatients compared with inpatient treatment. Methods: We did an open-label, multicentre, two-arm, randomised controlled trial at seven sites across Bangladesh, Ethiopia, India, Nigeria, Pakistan, and Tanzania. Young infants presenting to study hospitals with one of three low-mortality-risk PSBI signs (ie, fast breathing if age <7 days, body temperature ≥38°C, or severe chest indrawing) were randomly assigned (1:1) to the outpatient treatment group (2-day injectable gentamicin plus 7-day oral amoxicillin) or the inpatient treatment group (7-day injectable ampicillin plus gentamicin, with supportive care). The primary outcome was poor clinical outcome, which was a composite of any one of the following: death, critical illness, signs of other serious infections, new PSBI signs on days 2, 4, 8, and 15 or persistence of the presenting sign on day 8 after randomisation. We evaluated superiority and non-inferiority using the Farrington–Manning score test. The trial is registered with the ISRCTN Registry (ISRCTN44033252). Findings: Between June 24, 2021, and April 26, 2024, 7001 young infants were enrolled and randomly assigned to the outpatient treatment group (n=3501) or the inpatient treatment group (n=3500), and were part of the intention-to-treat (ITT) population. Poor clinical outcomes occurred in 269 (7·7%) of 3501 outpatients and 272 (7·8%) of 3500 inpatients in the ITT analysis (risk difference –0·0009 [95% CI –0·0134 to 0·0116]; p=1·0000 for superiority analysis). Deaths were significantly lower in the outpatient group (nine [0·3%] of 3501) than in the inpatient group (23 [0·7%] of 3500; risk difference –0·0040 [–0·0072 to –0·0008]). In the per-protocol analysis, outpatient treatment (266 [7·7%] of 3455) was non-inferior to inpatient treatment (269 [7·9%] of 3416) for poor clinical outcomes (risk difference –0·0018 [–0·0144 to 0·0109]; p=0·0012 for non-inferiority). Apart from deaths, there were no treatment-related serious adverse events. Interpretation: Outpatient treatment (gentamicin injection and oral amoxicillin) for infants with a single low-mortality-risk PSBI sign was non-inferior to standard inpatient treatment, with significantly lower mortality in the outpatient treatment group. Funding: Bill and Melinda Gates Foundation.
AB - Background: Research has shown low mortality in young infants with a single low-mortality-risk possible serious bacterial infection (PSBI) sign. Outpatient treatment of young infants (age <2 months) with a single low-mortality-risk PSBI sign might be as effective and safe as hospitalisation. Outpatient treatment overcomes the challenges of hospitalisation and improves access in low-resource settings. Our aim was to assess clinical outcomes in patients with one low-mortality-risk PSBI sign treated as outpatients compared with inpatient treatment. Methods: We did an open-label, multicentre, two-arm, randomised controlled trial at seven sites across Bangladesh, Ethiopia, India, Nigeria, Pakistan, and Tanzania. Young infants presenting to study hospitals with one of three low-mortality-risk PSBI signs (ie, fast breathing if age <7 days, body temperature ≥38°C, or severe chest indrawing) were randomly assigned (1:1) to the outpatient treatment group (2-day injectable gentamicin plus 7-day oral amoxicillin) or the inpatient treatment group (7-day injectable ampicillin plus gentamicin, with supportive care). The primary outcome was poor clinical outcome, which was a composite of any one of the following: death, critical illness, signs of other serious infections, new PSBI signs on days 2, 4, 8, and 15 or persistence of the presenting sign on day 8 after randomisation. We evaluated superiority and non-inferiority using the Farrington–Manning score test. The trial is registered with the ISRCTN Registry (ISRCTN44033252). Findings: Between June 24, 2021, and April 26, 2024, 7001 young infants were enrolled and randomly assigned to the outpatient treatment group (n=3501) or the inpatient treatment group (n=3500), and were part of the intention-to-treat (ITT) population. Poor clinical outcomes occurred in 269 (7·7%) of 3501 outpatients and 272 (7·8%) of 3500 inpatients in the ITT analysis (risk difference –0·0009 [95% CI –0·0134 to 0·0116]; p=1·0000 for superiority analysis). Deaths were significantly lower in the outpatient group (nine [0·3%] of 3501) than in the inpatient group (23 [0·7%] of 3500; risk difference –0·0040 [–0·0072 to –0·0008]). In the per-protocol analysis, outpatient treatment (266 [7·7%] of 3455) was non-inferior to inpatient treatment (269 [7·9%] of 3416) for poor clinical outcomes (risk difference –0·0018 [–0·0144 to 0·0109]; p=0·0012 for non-inferiority). Apart from deaths, there were no treatment-related serious adverse events. Interpretation: Outpatient treatment (gentamicin injection and oral amoxicillin) for infants with a single low-mortality-risk PSBI sign was non-inferior to standard inpatient treatment, with significantly lower mortality in the outpatient treatment group. Funding: Bill and Melinda Gates Foundation.
UR - https://www.scopus.com/pages/publications/105019113519
U2 - 10.1016/S2214-109X(25)00243-8
DO - 10.1016/S2214-109X(25)00243-8
M3 - Article
C2 - 41109260
AN - SCOPUS:105019113519
SN - 2572-116X
VL - 13
SP - e1892-e1902
JO - The Lancet Global Health
JF - The Lancet Global Health
IS - 11
ER -