PMCCPMCCPMCC

Search tips
Search criteria 

Advanced

 
Logo of apatholLink to Publisher's site
 
Acad Pathol. 2017 Jan-Dec; 4: 2374289517722152.
Published online 2017 September 6. doi:  10.1177/2374289517722152
PMCID: PMC5590695

Using Focused Laboratory Management and Quality Improvement Projects to Enhance Resident Training and Foster Scholarship

Abstract

Training in patient safety, quality, and management is widely recognized as an important element of graduate medical education. These concepts have been intertwined in pathology graduate medical education for many years, although training programs face challenges in creating explicit learning opportunities in these fields. Tangibly involving pathology residents in management and quality improvement projects has the potential to teach and reinforce key concepts and further fulfill Accreditation Council for Graduate Medical Education goals for pursuing projects related to patient safety and quality improvement. In this report, we present our experience at a pathology residency program (University of Iowa) in engaging pathology residents in projects related to practical issues of laboratory management, process improvement, and informatics. In this program, at least 1 management/quality improvement project, typically performed during a clinical chemistry/management rotation, was required and ideally resulted in a journal publication. The residency program also initiated a monthly management/informatics series for pathology externs, residents, and fellows that covers a wide range of topics. Since 2010, all pathology residents at the University of Iowa have completed at least 1 management/quality improvement project. Many of the projects involved aspects of laboratory test utilization, with some projects focused on other areas such as human resources, informatics, or process improvement. Since 2012, 31 peer-reviewed journal articles involving effort from 26 residents have been published. Multiple projects resulted in changes in ongoing practice, particularly within the hospital electronic health record. Focused management/quality improvement projects involving pathology residents can result in both meaningful quality improvement and scholarly output.

Keywords: clinical laboratory information systems, data mining, graduate medical education, leadership, management, medical informatics, pathology education, quality improvement

Introduction

Management, leadership, and informatics skills are increasingly important for physicians in academic, private practice, and industry jobs.1 Specifically, in the field of pathology, multiple surveys have found that recent graduates of pathology training programs are often viewed as deficient in leadership and management skills.2-4 The value and necessity of informatics skills has increased along with the complexity of laboratory information systems (LISs), electronic health records (EHRs), and technology (eg, digital pathology).5-7 This necessity was codified with inclusion of laboratory management and informatics in The Pathology Milestones developed jointly by the Accreditation Council for Graduate Medical Education (ACGME) and the American Board of Pathology (especially milestones Systems-Based Practice 4-7, Practice-Based Learning and Improvement 2).8 Despite the obvious necessity, teaching management, leadership, and informatics during residency training can be challenging.9-12 Anatomic pathology (AP) rotations are often very busy with clinical workload, resulting in limited time to focus on management and informatics issues. As a result, management activities are often delegated to clinical pathology (CP) rotations or elective time. Discrete rotations remain uncommon, and this training is more commonly integrated with subspecialties such as clinical chemistry or informatics.13-19 Various groups have published proposed curricula as guides for pathology residency programs to design educational content for laboratory management, leadership, and informatics.9,12,17,19 Examples of approaches include residency rotations with managerial responsibilities (eg, CP “superblocks” that mimic the broad CP coverage that may occur in private practice pathology or smaller academic centers) or focused rotations (elective or required) in laboratory management.15,17,18,20

Didactic sessions and assigned readings are a common means to teach management and leadership. Although this approach can provide background knowledge, residents may find it challenging to understand how these activities relate to pathology practice. Focused management/quality improvement (QI) projects are an approach to allow residents to apply and reinforce knowledge.13,17 As noted earlier, these activities also align with ACGME Milestone goals for integrating training-related patient safety and QI.21,22 In this report, we present our experience with the use of focused management and QI projects in the pathology residency program at the University of Iowa. As we will describe, these projects resulted not only in real-world education experiences with associated changes in laboratory practice but have also yielded substantial scholarly activity for both trainees and faculty.

Material and Methods

Institutional Setting

The University of Iowa Hospitals and Clinics (UIHC) is a 734-bed tertiary/quaternary care academic medical center located in Iowa City, Iowa. The University of Iowa Department of Pathology has an ACGME-accredited AP/CP pathology residency program for 20 residents. The department also has a medical student externship program (analogous to a postsophomore pathology fellowship in which 6 students spend a year doing clinical work in pathology outside the typical medical school curriculum) and fellowship programs in cytopathology, hematopathology, microbiology, molecular genetic pathology, surgical pathology, and transfusion medicine (approximately 10 fellows/year in total for all fellowships). The Department of Pathology manages pathology services throughout the medical center and affiliated outlying outpatient clinics, including AP laboratories (cytopathology, surgical pathology, and autopsy pathology), a centralized core clinical laboratory (clinical chemistry, flow cytometry, and hematopathology), clinical microbiology/molecular pathology laboratory, and blood center (donor center, blood bank, tissue/cellular therapy, and therapeutic apheresis).

Structure of Laboratory Management/Quality Improvement Projects

The retrospective time period discussed here covers July 1, 2010, to May 6, 2017. Over this time, residents were expected to complete at least 1 management/QI project. The project was expected to culminate in a conference presentation and/or scholarly publication. The primary faculty responsible for overseeing this program was the Vice Chair of Clinical Pathology and Laboratory Services and the director of the clinical chemistry/management pathology resident rotation (M.D.K.). Until June 30, 2016, clinical chemistry/management consisted of two 5½-week rotations, with the second rotation typically occurring in the third or fourth year of residency training. On July 1, 2016, the residency switched to 4-week blocks, with chemistry/management now having a total of three 4-week blocks during residency training. The possible parameters for the management/QI projects were broad, but emphasis was placed on projects that would yield tangible changes in laboratory practice, standard operating procedures, EHR (eg, test names, warning prompts, or alerts), and/or LIS. Although publication was not required, there was a preference for projects which would have broader interest and thus might be publishable in the general medical or pathology literature. Many of the projects were related to the core laboratory or broader laboratory utilization issues. A small number of projects were focused in AP. A summary of the parameters for the projects is listed in Table 1.

Table 1.
Parameters for Pathology Resident Management/Quality Improvement Projects.

Faculty Development

An additional factor considered in this initiative was faculty development. Several faculty development meetings were held to discuss strategies and barriers for faculty in fostering and mentoring residents in scholarly projects. Much of this discussion occurred at a regular series of faculty development meetings focused on mentoring and career development, especially for clinical and junior faculty. Barriers identified included competing demands on faculty time, minimal prior experience of many residents with scholarly projects, and resident overcommitment with too many projects. Strategies for faculty to utilize in mentoring resident projects to completion were discussed in this setting.

Informatics Capabilities

Since May 2009, the EHR for UIHC has been Epic (Epic Systems, Inc, Madison, Wisconsin), which contains historical data back to 1996. The LIS for all UIHC pathology laboratories until August 2, 2014, was Cerner “Classic” (Kansas City, Missouri). On August 2, 2014, the pathology laboratories adopted Epic Beaker Clinical Pathology,23 retaining Cerner as the LIS for AP, blood center, and some parts of hematopathology and molecular pathology. In October 2015, the pathology laboratories went to Epic Beaker Anatomic Pathology and Haemonetics for the AP and blood center LISs, respectively. A key to success for many of the projects described in this report was the ability to utilize Reporting Workbench functionality within Epic. This system allowed for data mining of laboratory orders, medications, and patient demographics for EHR data back to 1996. Some searches required data mining within Cerner or the clinical laboratory middleware system (Instrument Manager; Data Innovations, Burlington, Vermont) that provided interfacing of instruments to Epic Beaker.23,24 For more sophisticated searches, a data warehouse (Starmaker, Park Street Solutions, Naperville, Illinois) was used; this database was available to pathology faculty and trainees.25 This warehouse allowed for queries that are either very difficult or even infeasible within Epic Reporting Workbench or other routinely available informatics resources. An additional resource for challenging queries was Healthcare Enterprise Decision Intelligence (HEDI), a data warehouse that had restricted access limited mostly to specialized hospital information technology (IT) staff. Creation of new HEDI searches requires a formal approval process through hospital IT.

Results

Enhancing the Laboratory Management and Informatics Curriculum at Iowa

At Iowa, much of the pathology residents’ curriculum in laboratory management and informatics occurs in the chemistry/management rotations. In addition, there is a monthly management/informatics seminar series for all trainees (pathology externs, residents, and fellows) that covers a wide range of management, human resources, and informatics topics.

  • The chemistry/management rotations include resident meetings with a variety of personnel involved in clinical laboratory management (laboratory managers, financial managers, quality assurance staff, informatics staff, and department safety officer). Residents are also involved in hospital-wide safety activities such as participating with the UIHC Safety Oversight Team tasked with root cause analysis for high-level safety events.
  • The monthly management/informatics program was originally overseen by 2 faculty members and is currently organized by a faculty member (M.D.K.) and the departmental education manager (A.S.B.). The series has included multiple sessions to provide skills related to pursuing scholarly projects such as effective literature searching, data mining from the EHR and LIS, use of data warehouse, choice of possible scholarly projects, use of citation reference managers, and selection of biomedical journals (Table 2). The inclusion of externs also provides opportunities for medical students to develop interest in and pursue similar projects.
    Table 2.
    Management Series Topics.

Scholarly Productivity From Management/Quality Improvement Projects

Since July 2010, all pathology residents at the University of Iowa have completed at least 1 management/QI project. Since 2012, 31 peer-reviewed journal articles involving effort from 26 pathology residents and 10 pathology faculty have been published. Many of the projects involved aspects of laboratory test utilization, with other projects focused on other areas such as human resource issues or informatics. Multiple projects resulted in changes within the hospital EHR. A small number of projects were focused in AP QI. The following sections provide examples of projects that resulted in publication. A summary of 32 projects is in Table 3.

Table 3.
Examples of Resident Management/Quality Improvement Projects.

Projects Focused on Laboratory Test Utilization

Laboratory test utilization was a main focus of the projects for 11 residents. Many of these projects stemmed from issues that residents confronted during their chemistry/management rotation. Two examples that resulted in a change in EHR include positive hepatitis B surface antigen tests from recent hepatitis B vaccination33 and ordering of angiotensin-converting enzyme (ACE) serum levels for diagnosis of sarcoidosis in patients on ACE inhibitor therapy (the medication dramatically lowers serum ACE, making the testing unreliable).32 For the hepatitis B surface antigen study, the primary patient population affected by this issue was adult hemodialysis, who undergo regular testing for hepatitis B surface antigen. In the most common scenario, the patient had hepatitis B vaccine administered by a nondialysis provider and then happened to have routine hepatitis B surface antigen testing within a week of the vaccine dose. Erroneous diagnosis of hepatitis B in a hemodialysis patient has expensive downstream consequences, including use of separate dialysis equipment for hepatitis B-positive patients. This issue has been nearly eliminated by a best-practice alert within the EHR (Figure 1A).33

Figure 1.
Examples of best-practice alerts in the electronic health record (EHR) to improve laboratory utilization.

Compared to the hepatitis B issue, the ordering of ACE serum levels in patients on ACE inhibitor therapy was much more widespread and occurred in a variety of inpatient units and outpatient clinics. The initiating case for this project was a clinician who called the pathology resident confused that an ACE level was undetectable for a patient despite high pretest probability for sarcoidosis. Subsequent investigation showed that the patient was on lisinopril (an ACE inhibitor), and thus, the ACE level was not reliable due to probable medication interference. Detailed chart review by the pathology resident for this project revealed multiple cases where the diagnosis of sarcoidosis was delayed following a low ACE value likely caused by ACE inhibitor therapy. Like the hepatitis B surface antigen issue, a best-practice alert within the EHR has nearly eliminated the problem (Figure 1B) and was additionally combined with a warning prompt (Figure 2A).32 Another example included inclusion of a best-practice alert for attempts by providers to order a germ line genetic test that had been performed previously (Figure 1C).30

Figure 2.
Examples of warning prompts (requiring acknowledgment by ordering provider) in the electronic health record (EHR) to improve laboratory utilization.

Multiple pathology residents completed projects related to utilization of send-out testing.30 In our institution, the CP resident on call serves as the gatekeeper for a number of restricted tests. The data gathered during the multiple projects allowed for more effective gatekeeping and warning prompts within the EHR. Some of the interventions have resulted in substantial institutional cost savings. Two projects identified erroneous clinician electronic order sets as the basis for specific misutilization problems. One example was the inclusion of 1,25-dihydroxyvitamin D (calcitriol) instead of 25-hydroxyvitamin D in order sets meant to assess routine nutritional status of vitamin D. In the conversion to a new EHR in May 2009 for UIHC, 43 order sets had the incorrect vitamin D test. This resulted in a dramatic increase in misutilization of 1,25-dihydroxyvitamin D, a send-out test that is not appropriate for routine assessment of vitamin D nutritional status.30 More scattered examples of misutilization in order sets included confusion between “look-alike” tests such as beta-2 glycoprotein/beta-2 microglobulin and magnesium/manganese. These type of errors were found to occur both sporadically and due to insertion of the incorrect test in an electronic order set. Correction of the order sets combined with targeted warning prompts have nearly eliminated these look-alike misorders (Figure 2B and and2C2C).30

Informatics-Based Projects

Five residents were involved in projects related to clinical laboratory informatics, including 2 by residents with very strong interest in informatics (one of whom subsequently completed a pathology informatics fellowship). One of the informatics projects significantly streamlined and reduced sign-out time for capillary protein electrophoresis, using a combination of “hot keys” and middleware interfacing.40 These changes helped support timely turnaround time for protein electrophoresis testing amid a markedly expanding UIHC multiple myeloma program. Two of the informatics projects focused on application of a data warehouse for pathology projects.25 These projects have provided the basis for ongoing work by pathology residents to improve data mining tools in both AP and CP. The data warehouse was particularly strong in queries that combined medications and specific laboratory results. An example was the ACE inhibitor project mentioned above.32 The EHR at UIHC at the time of this project contained 123 distinct medication order options for 9 different ACE inhibitors in the time period of retrospective analysis. Each of these orders is a separate search item in the standard EHR reporting tools system. The data warehouse allowed for more efficient searching using SNOMED terminology (ie, single search for all ACE inhibitors). Once constructed, retrieval of all inpatient and outpatient encounters in a 5-year period that included both a completed ACE level order and an active ACE inhibitor prescription took less than 1 minute for the data warehouse to complete. Similar searches in toxicology (eg, how many amphetamine-positive screening immunoassays occur in patients on specific drugs known to cross-react) and microbiology (eg, how many positive blood cultures occur in patients with neutropenia) are also very quick for the data warehouse once constructed.25

Toxicology and Drug Monitoring Projects

Thirteen pathology residents worked on projects related to toxicology and therapeutic drug monitoring. Four residents tackled various aspects of the algorithm for evaluating toxic alcohol and glycol ingestion (ethylene glycol, methanol, isopropanol). The UIHC is the only institution within the state of Iowa to perform 24/7 testing for toxic alcohols. The osmolal gap-based algorithm that was used at UIHC for evaluating toxic alcohols through 2010 was noted to have frequent false positives for ethanol, resulting in many calls to the pathology resident on call. Many of these calls were in the evening and early morning, given that toxic ingestions often occur outside standard business hours. As a result of multiple projects, the toxic alcohols algorithm was significantly modified, eliminating an estimated 600 resident calls/year.41 Further modifications to the algorithm incorporated a rapid ethylene glycol assay.42,43

Four residents worked on a series of projects related to newborn drug testing.44 This was done in collaboration with the Department of Pediatrics and required substantial chart and literature review. Newborn drug testing is an ethically and technically challenging area of medicine, with the results impacting medical and social services decisions. Two of the most tangible outcomes for the projects were changes in the screening criteria used by pediatricians and family medicine providers for neonatal drug testing and a switch to umbilical cord tissue instead of meconium as the primary specimen at UIHC.44-46

Three residents worked on projects related to use of hair toxicology in potential child abuse cases. Similar to the newborn drug testing projects, these projects required extensive chart review, including determination of whether laboratory results resulted in child abuse reports from providers at UIHC. This analysis showed a high rate of illicit drug exposure in this population.47

Other Clinical Pathology Projects

Multiple projects focused on various aspects of assay validation, modification, or discontinuation. These included validation of plasma as an acceptable specimen for κ and λ free light chain analysis,34 comparison of diazo and vanadate oxidase direct bilirubin assays,35 validation of hematopoietic progenitor count on automated hematology analyzer for use in stem cell transplant,51 and introduction of lamellar bodies assay for fetal lung maturity testing. A transfusion medicine-related project involved innovative use of an inexpensive device to limit blood loss for Jehovah’s Witness patients.52 One project involved collaboration with laboratory managers to look at areas for improvement in clinical laboratory staff recruitment and retention. Lastly, 1 project examined areas for improvement in pathology for the transgender patient population.54

Anatomic Pathology Quality Improvement

A few projects focused on AP quality or process improvement. Most often these were additional projects after the first one was completed during the clinical chemistry/management rotation. One resident worked on a multiplatform comparison of molecular oncology testing using various cytologic preparations versus formalin-fixed, paraffin-embedded tissue blocks. This analysis demonstrated that a variety of cytologic preparations were reliable sources for molecular oncology testing on multiple different platforms.26 Two residents worked on a project to evaluate the effect of changes in grossing and histologic processing of gastrointestinal biopsy specimens. Their low-cost process change leads to a 17% reduction in the number of blocks used for these specimens and a decrease of 3% total blocks processed by our histology laboratory.28 One resident participated in a multidepartmental study with pathology and otolaryngology colleagues to evaluate the accuracy of fine needle aspiration (FNA) in comparison with imaging in the preoperative workup of salivary gland masses. They demonstrated that FNA is a reliable method to preoperatively assess both benign and malignant salivary gland lesions with higher sensitivity and specificity than imaging.27

Discussion

Training in patient safety, quality, and management is a key component of GME training throughout all specialties. However, training programs often find it challenging to create robust learning opportunities in these domains. Focused management/QI projects are one approach to teach and engage trainees in management, quality, safety, and informatics. This strategy also has the added benefit of increasing scholarship opportunities for clinical faculty.

Within the field of pathology, these activities can be especially valuable in educating pathology residents in concepts of laboratory management, regulatory affairs, and the interface of pathology results with electronic systems such as EHRs and LISs.13,17 These activities also align with ACGME goals (Milestones) for pathology resident training in QI and patient safety.21,22 Pathology projects can expose residents to operational issues, laboratory statistics, process improvement, and assay validation/introduction. While the possibilities for management/QI projects are theoretically limitless, it can be challenging to select projects that are both feasible and suitable for generating scholarly activity. Many projects extend beyond a single resident rotation, limiting continuity and potentially creating obstacles to project completion.

At the University of Iowa, we have made a concerted effort to improve training in laboratory management and informatics. We have used the monthly management seminar series to present a variety of topics that include design of scholarly projects, informatics resources, and QI. To increase scholarly activity from management/QI projects, a faculty member (M.D.K.) provides primary oversight for the projects and can either directly supervise the resident or facilitate a project with a different faculty member.

An important part of the process has been faculty engagement. A series of faculty development meetings were held to discuss strategies and barriers for faculty in mentoring residents in scholarly activity with the goal of improving initiation and completion of scholarly projects involving residents. A primary goal was to enhance resident participation in scholarship. Much of this discussion occurred at a regular series of faculty meetings focused on mentoring and career development. Barriers identified included competing demands on faculty time, minimal prior experience of many residents with scholarly projects, and resident overcommitment with too many projects. Other strategies for faculty to utilize while mentoring trainees on projects include setting defined dates for follow-up and explicit expectations for work to be completed by those dates. This becomes particularly relevant for projects that extend past the end of a rotation. In the current environment of increasing clinical demands, it has become challenging for many clinical faculty to generate scholarly output, so being able to successfully mentor trainee projects is critical for faculty success as well. Often GME activities are time-consuming for clinical faculty and decrease time for faculty to invest in scholarly activities. These projects provide an opportunity to combine education with scholarship.

As detailed above, we have been successful at Iowa in generating significant scholarly activity from management/QI projects. Achieving this goal has required some creativity, sometimes by combining efforts from multiple residents into a single publication. This has worked particularly well for projects related to laboratory utilization or complex projects that require time-intensive chart or data review that extend past rotation length. For laboratory utilization, individual residents can each tackle single focused subprojects (eg, look-alike labs, utilization of specific high-priced send-out tests, etc) that all contribute to a broader goal. We have also found that projects facilitate good collaboration across departments. Examples include work with pediatrics on newborn drug testing, collaboration with the physicians involved in transgender patient care, and work with otolaryngology physicians on assessing accuracy of FNA in preoperative workup of salivary gland masses.

Conclusions

While the primary goal of the focused laboratory management or QI projects is to enhance resident education and create opportunity for scholarship, these projects have tangible outcomes that have resulted in changes to our practice and improvements at our institution. The resulting scholarship benefits not only the trainees but also the faculty. These projects provide opportunities for faculty to merge education and scholarship. Focused management/QI projects involving pathology residents can result in both meaningful QI and scholarly output.

Footnotes

Declaration of Conflicting Interests: The author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.

Funding: The author(s) received no financial support for the research, authorship, and/or publication of this article.

References

1. Brimhall BB, Wright LD, McGregor KL, Hernandez JS. Critical leadership and management skills for pathology practice. Arch Pathol Lab Med. 2007;131:1547–1554. doi:10.1043/1543-2165(2007)131[1547: CLAMSF]2.0.CO;2. PMID: 17922591. [PubMed]
2. Brugnara C, Fenton T, Winkelman JW. Management training for pathology residents. I. Results of a national survey. Am J Clin Pathol. 1994;101:559–563. PMID: 8178760. [PubMed]
3. Goldberg-Kahn B, Sims KL, Darcy TP. Survey of management training in United States and Canadian pathology residency programs. Am J Clin Pathol. 1997;108:96–100. PMID: 9208985. [PubMed]
4. Kass ME, Crawford JM, Bennett B, et al. Adequacy of pathology resident training for employment: a survey report from the Future of Pathology Task Group. Arch Pathol Lab Med. 2007;131:545–555. doi:10.1043/1543-2165(2007)131[545: AOPRTF]2.0.CO;2. PMID: 17425382. [PubMed]
5. Henricks WH, Healy JC. Informatics training in pathology residency programs. Am J Clin Pathol. 2002;118:172–178. doi:10.1309/4CE8-N2MX-DFG6-N8H9. PMID: 12162674. [PubMed]
6. Riben M. The challenge of integrating informatics training during residency. Am J Clin Pathol. 2014;142:732–734. doi:10.1309/AJCPZK30STQFJHSH. PMID: 25389323. [PubMed]
7. Sinard JH, Powell SZ, Karcher DS. Pathology training in informatics: evolving to meet a growing need. Arch Pathol Lab Med. 2014;138:505–511. doi:10.5858/arpa.2013-0328-RA. PMID: 24678681. [PubMed]
8. The Pathology Milestone project. J Grad Med Educ. 2014;6:182–203. doi:10.4300/JGME-06-01s1-09. PMID: 24701282. [PMC free article] [PubMed]
9. Hemmer PR, Karon BS, Hernandez JS, Cuthbert C, Fidler ME, Tazelaar HD. Leadership and management training for residents and fellows: a curriculum for future medical directors. Arch Pathol Lab Med. 2007;131:610–614. doi:10.1043/1543-2165(2007)131[610: LAMTFR]2.0.CO;2. PMID: 17425393. [PubMed]
10. Horowitz RE, Naritoku W, Wagar EA. Management training for pathology residents: a regional approach. Arch Pathol Lab Med. 2004;128:59–63. doi:10.1043/1543-2165(2004)128<59: MTFPR>2.0.CO;2. PMID: 14692810. [PubMed]
11. Weiss RL, Hassell LA, Parks ER. Progress toward improved leadership and management training in pathology. Arch Pathol Lab Med. 2014;138:492–497. doi:10.5858/arpa.2013-0288-RA. PMID: 24678679. [PubMed]
12. Weiss RL, McKenna BJ, Lord-Toof M, Thompson NN.; Work Group Members. A consensus curriculum for laboratory management training for pathology residents. Am J Clin Pathol. 2011;136:671–678. doi:10.1309/AJCPWABWFBU9EYXR. PMID: 22031303. [PubMed]
13. Farnsworth JR, Weiss RL. A mentor-based laboratory management elective for residents. Am J Clin Pathol. 1999;111:156–160. PMID: 9930135. [PubMed]
14. Haber MH, Clifford SS, Britton CT. A management informatics rotation for pathology residents. Am J Clin Pathol. 1991;95:S38–S41. PMID: 1759998. [PubMed]
15. Ranheim EA. A novel program for clinical pathology training for residents emphasizing high-impact and attending-level learning opportunities. Hum Pathol. 2014;45:206–212. doi:10.1016/j.humpath.2013.08.012. PMID: 24196188. [PubMed]
16. Rishi A, Hoda ST, Crawford JM. A required rotation in clinical laboratory management for pathology residents: five-year experience at Hofstra Northwell School of Medicine. Acad Pathol. 2016;3:1–13. [PMC free article] [PubMed]
17. Sims KL, Darcy TP. A leadership-management training curriculum for pathology residents. Am J Clin Pathol. 1997;108:90–95. PMID: 9208984. [PubMed]
18. Weiss RL. A clinical laboratory management elective for pathology residents. Arch Pathol Lab Med. 1992;116:108–110. PMID: 1734828. [PubMed]
19. Winkelman JW, Brugnara C. Management training for pathology residents. II. Experience with a focused curriculum. Am J Clin Pathol. 1994;101:564–568. PMID: 8178761. [PubMed]
20. Spitzer ED, Pierce GF, McDonald JM. A laboratory medicine residency training program that includes clinical consultation and research. Arch Pathol Lab Med. 1990;114:360–362. PMID: 2322095. [PubMed]
21. Naritoku WY, Alexander CB. Pathology milestones. J Grad Med Educ. 2014;6:180–181. doi:10.4300/JGME-06-01s1-10. PMID: 24701281. [PMC free article] [PubMed]
22. Naritoku WY, Alexander CB, Bennett BD, et al. The pathology milestones and the next accreditation system. Arch Pathol Lab Med. 2014;138:307–315. doi:10.5858/arpa.2013-0260-SA. PMID: 24576024. [PubMed]
23. Krasowski MD, Wilford JD, Howard W, et al. Implementation of Epic Beaker Clinical Pathology at an academic medical center. J Pathol Inform. 2016;7:7 doi:10.4103/2153-3539.175798. PMID: 26955505. [PMC free article] [PubMed]
24. Krasowski MD, Davis SR, Drees D, et al. Autoverification in a core clinical chemistry laboratory at an academic medical center. J Pathol Inform. 2014;5:13 doi:10.4103/2153-3539.129450. PMID: 24843824. [PMC free article] [PubMed]
25. Krasowski MD, Schriever A, Mathur G, Blau JL, Stauffer SL, Ford BA. Use of a data warehouse at an academic medical center for clinical pathology quality improvement, education, and research. J Pathol Inform. 2015;6:45 doi:10.4103/2153-3539.161615. PMID: 26284156. [PMC free article] [PubMed]
26. Gailey MP, Stence AA, Jensen CS, Ma D. Multiplatform comparison of molecular oncology tests performed on cytology specimens and formalin-fixed, paraffin-embedded tissue. Cancer Cytopathol. 2015;123:30–39. doi:10.1002/cncy.21476. PMID: 25186473. [PubMed]
27. Tryggvason G, Hulstein SL, Karnell LH, et al. In response to accuracy of fine-needle aspiration and imaging in the preoperative workup of salivary gland mass lesions treated surgically. Laryngoscope. 2013;123:2330 doi:10.1002/lary.23991. PMID: 23813297. [PubMed]
28. Steussy B, Gailey M, Becker K, et al. Low-cost workflow improvement reduces gastrointestinal block use 17% by altering classic histotechnology testing. Am J Clin Pathol. 2015;143:861–864. doi:10.1309/AJCP3YSXDK9JJFMN. PMID: 25972328. [PubMed]
29. Lynch DW, Stauffer SL, Rosenthal NS. Adequacy of powered vs manual bone marrow biopsy specimens: a retrospective review of sequential marrow aspirates and biopsies in 68 patients. Am J Clin Pathol. 2015;143:535–539. doi:10.1309/AJCP67WITVPVVTNF. PMID: 25780005. [PubMed]
30. Krasowski MD, Chudzik D, Dolezal A, et al. Promoting improved utilization of laboratory testing through changes in an electronic medical record: experience at an academic medical center. BMC Med Inform Decis Mak. 2015;15:11 doi:10.1186/s12911-015-0137-7. PMID: 25880934. [PMC free article] [PubMed]
31. Genzen JR, Gosselin JT, Wilson TC, Racila E, Krasowski MD. Analysis of vitamin D status at two academic medical centers and a national reference laboratory: result patterns vary by age, gender, season, and patient location. BMC Endocr Disord. 2013;13:52 doi:10.1186/1472-6823-13-52. PMID: 24188187. [PMC free article] [PubMed]
32. Krasowski MD, Savage J, Ehlers A, et al. Ordering of the serum angiotensin-converting enzyme (ACE) test in patients receiving ACE inhibitor therapy: an avoidable but common error. Chest. 2015;148:1447–1453. doi:10.1378/chest.15-1061. PMID: 26225637. [PubMed]
33. Rysgaard CD, Morris CS, Drees D, et al. Positive hepatitis B surface antigen tests due to recent vaccination: a persistent problem. BMC Clin Pathol. 2012;12:15 doi:10.1186/1472-6890-12-15. PMID: 23006828. [PMC free article] [PubMed]
34. Nelson LS, Steussy B, Morris CS, Krasowski MD. Effect of specimen type on free immunoglobulin light chains analysis on the Roche Diagnostics cobas 800 analyzer. Springerplus. 2015;4:760. [PMC free article] [PubMed]
35. Dhungana N, Morris C, Krasowski MD. Operational impact of using a vanadate oxidase method for direct bilirubin measurements at an academic medical center clinical laboratory. Pract Lab Med. 2017;8:77–85. [PMC free article] [PubMed]
36. Kurt-Mangold M, Drees D, Krasowski MD. Extremely high myoglobin plasma concentrations producing hook effect in a critically ill patient. Clin Chim Acta. 2012;414:179–181. doi:10.1016/j.cca.2012.08.024. PMID: 22960204. [PubMed]
37. Kurt-Mangold M, Van Voorhis BJ, Krasowski MD. Persistent human chorionic gonadotropin after methotrexate treatment and an emergency surgical procedure for ectopic pregnancy. Lab Med. 2015;46:254–258. doi:10.1309/LMTDRFGJVJIM3VNM. PMID: 26199268. [PubMed]
38. Ogrin C, Ford BA, Stauffer SL, Krasowski MD, Azar AE. Positive test for antithyroglobulin antibodies due to administration of immunoglobulin replacement therapy in a patient with thyroid cancer. Endocr Pract. 2015;21:966–971. doi:10.4158/EP14533.CR. PMID: 26151422. [PubMed]
39. Krasowski MD, Drees D, Morris CS, Maakestad J, Blau JL, Ekins S. Cross-reactivity of steroid hormone immunoassays: clinical significance and two-dimensional molecular similarity prediction. BMC Clin Pathol. 2014;14:33 doi:10.1186/1472-6890-14-33. PMID: 25071417. [PMC free article] [PubMed]
40. Mathur G, Haugen TH, Davis SL, Krasowski MD. Streamlined sign-out of capillary protein electrophoresis using middleware and an open-source macro application. J Pathol Inform. 2014;5:36 doi:10.4103/2153-3539.141990. PMID: 25337433. [PMC free article] [PubMed]
41. Krasowski MD, Wilcoxon RM, Miron J. A retrospective analysis of glycol and toxic alcohol ingestion: utility of anion and osmolal gaps. BMC Clin Pathol. 2012;12:1 doi:10.1186/1472-6890-12 -1. PMID: 22240170. [PMC free article] [PubMed]
42. Rooney SL, Ehlers A, Krasowski MD. Reply to Dr. Kim and colleagues regarding use of a rapid ethylene glycol assay. J Med Toxicol. 2016;12:326–327. doi:10.1007/s13181-016-0548-6. PMID: 27055453. [PMC free article] [PubMed]
43. Rooney SL, Ehlers A, Morris C, et al. Use of a rapid ethylene glycol assay: a 4-year retrospective study at an academic medical center. J Med Toxicol. 2016;12:172–179. doi:1007/s13181-015-0516-6 [pii]. PMID: 26553280. [PMC free article] [PubMed]
44. Wood KE, Sinclair LL, Rysgaard CD, Strathmann FG, McMillin GA, Krasowski MD. Retrospective analysis of the diagnostic yield of newborn drug testing. BMC Pregnancy Childbirth. 2014;14:250 doi:10.1186/1471-2393-14-250. PMID: 25073780. [PMC free article] [PubMed]
45. Marin SJ, Metcalf A, Krasowski MD, et al. Detection of neonatal drug exposure using umbilical cord tissue and liquid chromatography time-of-flight mass spectrometry. Ther Drug Monit. 2014;36:119–124. doi:10.1097/FTD.0b013e3182a0d18c. PMID: 24061447. [PubMed]
46. Palmer KL, Wood KE, Krasowski MD. Evaluating a switch from meconium to umbilical cord tissue for newborn drug testing: a retrospective study at an academic medical center. Clin Biochem. 2017;50:255–261. doi:10.1016/j.clinbiochem.2016.11.026. PMID: 27890824. [PubMed]
47. Stauffer SL, Wood SM, Krasowski MD. Diagnostic yield of hair and urine toxicology testing in potential child abuse cases. J Forensic Leg Med. 2015;33:61–67. doi:10.1016/j.jflm.2015.04.010. PMID: 26048499. [PubMed]
48. Palmer KL, Krasowski MD. Hair testing for illicit drugs: do the advantages of this matrix outweigh the disadvantages? Clinical and Forensic Toxicology News. December 1-4, 2015:1–4.
49. Humble RM, Ehlers A, Pakalniskis BL, et al. Therapeutic drug monitoring of pentobarbital: experience at an academic medical center. Ther Drug Monit. 2015;7:783–791. [PubMed]
50. Fierro-Fine AC, Harland K, House HR, Krasowski MD. Ethanol values during college football season: university policy change and emergency department blood ethanol values from 2006 through 2014. Lab Med. 2016;47:300–305. doi:10.1093/labmed/lmw028. PMID: 27572874. [PubMed]
51. Steussy BW, Capper M, Krasowski MD, Rosenthal NS, Schlueter AJ. Algorithms utilizing peripheral blood hematopoietic progenitor cell counts in lieu of some CD34+ cell counts predict successful peripheral blood stem cell collections with substantial time and cost savings. ISBT Sci Series. 2016;11:153–162.
52. Dunseth C, Collins L, Reddy S, Schlueter AJ. Use of a simple, inexpensive device for collection of blood during acute normovolaemic haemodilution in a Jehovah’s Witness patient. Vox Sang. 2016;110:202–205. doi:10.1111/vox.12350. PMID: 26509493. [PubMed]
53. Dunseth CD, Ford BA, Krasowski MD. Traditional versus reverse syphilis algorithm: a comparison at a large academic medical center. Pract Lab Med. 2017;8:52–59. [PMC free article] [PubMed]
54. Gupta S, Imborek KL, Krasowski MD. Challenges in transgender healthcare: the pathology perspective. Lab Med. 2016;47:180–188. doi:10.1093/labmed/lmw020 [pii]. PMID: 27287942. [PMC free article] [PubMed]

Articles from Academic Pathology are provided here courtesy of SAGE Publications