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臨床試験の効率化を目的とした電子カルテからe-CRFへのデータ転送の方向性
http://hdl.handle.net/2297/18243
http://hdl.handle.net/2297/182436db07da6-749c-43ba-b4b9-f2d4e912bb1f
| 名前 / ファイル | ライセンス | アクション |
|---|---|---|
PH-PR-MIYAMOTO-K-91.pdf (1.0 MB)
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| Item type | 学術雑誌論文 / Journal Article(1) | |||||
|---|---|---|---|---|---|---|
| 公開日 | 2017-10-04 | |||||
| タイトル | ||||||
| タイトル | 臨床試験の効率化を目的とした電子カルテからe-CRFへのデータ転送の方向性 | |||||
| タイトル | ||||||
| タイトル | Directivity of data transmission from EMR to e-CRF for improving efficiency of clinical research | |||||
| 言語 | en | |||||
| 言語 | ||||||
| 言語 | jpn | |||||
| 資源タイプ | ||||||
| 資源タイプ識別子 | http://purl.org/coar/resource_type/c_6501 | |||||
| 資源タイプ | journal article | |||||
| 著者 |
吉冨, 克則
× 吉冨, 克則× 古川, 裕之× 宮本, 謙一 |
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| 書誌情報 |
臨床薬理 = Japanese journal of clinical pharmacology 巻 39, 号 3, p. 91-97, 発行日 2008-05-01 |
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| ISSN | ||||||
| 収録物識別子タイプ | ISSN | |||||
| 収録物識別子 | 0388-1601 | |||||
| ISSN | ||||||
| 収録物識別子タイプ | ISSN | |||||
| 収録物識別子 | http://www.jstage.jst.go.jp/article/jscpt/39/3/39_91/_article/-char/ja | |||||
| NCID | ||||||
| 収録物識別子タイプ | NCID | |||||
| 収録物識別子 | AN0025404X | |||||
| DOI | ||||||
| 関連タイプ | isIdenticalTo | |||||
| 識別子タイプ | DOI | |||||
| 関連識別子 | 10.3999/jscpt.39.91 | |||||
| 出版者 | ||||||
| 出版者 | 日本臨床薬理学会 = The Japanese Society of Clinical Pharmacology and Therapeutics | |||||
| 抄録 | ||||||
| 内容記述タイプ | Abstract | |||||
| 内容記述 | In the current clinical trials, clinical data which was originally recorded on source data is transcribed into CRF by physicians or CRCs, and CRAs verify source data and CRF. However, transcription and verification are labor-intensive jobs. If the information of source data could be electronically transmitted to CRF, transcription and verification jobs are unnecessary. However, transmission of all necessary data is difficult. Therefore, we carried out surveys for CRCs and CRAs about which data items should be transmitted and what problems might occur. We obtained responses from 370 CRCs and 252 CRAs. It was suggested that data items which can improve efficiency of clinical trials are "Concomitant Medications", "Medical History/Complications", "Laboratory Test Results", "Adverse Event", and "Vital Signs". And various problems were listed ; in paticular, CRCs were concerned about "Security" and CRAs were concerned about "Reliability and Assurance of the System". | |||||
| 権利 | ||||||
| 権利情報 | Copyright (c) 2009 日本臨床薬理学会 | |||||
| 著者版フラグ | ||||||
| 出版タイプ | VoR | |||||
| 出版タイプResource | http://purl.org/coar/version/c_970fb48d4fbd8a85 | |||||
| 関連URI | ||||||
| 識別子タイプ | URI | |||||
| 関連識別子 | http://www.jscpt.jp/ | |||||
