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首页> 外文期刊>Pharmacoepidemiology and drug safety >Validity of diagnostic codes to identify cases of severe acute liver injury in the U.S. Food and Drug Administration's Mini-Sentinel Distributed Database.
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Validity of diagnostic codes to identify cases of severe acute liver injury in the U.S. Food and Drug Administration's Mini-Sentinel Distributed Database.

机译:诊断码鉴定美国食品和药物管理局迷你哨兵分布式数据库严重急性肝损伤病例的有效性。

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摘要

The validity of International Classification of Diseases, Ninth Revision, Clinical Modification (ICD-9-CM) codes to identify diagnoses of severe acute liver injury (SALI) is not well known. We examined the positive predictive values (PPVs) of hospital ICD-9-CM diagnoses in identifying SALI among health plan members in the Mini-Sentinel Distributed Database (MSDD) for patients without liver/biliary disease and for those with chronic liver disease (CLD).We selected random samples of members (149 without liver/biliary disease; 75 with CLD) with a principal hospital diagnosis suggestive of SALI (ICD-9-CM 570, 572.2, 572.4, 572.8, 573.3, 573.8, or V42.7) in the MSDD (2009-2010). Medical records were reviewed by hepatologists to confirm SALI events. PPVs of codes and code combinations for confirmed SALI were determined by CLD status.Among 105 members with available records and no liver/biliary disease, SALI was confirmed in 26 (PPV, 24.7%; 95%CI, 16.9-34.1%). Combined hospital diagnoses of acute hepatic necrosis (570) and liver disease sequelae (572.8) had high PPV (100%; 95%CI, 59.0-100%) and identified 7/26 (26.9%) events. Among 46 CLD members with available records, SALI was confirmed in 19 (PPV, 41.3%; 95%CI, 27.0-56.8%). Acute hepatic necrosis (570) or hepatorenal syndrome (572.4) plus any other SALI code had a PPV of 83.3% (95%CI, 51.6-97.9%) and identified 10/19 (52.6%) events.Most individual hospital ICD-9-CM diagnoses had low PPV for confirmed SALI events. Select code combinations had high PPV but did not capture all events. Copyright ? 2013 John Wiley & Sons, Ltd.
机译:国际疾病分类的有效性,第九修正,临床修改(ICD-9-CM)判断诊断严重急性肝损伤(SALI)的诊断并不众所周知。我们研究了医院ICD-9-CM的阳性预测值(PPV)诊断,诊断迷你哨兵分布式数据库(MSDD)中的卫生计划成员之间的萨利,为没有肝脏/胆道疾病的患者,以及慢性肝病的患者(CLD )。我们选择了成员的随机样本(149,没有肝脏/胆管; 75种,CLD),萨利的主要医院诊断(ICD-9-CM 570,572.2,572.4,572.8,573.3,573.8或V42.7 )在MSDD(2009-2010)中。肝脏学家审查了病程以确认Sali事件。通过CLD状态确定了CODES和CODE组合的PPV。CLD状态确定了可用记录的105个成员,没有肝脏/胆道疾病,SALI在26例(PPV,24.7%; 95%CI,16.9-34.1%)。急性肝脏坏死(570)和肝病后遗症(572.8)的组合医院诊断具有高PPV(100%; 95%CI,59.0-100%),并确定7/26(26.9%)事件。在有可用记录的46个CLD成员中,萨利于19名(PPV,41.3%; 95%CI,27.0-56.8%)。急性肝脏坏死(570)或Hepatorenal综合征(572.4)加上任何其他Sali码的PPV为83.3%(95%CI,51.6-97.9%),并确定了10/19(52.6%)事件。最具个体医院ICD-9 -CM诊断具有低PPV的确认Sali事件。选择代码组合具有高PPV,但未捕获所有事件。版权? 2013年John Wiley&Sons,Ltd。

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