Risk factors for community-acquired bacterial infection among young infants in South Asia: a longitudinal cohort study with nested case–control analysis
ObjectiveRisk factors predisposing infants to community-acquired bacterial infections during the first 2 months of life are poorly understood in South Asia. Identifying risk factors for infection could lead to improved preventive measures and antibiotic stewardship.MethodsFive sites in Bangladesh, I...
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| Published in: | BMJ global health Vol. 7; no. 11; p. e009706 |
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| Main Authors: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
| Format: | Journal Article |
| Language: | English |
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England
BMJ Publishing Group Ltd
01.11.2022
BMJ Publishing Group LTD BMJ Publishing Group |
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| ISSN: | 2059-7908, 2059-7908 |
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| Abstract | ObjectiveRisk factors predisposing infants to community-acquired bacterial infections during the first 2 months of life are poorly understood in South Asia. Identifying risk factors for infection could lead to improved preventive measures and antibiotic stewardship.MethodsFive sites in Bangladesh, India and Pakistan enrolled mother–child pairs via population-based pregnancy surveillance by community health workers. Medical, sociodemographic and epidemiological risk factor data were collected. Young infants aged 0–59 days with signs of possible serious bacterial infection (pSBI) and age-matched controls provided blood and respiratory specimens that were analysed by blood culture and real-time PCR. These tests were used to build a Bayesian partial latent class model (PLCM) capable of attributing the probable cause of each infant’s infection in the ANISA study. The collected risk factors from all mother–child pairs were classified and analysed against the PLCM using bivariate and stepwise logistic multivariable regression modelling to determine risk factors of probable bacterial infection.ResultsAmong 63 114 infants born, 14 655 were assessed and 6022 had signs of pSBI; of these, 81% (4859) provided blood samples for culture, 71% (4216) provided blood samples for quantitative PCR (qPCR) and 86% (5209) provided respiratory qPCR samples. Risk factors associated with bacterial-attributed infections included: low (relative risk (RR) 1.73, 95% credible interval (CrI) 1.42 to 2.11) and very low birth weight (RR 5.77, 95% CrI 3.73 to 8.94), male sex (RR 1.27, 95% CrI 1.07 to 1.52), breathing problems at birth (RR 2.50, 95% CrI 1.96 to 3.18), premature rupture of membranes (PROMs) (RR 1.27, 95% CrI 1.03 to 1.58) and being in the lowest three socioeconomic status quintiles (first RR 1.52, 95% CrI 1.07 to 2.16; second RR 1.41, 95% CrI 1.00 to 1.97; third RR 1.42, 95% CrI 1.01 to 1.99).ConclusionDistinct risk factors: birth weight, male sex, breathing problems at birth and PROM were significantly associated with the development of bacterial sepsis across South Asian community settings, supporting refined clinical discernment and targeted use of antimicrobials. |
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| AbstractList | Objective Risk factors predisposing infants to community-acquired bacterial infections during the first 2 months of life are poorly understood in South Asia. Identifying risk factors for infection could lead to improved preventive measures and antibiotic stewardship.Methods Five sites in Bangladesh, India and Pakistan enrolled mother–child pairs via population-based pregnancy surveillance by community health workers. Medical, sociodemographic and epidemiological risk factor data were collected. Young infants aged 0–59 days with signs of possible serious bacterial infection (pSBI) and age-matched controls provided blood and respiratory specimens that were analysed by blood culture and real-time PCR. These tests were used to build a Bayesian partial latent class model (PLCM) capable of attributing the probable cause of each infant’s infection in the ANISA study. The collected risk factors from all mother–child pairs were classified and analysed against the PLCM using bivariate and stepwise logistic multivariable regression modelling to determine risk factors of probable bacterial infection.Results Among 63 114 infants born, 14 655 were assessed and 6022 had signs of pSBI; of these, 81% (4859) provided blood samples for culture, 71% (4216) provided blood samples for quantitative PCR (qPCR) and 86% (5209) provided respiratory qPCR samples. Risk factors associated with bacterial-attributed infections included: low (relative risk (RR) 1.73, 95% credible interval (CrI) 1.42 to 2.11) and very low birth weight (RR 5.77, 95% CrI 3.73 to 8.94), male sex (RR 1.27, 95% CrI 1.07 to 1.52), breathing problems at birth (RR 2.50, 95% CrI 1.96 to 3.18), premature rupture of membranes (PROMs) (RR 1.27, 95% CrI 1.03 to 1.58) and being in the lowest three socioeconomic status quintiles (first RR 1.52, 95% CrI 1.07 to 2.16; second RR 1.41, 95% CrI 1.00 to 1.97; third RR 1.42, 95% CrI 1.01 to 1.99).Conclusion Distinct risk factors: birth weight, male sex, breathing problems at birth and PROM were significantly associated with the development of bacterial sepsis across South Asian community settings, supporting refined clinical discernment and targeted use of antimicrobials. Risk factors predisposing infants to community-acquired bacterial infections during the first 2 months of life are poorly understood in South Asia. Identifying risk factors for infection could lead to improved preventive measures and antibiotic stewardship. Five sites in Bangladesh, India and Pakistan enrolled mother-child pairs via population-based pregnancy surveillance by community health workers. Medical, sociodemographic and epidemiological risk factor data were collected. Young infants aged 0-59 days with signs of possible serious bacterial infection (pSBI) and age-matched controls provided blood and respiratory specimens that were analysed by blood culture and real-time PCR. These tests were used to build a Bayesian partial latent class model (PLCM) capable of attributing the probable cause of each infant's infection in the ANISA study. The collected risk factors from all mother-child pairs were classified and analysed against the PLCM using bivariate and stepwise logistic multivariable regression modelling to determine risk factors of probable bacterial infection. Among 63 114 infants born, 14 655 were assessed and 6022 had signs of pSBI; of these, 81% (4859) provided blood samples for culture, 71% (4216) provided blood samples for quantitative PCR (qPCR) and 86% (5209) provided respiratory qPCR samples. Risk factors associated with bacterial-attributed infections included: low (relative risk (RR) 1.73, 95% credible interval (CrI) 1.42 to 2.11) and very low birth weight (RR 5.77, 95% CrI 3.73 to 8.94), male sex (RR 1.27, 95% CrI 1.07 to 1.52), breathing problems at birth (RR 2.50, 95% CrI 1.96 to 3.18), premature rupture of membranes (PROMs) (RR 1.27, 95% CrI 1.03 to 1.58) and being in the lowest three socioeconomic status quintiles (first RR 1.52, 95% CrI 1.07 to 2.16; second RR 1.41, 95% CrI 1.00 to 1.97; third RR 1.42, 95% CrI 1.01 to 1.99). Distinct risk factors: birth weight, male sex, breathing problems at birth and PROM were significantly associated with the development of bacterial sepsis across South Asian community settings, supporting refined clinical discernment and targeted use of antimicrobials. ObjectiveRisk factors predisposing infants to community-acquired bacterial infections during the first 2 months of life are poorly understood in South Asia. Identifying risk factors for infection could lead to improved preventive measures and antibiotic stewardship.MethodsFive sites in Bangladesh, India and Pakistan enrolled mother–child pairs via population-based pregnancy surveillance by community health workers. Medical, sociodemographic and epidemiological risk factor data were collected. Young infants aged 0–59 days with signs of possible serious bacterial infection (pSBI) and age-matched controls provided blood and respiratory specimens that were analysed by blood culture and real-time PCR. These tests were used to build a Bayesian partial latent class model (PLCM) capable of attributing the probable cause of each infant’s infection in the ANISA study. The collected risk factors from all mother–child pairs were classified and analysed against the PLCM using bivariate and stepwise logistic multivariable regression modelling to determine risk factors of probable bacterial infection.ResultsAmong 63 114 infants born, 14 655 were assessed and 6022 had signs of pSBI; of these, 81% (4859) provided blood samples for culture, 71% (4216) provided blood samples for quantitative PCR (qPCR) and 86% (5209) provided respiratory qPCR samples. Risk factors associated with bacterial-attributed infections included: low (relative risk (RR) 1.73, 95% credible interval (CrI) 1.42 to 2.11) and very low birth weight (RR 5.77, 95% CrI 3.73 to 8.94), male sex (RR 1.27, 95% CrI 1.07 to 1.52), breathing problems at birth (RR 2.50, 95% CrI 1.96 to 3.18), premature rupture of membranes (PROMs) (RR 1.27, 95% CrI 1.03 to 1.58) and being in the lowest three socioeconomic status quintiles (first RR 1.52, 95% CrI 1.07 to 2.16; second RR 1.41, 95% CrI 1.00 to 1.97; third RR 1.42, 95% CrI 1.01 to 1.99).ConclusionDistinct risk factors: birth weight, male sex, breathing problems at birth and PROM were significantly associated with the development of bacterial sepsis across South Asian community settings, supporting refined clinical discernment and targeted use of antimicrobials. Risk factors predisposing infants to community-acquired bacterial infections during the first 2 months of life are poorly understood in South Asia. Identifying risk factors for infection could lead to improved preventive measures and antibiotic stewardship.OBJECTIVERisk factors predisposing infants to community-acquired bacterial infections during the first 2 months of life are poorly understood in South Asia. Identifying risk factors for infection could lead to improved preventive measures and antibiotic stewardship.Five sites in Bangladesh, India and Pakistan enrolled mother-child pairs via population-based pregnancy surveillance by community health workers. Medical, sociodemographic and epidemiological risk factor data were collected. Young infants aged 0-59 days with signs of possible serious bacterial infection (pSBI) and age-matched controls provided blood and respiratory specimens that were analysed by blood culture and real-time PCR. These tests were used to build a Bayesian partial latent class model (PLCM) capable of attributing the probable cause of each infant's infection in the ANISA study. The collected risk factors from all mother-child pairs were classified and analysed against the PLCM using bivariate and stepwise logistic multivariable regression modelling to determine risk factors of probable bacterial infection.METHODSFive sites in Bangladesh, India and Pakistan enrolled mother-child pairs via population-based pregnancy surveillance by community health workers. Medical, sociodemographic and epidemiological risk factor data were collected. Young infants aged 0-59 days with signs of possible serious bacterial infection (pSBI) and age-matched controls provided blood and respiratory specimens that were analysed by blood culture and real-time PCR. These tests were used to build a Bayesian partial latent class model (PLCM) capable of attributing the probable cause of each infant's infection in the ANISA study. The collected risk factors from all mother-child pairs were classified and analysed against the PLCM using bivariate and stepwise logistic multivariable regression modelling to determine risk factors of probable bacterial infection.Among 63 114 infants born, 14 655 were assessed and 6022 had signs of pSBI; of these, 81% (4859) provided blood samples for culture, 71% (4216) provided blood samples for quantitative PCR (qPCR) and 86% (5209) provided respiratory qPCR samples. Risk factors associated with bacterial-attributed infections included: low (relative risk (RR) 1.73, 95% credible interval (CrI) 1.42 to 2.11) and very low birth weight (RR 5.77, 95% CrI 3.73 to 8.94), male sex (RR 1.27, 95% CrI 1.07 to 1.52), breathing problems at birth (RR 2.50, 95% CrI 1.96 to 3.18), premature rupture of membranes (PROMs) (RR 1.27, 95% CrI 1.03 to 1.58) and being in the lowest three socioeconomic status quintiles (first RR 1.52, 95% CrI 1.07 to 2.16; second RR 1.41, 95% CrI 1.00 to 1.97; third RR 1.42, 95% CrI 1.01 to 1.99).RESULTSAmong 63 114 infants born, 14 655 were assessed and 6022 had signs of pSBI; of these, 81% (4859) provided blood samples for culture, 71% (4216) provided blood samples for quantitative PCR (qPCR) and 86% (5209) provided respiratory qPCR samples. Risk factors associated with bacterial-attributed infections included: low (relative risk (RR) 1.73, 95% credible interval (CrI) 1.42 to 2.11) and very low birth weight (RR 5.77, 95% CrI 3.73 to 8.94), male sex (RR 1.27, 95% CrI 1.07 to 1.52), breathing problems at birth (RR 2.50, 95% CrI 1.96 to 3.18), premature rupture of membranes (PROMs) (RR 1.27, 95% CrI 1.03 to 1.58) and being in the lowest three socioeconomic status quintiles (first RR 1.52, 95% CrI 1.07 to 2.16; second RR 1.41, 95% CrI 1.00 to 1.97; third RR 1.42, 95% CrI 1.01 to 1.99).Distinct risk factors: birth weight, male sex, breathing problems at birth and PROM were significantly associated with the development of bacterial sepsis across South Asian community settings, supporting refined clinical discernment and targeted use of antimicrobials.CONCLUSIONDistinct risk factors: birth weight, male sex, breathing problems at birth and PROM were significantly associated with the development of bacterial sepsis across South Asian community settings, supporting refined clinical discernment and targeted use of antimicrobials. |
| Author | Diaz, Maureen H Hossain, Tanvir Waller, Jessica L Soofi, Sajid Isaac, Rita Baqui, Abdullah H Winchell, Jonas M Mullany, Luke C Weber, Martin W Qazi, Shamim A Arvay, Melissa L Connor, Nicholas E Saha, Samir K Islam, Maksuda Darmstadt, Gary L El Arifeen, Shams Shang, Nong Nisar, Imran Sadeq-ur Rahman, Qazi Bose, Anuradha Panigrahi, Pinaki Hibberd, Patricia Nawshad Uddin Ahmed, A S M Bhutta, Zulfiqar A Schrag, Stephanie J Hossain, Mohammad Belal Panigrahi, Kalpana Zaidi, Anita K M Mitra, Dipak K Islam, Mohammad Shahidul Satpathy, Radhanath Hamer, Davidson H |
| AuthorAffiliation | 8 Department of Pediatrics , Georgetown University Medical Center , Washington , DC , USA 5 Centre for Global Child Health , The Hospital for Sick Children , Toronto , Ontario , Canada 15 Section of Infectious Diseases, Department of Medicine , Boston University School of Medicine , Boston , Massachusetts , USA 3 Department of International Health , Johns Hopkins Bloomberg School of Public Health , Baltimore , Maryland , USA 1 Department of Microbiology , Child Health Research Foundation , Dhaka , Bangladesh 11 Department of Public Health , North South University , Dhaka , Bangladesh 6 Institute for Global Health and Development , The Aga Khan University , Karachi , Pakistan 17 Department of Pediatrics , Stanford University School of Medicine , Stanford , California , USA 10 Christian Medical College , Vellore , India 12 International Centre for Diarrhoeal Disease Research, Bangladesh , Dhaka , Bangladesh 7 Department of Pediatrics and Child Health , The Aga Khan University , Karachi , Pakistan 9 |
| AuthorAffiliation_xml | – name: 14 Department of Global Health , Boston University School of Public Health , Boston , Massachusetts , USA – name: 1 Department of Microbiology , Child Health Research Foundation , Dhaka , Bangladesh – name: 17 Department of Pediatrics , Stanford University School of Medicine , Stanford , California , USA – name: 4 Division of Bacterial Diseases , Centers for Disease Control and Prevention , Atlanta , Georgia , USA – name: 9 AIPH University , Bhubaneswar , India – name: 5 Centre for Global Child Health , The Hospital for Sick Children , Toronto , Ontario , Canada – name: 13 Child and Adolescent Health and Development Division , WHO Regional Office for Europe , Copenhagen , Denmark – name: 16 Consultant and Researcher , (Retired WHO staff) , Geneva , Switzerland – name: 15 Section of Infectious Diseases, Department of Medicine , Boston University School of Medicine , Boston , Massachusetts , USA – name: 6 Institute for Global Health and Development , The Aga Khan University , Karachi , Pakistan – name: 7 Department of Pediatrics and Child Health , The Aga Khan University , Karachi , Pakistan – name: 2 Department of Clinical Research , London School of Hygiene & Tropical Medicine , London , UK – name: 12 International Centre for Diarrhoeal Disease Research, Bangladesh , Dhaka , Bangladesh – name: 3 Department of International Health , Johns Hopkins Bloomberg School of Public Health , Baltimore , Maryland , USA – name: 10 Christian Medical College , Vellore , India – name: 11 Department of Public Health , North South University , Dhaka , Bangladesh – name: 8 Department of Pediatrics , Georgetown University Medical Center , Washington , DC , USA |
| Author_xml | – sequence: 1 givenname: Nicholas E orcidid: 0000-0002-5013-407X surname: Connor fullname: Connor, Nicholas E email: connorne@tcd.ie organization: Department of Clinical Research, London School of Hygiene & Tropical Medicine, London, UK – sequence: 2 givenname: Mohammad Shahidul surname: Islam fullname: Islam, Mohammad Shahidul organization: Department of Microbiology, Child Health Research Foundation, Dhaka, Bangladesh – sequence: 3 givenname: Luke C surname: Mullany fullname: Mullany, Luke C organization: Department of International Health, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, USA – sequence: 4 givenname: Nong surname: Shang fullname: Shang, Nong organization: Division of Bacterial Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia, USA – sequence: 5 givenname: Zulfiqar A surname: Bhutta fullname: Bhutta, Zulfiqar A organization: Institute for Global Health and Development, The Aga Khan University, Karachi, Pakistan 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Weber fullname: Weber, Martin W organization: Child and Adolescent Health and Development Division, WHO Regional Office for Europe, Copenhagen, Denmark – sequence: 24 givenname: Davidson H surname: Hamer fullname: Hamer, Davidson H organization: Section of Infectious Diseases, Department of Medicine, Boston University School of Medicine, Boston, Massachusetts, USA – sequence: 25 givenname: Patricia surname: Hibberd fullname: Hibberd, Patricia organization: Section of Infectious Diseases, Department of Medicine, Boston University School of Medicine, Boston, Massachusetts, USA – sequence: 26 givenname: A S M surname: Nawshad Uddin Ahmed fullname: Nawshad Uddin Ahmed, A S M organization: Department of Microbiology, Child Health Research Foundation, Dhaka, Bangladesh – sequence: 27 givenname: Maksuda surname: Islam fullname: Islam, Maksuda organization: Department of Microbiology, Child Health Research Foundation, Dhaka, Bangladesh – sequence: 28 givenname: Mohammad Belal surname: Hossain fullname: Hossain, Mohammad Belal organization: Department of Microbiology, Child Health Research Foundation, Dhaka, Bangladesh – sequence: 29 givenname: Shamim A surname: Qazi fullname: Qazi, Shamim A organization: Consultant and Researcher, (Retired WHO staff), Geneva, Switzerland – sequence: 30 givenname: Shams surname: El Arifeen fullname: El Arifeen, Shams organization: International Centre for Diarrhoeal Disease Research, Bangladesh, Dhaka, Bangladesh – sequence: 31 givenname: Gary L orcidid: 0000-0002-7522-5824 surname: Darmstadt fullname: Darmstadt, Gary L organization: Department of Pediatrics, Stanford University School of Medicine, Stanford, California, USA – sequence: 32 givenname: Samir K surname: Saha fullname: Saha, Samir K organization: Department of Microbiology, Child Health Research Foundation, Dhaka, Bangladesh |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/36319031$$D View this record in MEDLINE/PubMed |
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| CitedBy_id | crossref_primary_10_1016_j_clp_2024_10_003 crossref_primary_10_1007_s00203_024_04107_z |
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| DOI | 10.1136/bmjgh-2022-009706 |
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| Issue | 11 |
| Keywords | paediatrics cohort study infections, diseases, disorders, injuries child health |
| Language | English |
| License | This is an open access article distributed in accordance with the Creative Commons Attribution 4.0 Unported (CC BY 4.0) license, which permits others to copy, redistribute, remix, transform and build upon this work for any purpose, provided the original work is properly cited, a link to the licence is given, and indication of whether changes were made. See: https://creativecommons.org/licenses/by/4.0/. Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY. Published by BMJ. |
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| Snippet | ObjectiveRisk factors predisposing infants to community-acquired bacterial infections during the first 2 months of life are poorly understood in South Asia.... Risk factors predisposing infants to community-acquired bacterial infections during the first 2 months of life are poorly understood in South Asia. Identifying... ObjectiveRisk factors predisposing infants to community-acquired bacterial infections during the first 2 months of life are poorly understood in South Asia.... Objective Risk factors predisposing infants to community-acquired bacterial infections during the first 2 months of life are poorly understood in South Asia.... |
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| SubjectTerms | Antibiotics Antimicrobial agents Bacteria Bacterial diseases Bacterial Infections Bayes Theorem Birth weight Blood Case-Control Studies child health Cohort analysis Cohort Studies cohort study Community-Acquired Infections - complications Community-Acquired Infections - epidemiology Female Humans India - epidemiology Infant Infant, Newborn Infants Infections infections, diseases, disorders, injuries Longitudinal Studies Male Original Research paediatrics Pediatrics Pregnancy Risk Factors Socioeconomics |
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| Title | Risk factors for community-acquired bacterial infection among young infants in South Asia: a longitudinal cohort study with nested case–control analysis |
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