Q-tracks: a College of American Pathologists program of continuous laboratory monitoring and longitudinal tracking.

CONTEXT Continuous monitoring of key laboratory indicators of quality by hundreds of laboratories in a standardized measurement program affords an opportunity to document the influence of longitudinal tracking on performance improvement by participants focused on that outcome. OBJECTIVE To describe the results of the first 2 years of participation in a unique continuous performance assessment program for pathology and laboratory medicine. DESIGN Participants in any of 6 modules in the 1999 and 2000 College of American Pathologists (CAP) Q-Tracks program collected data according to defined methods and sampling intervals on standardized input forms. Data were submitted quarterly to CAP for statistical analysis. Interinstitutional comparison reports returned in 6 weeks provided each laboratory with its performance profile of key indicators and its percentile ranking compared with all participants in that quarter. This also included longitudinal comparisons of performance during previous cumulative quarters. Control charts graphically displayed data with flags identifying performance points that were out of statistical control. SETTING Hospital-based laboratories in the United States (98%), Canada, and Australia. PARTICIPANTS Voluntary subscriber laboratories in the CAP Q-Tracks performance measurement program: roughly 70% from hospitals of 300 occupied beds or fewer, 65% from private, nonprofit institutions, slightly more than half located in cities, one third from teaching hospitals, and 20% with pathology residency training programs. MAIN OUTCOME MEASURES Each module measured several major and additional minor quality indicators and unbenchmarked individualized data for internal use. RESULTS Participants in 4 of 6 Q-Tracks continuous monitors demonstrated statistically significant performance improvement trends in 1999 and 2000, which were most marked for laboratories that continued participation throughout both years. These monitors were wristband patient identification, laboratory specimen acceptability, blood product wastage, and intraoperative frozen section consultation. CONCLUSIONS Key continuous indicators chosen on the basis of a decade's experience in the CAP Q-Probes quality improvement program are useful measurement and benchmarking tools for laboratories to improve performance. In general, measures in which there is a broad range of demonstrable performance initially are most optimal for subsequent improvement using continuous monitoring. These studies have shown that quality is not static, but rather is a moving benchmark of performance as seen in the redefinition of benchmarks over time by participants in the first 2 years of the CAP Q-Tracks program.

[1]  B. Jones,et al.  Quality management in gynecologic cytology using interlaboratory comparison. , 2009, Archives of pathology & laboratory medicine.

[2]  Howanitz Pj,et al.  Chemistry specimen acceptability: a College of American Pathologists Q-Probes study of 453 laboratories. , 1997 .

[3]  L Goldman,et al.  Contaminant blood cultures and resource utilization. The true consequences of false-positive results. , 1991, JAMA.

[4]  E. Spitznagel,et al.  A randomized trial of povidone-iodine compared with iodine tincture for venipuncture site disinfection: effects on rates of blood culture contamination. , 1999, The American journal of medicine.

[5]  P Bachner,et al.  Wristband identification error reporting in 712 hospitals. A College of American Pathologists' Q-Probes study of quality issues in transfusion practice. , 1993, Archives of pathology & laboratory medicine.

[6]  Argie Leach,et al.  Assessing the Competence of Specimen-Processing Personnel , 2000 .

[7]  D Nevalainen,et al.  Evaluating laboratory performance on quality indicators with the six sigma scale. , 2000, Archives of pathology & laboratory medicine.

[8]  R. Zarbo,et al.  Interinstitutional comparison of frozen section consultations. A college of American Pathologists Q-Probes study of 90,538 cases in 461 institutions. , 1996, Archives of pathology & laboratory medicine.

[9]  F. Meier,et al.  Blood culture contamination: a College of American Pathologists Q-Probes study involving 640 institutions and 497134 specimens from adult patients. , 1998, Archives of pathology & laboratory medicine.

[10]  M. Schiffman,et al.  Interobserver reproducibility of cervical cytologic and histologic interpretations: realistic estimates from the ASCUS-LSIL Triage Study. , 2001, JAMA.

[11]  R. Brant,et al.  Reduction in blood culture contamination rate by feedback to phlebotomists. , 1997, Archives of pathology & laboratory medicine.

[12]  R. Zarbo,et al.  Interinstitutional comparison of frozen section consultation in small hospitals: a College of American Pathologists Q-Probes study of 18,532 frozen section consultation diagnoses in 233 small hospitals. , 1996, Archives of pathology & laboratory medicine.

[13]  R G Carey,et al.  Measuring Health Care Quality , 2000, Evaluation & the health professions.

[14]  Jane C. Dale,et al.  Wristband Errors in Small Hospitals: A College of American Pathologists’ Q-Probes Study of Quality Issues in Patient Identification , 1997 .

[15]  F. Meier,et al.  Complete blood count specimen acceptability. A College of American Pathologists Q-Probes study of 703 laboratories. , 1995, Archives of pathology & laboratory medicine.

[16]  S. Woodhouse,et al.  Managed discontinuity of care: The value and fate of cytohistologic correlation , 1997 .

[17]  S. Narayanan,et al.  The preanalytic phase. An important component of laboratory medicine. , 2000, American journal of clinical pathology.

[18]  Jones Ba,et al.  Cervical biopsy-cytology correlation. A College of American Pathologists Q-Probes study of 22 439 correlations in 348 laboratories. , 1996 .

[19]  P J Howanitz,et al.  Interinstitutional comparison of frozen-section consultation. A College of American Pathologists Q-Probe study of 79,647 consultations in 297 North American institutions. , 1991, Archives of pathology & laboratory medicine.

[20]  S. Selvaggi Implications of low diagnostic reproducibility of cervical cytologic and histologic diagnoses. , 2001, JAMA.

[21]  A. Morselli-Labate,et al.  Intralaboratory quality assurance in cervical/vaginal cytology: Evaluation of intercytologist diagnostic reproducibility , 1997, Diagnostic cytopathology.