Literature DB >> 30659653

Bleeding assessment in female patients with the Hermansky-Pudlak syndrome-A case series.

Joel Rivera-Concepción1, Jorge Acevedo-Canabal1, Antonio Burés2, Gustavo Vargas2, Carmen Cadilla2, Natalio J Izquierdo3.   

Abstract

INTRODUCTION: The Hermansky-Pudlak syndrome (HPS) is an autosomal recessive rare disorder characterized by oculocutaneous albinism, bleeding diathesis, chronic granulomatous colitis and/or pulmonary fibrosis. HPS is the most common single-gene disorder in Puerto Rico with a prevalence of 1:1,800 in the Northwest of the island. Risk of menorrhagia and post-partum hemorrhage (PPH) in cases of women with HPS have been described in the medical literature, but data regarding comprehensive description of bleeding diathesis remains lacking. For this reason, we aim to identify bleeding events using the International Society on Thrombosis and Hemostasis Bleeding Assessment Tool (ISTH-BAT), a standardized quantitative tool that translates the range of severity of bleeding symptoms into a cumulative bleeding score (BS).
OBJECTIVE: To use the ISTH-BAT in HPS in order to describe bleeding symptoms and allow for comparison with other inherited bleeding disorders.
METHODS: Puerto Rican females and adult participants with HPS based on genetic linkage were enrolled. The ISTH-BAT was administered and results were identified using descriptive statistical analysis.
RESULTS: Questionnaire answers of twelve women with HPS-1 and HPS-3 were evaluated. Participants' mean BS was HPS-1 (11.4) and HPS-3 (8.0) Participants with HPS-1 and HPS-3 reported abnormal bleeding events that presented during dental extractions, menorrhagia, surgical interventions, gastrointestinal, oral cavity and post-partum. Patients with history of pulmonary fibrosis (PF) showed a higher mean bleeding score than those who had no history of PF.
CONCLUSIONS: Female patients with HPS type 1 and 3 experienced abnormal bleeding events according to the ISTH-BAT bleeding score. Bleeding medications were inconsistently used and varied independently from healthcare professionals. The benefits of this study were to understand the history of bleeding complications in patients with HPS type 1 and 3 using an international validated system. The results of this study will help design strategies to improve the care we provide to this population.
© 2019 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

Entities:  

Keywords:  Hermansky Pudlak syndrome; ISTH-BAT; bleeding diathesis; hereditary bleeding disorders

Mesh:

Year:  2019        PMID: 30659653      PMCID: PMC6545108          DOI: 10.1111/ejh.13210

Source DB:  PubMed          Journal:  Eur J Haematol        ISSN: 0902-4441            Impact factor:   2.997


  15 in total

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Journal:  Nat Genet       Date:  2001-08       Impact factor: 38.330

2.  Hermansky-Pudlak syndrome: the importance of molecular subtyping.

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Review 3.  Modern management of severe platelet function disorders.

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4.  Albinism associated with hemorrhagic diathesis and unusual pigmented reticular cells in the bone marrow: report of two cases with histochemical studies.

Authors:  F HERMANSKY; P PUDLAK
Journal:  Blood       Date:  1959-02       Impact factor: 22.113

5.  Albinism and Hermansky-Pudlak syndrome in Puerto Rico.

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Journal:  Bol Asoc Med P R       Date:  1990-08

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9.  Variable response of Hermansky-Pudlak syndrome to prophylactic administration of 1-desamino 8D-arginine in subsequent pregnancies.

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10.  Two successful vaginal births after cesarean section in a patient with Hermansky-Pudlak syndrome who was treated with 1-deamino-8-arginine-vasopression during labor.

Authors:  Ronald D Beesley; Randal D Robinson; Theresa L Stewart
Journal:  Mil Med       Date:  2008-10       Impact factor: 1.437

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  2 in total

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Review 2.  Women With Congenital Hypofibrinogenemia/Afibrinogenemia: From Birth to Death.

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