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Group B Streptococcal Colonization among Pregnant Women and Neonates in a Tertiary Care Hospital in South India
OBJECTIVES: To assess the prevalence of maternal and neonatal group B Streptococcal colonization, incidence of neonatal systemic illness, and antibiotic sensitivity of isolates. METHODS: This prospective cohort study was conducted in a South Indian tertiary care hospital. Rectovaginal swabs from pre...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer India
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9017074/ https://www.ncbi.nlm.nih.gov/pubmed/35438474 http://dx.doi.org/10.1007/s12098-022-04120-4 |
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author | Warrier, Lakshmi M. Joy, Sapna C, Raja Rajeswari Bashir, Rani Ameena |
author_facet | Warrier, Lakshmi M. Joy, Sapna C, Raja Rajeswari Bashir, Rani Ameena |
author_sort | Warrier, Lakshmi M. |
collection | PubMed |
description | OBJECTIVES: To assess the prevalence of maternal and neonatal group B Streptococcal colonization, incidence of neonatal systemic illness, and antibiotic sensitivity of isolates. METHODS: This prospective cohort study was conducted in a South Indian tertiary care hospital. Rectovaginal swabs from pregnant mothers at 36(0/7)–37(6/7) wk gestation and throat and rectal swabs from their neonates at 48 h of age were collected. Presence of group B Streptococcus (GBS) was identified by broth enrichment step, and traditional microbiologic methods and antibiotic sensitivity of isolates was noted. All mothers received intrapartum antibiotic prophylaxis (IAP). Culture-positive sepsis, clinical sepsis, pneumonia, meningitis, and urinary tract infection were defined as neonatal systemic illness. Neonates of colonized mothers were followed at 3 mo for late-onset sepsis. RESULTS: Of the 310 mothers, 40 were GBS colonized (prevalence: 12.9%; 95% CI 9.2%, 17.6%). None of the neonates were colonized. Maternal GBS colonization was significantly associated with premature rupture of membrane (RR - 2.93, 95% CI - 1.66–5.16) and neonatal systemic illness (RR - 2.78, 95% CI - 1.39–5.54). Positive correlation was noted between duration of IAP ≤ 4 h and neonatal illness and between maternal GBS colonization and Apgar at 1 min ≤ 4. Clindamycin resistance was noted in 20%. All neonates remained well at 3 mo follow-up. CONCLUSION: High maternal colonization alerts the need for GBS screening in India. Clindamycin resistance among GBS isolates questions its effectiveness as alternative therapy in penicillin allergy. |
format | Online Article Text |
id | pubmed-9017074 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer India |
record_format | MEDLINE/PubMed |
spelling | pubmed-90170742022-04-19 Group B Streptococcal Colonization among Pregnant Women and Neonates in a Tertiary Care Hospital in South India Warrier, Lakshmi M. Joy, Sapna C, Raja Rajeswari Bashir, Rani Ameena Indian J Pediatr Original Article OBJECTIVES: To assess the prevalence of maternal and neonatal group B Streptococcal colonization, incidence of neonatal systemic illness, and antibiotic sensitivity of isolates. METHODS: This prospective cohort study was conducted in a South Indian tertiary care hospital. Rectovaginal swabs from pregnant mothers at 36(0/7)–37(6/7) wk gestation and throat and rectal swabs from their neonates at 48 h of age were collected. Presence of group B Streptococcus (GBS) was identified by broth enrichment step, and traditional microbiologic methods and antibiotic sensitivity of isolates was noted. All mothers received intrapartum antibiotic prophylaxis (IAP). Culture-positive sepsis, clinical sepsis, pneumonia, meningitis, and urinary tract infection were defined as neonatal systemic illness. Neonates of colonized mothers were followed at 3 mo for late-onset sepsis. RESULTS: Of the 310 mothers, 40 were GBS colonized (prevalence: 12.9%; 95% CI 9.2%, 17.6%). None of the neonates were colonized. Maternal GBS colonization was significantly associated with premature rupture of membrane (RR - 2.93, 95% CI - 1.66–5.16) and neonatal systemic illness (RR - 2.78, 95% CI - 1.39–5.54). Positive correlation was noted between duration of IAP ≤ 4 h and neonatal illness and between maternal GBS colonization and Apgar at 1 min ≤ 4. Clindamycin resistance was noted in 20%. All neonates remained well at 3 mo follow-up. CONCLUSION: High maternal colonization alerts the need for GBS screening in India. Clindamycin resistance among GBS isolates questions its effectiveness as alternative therapy in penicillin allergy. Springer India 2022-04-19 2022 /pmc/articles/PMC9017074/ /pubmed/35438474 http://dx.doi.org/10.1007/s12098-022-04120-4 Text en © Dr. K C Chaudhuri Foundation 2022 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Original Article Warrier, Lakshmi M. Joy, Sapna C, Raja Rajeswari Bashir, Rani Ameena Group B Streptococcal Colonization among Pregnant Women and Neonates in a Tertiary Care Hospital in South India |
title | Group B Streptococcal Colonization among Pregnant Women and Neonates in a Tertiary Care Hospital in South India |
title_full | Group B Streptococcal Colonization among Pregnant Women and Neonates in a Tertiary Care Hospital in South India |
title_fullStr | Group B Streptococcal Colonization among Pregnant Women and Neonates in a Tertiary Care Hospital in South India |
title_full_unstemmed | Group B Streptococcal Colonization among Pregnant Women and Neonates in a Tertiary Care Hospital in South India |
title_short | Group B Streptococcal Colonization among Pregnant Women and Neonates in a Tertiary Care Hospital in South India |
title_sort | group b streptococcal colonization among pregnant women and neonates in a tertiary care hospital in south india |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9017074/ https://www.ncbi.nlm.nih.gov/pubmed/35438474 http://dx.doi.org/10.1007/s12098-022-04120-4 |
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