Evidence-based Diagnostics: Adult Septic Arthritis

被引:0
作者
Carpenter, Christopher R. [1 ]
Schuur, Jeremiah D. [2 ]
Everett, Worth W. [3 ]
Pines, Jesse M. [4 ]
机构
[1] Washington Univ, Sch Med, Div Emergency Med, St Louis, MO 63130 USA
[2] Brigham & Womens Hosp, Dept Emergency Med, Salt Lake City, UT USA
[3] Skagit Valley Hosp, Dept Emergency Med, Mt Vernon, IA USA
[4] George Washington Univ, Dept Emergency Med, Washington, DC USA
基金
美国医疗保健研究与质量局;
关键词
FLUID LACTIC-ACID; EMERGENCY-DEPARTMENT PATIENTS; SYNOVIAL-FLUID; BACTERIAL ARTHRITIS; INFECTIOUS ARTHRITIS; SERUM PROCALCITONIN; THRESHOLD APPROACH; LIKELIHOOD RATIOS; LABORATORY TESTS; DECISION-MAKING;
D O I
10.1111/j.1553-2712.2011.01121.x
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Background: Acutely swollen or painful joints are common complaints in the emergency department (ED). Septic arthritis in adults is a challenging diagnosis, but prompt differentiation of a bacterial etiology is crucial to minimize morbidity and mortality. Objectives: The objective was to perform a systematic review describing the diagnostic characteristics of history, physical examination, and bedside laboratory tests for nongonococcal septic arthritis. A secondary objective was to quantify test and treatment thresholds using derived estimates of sensitivity and specificity, as well as best-evidence diagnostic and treatment risks and anticipated benefits from appropriate therapy. Methods: Two electronic search engines (PUBMED and EMBASE) were used in conjunction with a selected bibliography and scientific abstract hand search. Inclusion criteria included adult trials of patients presenting with monoarticular complaints if they reported sufficient detail to reconstruct partial or complete 2 x 2 contingency tables for experimental diagnostic test characteristics using an acceptable criterion standard. Evidence was rated by two investigators using the Quality Assessment Tool for Diagnostic Accuracy Studies (QUADAS). When more than one similarly designed trial existed for a diagnostic test, meta-analysis was conducted using a random effects model. Interval likelihood ratios (LRs) were computed when possible. To illustrate one method to quantify theoretical points in the probability of disease whereby clinicians might cease testing altogether and either withhold treatment (test threshold) or initiate definitive therapy in lieu of further diagnostics (treatment threshold), an interactive spreadsheet was designed and sample calculations were provided based on research estimates of diagnostic accuracy, diagnostic risk, and therapeutic risk/benefits. Results: The prevalence of nongonococcal septic arthritis in ED patients with a single acutely painful joint is approximately 27% (95% confidence interval [CI] = 17% to 38%). With the exception of joint surgery (positive likelihood ratio [+LR] = 6.9) or skin infection overlying a prosthetic joint (+LR = 15.0), history, physical examination, and serum tests do not significantly alter posttest probability. Serum inflammatory markers such as white blood cell (WBC) counts, erythrocyte sedimentation rate (ESR), and C-reactive protein (CRP) are not useful acutely. The interval LR for synovial white blood cell (sWBC) counts of 0 x 10(9)-25 x 10(9)/L was 0.33; for 25 x 10(9)-50 x 10(9)/L, 1.06; for 50 x 10(9)-100 x 10(9)/L, 3.59; and exceeding 100 x 10(9)/L, infinity. Synovial lactate may be useful to rule in or rule out the diagnosis of septic arthritis with a +LR ranging from 2.4 to infinity, and negative likelihood ratio (-LR) ranging from 0 to 0.46. Rapid polymerase chain reaction (PCR) of synovial fluid may identify the causative organism within 3 hours. Based on 56% sensitivity and 90% specificity for sWBC counts of >50 x 10(9)/L in conjunction with best-evidence estimates for diagnosis-related risk and treatment-related risk/benefit, the arthrocentesis test threshold is 5%, with a treatment threshold of 39%. Conclusions: Recent joint surgery or cellulitis overlying a prosthetic hip or knee were the only findings on history or physical examination that significantly alter the probability of nongonococcal septic arthritis. Extreme values of sWBC (>50 x 10(9)/L) can increase, but not decrease, the probability of septic arthritis. Future ED-based diagnostic trials are needed to evaluate the role of clinical gestalt and the efficacy of nontraditional synovial markers such as lactate. ACADEMIC EMERGENCY MEDICINE 2011; 18:782-796 (C) 2011 by the Society for Academic Emergency Medicine
引用
收藏
页码:782 / 796
页数:15
相关论文
共 92 条
  • [61] Parrillo SJ, 2010, CLIN PROCEDURES EMER, P971
  • [62] THE THRESHOLD APPROACH TO CLINICAL DECISION-MAKING
    PAUKER, SG
    KASSIRER, JP
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1980, 302 (20) : 1109 - 1117
  • [63] Pretest probability estimates: A pitfall to the clinical utility of evidence-based medicine?
    Phelps, MA
    Levitt, MA
    [J]. ACADEMIC EMERGENCY MEDICINE, 2004, 11 (06) : 692 - 694
  • [64] Pines J., 2008, Evidence-based emergency care: diagnostic testing and clinical decision rules
  • [65] Could our pretest probabilities become evidence based? A prospective survey of hospital practice
    Richardson, WS
    Polashenski, WA
    Robbins, BW
    [J]. JOURNAL OF GENERAL INTERNAL MEDICINE, 2003, 18 (03) : 203 - 208
  • [66] SYNOVIAL-FLUID LACTIC-ACID MEASUREMENT IN THE DIAGNOSIS AND MANAGEMENT OF SEPTIC ARTHRITIS
    RIORDAN, T
    DOYLE, D
    TABAQCHALI, S
    [J]. JOURNAL OF CLINICAL PATHOLOGY, 1982, 35 (04) : 390 - 394
  • [67] ACUTE NON-GONOCOCCAL INFECTIOUS ARTHRITIS - EVALUATION OF RISK-FACTORS, THERAPY, AND OUTCOME
    ROSENTHAL, J
    BOLE, GG
    ROBINSON, WD
    [J]. ARTHRITIS AND RHEUMATISM, 1980, 23 (08): : 889 - 897
  • [68] Evidence of bias and variation in diagnostic accuracy studies
    Rutjes, AWS
    Reitsma, JB
    Di Nisio, M
    Smidt, N
    van Rijn, JC
    Bossuyt, PMM
    [J]. CANADIAN MEDICAL ASSOCIATION JOURNAL, 2006, 174 (04) : 469 - 476
  • [69] Saraux A, 1997, BRIT J RHEUMATOL, V36, P333
  • [70] BACTERIAL ARTHRITIS - ARE FEVER, RIGORS, LEUKOCYTOSIS AND BLOOD CULTURES OF DIAGNOSTIC-VALUE
    SCHLAPBACH, P
    AMBORD, C
    BLOCHLINGER, AM
    GERBER, NJ
    [J]. CLINICAL RHEUMATOLOGY, 1990, 9 (01) : 69 - 72