Margaretten Mary E, Kohlwes Jeffrey, Moore Dan, Bent Stephen
Division of Rheumatology, Prime Program, Department of Medicine, University of California, San Francisco, CA 94143-0633, USA.
JAMA. 2007 Apr 4;297(13):1478-88. doi: 10.1001/jama.297.13.1478.
In patients who present with an acutely painful and swollen joint, prompt identification and treatment of septic arthritis can substantially reduce morbidity and mortality.
To review the accuracy and precision of the clinical evaluation for the diagnosis of nongonococcal bacterial arthritis.
Structured PubMed and EMBASE searches (1966 through January 2007), limited to human, English-language articles and using the following Medical Subject Headings terms: arthritis, infectious, physical examination, medical history taking, diagnostic tests, and sensitivity and specificity.
Studies were included if they contained original data on the accuracy or precision of historical items, physical examination, serum, or synovial fluid laboratory data for diagnosing septic arthritis.
Three authors independently abstracted data from the included studies.
Fourteen studies involving 6242 patients, of whom 653 met the gold standard for the diagnosis of septic arthritis, satisfied all inclusion criteria. Two studies examined risk factors and found that age, diabetes mellitus, rheumatoid arthritis, joint surgery, hip or knee prosthesis, skin infection, and human immunodeficiency virus type 1 infection significantly increase the probability of septic arthritis. Joint pain (sensitivity, 85%; 95% confidence interval [CI], 78%-90%), a history of joint swelling (sensitivity, 78%; 95% CI, 71%-85%), and fever (sensitivity, 57%; 95% CI, 52%-62%) are the only findings that occur in more than 50% of patients. Sweats (sensitivity, 27%; 95% CI, 20%-34%) and rigors (sensitivity, 19%; 95% CI, 15%-24%) are less common findings in septic arthritis. Of all laboratory findings readily available to the clinician, the 2 most powerful were the synovial fluid white blood cell (WBC) count and percentage of polymorphonuclear cells from arthrocentesis. The summary likelihood ratio (LR) increased as the synovial fluid WBC count increased (for counts <25,000/microL: LR, 0.32; 95% CI, 0.23-0.43; for counts > or =25,000/microL: LR, 2.9; 95% CI, 2.5-3.4; for counts >50,000/microL: LR, 7.7; 95% CI, 5.7-11.0; and for counts >100,000/microL: LR, 28.0; 95% CI, 12.0-66.0). On the same synovial fluid sample, a polymorphonuclear cell count of at least 90% suggests septic arthritis with an LR of 3.4 (95% CI, 2.8-4.2), while a polymorphonuclear cell count of less than 90% lowers the likelihood (LR, 0.34; 95% CI, 0.25-0.47).
Clinical findings identify patients with peripheral, monoarticular arthritis who might have septic arthritis. However, the synovial WBC and percentage of polymorphonuclear cells from arthrocentesis are required to assess the likelihood of septic arthritis before the Gram stain and culture test results are known.
对于出现关节急性疼痛和肿胀的患者,及时识别和治疗化脓性关节炎可显著降低发病率和死亡率。
回顾临床评估诊断非淋菌性细菌性关节炎的准确性和精确性。
对PubMed和EMBASE进行结构化检索(1966年至2007年1月),限于人类英文文章,并使用以下医学主题词:关节炎、感染性、体格检查、病史采集、诊断试验以及敏感性和特异性。
如果研究包含关于历史项目、体格检查、血清或滑液实验室数据诊断化脓性关节炎的准确性或精确性的原始数据,则纳入研究。
三位作者独立从纳入研究中提取数据。
14项研究涉及6242例患者,其中653例符合化脓性关节炎诊断的金标准,满足所有纳入标准。两项研究检查了危险因素,发现年龄、糖尿病、类风湿关节炎、关节手术、髋或膝关节假体、皮肤感染和1型人类免疫缺陷病毒感染显著增加化脓性关节炎的可能性。关节疼痛(敏感性85%;95%置信区间[CI],78% - 90%)、关节肿胀史(敏感性78%;95% CI,71% - 85%)和发热(敏感性57%;95% CI,52% - 62%)是仅在超过50%的患者中出现的表现。盗汗(敏感性27%;95% CI,20% - 34%)和寒战(敏感性19%;95% CI,15% - 24%)在化脓性关节炎中较少见。对于临床医生可获得的所有实验室检查结果,最具诊断价值的两项是滑液白细胞(WBC)计数和关节穿刺抽出液中多形核细胞百分比。随着滑液WBC计数增加,汇总似然比(LR)升高(计数<25,000/μL:LR,0.32;95% CI,0.23 - 0.43;计数≥25,000/μL:LR,2.9;95% CI,2.5 - 3.4;计数>50,000/μL:LR,7.7;95% CI,5.7 - 11.0;计数>100,000/μL:LR,28.0;95% CI,12.0 - 66.0)。在同一滑液样本中,多形核细胞计数至少90%提示化脓性关节炎,LR为3.4(95% CI,2.8 - 4.2),而多形核细胞计数低于90%则降低可能性(LR,0.34;95% CI,0.25 - 0.47)。
临床检查结果可识别可能患有化脓性关节炎的外周单关节关节炎患者。然而,在革兰氏染色和培养试验结果出来之前,需要通过关节穿刺获得的滑液白细胞计数和多形核细胞百分比来评估化脓性关节炎的可能性。