Quality of periprocedural care in patients with von Willebrand disease

被引:3
作者
Seaman, Craig D. [1 ,2 ]
Bertolet, Marnie [3 ,4 ,5 ]
Zhang, Jun [6 ]
Ragni, Margaret V. [1 ,2 ]
机构
[1] Univ Pittsburgh, Dept Med, Ctr Med, Div Hematol Oncol, Pittsburgh, PA USA
[2] Hemophilia Ctr Western Penn, Pittsburgh, PA USA
[3] Dept Epidemiol, Pittsburgh, PA USA
[4] Dept Biostat, Pittsburgh, PA USA
[5] Clin & Translat Sci Inst, Pittsburgh, PA USA
[6] Univ Pittsburgh, Dept Biostat, Pittsburgh, PA 15261 USA
基金
美国国家卫生研究院;
关键词
haemophilia treatment centre; surgery; von Willebrand disease; HEMOPHILIA;
D O I
10.1111/hae.14389
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction While it has been shown that haemophilia patients receiving care at Haemophilia Treatment Centres (HTCs) experience decreased morbidity and mortality, little research has been done on the outcomes of patients with von Willebrand disease (VWD). Aim To compare the quality of periprocedural care received by patients with VWD at HTCs and non-HTCs. Methods We performed a retrospective chart review on all adult VWD patients undergoing an invasive procedure from 2015 to 2017. Quality of periprocedural care was measured using the following surrogate outcomes: periprocedural VWD-specific therapy use per 2007 National Heart, Lung, and Blood Institute (NHLBI) guidelines, procedural estimated blood loss (EBL), and post-procedure bleeding. Comparisons were performed according to the setting of care at the time of the invasive procedure, HTC versus non-HTC. Results There were 668 invasive procedures performed on 305 patients, of which 8.2% were HTC cases. Non-type 1 VWD was more likely in HTC cases. VWD-specific therapy was used per NHLBI guidelines in 100% of HTC cases compared with 10.6% of non-HTC cases. Procedural EBL > = 100 ml was more likely to occur in HTC differences cases (OR = 2.34; 95% CI, 1.05 to 5.25). There was no difference in post-procedure bleeding between the two groups (OR = 1.26, 95% CI, .20- 7.86). Conclusion Despite widespread periprocedural use of VWD-specific therapy outside established guidelines at non-HTCs, there was no difference in periprocedural bleeding. Possible explanations include diagnostic error, in disease severity and procedure types, and dataset limitations. Additional studies are needed to investigate this further and compare other patient care outcomes between HTCs and non-HTCs.
引用
收藏
页码:830 / 836
页数:7
相关论文
共 16 条
[1]   US Hemophilia Treatment Center population trends 1990-2010: patient diagnoses, demographics, health services utilization [J].
Baker, J. R. ;
Riske, B. ;
Drake, J. H. ;
Forsberg, A. D. ;
Atwood, R. ;
Voutsis, M. ;
Shearer, R. .
HAEMOPHILIA, 2013, 19 (01) :21-26
[2]  
Centers for Disease Control and Prevention, 2020, WILL DIS DAT STAT WI
[3]   Clinical and laboratory variability in a cohort of patients diagnosed with type 1 VWD in the United States [J].
Flood, Veronica H. ;
Christopherson, Pamela A. ;
Gill, Joan Cox ;
Friedman, Kenneth D. ;
Haberichter, Sandra L. ;
Bellissimo, Daniel B. ;
Udani, Rupa A. ;
Dasgupta, Mahua ;
Hoffmann, Raymond G. ;
Ragni, Margaret V. ;
Shapiro, Amy D. ;
Lusher, Jeanne M. ;
Lentz, Steven R. ;
Abshire, Thomas C. ;
Leissinger, Cindy ;
Hoots, W. Keith ;
Manco-Johnson, Marilyn J. ;
Gruppo, Ralph A. ;
Boggio, Lisa N. ;
Montgomery, Kate T. ;
Goodeve, Anne C. ;
James, Paula D. ;
Lillicrap, David ;
Peake, Ian R. ;
Montgomery, Robert R. .
BLOOD, 2016, 127 (20) :2481-2488
[4]   Common VWF exon 28 polymorphisms in African Americans affecting the VWF activity assay by ristocetin cofactor [J].
Flood, Veronica H. ;
Gill, Joan Cox ;
Morateck, Patricia A. ;
Christopherson, Pamela A. ;
Friedman, Kenneth D. ;
Haberichter, Sandra L. ;
Branchford, Brian R. ;
Hoffmann, Raymond G. ;
Abshire, Thomas C. ;
Di Paola, Jorge A. ;
Hoots, W. Keith ;
Leissinger, Cindy ;
Lusher, Jeanne M. ;
Ragni, Margaret V. ;
Shapiro, Amy D. ;
Montgomery, Robert R. .
BLOOD, 2010, 116 (02) :280-286
[5]   Automated assays for von Willebrand factor activity [J].
Higgins, Russell A. ;
Goodwin, Andrew J. .
AMERICAN JOURNAL OF HEMATOLOGY, 2019, 94 (04) :496-503
[6]  
Hoots W Keith, 2003, Curr Hematol Rep, V2, P395
[7]   Von Willebrand disease in the emergency department [J].
Livesey, K. ;
Yealy, D. M. ;
Li, J. ;
Moore, C. G. ;
Ragni, M. V. .
HAEMOPHILIA, 2016, 22 (02) :263-267
[8]  
Medical and Scientific Advisory Council, 2020, MASAC REC C TREATM I
[9]  
Nichols, 2007, NIH PUB
[10]   Comprehensive care for hemophilia and other inherited bleeding disorders [J].
Page, David .
TRANSFUSION AND APHERESIS SCIENCE, 2019, 58 (05) :565-568