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开发澳大利亚黑色素瘤临床结局登记处(MelCOR)的黑色素瘤临床质量指标:一项改良 Delphi 研究。

Development of melanoma clinical quality indicators for the Australian melanoma clinical outcomes registry (MelCOR): A modified Delphi study.

机构信息

Victorian Melanoma Service, Alfred Hospital, Melbourne, Victoria, Australia.

School of Public Health and Preventive Medicine, Monash University, Melbourne, Victoria, Australia.

出版信息

Australas J Dermatol. 2022 Aug;63(3):344-351. doi: 10.1111/ajd.13848. Epub 2022 Apr 29.

Abstract

BACKGROUND

Clinical quality registries aim to identify significant variations in care and provide anonymised feedback to institutions to improve patient outcomes. Thirty-six Australian organisations with an interest in melanoma, raised funds through three consecutive Melanoma Marches, organised by Melanoma Institute Australia, to create a national Melanoma Clinical Outcomes Registry (MelCOR). This study aimed to formally develop valid clinical quality indicators for the diagnosis and early management of cutaneous melanoma as an important step in creating the registry.

METHODS

Potential clinical quality indicators were identified by examining the literature, including Australian and international melanoma guidelines, and by consulting with key melanoma and registry opinion leaders. A modified two-round Delphi survey method was used, with participants invited from relevant health professions routinely managing melanoma as well as relevant consumer organisations.

RESULTS

Nineteen participants completed at least one round of the Delphi process. 12 of 13 proposed clinical quality indictors met the validity criteria. The clinical quality indicators included acceptable biopsy method, appropriate excision margins, standardised pathology reporting, indications for sentinel lymph node biopsy, and involvement of multidisciplinary care and referrals.

CONCLUSION

This study provides a multi-stakeholder consensus for important clinical quality indicators that define optimal practice that will now be used in the Australian Melanoma Clinical Outcomes Registry (MelCOR).

摘要

背景

临床质量登记册旨在识别护理中的显著差异,并向医疗机构提供匿名反馈,以改善患者的治疗效果。36 家对黑色素瘤感兴趣的澳大利亚机构通过澳大利亚黑色素瘤研究所组织的三次连续黑色素瘤游行筹集资金,创建了一个全国性的黑色素瘤临床结果登记册(MelCOR)。本研究旨在通过检查文献,包括澳大利亚和国际黑色素瘤指南,并咨询黑色素瘤和登记册的主要意见领袖,正式制定用于诊断和早期管理皮肤黑色素瘤的有效临床质量指标,这是创建登记册的重要步骤。

方法

通过检查文献,包括澳大利亚和国际黑色素瘤指南,并咨询黑色素瘤和登记册的主要意见领袖,确定潜在的临床质量指标。采用改良的两轮德尔菲调查方法,邀请相关卫生专业人员(常规管理黑色素瘤)和相关消费者组织参与。

结果

19 名参与者至少完成了一轮德尔菲调查过程。13 个拟议的临床质量指标中有 12 个符合有效性标准。临床质量指标包括可接受的活检方法、适当的切除边缘、标准化的病理报告、前哨淋巴结活检的适应证,以及多学科护理和转诊的参与。

结论

本研究为定义最佳实践的重要临床质量指标提供了多利益相关者共识,这些指标将在澳大利亚黑色素瘤临床结果登记册(MelCOR)中使用。

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