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风湿性多肌痛和巨细胞动脉炎——诊断困难。

Polymyalgia rheumatica and giant cell arteritis--a difficult diagnosis.

作者信息

Jones J G, Hazleman B L

出版信息

J R Coll Gen Pract. 1981 May;31(226):283-9.

Abstract

This five-year study of 108 patients with giant cell arteritis and/or polymyalgia rheumatica drawn from all departments of a district general hospital emphasizes the difficulties of diagnosis. A correct diagnosis was made by the referring doctor in 33 per cent of patients and on initial attendance at hospital in 67 per cent of patients. Symptoms were present for more than three months before referral to hospital in 39 per cent of patients, and the delay before diagnosis at hospital was greater than one month in 20 per cent. Systemic illness (present in 83 per cent of cases), anaemia (33 per cent), elevated alkaline phosphatase (73 per cent) and raised immunoglobulin levels (48 per cent) caused diagnostic problems in 28 patients at primary care level and in 23 patients at hospital.

摘要

这项对一家地区综合医院各科室108例巨细胞动脉炎和/或风湿性多肌痛患者进行的为期五年的研究强调了诊断的困难。转诊医生对33%的患者做出了正确诊断,67%的患者在初次就诊时被正确诊断。39%的患者在转诊至医院前症状已持续三个月以上,20%的患者在医院诊断前的延迟超过一个月。全身性疾病(83%的病例存在)、贫血(33%)、碱性磷酸酶升高(73%)和免疫球蛋白水平升高(48%)在基层医疗水平上给28例患者和在医院给23例患者造成了诊断难题。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39b1/1971040/89fb60473cec/jroyalcgprac00101-0033-a.jpg

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