ガイドラインの簡潔な言語版の開発プロセス 勧告:範囲の見直し
Alena Langaufova1, Tereza Friessova1, Dana Dolanova1
1Department of Health Sciences, Faculty of Medicine, Masaryk University, Brno, Czech Republic.
Journal of evaluation in clinical practice
|August 28, 2025
まとめ
医療ガイドラインの簡潔な言語の勧告 (PLR) を策定するには,方法論的な証拠が必要です. このレビューは,多様な聴衆のための理解可能な健康情報の作成と実施を支援する証拠をまとめています.
科学分野:
- 健康に関する情報
- 証拠の統合
- ガイドライン開発
背景:
- 複雑な健康ガイドラインを入手できるようにするには,シンプルな言語の勧告 (PLR) が不可欠です.
- 明確で分かりやすい健康情報は 患者の関わりと情報に基づいた意思決定に不可欠です
研究 の 目的:
- 医療の文脈でシンプルな言語の勧告 (PLRs) を開発するための方法論的証拠を統合する.
- 理解しやすい健康ガイドラインを作成するためのベストプラクティスとリソースを特定する.
主な方法:
- JBIの基準とPRISMA-ScRのガイドラインに従ってスコーピングレビューの方法論が採用されました.
- 主要なデータベース (MEDLINE,Embase) とガイドライン開発者のリポジトリで体系的な検索が行われました.
- データは独立して抽出され 物語的に合成されました
主要な成果:
- ガイドライン開発者からの9つの記事と8つの文書が含まれており,PLRの開発と方法論を詳細に説明しています.
- インフォグラフィックと患者の関与は,さまざまなターゲットグループ (患者,公衆,政策立案者,医療提供者) のためのPLR作成において一般的です.
- GIN Public Toolkit,RIGHT-PVG,およびDISCERNのようなリソースは,PLRの開発をサポートすることができます.
結論:
- 医療のPLRの開発と実施には政策支援が推奨されています.
- コミュニケーション戦略の報告とPLRの理解性と実行可能性の検証は極めて重要です.
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