Literature DB >> 26714028

Perioperative treatment of hemophilia A patients: blood group O patients are at risk of bleeding complications.

H C A M Hazendonk1, J Lock1, R A A Mathôt2, K Meijer3, M Peters4, B A P Laros-van Gorkom5, F J M van der Meer6, M H E Driessens7, F W G Leebeek8, K Fijnvandraat4, M H Cnossen1.   

Abstract

UNLABELLED: ESSENTIALS: Targeting of factor VIII values is a challenge during perioperative replacement therapy in hemophilia. This study aims to identify the extent and predictors of factor VIII underdosing and overdosing. Blood group O predicts underdosing and is associated with perioperative bleeding. To increase quality of care and cost-effectiveness of treatment, refining of dosing is obligatory.
BACKGROUND: Perioperative administration of factor VIII (FVIII) concentrate in hemophilia A may result in both underdosing and overdosing, leading to respectively a risk of bleeding complications and unnecessary costs.
OBJECTIVES: This retrospective observational study aims to identify the extent and predictors of underdosing and overdosing in perioperative hemophilia A patients (FVIII levels < 0.05 IU mL(-1)). PATIENTS AND METHODS: One hundred nineteen patients undergoing 198 elective, minor, or major surgical procedures were included (median age 40 years, median body weight 75 kg). Perioperative management was evaluated by quantification of perioperative infusion of FVIII concentrate and achieved FVIII levels. Predictors of underdosing and (excessive) overdosing were analyzed by logistic regression analysis. Excessive overdosing was defined as upper target level plus ≥ 0.20 IU mL(-1).
RESULTS: Depending on postoperative day, 7-45% of achieved FVIII levels were under and 33-75% were above predefined target ranges as stated by national guidelines. A potential reduction of FVIII consumption of 44% would have been attained if FVIII levels had been maintained within target ranges. Blood group O and major surgery were predictive of underdosing (odds ratio [OR] 6.3, 95% confidence interval [CI] 2.7-14.9; OR 3.3, 95% CI 1.4-7.9). Blood group O patients had more bleeding complications in comparison to patients with blood group non-O (OR 2.02, 95% CI 1.00-4.09). Patients with blood group non-O were at higher risk of overdosing (OR 1.5, 95% CI 1.1-1.9). Additionally, patients treated with bolus infusions were at higher risk of excessive overdosing (OR 1.8, 95% CI 1.3-2.4).
CONCLUSION: Quality of care and cost-effectiveness can be improved by refining of dosing strategies based on individual patient characteristics such as blood group and mode of infusion.
© 2015 International Society on Thrombosis and Haemostasis.

Entities:  

Keywords:  ABO blood group system; factor VIII; hemophilia A; perioperative period; surgery

Mesh:

Substances:

Year:  2016        PMID: 26714028     DOI: 10.1111/jth.13242

Source DB:  PubMed          Journal:  J Thromb Haemost        ISSN: 1538-7836            Impact factor:   5.824


  14 in total

1.  A population pharmacokinetic model for perioperative dosing of factor VIII in hemophilia A patients.

Authors:  Hendrika Hazendonk; Karin Fijnvandraat; Janske Lock; Mariëtte Driessens; Felix van der Meer; Karina Meijer; Marieke Kruip; Britta Laros-van Gorkom; Marjolein Peters; Saskia de Wildt; Frank Leebeek; Marjon Cnossen; Ron Mathôt
Journal:  Haematologica       Date:  2016-07-06       Impact factor: 9.941

2.  O blood type is a risk factor for upper gastrointestinal bleeding.

Authors:  Massimo Franchini; Thomas Togliani; Rosalia Turdo; Giuseppe Lucchini; Carlo Bonfanti; Ivano Giacomini; Mario Luppi; Stefano Pilati
Journal:  J Thromb Thrombolysis       Date:  2018-01       Impact factor: 2.300

3.  Pharmacokinetic-guided dosing of factor VIII concentrate in a patient with haemophilia during renal transplantation.

Authors:  Hendrika C A M Hazendonk; Marieke J H A Kruip; Ron A A Mathôt; Marjon H Cnossen
Journal:  BMJ Case Rep       Date:  2016-09-22

4.  Recombinant Factor VIII Measurement in a Hemophilia A Patient Undergoing Cardiopulmonary Bypass-Supported Cardiac Surgery.

Authors:  Jennifer Bezaire; Dorothy Thomson; Erick McNair
Journal:  J Extra Corpor Technol       Date:  2018-09

5.  New Surgical Technologies Could Facilitate Surgical Hemostasis in Hemophilic Patients.

Authors:  Milcho J Panovski; Igor V Fildishevski; Ljubomir Lj Ognjenovic; Violeta I Dejanova-Ilijevska
Journal:  Open Access Maced J Med Sci       Date:  2017-05-25

6.  Desmopressin treatment combined with clotting factor VIII concentrates in patients with non-severe haemophilia A: protocol for a multicentre single-armed trial, the DAVID study.

Authors:  Lisette M Schütte; Marjon H Cnossen; Reinier M van Hest; Mariette H E Driessens; Karin Fijnvandraat; Suzanne Polinder; Erik A M Beckers; Michiel Coppens; Jeroen Eikenboom; Britta A P Laros-van Gorkom; Karina Meijer; Laurens Nieuwenhuizen; Evelien P Mauser-Bunschoten; Frank W G Leebeek; Ron A A Mathôt; Marieke J H A Kruip
Journal:  BMJ Open       Date:  2019-04-23       Impact factor: 2.692

Review 7.  Population Pharmacokinetics of Clotting Factor Concentrates and Desmopressin in Hemophilia.

Authors:  Tim Preijers; Lisette M Schütte; Marieke J H A Kruip; Marjon H Cnossen; Frank W G Leebeek; Reinier M van Hest; Ron A A Mathôt
Journal:  Clin Pharmacokinet       Date:  2021-01       Impact factor: 6.447

8.  Rare but not Abdicated: Status of Haemophilia in foothills of Himalaya, Uttarakhand: A cross-sectional study.

Authors:  Vyas K Rathaur; N K V Vigneshwar; Ayesha Imran; Monika Pathania; Sonam Agrawal; Swathi Chacham; Prashant K Verma; Nowneet K Bhat
Journal:  J Family Med Prim Care       Date:  2021-04-08

Review 9.  Performing and interpreting individual pharmacokinetic profiles in patients with Hemophilia A or B: Rationale and general considerations.

Authors:  Alfonso Iorio; Andrea N Edginton; Victor Blanchette; Jan Blatny; Ana Boban; Marjon Cnossen; Peter Collins; Stacy E Croteau; Katheljin Fischer; Daniel P Hart; Shinya Ito; Joan Korth-Bradley; Stefan Lethagen; David Lillicrap; Mike Makris; Ron Mathôt; Massimo Morfini; Ellis J Neufeld; Jeffrey Spears
Journal:  Res Pract Thromb Haemost       Date:  2018-05-20

10.  Pharmacodynamic monitoring of factor VIII replacement therapy in hemophilia A: Combining thrombin and plasmin generation.

Authors:  Lars L F G Valke; Laura H Bukkems; Wideke Barteling; Britta A P Laros-van Gorkom; Nicole M A Blijlevens; Ron A A Mathôt; Waander L van Heerde; Saskia E M Schols
Journal:  J Thromb Haemost       Date:  2020-10-21       Impact factor: 16.036

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