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Current knowledge of medical complications in adults with achondroplasia: A scoping review
This article provides an overview of the current knowledge on medical complications, health characteristics, and psychosocial issues in adults with achondroplasia. We have used a scoping review methodology particularly recommended for mapping and summarizing existing research evidence, and to identi...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6972520/ https://www.ncbi.nlm.nih.gov/pubmed/30916780 http://dx.doi.org/10.1111/cge.13542 |
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author | Fredwall, Svein O. Maanum, Grethe Johansen, Heidi Snekkevik, Hildegun Savarirayan, Ravi Lidal, Ingeborg B. |
author_facet | Fredwall, Svein O. Maanum, Grethe Johansen, Heidi Snekkevik, Hildegun Savarirayan, Ravi Lidal, Ingeborg B. |
author_sort | Fredwall, Svein O. |
collection | PubMed |
description | This article provides an overview of the current knowledge on medical complications, health characteristics, and psychosocial issues in adults with achondroplasia. We have used a scoping review methodology particularly recommended for mapping and summarizing existing research evidence, and to identify knowledge gaps. The review process was conducted in accordance with the PRISMA‐ScR guidelines (Preferred Reporting Items for Systematic reviews and Meta‐Analyses Extension for Scoping Reviews). The selection of studies was based on criteria predefined in a review protocol. Twenty‐nine publications were included; 2 reviews, and 27 primary studies. Key information such as reference details, study characteristics, topics of interest, main findings and the study author's conclusion are presented in text and tables. Over the past decades, there has only been a slight increase in publications on adults with achondroplasia. The reported morbidity rates and prevalence of medical complications are often based on a few studies where the methodology and representativeness can be questioned. Studies on sleep‐related disorders and pregnancy‐related complications were lacking. Multicenter natural history studies have recently been initiated. Future studies should report in accordance to methodological reference standards, to strengthen the reliability and generalizability of the findings, and to increase the relevance for implementing in clinical practice. |
format | Online Article Text |
id | pubmed-6972520 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-69725202020-01-27 Current knowledge of medical complications in adults with achondroplasia: A scoping review Fredwall, Svein O. Maanum, Grethe Johansen, Heidi Snekkevik, Hildegun Savarirayan, Ravi Lidal, Ingeborg B. Clin Genet Reviews This article provides an overview of the current knowledge on medical complications, health characteristics, and psychosocial issues in adults with achondroplasia. We have used a scoping review methodology particularly recommended for mapping and summarizing existing research evidence, and to identify knowledge gaps. The review process was conducted in accordance with the PRISMA‐ScR guidelines (Preferred Reporting Items for Systematic reviews and Meta‐Analyses Extension for Scoping Reviews). The selection of studies was based on criteria predefined in a review protocol. Twenty‐nine publications were included; 2 reviews, and 27 primary studies. Key information such as reference details, study characteristics, topics of interest, main findings and the study author's conclusion are presented in text and tables. Over the past decades, there has only been a slight increase in publications on adults with achondroplasia. The reported morbidity rates and prevalence of medical complications are often based on a few studies where the methodology and representativeness can be questioned. Studies on sleep‐related disorders and pregnancy‐related complications were lacking. Multicenter natural history studies have recently been initiated. Future studies should report in accordance to methodological reference standards, to strengthen the reliability and generalizability of the findings, and to increase the relevance for implementing in clinical practice. Blackwell Publishing Ltd 2019-04-22 2020-01 /pmc/articles/PMC6972520/ /pubmed/30916780 http://dx.doi.org/10.1111/cge.13542 Text en © 2019 The Authors. Clinical Genetics published by John Wiley & Sons A/S. Published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Reviews Fredwall, Svein O. Maanum, Grethe Johansen, Heidi Snekkevik, Hildegun Savarirayan, Ravi Lidal, Ingeborg B. Current knowledge of medical complications in adults with achondroplasia: A scoping review |
title | Current knowledge of medical complications in adults with achondroplasia: A scoping review |
title_full | Current knowledge of medical complications in adults with achondroplasia: A scoping review |
title_fullStr | Current knowledge of medical complications in adults with achondroplasia: A scoping review |
title_full_unstemmed | Current knowledge of medical complications in adults with achondroplasia: A scoping review |
title_short | Current knowledge of medical complications in adults with achondroplasia: A scoping review |
title_sort | current knowledge of medical complications in adults with achondroplasia: a scoping review |
topic | Reviews |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6972520/ https://www.ncbi.nlm.nih.gov/pubmed/30916780 http://dx.doi.org/10.1111/cge.13542 |
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