真实世界环境中的全国性黑色素瘤登记数据库：范围界定审查协议

medRxiv - Dermatology Pub Date : 2024-08-29 DOI:10.1101/2024.08.28.24311481

Songchun Yang, Dilan Deng, Wenrui Lin, Xiaozhen Chen, Shuang Zhao, Lixia Lu, Yi Xiao, Minxue Shen, Mingliang Chen, Xiang Chen, Juan Su

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引用次数: 0

摘要

导言病人登记数据库是解决各种研究问题的重要工具。一些国家已经建立了全国性的黑色素瘤登记数据库。然而，目前还没有对这些数据库进行总结和比较的报告。本范围综述旨在回答一个广泛的问题，即当代全国性黑色素瘤登记数据库是如何在不同国家开展工作的。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

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Nationwide melanoma registry databases in real-world settings: a scoping review protocol

Introduction A patient registry database is an important tool to address a wide range of research questions. Several countries have established nationwide melanoma registry databases. However, there is no report on summarising and comparing these databases. This scoping review aims to answer a broad question on how contemporary nationwide melanoma registry databases were conducted across different countries.

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medRxiv - Dermatology

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