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Myxedema psychosis: A protocol for a systematic review and a pooled analysis
BACKGROUND: Myxedema psychosis (MP) is a rare presentation of hypothyroidism. Although known for >70 years, a significant lack of systematic literature describing this condition exists. This limits the clinician's ability to identify and manage this entity properly. Hence, we aimed to system...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7328932/ https://www.ncbi.nlm.nih.gov/pubmed/32590756 http://dx.doi.org/10.1097/MD.0000000000020778 |
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author | Mohamed, Mouhand F.H. Siepmann, Timo Suwileh, Salah Mohammed, Mohammed H. Mohamed, Samreen Abdalla, Lina O. Elzouki, Abdel-Naser Mahmoud, Mohamed H. Al-Mohanadi, Dabia Danjuma, Mohammed |
author_facet | Mohamed, Mouhand F.H. Siepmann, Timo Suwileh, Salah Mohammed, Mohammed H. Mohamed, Samreen Abdalla, Lina O. Elzouki, Abdel-Naser Mahmoud, Mohamed H. Al-Mohanadi, Dabia Danjuma, Mohammed |
author_sort | Mohamed, Mouhand F.H. |
collection | PubMed |
description | BACKGROUND: Myxedema psychosis (MP) is a rare presentation of hypothyroidism. Although known for >70 years, a significant lack of systematic literature describing this condition exists. This limits the clinician's ability to identify and manage this entity properly. Hence, we aimed to systematically review the literature and summarize the presentation, diagnosis, management, and outcomes of this rare entity. METHODS: Systematic review following PRISMA guidance. We will perform a comprehensive search of PubMed, Medline, Embase, Google Scholar (first 300 hits), and Cochrane databases for published observational studies, case series, and case reports. We will use descriptive statistics to provide summary estimates of demographics, common presenting features, laboratory test results, imaging findings, treatment administered, and outcomes. Moreover, continuous variables will be compared by the Wilcoxon Mann Whitney test, whereas categorical variables will be assessed by the χ(2) test. Bivariate and multivariate regression will be performed to assess risk factors associated with poor outcome. A scoping review revealed that a meta-analysis might not be feasible owing to the paucity of systematic studies describing the condition. RESULTS: This is the first systematic review examining this rare entity. Thus, the result of which will be significant. We hope that this review will help in identifying relevant predictive clinical or laboratory characteristics. Additionally, it identifies the best treatment strategies. The findings of this review will help increase our knowledge of this condition so as to recognize this condition promptly. Also, it will assist in differentiating MP from masqueraders, such as Hashimoto encephalopathy (HE). The results of this review will be published in a peer-reviewed journal. CONCLUSION: This is the first systematic review exploring MP demographics, diagnosis treatment, and outcomes. The information gathered by this review will be necessary for patients, clinicians, researchers, and guideline makers. PROSPERO REGISTRATION NUMBER: CRD42020160310 |
format | Online Article Text |
id | pubmed-7328932 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-73289322020-07-09 Myxedema psychosis: A protocol for a systematic review and a pooled analysis Mohamed, Mouhand F.H. Siepmann, Timo Suwileh, Salah Mohammed, Mohammed H. Mohamed, Samreen Abdalla, Lina O. Elzouki, Abdel-Naser Mahmoud, Mohamed H. Al-Mohanadi, Dabia Danjuma, Mohammed Medicine (Baltimore) 4300 BACKGROUND: Myxedema psychosis (MP) is a rare presentation of hypothyroidism. Although known for >70 years, a significant lack of systematic literature describing this condition exists. This limits the clinician's ability to identify and manage this entity properly. Hence, we aimed to systematically review the literature and summarize the presentation, diagnosis, management, and outcomes of this rare entity. METHODS: Systematic review following PRISMA guidance. We will perform a comprehensive search of PubMed, Medline, Embase, Google Scholar (first 300 hits), and Cochrane databases for published observational studies, case series, and case reports. We will use descriptive statistics to provide summary estimates of demographics, common presenting features, laboratory test results, imaging findings, treatment administered, and outcomes. Moreover, continuous variables will be compared by the Wilcoxon Mann Whitney test, whereas categorical variables will be assessed by the χ(2) test. Bivariate and multivariate regression will be performed to assess risk factors associated with poor outcome. A scoping review revealed that a meta-analysis might not be feasible owing to the paucity of systematic studies describing the condition. RESULTS: This is the first systematic review examining this rare entity. Thus, the result of which will be significant. We hope that this review will help in identifying relevant predictive clinical or laboratory characteristics. Additionally, it identifies the best treatment strategies. The findings of this review will help increase our knowledge of this condition so as to recognize this condition promptly. Also, it will assist in differentiating MP from masqueraders, such as Hashimoto encephalopathy (HE). The results of this review will be published in a peer-reviewed journal. CONCLUSION: This is the first systematic review exploring MP demographics, diagnosis treatment, and outcomes. The information gathered by this review will be necessary for patients, clinicians, researchers, and guideline makers. PROSPERO REGISTRATION NUMBER: CRD42020160310 Wolters Kluwer Health 2020-06-26 /pmc/articles/PMC7328932/ /pubmed/32590756 http://dx.doi.org/10.1097/MD.0000000000020778 Text en Copyright © 2020 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by/4.0 This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0 |
spellingShingle | 4300 Mohamed, Mouhand F.H. Siepmann, Timo Suwileh, Salah Mohammed, Mohammed H. Mohamed, Samreen Abdalla, Lina O. Elzouki, Abdel-Naser Mahmoud, Mohamed H. Al-Mohanadi, Dabia Danjuma, Mohammed Myxedema psychosis: A protocol for a systematic review and a pooled analysis |
title | Myxedema psychosis: A protocol for a systematic review and a pooled analysis |
title_full | Myxedema psychosis: A protocol for a systematic review and a pooled analysis |
title_fullStr | Myxedema psychosis: A protocol for a systematic review and a pooled analysis |
title_full_unstemmed | Myxedema psychosis: A protocol for a systematic review and a pooled analysis |
title_short | Myxedema psychosis: A protocol for a systematic review and a pooled analysis |
title_sort | myxedema psychosis: a protocol for a systematic review and a pooled analysis |
topic | 4300 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7328932/ https://www.ncbi.nlm.nih.gov/pubmed/32590756 http://dx.doi.org/10.1097/MD.0000000000020778 |
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