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Procedural outcomes in children with mild type 1 von Willebrand disease.


ABSTRACT:

Background

In patients with mild type 1 von Willebrand disease (VWD), treatment guidelines suggest individualization of surgical management. However, these conditional recommendations are based on very low-certainty evidence due to limited data on surgical outcomes in this population.

Objectives

To characterize procedural bleeding prophylaxis strategies and outcomes in children with mild type 1 VWD.

Methods

This is a retrospective cohort study that included patients aged between 0 and 21 years with mild type 1 VWD (defined as von Willebrand factor antigen and/or an activity of 30-50 IU/dL) who underwent a procedure from July 1, 2017, to July 1, 2022. Demographic, surgical, medication, and bleeding data were collected by manual chart review.

Results

A total of 161 procedures were performed in 108 patients. The population was primarily female (75%), White (77.8%), and non-Hispanic (79.6%). Median age was 15.8 years (IQR, 8.2-17.6). Fifty-nine surgeries were classified as major, 66 as minor, and 36 as dental. For most procedures, patients received only antifibrinolytics for bleeding prophylaxis (n = 128, 79.5%); desmopressin was used in 17 (10.6%) procedures, and von Willebrand factor concentrate was used in 12 (7.5%) procedures. Bleeding complications occurred in 8 (5.0%) procedures: these included 1 major, 4 clinically relevant nonmajor, and 3 minor bleeding events. No patient required blood transfusion or an additional procedure to achieve hemostasis. Most bleeding complications were seen following intrauterine device (IUD) placement (5/8). Nearly 30% of patients who underwent IUD placement reported bleeding.

Conclusion

Pediatric patients with mild type 1 VWD can safely undergo procedures using a tailored approach. Bleeding complications were uncommon, with the majority following IUD placement.

SUBMITTER: Heery S 

PROVIDER: S-EPMC10909640 | biostudies-literature | 2024 Jan

REPOSITORIES: biostudies-literature

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Publications

Procedural outcomes in children with mild type 1 von Willebrand disease.

Heery Samuel S   Zimowski Karen K   Mason Sadie F SF   White Michael H MH   DiGiandomenico Stefanie S   Trotter Caroline C   Sidonio Robert F RF   Brown Megan C MC  

Research and practice in thrombosis and haemostasis 20240101 1


<h4>Background</h4>In patients with mild type 1 von Willebrand disease (VWD), treatment guidelines suggest individualization of surgical management. However, these conditional recommendations are based on very low-certainty evidence due to limited data on surgical outcomes in this population.<h4>Objectives</h4>To characterize procedural bleeding prophylaxis strategies and outcomes in children with mild type 1 VWD.<h4>Methods</h4>This is a retrospective cohort study that included patients aged be  ...[more]

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