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眼部药物不良反应上市后监测中的科学挑战。

Scientific challenges in postmarketing surveillance of ocular adverse drug reactions.

作者信息

Fraunfelder Frederick W, Fraunfelder Frederick T

机构信息

Casey Eye Institute, Oregon Health and Science University, 3375 SW Terwilliger Blvd., Portland, OR 97239, USA.

出版信息

Am J Ophthalmol. 2007 Jan;143(1):145-149. doi: 10.1016/j.ajo.2006.10.005. Epub 2006 Nov 13.

Abstract

PURPOSE

To highlight the challenges of postmarketing surveillance for drug-related adverse events in the practice of ophthalmology.

DESIGN

A retrospective review of the medical literature and postmarketing surveillance databases.

METHODS

MEDLINE literature review of sildenafil-associated or amiodarone-associated optic neuropathy and chloramphenicol-associated blood dyscrasias.

RESULTS

Sildenafil, amiodarone, and chloramphenicol may all cause adverse ocular events; however, the data are not conclusive.

CONCLUSIONS

Reports in peer-reviewed medical journals may be proven incorrect over time. For drug-induced adverse ocular events, there is little true science after the drug reaches the marketplace, so the percentage of incorrect conclusions may be high. Clinicians should be wary of reports of adverse ocular effects until data are confirmed by multiple authors over the long-term. Even so, spontaneous reports from postmarketing surveillance databases may be the first and only signal of an adverse ocular event.

摘要

目的

强调眼科实践中药物相关不良事件上市后监测的挑战。

设计

对医学文献和上市后监测数据库进行回顾性分析。

方法

对西地那非相关或胺碘酮相关视神经病变以及氯霉素相关血液系统疾病进行MEDLINE文献综述。

结果

西地那非、胺碘酮和氯霉素均可能导致眼部不良事件;然而,数据并不确凿。

结论

同行评审医学期刊上的报道可能会随着时间的推移被证明是错误的。对于药物引起的眼部不良事件,药物上市后几乎没有真正的科学研究,因此错误结论的比例可能很高。在数据得到多位作者长期证实时,临床医生应警惕眼部不良影响的报道。即便如此,上市后监测数据库的自发报告可能是眼部不良事件的首个也是唯一信号。

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