CAP Laboratory Improvement Programs. Clinical Consequences of Specimen Rejection

CAP Laboratory Improvement Programs Clinical Consequences of Specimen Rejection A College of American Pathologists Q-Probes Analysis of 78 Clinical Laboratories Donald S. Karcher, MD; Christopher M. Lehman, MD Context. Clinical laboratory specimens may be rejected as unsuitable for analysis for a variety of reasons and specimen rejection may have significant clinical consequences. Objective. To quantify the clinical consequences of specimen rejection and determine the impact of laboratories policies and practices on these consequences. Design. Participants prospectively reviewed consecutive blood and urine specimens submitted to the chemistry and/or hematology laboratories to identify rejected specimens. For each rejected specimen, the patient s age, specimen type, testing priority, rejection reason, time from specimen receipt to receipt of recollected/relabeled specimen, recollection method, and test result time were recorded. Specimen/test abandonment was determined by failure to recollect or relabel a rejected specimen. Each laboratory s policy regarding relabeling of incorrectly labeled specimens was recorded, along with how many relabeled specimens were subsequently discovered to be mislabeled. Results. Specimen rejection led to a (1) high rate of specimen recollection, (2) delay in result availability (median of 65 minutes), and (3) high rate of specimen/ test abandonment. Longer test result delay was associated with higher hospital bed size; and higher test abandonment rate, with failure of the laboratory to request specimen recollection. Relabeling of incorrectly labeled specimens was found to be of little benefit and was associated with a substantial percentage of subsequently mislabeled specimens. Conclusions. Specimen rejection has significant clinical consequences, including patient discomfort, significant delay in result availability, and high rate of specimen/test abandonment. Allowing routine relabeling of incorrectly labeled specimens is a dangerous practice, with little measureable benefit and with an increased risk to patient safety. (Arch Pathol Lab Med. 2014;138:1003 1008; doi: 10.5858/arpa.2013-0331-CP) Specimens submitted to the clinical laboratory may be rejected as unsuitable for analysis for a variety of reasons, including inaccurate or inadequate labeling of the specimen and defects in specimen quality or quantity. Specimens submitted to the chemistry and hematology laboratories are typically rejected at an approximate mean rate of 1.0% or less of all specimens submitted, with the rate usually higher for inpatients and patients in the emergency department than for outpatients. 1 4 Specimen rejection may have significant consequences for patients and their clinical management. Patients whose specimens are rejected are frequently subjected to repeated specimen collection, resulting in inconvenience, the discomfort of repeated phlebotomy or other collection procedures, and/or the potential need for blood transfusion due to excessive iatrogenic blood loss. Specimen rejection and the need for specimen recollection or correction also ultimately lead to a delay in specimen analysis and the availability of test results and may lead to abandonment of the test(s) requested. The prolonged turnaround time is clinically most significant for tests ordered with a stat testing priority, but similar delays may also impact routine and other nonstat tests. This study was designed to quantify the effect of laboratory specimen rejection on the need to recollect specimens, the delay in test result availability, and the rate of test abandonment, and to determine the impact on test result availability of the (1) reason for specimen rejection, (2) detection method used for mislabeled specimens, and (3) the laboratory s policy regarding resolution of improperly labeled specimens. In addition, an attempt was made to measure the accuracy of relabeling of incorrectly labeled specimens, if allowed by the laboratory. Accepted for publication October 7, 2013. From the Department of Pathology, The George Washington University Medical Center, Washington, DC (Dr Karcher); and the Department of Pathology, University of Utah School of Medicine, Salt Lake City (Dr Lehman). MATERIALS AND METHODS Study Design The authors have no relevant financial interest in the products or companies described in this article. Participants prospectively reviewed consecutive blood and urine Reprints: Donald S. Karcher, MD, Department of Pathology, The specimens submitted to the central chemistry and/or hematology George Washington University Medical Center, 2100 W Pennsylvania (including coagulation) laboratory sections to identify specimens Ave, NW, 5th Floor, Suite 5027, Washington, DC 20037 (e-mail: dkarcher@mfa.gwu.edu). that were rejected for any reason. This process was conducted on all laboratory shifts until 80 rejected specimens that fit the study Arch Pathol Lab Med Vol 138, August 2014 Specimen Rejection Karcher & Lehman 1003

Table 1. Definitions of Terms Provided to Participants Test accession: A test order that resulted in a unique laboratory accession number. Rejected specimen: A specimen that was found for any reason to be unsuitable for analysis before initiation of testing or a specimen found, before or after completion of testing, to be mislabeled or otherwise inappropriate as a result of comparison of the specimen label to the requisition form or electronic test order, or comparison of the current test results to previous laboratory results for the same patient (delta check analysis) or to the patient s clinical status. Improperly labeled specimen: A specimen that was (1) unlabeled, (2) incompletely labeled (does not include the minimum information required by institutional guidelines), (3) labeled with information not in adequate agreement with the accompanying requisition form or electronic test order, or (4) mislabeled (ie, found to not be from the intended patient, by any method of detection). Inappropriate or inadequate specimen: A specimen found to be unsuitable for analysis as a result of (1) hemolysis, (2) unintended clotting, (3) inadequate quantity, (4) inappropriate anticoagulant and/or collection container, (5) improper method of collection, (6) excessive time from collection to receipt in the laboratory, or (7) inappropriate storage conditions before receipt in the laboratory. Laboratory check of specimen label ( lab check ): Means of detecting mislabeled specimens by laboratory personnel proactively comparing the specimen label to the accompanying requisition form or electronic test order. Delta check: Means of detecting mislabeled specimens by laboratory personnel and/or the laboratory information system comparing test results to previous results for the same patient. Laboratory correlation with clinical picture ( clinical picture lab ): Means of detecting mislabeled specimens by laboratory personnel proactively comparing test results to the patient s clinical picture. Feedback from patient s clinical care team ( feedback from caregiver ): Detection of a mislabeled specimen by feedback received from the patient s clinical care team indicating that the test result(s) is(are) inappropriate for the patient s clinical picture. Note: Although this would occur after initial test result(s) had already been reported, this was still considered rejection of the original specimen and included in the study. Corrected specimen: A specimen found to be improperly labeled and then allowed to be relabeled correctly without requiring recollection. Recollected specimen: A specimen recollected in direct response to rejection of a specimen previously collected for the same test(s). Note: For the purposes of this study, any specimen recollected more than 6 hours after a specimen was rejected was not considered to be in direct response to the previous rejection and was excluded. Abandoned specimen: When a specimen was rejected and neither a recollected nor relabeled specimen was received within 6 hours of the time of rejection, the original specimen/test was considered to be abandoned. Laboratory-abandoned specimen: Specimen abandoned (see Abandoned specimen above) when the laboratory did not request a recollected or relabeled specimen. Provider-abandoned specimen: Specimen abandoned (see Abandoned specimen above) when the provider did not provide a recollected or relabeled specimen after having been requested to do so by the laboratory. inclusion criteria were identified or until 6 weeks elapsed, whichever came first. Definitions of terms provided to participants are listed in Table 1. Specimens included in the study were those received from inpatients and emergency department patients older than 6 months for on-site analysis. The following specimen types were excluded from the study: point-of-care, blood bank, bone marrow, specimens received in the form of pre-prepared smears, and specimens submitted for highly specialized testing (ie, flow cytometry, molecular DNA/RNA, cytogenetic analysis). Participants provided the total number of chemistry and hematology accessions separately for the study period. For each rejected specimen included in the study, the following information was recorded: patient age, specimen type, laboratory testing section, test priority, time of specimen receipt and time of specimen rejection, rejection reason, detection method used for rejection due to improper labeling, whether or not a recollected or relabeled specimen was requested by the laboratory, time of recollected/ relabeled request, time of recollected/relabeled specimen receipt, recollection method for blood and urine specimens, if applicable, and result time. Participants were also asked to provide information regarding their laboratory s policies and practices in the following areas: presence of a detailed written policy regarding the detection and/or handling of rejected specimens, method(s) used to detect improperly labeled specimens, whether or not improperly labeled blood and/or urine specimens are allowed to be relabeled, and the nature of recommendation(s) made to providers when a specimen is rejected. Statistical Analysis Five performance indicators were calculated for this study: specimen rejection rate, median processing delay, percentage of laboratory-abandoned specimens, percentage of provider-abandoned specimens (see Table 1), and percentage of relabeled specimens subsequently determined to not be from the intended patient (wrong specimen in container). Median processing delay was defined as the interval between the original and recollected/ relabeled specimen receipt times. Individual associations between the first 4 performance indicators with demographic and practice variables were tested by using Kruskal-Wallis tests for discrete-valued independent variables and regression analysis for the continuous independent variables. The 2 abandoned rates were skewed so a log transformation was used for the regression-based analyses. Variables with significant associations for the individual associations (P,.10) were then included in a forward selection multivariate regression model. A significance level of.05 was used for the final multivariate models. All analyses were run by using SAS 9.1 (SAS Institute, Cary, North Carolina). RESULTS Table 2 lists the characteristics of the 78 institutions submitting data for this study. A total of 4794 rejected specimens were identified from 2 054 702 accessions. Most of the participating institutions (94%) are located in the United States, with the remaining in Saudi Arabia (2), Canada, Jordan, and Spain. Of the participating institutions, 39% are teaching hospitals and 27% have pathology residency training programs. Table 3 illustrates the distribution of 4 of the 5 performance indicators among participants. The overall specimen rejection rate was 0.2%, with the 90th percentile at 0.1%, median at 0.3%, and 10th percentile at 1.5%. The overall median specimen processing delay due to specimen rejection was 65 minutes, with a median of 54 minutes for stat specimens and 88 minutes for nonstat specimens. Of the 4794 rejected specimens, 537 (11.2%) were abandoned by either the laboratory not requesting a recollected or relabeled specimen (laboratory abandoned) or by the 1004 Arch Pathol Lab Med Vol 138, August 2014 Specimen Rejection Karcher & Lehman

Table 3. Table 2. Institution Characteristics Count Percentage Occupied bed size 0 150 27 37.5 151 300 22 30.6 301 450 14 19.4 451 600 5 6.9.600 4 5.6 Institution location City 40 54.1 Rural 17 23.0 Suburban 16 21.6 Federal installation 1 1.4 Government affiliation Nongovernmental 60 82.2 Governmental, nonfederal 8 11.0 Governmental, federal 5 6.8 Institution type Voluntary, nonprofit hospital 47 64.4 County hospital 5 6.8 Nongovernmental, university hospital 5 6.8 Proprietary hospital 5 6.8 Veterans hospital 3 4.1 State acute hospital 2 2.7 Children s hospital 1 1.4 Department of Defense 1 1.4 Governmental, nonfederal university 1 1.4 hospital Indian Health Service 1 1.4 Private, independent laboratory 1 1.4 System/integrated delivery network 1 1.4 Distribution of Performance Indicators N All Institutions Percentiles 10th 25th Median (50th) 75th 90th Rate of specimen rejection, % 77 1.5 0.6 0.3 0.2 0.1 Median specimen processing delay, min 72 93.0 80.8 65.5 51.5 41.0 Laboratory-abandoned 73 31.3 11.3 1.3 0.0 0.0 specimens, % Provider-abandoned specimens following laboratory request for correction/ recollection, % 72 23.8 14.0 5.0 0.0 0.0 Table 4. Information Relating to the Rejected Specimens Included in This Study a Count Percentage Patient age, y 0 10 304 6.3 11 20 180 3.7 21 40 645 13.3 41 60 1286 26.5 61 80 1679 34.7 81 100 751 15.5 Specimen type Blood 4674 96.5 Urine 170 3.5 Laboratory testing location Chemistry 2462 50.9 Hematology 2374 49.1 Test priority Stat 2542 52.7 Nonstat 2192 45.5 Not applicable 85 1.8 Rejection reason Inappropriate/inadequate specimen 4445 92.4 Improperly labeled 367 7.6 Improper labeling detection method Laboratory check 268 73.6 Feedback from caregiver 36 9.9 Delta check 33 9.1 Clinical picture laboratory 12 3.3 Not applicable 8 2.2 Other 7 1.9 Response to specimen rejection Recollected specimen 4206 87.7 Abandoned specimen (neither 537 11.2 recollected nor relabeled/corrected) Relabeled/corrected specimen 51 1.1 Blood recollection method Phlebotomy 3151 86.8 Line draw 479 13.2 Urine recollection method Urine cup 69 86.3 Catheterization 11 13.8 a See Table 1 for definition of terms. provider or caregiver team not complying with the laboratory request (provider abandoned). The median laboratory abandonment rate was 1.3%. The median provider abandonment rate was 5%. Nonstat and urine specimens were significantly more likely to be abandoned, with approximately equal likelihood for laboratory- and provider-abandoned specimens. Table 4 details information relating to the rejected specimens. A substantial majority (96.5%) of rejected specimens were blood, with essentially equal numbers of chemistry and hematology specimens. The reason for most rejected specimens (92.4%) was inappropriate/inadequate specimen. The remaining 7.6% were rejected owing to improper labeling. Regarding specimens found to be improperly labeled, most (73.6%) were detected by laboratory review ( lab check ), 9.9% by feedback from caregiver, and 9.1% by delta check (see Table 1). Most rejected specimens (87.7%) were ultimately recollected, 1.1% were relabeled/corrected, and 11.2% were abandoned (neither recollected nor relabeled/corrected). The first 4 performance indicators were tested for associations with institutional demographic and laboratory policy variables. A P value of less than.05 was considered statistically significant. Institutional and/or laboratory policy relationships were found with 3 of the first 4 performance indicators. No relationships were found with the rate of specimen rejection. The significant associations, detailed in Table 5, were as follows: longer specimen processing delays tended to occur in institutions with higher occupied bed size; higher rates of laboratory-abandoned specimens tended to occur in laboratories that communicate to the patient s caregiver that the specimen is rejected without providing any direction for specimen replacement; and higher rates of provider-abandoned specimens tended to occur in institutions that train pathology residents/fellows or Arch Pathol Lab Med Vol 138, August 2014 Specimen Rejection Karcher & Lehman 1005

Table 5. Statistically Significant Relationships Between 3 Performance Indicators and Demographic or Practice Variables No. of Institutions 10th Percentile Median 90th Percentile Median specimen processing delay, min Occupied bed size (P ¼.005) 0 150 27 33 51 84 151 300 22 55 71 83 301 450 14 55 67 111.450 9 51 91 263 Rejected specimens abandoned by laboratory, % Laboratory only communicates that the specimen is rejected when reporting a rejected specimen to the patient s caregiver (P ¼.01) Yes 21 0.0 10.0 47.5 No 49 0.0 1.3 24.4 Rejected specimens abandoned by provider, % Laboratory trains pathology residents/fellows (P ¼.007) Yes 20 0.0 15.0 44.8 No 51 0.0 3.8 14.1 Laboratory allows any improperly labeled chemistry or hematology blood specimen to be relabeled without requiring the specimen to be recollected (P ¼.01) Yes 30 0.0 0.0 18.3 No 40 0.0 6.9 31.1 that do not allow improperly labeled chemistry or hematology blood specimens to be relabeled without requiring the specimen to be recollected. Table 6 summarizes responses received from participants regarding their policies and practices related to detection and resolution of rejected specimens. Of the participating laboratories, 45% reported that they allow improperly labeled blood specimens (see Table 1) to be relabeled (among these, 85% when incompletely labeled, 59% when mislabeled, and 38% when unlabeled). Likewise, 37% allow improperly labeled urine specimens to be relabeled (among these, 89% when incompletely labeled, 57% when mislabeled, and 36% when unlabeled). Regarding the laboratories that allow relabeling of specimens and the relabeled specimens included in this study, the following were found: (1) These laboratories reported no better performance regarding specimen processing delay, but a slightly lower rate of provider-abandoned specimens (see Table 5); (2) of the 51 improperly labeled specimens that were relabeled, 20 specimens (39%) were subsequently discovered to not be from the intended patient (wrong specimen in container). Of the 6 laboratories that reported the 20 relabeled specimens with wrong specimen in container, 4 allowed relabeling of unlabeled blood and/or urine specimens, and 2 stated that they did not allow relabeling of any improperly labeled specimens (ie, there was an apparent breach of policy). Among the 51 improperly labeled specimens allowed to be relabeled, there was no statistically significant difference in the rate of relabeling between stat and routine test priorities. COMMENT Defects in laboratory specimens that result in specimen rejection are a cause of inconvenience and discomfort to patients, lead to a delay in the availability of often critical laboratory results, and, if the methods used to detect specimen defects are not effective, may also represent a major compromise of patient safety. To address the potential harm to patients from misidentification, including mislabeling of laboratory specimens, the Joint Commission 5 has for the past several years designated accurate patient identification as one of its national patient safety goals. This study clearly documents the consequences of laboratory specimen defects and resulting specimen rejection. Prospective analysis performed by 78 institutions of a total of 2 054 702 specimen accessions revealed an overall specimen rejection rate of 0.2%. This is generally in line with the rate reported in past studies of specimen rejection, 1 4 which have typically shown rates of less than 0.3% and up to 0.75%, with lower rejection rates reported in more recent studies. 3,4 The first and most direct consequence of specimen rejection is the need to collect a new specimen from the patient. In this study, 86.8% of rejected blood specimens led to repeated phlebotomy. Likewise, 13.8% of rejected urine specimens required recatheterization of the patient to collect a new urine sample. Both of these repeated procedures are associated with inconvenience and discomfort for the patient, and both introduce the potential for patient complications. Another well-known consequence of specimen rejection is a delay in the performance and reporting of the results of the ordered tests. In this study, the median specimen processing delay was 65 minutes, with a range of 41 minutes (90th percentile) to 93 minutes (10th percentile). The median processing delay was longer for tests with routine priority (88 minutes) but was still 54 minutes for stat tests. This indicates that delays in availability of urgent and sometimes critical test results of nearly a full hour are commonly seen when stat specimens must be rejected. An interesting association with even longer specimen processing delay (median ¼ 91 minutes) was hospital occupied bed size, specifically with bed size of greater than 450 beds. No definite explanation for this association was apparent; however, this may be a function of the greater complexity of very large hospitals, which could contribute to less effective communication among patient care staff members and slower response time to special requests, such as for recollection of a rejected laboratory specimen. Although not specifically assessed in this study, longer delays in test result availability in the largest hospitals, where the clinical acuity 1006 Arch Pathol Lab Med Vol 138, August 2014 Specimen Rejection Karcher & Lehman

Table 6. Laboratory Policies and Practices Relating to Rejected Specimens Count Percentage Does your laboratory have a detailed written policy/procedure regarding the detection and/or handling of the following? a (N ¼ 74) Improperly labeled (including mislabeled) specimens 73 98.6 Inappropriate/inadequate specimens 71 95.9 Neither 0 0.0 What methods are used by your laboratory to detect improperly labeled (including mislabeled) specimens? a (N ¼ 75) Laboratory check of specimen label 74 98.7 Delta check 68 90.7 Feedback from patient s clinical care team 60 80.0 Laboratory correlation with the clinical picture 42 56.0 If you indicated delta check above, which method is used in your laboratory to perform delta checks? Automated/preprogrammed comparison using laboratory information system 48 70.6 Both manual and automated comparison 17 25.0 Manual comparison by laboratory personnel 3 4.4 Does your laboratory allow any improperly labeled blood specimens submitted to the central chemistry or hematology laboratories to be relabeled correctly without requiring the specimen to be recollected? Yes 34 45.3 No 41 54.7 If blood specimens are allowed to be relabeled correctly, for which of the following circumstances? a (N ¼ 34) Incompletely labeled specimens 29 85.3 Mislabeled specimens 20 58.8 Unlabeled specimens 13 38.2 Does your laboratory allow any improperly labeled urine specimens submitted to the central chemistry or hematology laboratories to be relabeled correctly without requiring the specimen to be recollected? Yes 28 37.3 No 47 62.7 If urine specimens are allowed to be relabeled correctly, for which of the following circumstances? a (N ¼ 28) Incompletely labeled specimens 25 89.3 Mislabeled specimens 16 57.1 Unlabeled specimens 10 35.7 When your laboratory reports a rejected chemistry or hematology specimen to a patient s caregiver, what may be communicated to the caregiver? a (N ¼ 74) The specimen is rejected 23 31.1 The specimen is rejected, please recollect 69 93.2 The specimen is rejected, please come to laboratory to correct labeling defect 20 27.0 Were any relabeled specimens encountered in this study subsequently discovered, by any means, to not be from the intended patient? Yes 6 9.0 No 61 91.0 If any relabeled specimens in this study were subsequently discovered to not be from the intended patient, how many were there? 1 2 33.3 4 2 33.3 5 2 33.3 a Multiple responses allowed. of patients is often higher, may have an even greater negative impact on patient safety and on the delivery of care to a larger number of critically ill patients. An additional significant consequence of laboratory specimen rejection is abandonment of the ordered test(s). Such abandonment may occur when the laboratory fails to request recollection or relabeling/correction of a defective specimen (laboratory abandonment) or when the provider or patient care team fails to comply with such a request (provider abandonment). The overall specimen abandonment rate in this study was 11.2%, meaning that these patients received no result(s) for the test(s) originally ordered. The laboratory abandonment rate was lower (median rate ¼ 1.3%) than when the provider abandoned the specimen (median rate ¼ 5%), but still significant. Specimen abandonment rates were significantly higher for all nonstat tests and for urine specimens. The association with nonstat priority may be a simple function of lower clinical urgency and a decision to wait for the next routine phlebotomy session or next urine collection opportunity to recollect a rejected specimen. Higher overall abandonment of urine specimens is likely a reflection of the difficulty in having patients produce urine samples on demand or in recollecting catheter urine specimens. Another association with higher specimen abandonment, this time by the provider, was institutions that train pathology residents/ fellows. Similar to the longer specimen processing delay seen in the largest hospitals, the higher rate of provider specimen abandonment may be related to the complexity and communication challenges typical in academic medical centers. A troubling finding in this study was the very high rate of mislabeled specimens that were the result of allowing providers and other patient care team members to relabel Arch Pathol Lab Med Vol 138, August 2014 Specimen Rejection Karcher & Lehman 1007

specimens that were received in the laboratory improperly labeled. Of the participating institutions, 45% allow relabeling of blood specimens and 37% allow relabeling of urine specimens. Among the institutions allowing specimen relabeling, this was reported to be allowed at higher rates for incompletely labeled specimens, but 59% and 38% of participating institutions allow correction of mislabeled or unlabeled blood specimens, respectively. Among these institutions, the percentage allowing correction of mislabeled or unlabeled urine specimens was similar (57% and 36%, respectively). When asked to indicate how many relabeled specimens ultimately turned out to not be from the intended patient (ie, wrong specimen in container), respondents reported that 39% of such specimens had this outcome. Though this may represent a slight overestimate of the true risk of a wrong specimen in container collection event (since multiple blood tubes may have been collected at the same time, but given different accession numbers and thus considered separate events), the incidence of wrong blood in container in this study is clearly concerning. An interesting sidelight to this finding was the fact that those institutions that allow specimen relabeling reported no significant shortening of the specimen processing delay resulting from specimen rejection, although they did report a slightly lower rate of specimen abandonment by the provider. Thus, allowing specimen relabeling resulted in little measurable advantage, yet this practice clearly introduced an increased risk to patient safety. These findings represent a strong indictment of the practice of routinely allowing relabeling of improperly labeled specimens. This practice has been increasingly discouraged in recent years, 6 8 a recommendation convincingly reinforced by this study. In summary, specimen rejection leads to a high rate of recollection of specimens, including repeated phlebotomy and recatheterization for urine, causing discomfort and potential complications in the affected patients. A major consequence of specimen rejection is a significant delay in availability of test results, of particular importance with stat tests and a situation potentially made worse in large and/or teaching hospitals, where a higher number of critically ill patients typically receive care. Specimen rejection also leads to frequent abandonment of the test(s) originally ordered, more so with nonstat tests and urine specimens. Finally, the practice of allowing relabeling of improperly labeled specimens is associated with little clinical benefit but introduces a significant likelihood of specimen mislabeling and potential harm to the patient. If laboratories choose to allow relabeling of blood and urine specimens, they should construct their policy thoughtfully, considering the relative risks and benefits, and perhaps restrict relabeling to correction of only the simplest labeling defects. The policy should also address relabeling of specimens that either cannot be recollected (eg, surgical pathology specimens), or that cannot be recollected without potential harm to the patient (eg, cerebrospinal fluid or other body cavity fluid specimens, bone marrow aspirate/biopsy specimens). References 1. Jones BA, Meier F, Howanitz PJ. Complete blood count specimen acceptability: a College of American Pathologists Q-Probes study of 703 laboratories. Arch Pathol Lab Med. 1995;119(3):203 208. 2. Jones BA, Calam RR, Howanitz PJ. Chemistry specimen acceptability: a College of American Pathologists Q-Probes study of 453 laboratories. Arch Pathol Lab Med. 1997;121(1):19 26. 3. Stark A, Jones BA, Chapman D, et al. Clinical laboratory specimen rejection association with the site of patient care and patients characteristics: findings from a single health care organization. Arch Pathol Lab Med. 2007; 131(4):588 592. 4. Zarbo RJ, Jones BA, Friedberg RC, et al. Q-Tracks: a College of American Pathologists program of continuous laboratory monitoring and longitudinal performance tracking. Arch Pathol Lab Med. 2002;126(9):1036 1044. 5. The Joint Commission. National patient safety goals for 2013. http://www. jointcommission.org/standards_information/npsgs.aspx, Published October 22, 2012. Accessed May 1, 2013. 6. Paxton A. Punching a hole in specimen ID errors. CAP Today. 2008;22(6):1 10. 7. Dunn EJ, Moga PJ. Patient misidentification in laboratory medicine: a qualitative analysis of 227 root cause analysis reports in the Veterans Health Administration. Arch Pathol Lab Med. 2010;134(2):244 255. 8. Astion M. Patient safety focus: mislabeled specimens. Clin Lab News. 2010; 36(1):15. 1008 Arch Pathol Lab Med Vol 138, August 2014 Specimen Rejection Karcher & Lehman