Will the history and physical examination help establish that irritable bowel syndrome is causing this patient's lower gastrointestinal tract symptoms?

被引:85
作者
Ford, Alexander C. [1 ]
Talley, Nicholas J. [2 ]
van Zanten, Sander J. O. Veldhuyzen [3 ]
Vakil, Nimish B. [4 ]
Simel, David L. [5 ,6 ]
Moayyedi, Paul [1 ]
机构
[1] McMaster Univ, Med Ctr, Div Gastroenterol, Hamilton, ON L8N 3Z5, Canada
[2] Mayo Clin, Dept Med, Jacksonville, FL 32224 USA
[3] Univ Alberta, Div Gastroenterol, Edmonton, AB, Canada
[4] Univ Wisconsin, Sch Med, Dept Med, Madison, WI USA
[5] Durham Vet Affairs Med Ctr, Dept Med, Durham, NC USA
[6] Duke Univ, Durham, NC USA
来源
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION | 2008年 / 300卷 / 15期
关键词
D O I
10.1001/jama.300.15.1793
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Context Many individuals experience lower gastrointestinal tract symptoms, most commonly attributable to functional conditions. These individuals are frequently diagnosed with irritable bowel syndrome ( IBS) based on their symptoms; however, some may require additional testing or referral to specialists before this diagnosis is made. Objective To systematically review the literature of the accuracy of individual symptoms and combinations of findings in diagnosing IBS. Data Sources Search of MEDLINE and EMBASE ( up to June 2008) for prospective studies reporting on unselected cohorts of adult patients with lower gastrointestinal tract symptoms recorded before investigation. Study Selection Studies prospectively evaluating accuracy of individual symptoms or combinations of findings compared with results from investigations of the lower gastrointestinal tract. Data Extraction Two authors independently assessed studies and extracted data to estimate likelihood ratios ( LRs) of individual symptoms and combinations of findings in diagnosing IBS. Results Ten studies evaluating 2355 patients were identified, with a summary prevalence of IBS following investigation of 57%. Individual symptom items yielded positive LRs from 1.2 ( 95% confidence interval [ CI], 0.93- 1.6) for passage of mucus per rectum to 2.1 ( 95% CI, 1.4- 3.0) for looser stools at onset of abdominal pain and negative LRs from 0.29 ( 95% CI, 0.12- 0.72) for no lower abdominal pain to 0.88 ( 95% CI, 0.72- 1.1) for no passage of mucus per rectum in diagnosing IBS. The Manning criteria had a summary positive LR of 2.9 ( 95% CI, 1.3- 6.4) and a summary negative LR of 0.29 ( 95% CI, 0.12- 0.71). The Rome I criteria had a positive LR of 4.8 ( 95% CI, 3.6- 6.5) and a negative LR of 0.34 ( 95% CI, 0.29- 0.41). The Kruis scoring system provided a summary positive LR of 8.6 ( 95% CI, 2.9- 26.0) and a summary negative LR of 0.26 ( 95% CI, 0.17- 0.41). The Rome II and III criteria have not been studied. Conclusions Individual symptoms have limited accuracy for diagnosing IBS in patients referred with lower gastrointestinal tract symptoms. The accuracy of the Manning criteria and Kruis scoring system were only modest. Despite strong advocacy for use of the Rome criteria, only the Rome I classification has been validated. Future research should concentrate on validating existing diagnostic criteria or developing more accurate ways of predicting a diagnosis of IBS without the need for investigation of the lower gastrointestinal tract.
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收藏
页码:1793 / 1805
页数:13
相关论文
共 61 条
  • [1] Agréus L, 2000, SCAND J GASTROENTERO, V35, P142
  • [2] Amer College Gastroenterology Func, 2002, AM J GASTROENTEROL, V97, pS1
  • [3] Aziz Q, 2000, J NEUROSCI, V20, P2657
  • [4] Banerjee Rupa, 2005, Indian J Gastroenterol, V24, P164
  • [5] A SIMPLE SCORE FOR THE IDENTIFICATION OF PATIENTS AT HIGH-RISK OF ORGANIC DISEASES OF THE COLON IN THE FAMILY DOCTOR CONSULTING ROOM
    BELLENTANI, S
    BALDONI, P
    PETRELLA, S
    TATA, C
    ARMOCIDA, C
    MARCHEGIANO, P
    SACCOCCIO, G
    MANENTI, F
    [J]. FAMILY PRACTICE, 1990, 7 (04) : 307 - 312
  • [6] Number of responses on a review of systems - Questionnaire predicts the diagnosis of functional gastrointestinal disorders
    Brown, WH
    Chey, WD
    Elta, GH
    [J]. JOURNAL OF CLINICAL GASTROENTEROLOGY, 2003, 36 (03) : 222 - 227
  • [7] *COCHR COLL, 2007, COCHR METH GROUP SYS
  • [8] METAANALYSIS IN CLINICAL-TRIALS
    DERSIMONIAN, R
    LAIRD, N
    [J]. CONTROLLED CLINICAL TRIALS, 1986, 7 (03): : 177 - 188
  • [9] Dogan UB, 1996, ACTA GASTRO-ENT BELG, V59, P225
  • [10] Drossman DA, 1999, GUT, V45, P1