このアイテムのアクセス数: 118
このアイテムのファイル:
ファイル | 記述 | サイズ | フォーマット | |
---|---|---|---|---|
s11136-017-1659-5.pdf | 748.69 kB | Adobe PDF | 見る/開く |
完全メタデータレコード
DCフィールド | 値 | 言語 |
---|---|---|
dc.contributor.author | Obbarius, Alexander | en |
dc.contributor.author | van Maasakkers, Lisa | en |
dc.contributor.author | Baer, Lee | en |
dc.contributor.author | Clark, David M. | en |
dc.contributor.author | Crocker, Anne G. | en |
dc.contributor.author | de Beurs, Edwin | en |
dc.contributor.author | Emmelkamp, Paul M. G. | en |
dc.contributor.author | Furukawa, Toshi A. | en |
dc.contributor.author | Hedman-Lagerlöf, Erik | en |
dc.contributor.author | Kangas, Maria | en |
dc.contributor.author | Langford, Lucie | en |
dc.contributor.author | Lesage, Alain | en |
dc.contributor.author | Mwesigire, Doris M. | en |
dc.contributor.author | Nolte, Sandra | en |
dc.contributor.author | Patel, Vikram | en |
dc.contributor.author | Pilkonis, Paul A. | en |
dc.contributor.author | Pincus, Harold A. | en |
dc.contributor.author | Reis, Roberta A. | en |
dc.contributor.author | Rojas, Graciela | en |
dc.contributor.author | Sherbourne, Cathy | en |
dc.contributor.author | Smithson, Dave | en |
dc.contributor.author | Stowell, Caleb | en |
dc.contributor.author | Woolaway-Bickel, Kelly | en |
dc.contributor.author | Rose, Matthias | en |
dc.contributor.alternative | 古川, 壽亮 | ja |
dc.date.accessioned | 2020-01-27T01:53:26Z | - |
dc.date.available | 2020-01-27T01:53:26Z | - |
dc.date.issued | 2017-12 | - |
dc.identifier.issn | 0962-9343 | - |
dc.identifier.issn | 1573-2649 | - |
dc.identifier.uri | http://hdl.handle.net/2433/245457 | - |
dc.description.abstract | Purpose: National initiatives, such as the UK Improving Access to Psychological Therapies program (IAPT), demonstrate the feasibility of conducting empirical mental health assessments on a large scale, and similar initiatives exist in other countries. However, there is a lack of international consensus on which outcome domains are most salient to monitor treatment progress and how they should be measured. The aim of this project was to propose (1) an essential set of outcome domains relevant across countries and cultures, (2) a set of easily accessible patient-reported instruments, and (3) a psychometric approach to make scores from different instruments comparable. Methods: Twenty-four experts, including ten health outcomes researchers, ten clinical experts from all continents, two patient advocates, and two ICHOM coordinators worked for seven months in a consensus building exercise to develop recommendations based on existing evidence using a structured consensus-driven modified Delphi technique. Results: The group proposes to combine an assessment of potential outcome predictors at baseline (47 items: demographics, functional, clinical status, etc.), with repeated assessments of disease-specific symptoms during the treatment process (19 items: symptoms, side effects, etc.), and a comprehensive annual assessment of broader treatment outcomes (45 items: remission, absenteeism, etc.). Further, it is suggested reporting disease-specific symptoms for depression and anxiety on a standardized metric to increase comparability with other legacy instruments. All recommended instruments are provided online (www.ichom.org). Conclusion: An international standard of health outcomes assessment has the potential to improve clinical decision making, enhance health care for the benefit of patients, and facilitate scientific knowledge. | en |
dc.format.mimetype | application/pdf | - |
dc.language.iso | eng | - |
dc.publisher | Springer Nature | en |
dc.rights | © The Author(s) 2017 This 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. | en |
dc.subject | Depression | en |
dc.subject | Anxiety | en |
dc.subject | Patient-reported outcomes | en |
dc.subject | Health-related quality of life | en |
dc.subject | Standardization | en |
dc.subject | Outcome Set | en |
dc.title | Standardization of health outcomes assessment for depression and anxiety: recommendations from the ICHOM Depression and Anxiety Working Group | en |
dc.type | journal article | - |
dc.type.niitype | Journal Article | - |
dc.identifier.jtitle | Quality of Life Research | en |
dc.identifier.volume | 26 | - |
dc.identifier.issue | 12 | - |
dc.identifier.spage | 3211 | - |
dc.identifier.epage | 3225 | - |
dc.relation.doi | 10.1007/s11136-017-1659-5 | - |
dc.textversion | publisher | - |
dc.identifier.pmid | 28786017 | - |
dcterms.accessRights | open access | - |
dc.identifier.pissn | 0962-9343 | - |
dc.identifier.eissn | 1573-2649 | - |
出現コレクション: | 学術雑誌掲載論文等 |

このリポジトリに保管されているアイテムはすべて著作権により保護されています。