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Neurologic complications after allogeneic transplantation: a meta‐analysis
OBJECTIVE: Neurologic adverse events remain challenging complications with poor morbidity and mortality post adult allogeneic hematopoietic cell transplantation (allo‐HCT) for hematologic diseases. We conducted a systematic review and meta‐analysis to determine their spectrum, incidence, and impact...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6801165/ https://www.ncbi.nlm.nih.gov/pubmed/31560177 http://dx.doi.org/10.1002/acn3.50909 |
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author | Gavriilaki, Maria Mainou, Maria Gavriilaki, Eleni Haidich, Anna‐Bettina Papagiannopoulos, Sotirios Sakellari, Ioanna Anagnostopoulos, Achilles Kimiskidis, Vasilis |
author_facet | Gavriilaki, Maria Mainou, Maria Gavriilaki, Eleni Haidich, Anna‐Bettina Papagiannopoulos, Sotirios Sakellari, Ioanna Anagnostopoulos, Achilles Kimiskidis, Vasilis |
author_sort | Gavriilaki, Maria |
collection | PubMed |
description | OBJECTIVE: Neurologic adverse events remain challenging complications with poor morbidity and mortality post adult allogeneic hematopoietic cell transplantation (allo‐HCT) for hematologic diseases. We conducted a systematic review and meta‐analysis to determine their spectrum, incidence, and impact on survival. METHODS: We searched MEDLINE, COCHRANE, EMBASE through March 2019 for all types of primary studies. Two independent reviewers screened, extracted data, and assessed risk of bias (RoB). RESULTS: We identified 552 eligible studies describing 57.972 patients; one randomized controlled trial, two case–control, 17 prospective, 86 retrospective cohort studies, 21 case series, and 425 case reports. RoB ranged from fair to high although case series were low‐risk. The majority of studies traced infectious or drug‐related neurologic manifestations. Infectious complications were present in 2.7% (95% CI 1.9–3.6) and 3.3% (95% CI 0.8–7.1) of patients in retrospective and prospective cohort studies, respectively. In retrospective studies, 3.4% (95% CI 2.1–4.9) of patients suffered from drug‐related neurologic events. In prospective cohorts the equivalent incidence was 13% (95% CI 4.2–24.8). Neurologic complications had a detrimental impact on survival. INTERPRETATION: Our study highlights the wide spectrum and significant impact of neurologic complications on survival post allo‐HCT. This systematic review summarizes existing data and provides the necessary background information for every physician involved in the management of these patients. |
format | Online Article Text |
id | pubmed-6801165 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-68011652019-10-22 Neurologic complications after allogeneic transplantation: a meta‐analysis Gavriilaki, Maria Mainou, Maria Gavriilaki, Eleni Haidich, Anna‐Bettina Papagiannopoulos, Sotirios Sakellari, Ioanna Anagnostopoulos, Achilles Kimiskidis, Vasilis Ann Clin Transl Neurol Research Articles OBJECTIVE: Neurologic adverse events remain challenging complications with poor morbidity and mortality post adult allogeneic hematopoietic cell transplantation (allo‐HCT) for hematologic diseases. We conducted a systematic review and meta‐analysis to determine their spectrum, incidence, and impact on survival. METHODS: We searched MEDLINE, COCHRANE, EMBASE through March 2019 for all types of primary studies. Two independent reviewers screened, extracted data, and assessed risk of bias (RoB). RESULTS: We identified 552 eligible studies describing 57.972 patients; one randomized controlled trial, two case–control, 17 prospective, 86 retrospective cohort studies, 21 case series, and 425 case reports. RoB ranged from fair to high although case series were low‐risk. The majority of studies traced infectious or drug‐related neurologic manifestations. Infectious complications were present in 2.7% (95% CI 1.9–3.6) and 3.3% (95% CI 0.8–7.1) of patients in retrospective and prospective cohort studies, respectively. In retrospective studies, 3.4% (95% CI 2.1–4.9) of patients suffered from drug‐related neurologic events. In prospective cohorts the equivalent incidence was 13% (95% CI 4.2–24.8). Neurologic complications had a detrimental impact on survival. INTERPRETATION: Our study highlights the wide spectrum and significant impact of neurologic complications on survival post allo‐HCT. This systematic review summarizes existing data and provides the necessary background information for every physician involved in the management of these patients. John Wiley and Sons Inc. 2019-09-27 /pmc/articles/PMC6801165/ /pubmed/31560177 http://dx.doi.org/10.1002/acn3.50909 Text en © 2019 The Authors. Annals of Clinical and Translational Neurology published by Wiley Periodicals, Inc on behalf of American Neurological Association. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Gavriilaki, Maria Mainou, Maria Gavriilaki, Eleni Haidich, Anna‐Bettina Papagiannopoulos, Sotirios Sakellari, Ioanna Anagnostopoulos, Achilles Kimiskidis, Vasilis Neurologic complications after allogeneic transplantation: a meta‐analysis |
title | Neurologic complications after allogeneic transplantation: a meta‐analysis |
title_full | Neurologic complications after allogeneic transplantation: a meta‐analysis |
title_fullStr | Neurologic complications after allogeneic transplantation: a meta‐analysis |
title_full_unstemmed | Neurologic complications after allogeneic transplantation: a meta‐analysis |
title_short | Neurologic complications after allogeneic transplantation: a meta‐analysis |
title_sort | neurologic complications after allogeneic transplantation: a meta‐analysis |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6801165/ https://www.ncbi.nlm.nih.gov/pubmed/31560177 http://dx.doi.org/10.1002/acn3.50909 |
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