Depression in adults with sickle cell disease: a systematic review of the methodological issues in assessing prevalence of depression
Abstract Background Sickle cell disease (SCD) as other chronic medical conditions is commonly complicated by depression or other psychiatric symptoms. Results reported in studies present a large variation. Thus, synthetic data are needed to understand impact of depression in adults with SCD. The aim...
| Main Authors: | , , , , |
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| Format: | Article |
| Language: | English |
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BMC
2021-04-01
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| Series: | BMC Psychology |
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| Online Access: | https://doi.org/10.1186/s40359-021-00543-4 |
| _version_ | 1818652763730477056 |
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| author | Damien Oudin Doglioni Vincent Chabasseur Frédéric Barbot Frédéric Galactéros Marie-Claire Gay |
| author_facet | Damien Oudin Doglioni Vincent Chabasseur Frédéric Barbot Frédéric Galactéros Marie-Claire Gay |
| author_sort | Damien Oudin Doglioni |
| collection | DOAJ |
| description | Abstract Background Sickle cell disease (SCD) as other chronic medical conditions is commonly complicated by depression or other psychiatric symptoms. Results reported in studies present a large variation. Thus, synthetic data are needed to understand impact of depression in adults with SCD. The aim of this literature review is to analyse the methodology used in the studies assessing depression and discuss the different prevalence levels reported. Methods Studies involving adults with SCD from 1999 to 2018 were included when providing data on prevalence of depression. It was defined by a psychometric assessment, a structured interview, or a medical record review. PRISMA recommendations were followed. Results 36 studies are included accordingly to our methodology. Prevalence variation is large, from 0% to more than 85%. We find that the type of assessment tool used plays a major role in this between studies variation. Also, methodological issues arise with respect to psychometric assessment. Moreover, differences emerge between continents, setting of recruitment or time of assessment. Conclusion All these issues are discussed to provide insight on depression in adults with sickle cell disease. Trial Registration PROSPERO Registration CRD42018100684. |
| first_indexed | 2024-12-17T02:27:11Z |
| format | Article |
| id | doaj.art-208845504b004c70b829138f325d79b4 |
| institution | Directory Open Access Journal |
| issn | 2050-7283 |
| language | English |
| last_indexed | 2024-12-17T02:27:11Z |
| publishDate | 2021-04-01 |
| publisher | BMC |
| record_format | Article |
| series | BMC Psychology |
| spelling | doaj.art-208845504b004c70b829138f325d79b42022-12-21T22:07:04ZengBMCBMC Psychology2050-72832021-04-019111410.1186/s40359-021-00543-4Depression in adults with sickle cell disease: a systematic review of the methodological issues in assessing prevalence of depressionDamien Oudin Doglioni0Vincent Chabasseur1Frédéric Barbot2Frédéric Galactéros3Marie-Claire Gay4EA4430 EvaCliPsy/ED139, Paris Nanterre UniversityEA4430 EvaCliPsy, Paris Nanterre UniversityINSERM Clinical Investigation Center 1429, Teaching Hospital Raymond Poincaré AP-HPRed Blood Cell Genetic Diseases Unit (UMGGR), Teaching Hospital Henri MondorEA4430 EvaCliPsy/ED139, Paris Nanterre UniversityAbstract Background Sickle cell disease (SCD) as other chronic medical conditions is commonly complicated by depression or other psychiatric symptoms. Results reported in studies present a large variation. Thus, synthetic data are needed to understand impact of depression in adults with SCD. The aim of this literature review is to analyse the methodology used in the studies assessing depression and discuss the different prevalence levels reported. Methods Studies involving adults with SCD from 1999 to 2018 were included when providing data on prevalence of depression. It was defined by a psychometric assessment, a structured interview, or a medical record review. PRISMA recommendations were followed. Results 36 studies are included accordingly to our methodology. Prevalence variation is large, from 0% to more than 85%. We find that the type of assessment tool used plays a major role in this between studies variation. Also, methodological issues arise with respect to psychometric assessment. Moreover, differences emerge between continents, setting of recruitment or time of assessment. Conclusion All these issues are discussed to provide insight on depression in adults with sickle cell disease. Trial Registration PROSPERO Registration CRD42018100684.https://doi.org/10.1186/s40359-021-00543-4Sickle cell diseaseDepressionPrevalenceMethodology |
| spellingShingle | Damien Oudin Doglioni Vincent Chabasseur Frédéric Barbot Frédéric Galactéros Marie-Claire Gay Depression in adults with sickle cell disease: a systematic review of the methodological issues in assessing prevalence of depression BMC Psychology Sickle cell disease Depression Prevalence Methodology |
| title | Depression in adults with sickle cell disease: a systematic review of the methodological issues in assessing prevalence of depression |
| title_full | Depression in adults with sickle cell disease: a systematic review of the methodological issues in assessing prevalence of depression |
| title_fullStr | Depression in adults with sickle cell disease: a systematic review of the methodological issues in assessing prevalence of depression |
| title_full_unstemmed | Depression in adults with sickle cell disease: a systematic review of the methodological issues in assessing prevalence of depression |
| title_short | Depression in adults with sickle cell disease: a systematic review of the methodological issues in assessing prevalence of depression |
| title_sort | depression in adults with sickle cell disease a systematic review of the methodological issues in assessing prevalence of depression |
| topic | Sickle cell disease Depression Prevalence Methodology |
| url | https://doi.org/10.1186/s40359-021-00543-4 |
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