scholarly journals Burkitt lymphoma of the maxilla in a HIV positive male – Presentation and review of diagnostic laboratory tests

2019 ◽  
Vol 5 (3) ◽  
pp. 100113
Author(s):  
William Alvarez ◽  
Li Han Lai ◽  
Shakira J. Grant ◽  
Daniel E. Sabath ◽  
Jasjit Dillon
2011 ◽  
Vol 47 (8) ◽  
pp. 415-417 ◽  
Author(s):  
Francisco Rodríguez-Frías ◽  
Brian Vila-Auli ◽  
María Homs-Riba ◽  
Rafael Vidal-Pla ◽  
José Luis Calpe-Calpe ◽  
...  

1986 ◽  
Vol 314 (19) ◽  
pp. 1233-1235 ◽  
Author(s):  
Bruce R. Smoller ◽  
Margot S. Kruskall

2020 ◽  
Vol 63 (8) ◽  
pp. 493-503
Author(s):  
Hye Ryun Lee ◽  
Sollip Kim ◽  
Yeo-Min Yun ◽  
Jae-Hyeok Heo ◽  
Kun Sei Lee ◽  
...  

A new diagnosis-related group (DRG) based payment system has been implemented in most public hospitals in Korea. We investigated the effects of the new DRG system and its incentive policy on the utilization rate of diagnostic laboratory tests. Three groups were categorized; 36 hospitals under the new DRG system (participant group), 72 hospitals (control-1) matching with 36 participants according to the number of beds, and 42 tertiary hospitals (control-2). The patients of acute myocardial infarction, cerebral infarction, type 2 diabetes mellitus, and gonarthrosis receiving total arthroplasty were included. We analyzed the mean length of stay and the number of diagnostic laboratory tests conducted during hospitalization of the three groups according to the new DRG system and the incentive policy rates under the new DRG system. Before participating in the new DRG system, the number of diagnostic laboratory tests in the participant group was less than that in the two control groups for all four diseases. However, although the participant group’s length of stay decreased under the new DRG system, the number of diagnostic laboratory tests increased as the maximum incentive policy rate increased. The increment of the number of diagnostic laboratory tests was prominent in the period of a maximum of 35% incentive policy rates. Finally, the number of diagnostic laboratory tests of the participant group was similar to or exceeded that of the control-2 group. The new DRG system’s incentive policy rates played a driving force on the increased utilization rate of the diagnostic laboratory test. For preparing in advance for the change in incentive policy rates, monitoring and guidelines for the utilization of diagnostic laboratory tests are necessary.


2018 ◽  
Vol 56 (10) ◽  
pp. 1743-1748 ◽  
Author(s):  
Pier Luigi Meroni ◽  
Maria Orietta Borghi

Abstract Autoantibodies are helpful tools not only for the diagnosis and the classification of systemic autoimmune rheumatic diseases (SARD) but also for sub-grouping patients and/or for monitoring disease activity or specific tissue/organ damage. Consequently, the role of the diagnostic laboratory in the management of SARD is becoming more and more important. The advent of new techniques raised the need of updating and harmonizing our use/interpretation of the assays. We discuss in this opinion paper some of these issues. Indirect immunofluorescence (IIF) was originally suggested as the reference technique for anti-nuclear antibody (ANA) detection as previous solid phase assays (SPA) displayed lower sensitivity. The new available SPA are now offering better results and can represent alternative or even complementary diagnostic tools for ANA detection. The improved sensitivity of SPA technology is also changing our interpretation of the results for other types of autoantibody assays, but we need updating their calibration and new reference materials are going to be obtained in order to harmonize the assays. There is growing evidence that the identification of autoantibody combinations or profiles is helpful in improving diagnosis, patients’ subgrouping and predictivity for disease evolution in the field of SARD. We report some explanatory examples to support the idea to make the use of these autoantibody profiles more and more popular. The technological evolution of the autoimmune assays is going to change our routine diagnostic laboratory tests for SARD and validation of new algorithms is needed in order to harmonize our approach to the issue.


PEDIATRICS ◽  
1980 ◽  
Vol 65 (6) ◽  
pp. 1197-1197
Author(s):  
Edward N. Squire ◽  
James K. Todd ◽  
Blaise E. Favara

It is an appropriate conclusion that our data should "mitigate enthusiasm for the prospective use of WBC parameters in the diagnosis of infection of the newborn infant." Such enthusiasm for a laboratory test is usually the result of the overzealous interpretation of inadequately controlled comparative studies suffering from small sample size, or inappropriate extrapolation of limited conclusions to expanded populations. Very few diagnostic laboratory tests are so sensitive and specific that they lack significant false-positive or false-negative results, and the aforementioned white blood cell studies are commonly referred to as nonspecific indicators of inflammation with just cause.


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