scholarly journals Evaluation of thrombophilia testing in the inpatient setting: A single institution retrospective review

PLoS ONE ◽  
2021 ◽  
Vol 16 (9) ◽  
pp. e0257687
Author(s):  
Chun Ting Siu ◽  
Zachary Wolfe ◽  
Martin DelaTorre ◽  
Erafat Rehim ◽  
Robert Decker ◽  
...  

Background Thrombophilia workup is typically inappropriate in the inpatient setting as testing may be skewed by anticoagulation, acute thrombosis, or acute illness. Objective To determine adherence of inpatient thrombophilia testing with institutional guidelines. Patients and methods A retrospective study to evaluate thrombophilia testing practices of adult patients who were admitted to Lehigh Valley Hospital at Cedar Crest with either venous thromboembolism or ischemic stroke in 2019. Testing included inherited and acquired thrombophilia. Patient charts were individually reviewed for three measured outcomes: 1) the number of appropriate thrombophilia testing in the inpatient setting; 2) the indications used for thrombophilia testing; 3) the proportion of positive thrombophilia tests with change in clinical management. Results 201 patients were included in our study. 26 patients (13%) were tested appropriately in accordance with institution guidelines and 175 (87%) patients were tested inappropriately. The most common reason for the inappropriate testing was testing during acute thrombosis. 28 of the 201 patients had positive thrombophilia tests, but the reviewers only noted 7 patients with change in clinical management—involving anticoagulation change. Conclusion Our study revealed that a majority of inpatient thrombophilia testing did not follow institutional guidelines for appropriate testing and did not change patient management. These thrombophilia tests are often overutilized and have minimal clinical utility in the inpatient setting.

Blood ◽  
2015 ◽  
Vol 126 (23) ◽  
pp. 4474-4474
Author(s):  
Harel Ronen ◽  
Nakul Singhal ◽  
Colette Spaccavento

Abstract Introduction Hereditary thrombophilia describes an inherited tendency to form venous or arterial thrombosis second to loss of natural anticoagulants. The optimal patient populations to test for these thrombophilic states are controversial. No accepted guidelines exist for whom to test, but consensus among many experts is that a targeted approach should be taken. Both the College of American Pathologists (CAP) and the American College of Medical Genetics (ACMG) suggest testing the following patients: Idiopathic VTE at <50 years old, recurrent VTE, and unusual sites of VTE (e.g., mesenteric, portal, hepatic) [1,2]. Hypercoagulable testing should not be done during acute thrombosis or while receiving anticoagulation. Given our clinical observations, we hypothesized that hypercoagulable testing is often done without the proper indication and performed at an inappropriate time at our institution. A single institution study was performed at our hospital from January '13 through August '13 reviewing inpatients that had Factor V Leiden and Prothrombin Gene mutations, Antithrombin, Protein C, and Protein S antigens or activities ordered, and evaluated as to whether or not they were ordered in concordance with the CAP and ACMG indications. Results from that study illustrated that of the 43 patients that had these tests ordered; only 13 were ordered based on appropriate indications from CAP and ACMG. Of those 13 patients, all were tested at an inappropriate time, either during an acute thrombosis or while on anticoagulation. The departments responsible for ordering the majority of the tests were Medicine, Neurology and Ob/Gyn., making up greater than 75% of the orders. In view of this information we designed an intervention to further educate the staff and to evaluate its outcome. Methods From September '14 through December '14, we educated the staff responsible for ordering these tests via instructional seminars. Each department was educated separately, and was given 30 minute lectures reviewing the utilities, indications and appropriate timing of ordering a thrombophilic workup. This was repeated several times over the course of the three month period. We then retrospectively reviewed charts of hospitalized patients at our hospital from January '15 through August '15. A patient must have had the following tests ordered to be included in the study: Factor V Leiden mutation, Prothrombin Gene mutation, Antithrombin, Protein C, and Protein S antigens or activities. Data compiled from electronic databases included age, clinical indication for hypercoagulable workup, ordering service, and whether or not anticoagulation was present during testing. These indications were then compared to the indications recommended by both the CAP and the ACMG listed above. If testing occurred for a non-approved indication, during acute thrombosis, or while patients were receiving anticoagulation it was deemed inappropriate. Results 22 patients had inpatient hypercoaguable testing sent over the time period of January '15 through June '15 as compared to 43 tested from January '13 through August '13, prior to the intervention. Of the 22 patients, 3/22 (14%) were tested appropriately according to the CAP and ACMG recommendations. However, all 3 patients had hypercoaguable testing sent inappropriately when timing was analyzed; all were tested during an acute thrombosis or while on anticoagulation. When comparing the current data to that prior to the intervention, there was a trend of decreasing number of hypercoaguable tests ordered. The departments given the seminar all had a decreasing trend in tests ordered. Despite this, the majority of the tests ordered after the interventions were still ordered incorrectly or while either on anticoagulant treatment or during an acute thrombosis. Discussion Hypercoagulable testing is being over utilized in the inpatient setting, largely because it is being performed for inappropriate indications and during suboptimal conditions. Principally, this is due to lack of knowledge on the indications and timing of ordering these thrombophilic tests. Here we demonstrate how education, in the form of lectures and seminars, can inform the staff on how and when to order these hypercoaguable panels. This study acts as a template to illustrate how education in the form of brief and repeated seminars can help change practice habits, provide better quality care and prevent inappropriate testing. Disclosures No relevant conflicts of interest to declare.


2021 ◽  
Vol 7 (3) ◽  
pp. 178
Author(s):  
Lea M Monday ◽  
Tommy Parraga Acosta ◽  
George Alangaden

Invasive candidiasis is a common healthcare-associated infection with high mortality and is difficult to diagnose due to nonspecific symptoms and limitations of culture based diagnostic methods. T2Candida, based on T2 magnetic resonance technology, is FDA approved for the diagnosis of candidemia and can rapidly detect the five most commonly isolated Candida sp. in approximately 5 h directly from whole blood. We discuss the preclinical and clinical studies of T2Candida for the diagnosis of candidemia and review the current literature on its use in deep-seated candidiasis, its role in patient management and prognosis, clinical utility in unique populations and non-blood specimens, and as an antifungal stewardship tool. Lastly, we summarize the strengths and limitations of this promising nonculture-based diagnostic test.


2019 ◽  
pp. 1-18
Author(s):  
Olga Kondrashova ◽  
Gwo-Yaw Ho ◽  
George Au-Yeung ◽  
Leakhena Leas ◽  
Tiffany Boughtwood ◽  
...  

PURPOSE The ALLOCATE study was designed as a pilot to demonstrate the feasibility and clinical utility of real-time targeted molecular profiling of patients with recurrent or advanced ovarian cancer for identification of potential targeted therapies. PATIENTS AND METHODS A total of 113 patients with ovarian cancer of varying histologies were recruited from two tertiary hospitals, with 99 patient cases suitable for prospective analysis. Targeted molecular and methylation profiling of fresh biopsy and archived tumor samples were performed by screening for mutations or copy-number variations in 44 genes and for promoter methylation of BRCA1 and RAD51C. RESULTS Somatic genomic or methylation events were identified in 85% of all patient cases, with potentially actionable events with defined targeted therapies (including four resistance events) detected in 60% of all patient cases. On the basis of these findings, six patients received molecularly guided therapy, three patients had unsuspected germline cancer–associated BRCA1/ 2 mutations and were referred for genetic counseling, and two intermediate differentiated (grade 2) serous ovarian carcinomas were reclassified as low grade, leading to changes in clinical management. Additionally, secondary reversion mutations in BRCA1/ 2 were identified in fresh biopsy samples of two patients, consistent with clinical platinum/poly (ADP-ribose) polymerase inhibitor resistance. Timely reporting of results if molecular testing is done at disease recurrence, as well as early referral for patients with platinum-resistant cancers, were identified as factors that could improve the clinical utility of molecular profiling. CONCLUSION ALLOCATE molecular profiling identified known genomic and methylation alterations of the different ovarian cancer subtypes and was deemed feasible and useful in routine clinical practice. Better patient selection and access to a wider range of targeted therapies or clinical trials will further enhance the clinical utility of molecular profiling.


2018 ◽  
Vol 46 (3-4) ◽  
pp. 154-167 ◽  
Author(s):  
Yejin Kim ◽  
Paul Rosenberg ◽  
Esther Oh

Background: Molecular imaging of brain amyloid for the diagnosis of Alzheimer’s disease (AD) using positron emission tomography (PET) has been approved for use in clinical practice by the Food and Drug Administration (FDA) since 2012. However, the clinical utility and diagnostic impact of amyloid PET imaging remain controversial. We conducted a review of the recent studies investigating clinical utility of amyloid PET imaging with focus on changes in diagnosis, diagnostic confidence, and patient management. Summary: A total of 16 studies were included in the final analysis. Overall rate of changes in diagnosis after amyloid PET ranged from 9 to 68% (pooled estimate of 31%, 95% CI 23–39%). All studies reported overall increase in diagnostic confidence or diagnostic certainty after amyloid PET. Changes in patient management ranged from 37 to 87%; the most common type of change in management reported was either the initiation or discontinuation of planned AD medications. Key Messages: Amyloid PET imaging led to moderate to significant changes in diagnosis, diagnostic confidence, and subsequent patient management. It may be most useful in patients with high level of diagnostic uncertainty even after the completing the standard workup.


TH Open ◽  
2020 ◽  
Vol 04 (03) ◽  
pp. e153-e162
Author(s):  
Manila Gaddh ◽  
En Cheng ◽  
Maha A.T. Elsebaie ◽  
Imre Bodó

Abstract Introduction Testing for inherited and acquired thrombophilias adds to the cost of care of patients with venous thromboembolism (VTE), though results may not influence patient management. Methods This is a single-center, retrospective study conducted at Emory University Hospitals from January to December 2015 to (1) determine the pattern of thrombophilia testing in patients with VTE, (2) study the impact of results of thrombophilia testing on clinical decision-making, and (3) determine the direct costs of thrombophilia testing in patients with VTE. Results Of the 266 eligible patients, 189 (71%) underwent testing; 51 (26.9%) tested positive and the results impacted management in 32 (16.9%) of tested patients. Patient undergoing testing were more likely to be younger than 40 years (30.9 vs. 18.2%), have had prior pregnancy loss (9.0 vs. 0%), or known family history of hypercoagulability (24.9 vs. 10.4%), and were less likely to have had provoked VTE (37 vs. 79.2%). The most common thrombophilias tested were antiphospholipid syndrome (60.1%), factor V Leiden (59.7%), and prothrombin gene mutation (57.5%). Direct costs of thrombophilia testing were $2,364.32 per patient, $12,331.55 to diagnose 1 positive, and $19,653.41 per patient-management affected. Conclusion We noted significant variability in selection of patients and panel of tests, sparse utilization of test results in patient management, but high cost associated with thrombophilia testing in patients with VTE. With guidelines advocating selective use of thrombophilia testing and attention to potential impact of test results in patient management, we propose the need for measures at institutional levels to improve test-ordering practices.


1995 ◽  
Vol 12 (1) ◽  
pp. 34-36
Author(s):  
Niall Quigley ◽  
Oscar Daly

AbstractObjective: Case notes on 116 patients aged 65 or more admitted to a general psychiatry hospital over a three month period were examined to assess the current use of haematological screening tests.Method: Retrospective justification for tests performed, rate of abnormal results, and consequences for patient management were assessed by case note review.Results: A total of 200 screening tests, 105 of which appeared justified, were performed; 66 patients were screened, of whom 85% had at least one abnormal result. Those who were older were less likely to be screened. There was no relationship between diagnosis and being screened. Of the 90 abnormal results received, less then one third affected clinical management.Conclusions: The financial and other costs of screening tests are discussed. The current use of haematological screening tests in this population appears erratic and often adds little to patient management.


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