The Eurocleft Project, 1996-2000
著者
書誌事項
The Eurocleft Project, 1996-2000
(Biomedical and health research, v. 43)
IOS Press , Ohmsha[distributor], c2000
- : IOS Press
- : Ohmsha
- タイトル別名
-
The Eurocleft Project, 1996-2000 : standards of care for cleft lip & plate in Europe
大学図書館所蔵 全3件
  青森
  岩手
  宮城
  秋田
  山形
  福島
  茨城
  栃木
  群馬
  埼玉
  千葉
  東京
  神奈川
  新潟
  富山
  石川
  福井
  山梨
  長野
  岐阜
  静岡
  愛知
  三重
  滋賀
  京都
  大阪
  兵庫
  奈良
  和歌山
  鳥取
  島根
  岡山
  広島
  山口
  徳島
  香川
  愛媛
  高知
  福岡
  佐賀
  長崎
  熊本
  大分
  宮崎
  鹿児島
  沖縄
  韓国
  中国
  タイ
  イギリス
  ドイツ
  スイス
  フランス
  ベルギー
  オランダ
  スウェーデン
  ノルウェー
  アメリカ
注記
Includes bibliographical references (p. 277-278)
"European Commission Directorate-General XII, science, research and development" -- cover
内容説明・目次
内容説明
"The European Register of Cleft Lip and Palate Services" will be produced as a result of the concerted action project: "Standards of Care for Cleft Lip and Palate in Europe: EUROCLEFT" funded by the European Commision under its BIOMED II and INCO COPERNICUS programmes. The project, aimed at developing a network of cleft care teams across Europe, ran for three years between 1996 and 1999 and aimed broadly to improve the effectiveness and efficiency of care for European children with clefts of the lip and/or palate. Clefts of the lip and/or palate are birth defects affecting 1:500 live births. Successful rehabilitation requires a complex multidisciplinary mix of services. The work of the project has shown that the organization of cleft care across Europe varies dramatically from highly centralized national teams to poorly coordinated local services. Clinical protocols of care also differ widely and are seldom evidence based. There is no commonly agreed method of quality assurance and resources for research on treatment and prevention are fragmented.
The Register will include: an inventory of services across Europe, with details of approximately 190 teams involved in cleft care, service organization, clinical protocols and special facilities for research; a set of common Policy Statements governing clinical practice for European cleft teams; a set of common Practice Guidelines describing minimum recommendations for care that all European children with clefts should be entitled to; and a set of common recommendations for Documentation governing minimum records that cleft teams should maintain systematic reviews of clinical trials in the literature. This publication will be circulated to all registered centres of the project, governments, health authorities and relevant professional bodies in an effort to raise the profile of cleft lip and palate care in Europe.
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