Literature DB >> 16443731

An audit of thrombophilia screens: results from the National Pathology Alliance benchmarking review.

S Lyons1, M J Galloway, J Osgerby, J Hanley.   

Abstract

AIMS: The National Pathology Alliance benchmarking review has completed six years of data collection and analysis of the workload and organisation of haematology laboratories in the UK. This study audits national practice of routine thrombophilia screening against the current standards, as set out in the British committee for standards in haematology (BCSH) guidelines on investigation of heritable thrombophilia.
METHODS: Each laboratory completed a standard data collection questionnaire about the number of routine thrombophilia assays performed each year. Information was collected on which thrombophilia tests were performed as part of a routine thrombophilia screen. These results were then compared against the BCSH guidelines on investigation of heritable thrombophilia.
RESULTS: Of the 57 National Health Service trusts that submitted data for review in 2002/2003, 47 performed a routine thrombophilia screen. Ten laboratories complied with the guidelines but 37 laboratories did not.
CONCLUSION: There was variation in practice in the tests used in routine thrombophilia screens. There is evidence that some laboratories deviate from what may be regarded as "evidence based practice". The lack of compliance with the guidelines was in general associated with the performance of additional tests not recommended in the guideline. In a minority of laboratories, a clinically significant diagnosis would be missed by the failure to include one or more tests in a thrombophilia screen.

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Mesh:

Year:  2006        PMID: 16443731      PMCID: PMC1860328          DOI: 10.1136/jcp.2005.025841

Source DB:  PubMed          Journal:  J Clin Pathol        ISSN: 0021-9746            Impact factor:   3.411


  9 in total

1.  Guidelines on the investigation and management of the antiphospholipid syndrome.

Authors:  M Greaves; H Cohen; S J MacHin; I Mackie
Journal:  Br J Haematol       Date:  2000-06       Impact factor: 6.998

2.  Investigation and management of heritable thrombophilia.

Authors: 
Journal:  Br J Haematol       Date:  2001-09       Impact factor: 6.998

3.  Red cell or serum folate? Results from the National Pathology Alliance benchmarking review.

Authors:  M Galloway; L Rushworth
Journal:  J Clin Pathol       Date:  2003-12       Impact factor: 3.411

Review 4.  Inherited thrombophilia: Part 1.

Authors:  D A Lane; P M Mannucci; K A Bauer; R M Bertina; N P Bochkov; V Boulyjenkov; M Chandy; B Dahlbäck; E K Ginter; J P Miletich; F R Rosendaal; U Seligsohn
Journal:  Thromb Haemost       Date:  1996-11       Impact factor: 5.249

Review 5.  Inherited thrombophilia: Part 2.

Authors:  D A Lane; P M Mannucci; K A Bauer; R M Bertina; N P Bochkov; V Boulyjenkov; M Chandy; B Dahlbäck; E K Ginter; J P Miletich; F R Rosendaal; U Seligsohn
Journal:  Thromb Haemost       Date:  1996-12       Impact factor: 5.249

6.  Modified APC resistance assay for patients on oral anticoagulants.

Authors:  M Trossaërt; J Conard; M H Horellou; M M Samama; H Ireland; T A Bayston; D A Lane
Journal:  Lancet       Date:  1994-12-17       Impact factor: 79.321

Review 7.  Dysfibrinogenemia and thrombosis.

Authors:  Timothy Hayes
Journal:  Arch Pathol Lab Med       Date:  2002-11       Impact factor: 5.534

Review 8.  A review of the technical, diagnostic, and epidemiologic considerations for protein S assays.

Authors:  Andrew J Goodwin; Frits R Rosendaal; Kandice Kottke-Marchant; Edwin G Bovill
Journal:  Arch Pathol Lab Med       Date:  2002-11       Impact factor: 5.534

Review 9.  Familial dysfibrinogenemia and thrombophilia. Report on a study of the SSC Subcommittee on Fibrinogen.

Authors:  F Haverkate; M Samama
Journal:  Thromb Haemost       Date:  1995-01       Impact factor: 5.249

  9 in total
  2 in total

1.  An audit of the indications for the reporting of blood films: results from the National Pathology Benchmarking Study.

Authors:  M J Galloway; J C Osgerby
Journal:  J Clin Pathol       Date:  2006-05       Impact factor: 3.411

2.  High prevalence of protein C, protein S, antithrombin deficiency, and Factor V Leiden mutation as a cause of hereditary thrombophilia in patients of venous thromboembolism and cerebrovascular accident.

Authors:  Nadir Ali; Muhammad Ayyub; Saleem Ahmed Khan
Journal:  Pak J Med Sci       Date:  2014 Nov-Dec       Impact factor: 1.088

  2 in total

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