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Non-typeable Haemophilus influenzae-associated early pregnancy loss: an emerging neonatal and maternal pathogen

OBJECTIVES: There is increasing evidence indicating an association between invasive non-typeable Haemophilus influenzae (NTHi) infection in pregnancy and early pregnancy loss. As the diagnosis relies on microbiological investigation of post-mortem placental and foetal samples, a significant proporti...

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Autores principales: Cevik, Muge, Moncayo-Nieto, Olga L., Evans, Margaret J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7292808/
https://www.ncbi.nlm.nih.gov/pubmed/31549360
http://dx.doi.org/10.1007/s15010-019-01359-6
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author Cevik, Muge
Moncayo-Nieto, Olga L.
Evans, Margaret J.
author_facet Cevik, Muge
Moncayo-Nieto, Olga L.
Evans, Margaret J.
author_sort Cevik, Muge
collection PubMed
description OBJECTIVES: There is increasing evidence indicating an association between invasive non-typeable Haemophilus influenzae (NTHi) infection in pregnancy and early pregnancy loss. As the diagnosis relies on microbiological investigation of post-mortem placental and foetal samples, a significant proportion of NTHi-related pregnancy loss remains unrecognised. To better characterise NTHi in septic abortion, we report NTHi cases associated with early pregnancy loss. METHODS: We reviewed all post-mortems at <24 weeks gestation with histologically proven acute chorioamnionitis on placental histology and enrolled cases with at least one matched foetal and placental sample culture positive for NTHi. The study was approved by the NHS Lothian Caldicott Guardian. RESULTS: In our cohort, invasive NTHi has accounted for 20% of infections associated with early pregnancy loss prior to 24 weeks gestation. All patients were young and healthy pregnant women at < 20 weeks' gestation who presented with abdominal pain, PV bleed /discharge and were septic at the time of presentation. One patient with previous history of miscarriage who presented with cervical incompetence had more severe pathology suggestive of early intrauterine pneumonia. CONCLUSION: The burden of invasive NTHi disease in early pregnancy loss is likely to be much larger than currently recognised. NTHi should be considered in pregnant women presenting with abdominal pain and PV bleed/discharge in whom clinical signs of sepsis are present. Active surveillance should be considered in this patient group including septic abortion to capture the true prevalence of this emerging pathogen to inform preventative and therapeutic approaches.
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spelling pubmed-72928082020-06-16 Non-typeable Haemophilus influenzae-associated early pregnancy loss: an emerging neonatal and maternal pathogen Cevik, Muge Moncayo-Nieto, Olga L. Evans, Margaret J. Infection Brief Report OBJECTIVES: There is increasing evidence indicating an association between invasive non-typeable Haemophilus influenzae (NTHi) infection in pregnancy and early pregnancy loss. As the diagnosis relies on microbiological investigation of post-mortem placental and foetal samples, a significant proportion of NTHi-related pregnancy loss remains unrecognised. To better characterise NTHi in septic abortion, we report NTHi cases associated with early pregnancy loss. METHODS: We reviewed all post-mortems at <24 weeks gestation with histologically proven acute chorioamnionitis on placental histology and enrolled cases with at least one matched foetal and placental sample culture positive for NTHi. The study was approved by the NHS Lothian Caldicott Guardian. RESULTS: In our cohort, invasive NTHi has accounted for 20% of infections associated with early pregnancy loss prior to 24 weeks gestation. All patients were young and healthy pregnant women at < 20 weeks' gestation who presented with abdominal pain, PV bleed /discharge and were septic at the time of presentation. One patient with previous history of miscarriage who presented with cervical incompetence had more severe pathology suggestive of early intrauterine pneumonia. CONCLUSION: The burden of invasive NTHi disease in early pregnancy loss is likely to be much larger than currently recognised. NTHi should be considered in pregnant women presenting with abdominal pain and PV bleed/discharge in whom clinical signs of sepsis are present. Active surveillance should be considered in this patient group including septic abortion to capture the true prevalence of this emerging pathogen to inform preventative and therapeutic approaches. Springer Berlin Heidelberg 2019-09-23 2020 /pmc/articles/PMC7292808/ /pubmed/31549360 http://dx.doi.org/10.1007/s15010-019-01359-6 Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Brief Report
Cevik, Muge
Moncayo-Nieto, Olga L.
Evans, Margaret J.
Non-typeable Haemophilus influenzae-associated early pregnancy loss: an emerging neonatal and maternal pathogen
title Non-typeable Haemophilus influenzae-associated early pregnancy loss: an emerging neonatal and maternal pathogen
title_full Non-typeable Haemophilus influenzae-associated early pregnancy loss: an emerging neonatal and maternal pathogen
title_fullStr Non-typeable Haemophilus influenzae-associated early pregnancy loss: an emerging neonatal and maternal pathogen
title_full_unstemmed Non-typeable Haemophilus influenzae-associated early pregnancy loss: an emerging neonatal and maternal pathogen
title_short Non-typeable Haemophilus influenzae-associated early pregnancy loss: an emerging neonatal and maternal pathogen
title_sort non-typeable haemophilus influenzae-associated early pregnancy loss: an emerging neonatal and maternal pathogen
topic Brief Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7292808/
https://www.ncbi.nlm.nih.gov/pubmed/31549360
http://dx.doi.org/10.1007/s15010-019-01359-6
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