Sociedad Americana de Hirudoterapia

Standardizing the management of heparin-induced thrombocytopenia

Protocol development published in Am J Health Syst Pharm (2008)

Última actualización: 18 de junio de 2026Revisado por: ASH Editorial Board
Artículo de investigación — revisión de evidenciaReferencia del artículo
Evidence: Research reportDesarrollo de fármacosEnsayos clínicosFugate S, Chiappe J · American journal of health-system pharmacy, 2008

Abstract

PURPOSE: An evidence-based heparin- induced thrombocytopenia (HIT) treatment protocol to standardize the management of confirmed or suspected HIT was developed. SUMMARY: In a retrospective review of 10 patients with known or suspected HIT over a two-year period, medical records were evaluated for baseline laboratory results, treatment selection, initial dosing and monitoring, discontinuation of heparin, and alternative therapies chosen. Six of 10 patients had antibody-confirmed HIT at admission. Nine patients received alternative anticoagulation therapy with one of two formulary direct thrombin inhibitor (DTI) agents, lepirudin and argatroban; 1 patient was given fondaparinux. Medical record analyses revealed deficiencies in both initial and transitional dose administration and renal function monitoring, order omissions, infusion-related medication errors, and treatments that were unsubstantiated, inappropriate, or lacking in regulatory approval. The new treatment protocol developed to assist physicians, pharmacists, and nurses with HIT management focused primarily on the two agents labeled for HIT, lepirudin and argatroban. The protocol established baseline levels for the selection of anticoagulation therapy as well as guidance in DTI selection, use, and monitoring. Guidelines for initial dosing and continuous infusion rates based on weight and detailed instructions in all aspects of therapy discontinuation (transition) were included. HIT treatments unsupported by data ensuring the efficacy and safety of therapies were excluded. Careful review of the relevant literature led to the inclusion of alternative anticoagulant treatments based on issues of safety, efficacy, cost, and convenience of dose forms. CONCLUSION: A treatment protocol for HIT was developed and implemented in a tertiary care hospital in an effort to improve the management of patients suffering from this complication.

Abstract sourced from PubMed (NCBI) for the cited record. See the original publication for the authoritative version.

Publication typeJournal Article
Indexed MeSH termsAnticoagulantsArginineClinical ProtocolsEvidence-Based MedicineFondaparinuxHeparinHirudinsHumansPipecolic AcidsPlatelet CountPlatelet Function TestsPolysaccharides

Resumen

Evidence-based HIT treatment protocol developed at tertiary care hospital after retrospective review of 10 patients; protocol focused on lepirudin and argatroban as primary FDA-labeled DTIs.

Por qué esto importa para la hirudoterapia

Este artículo describe el desarrollo e implementación de un protocolo de tratamiento basado en evidencia para la trombocitopenia inducida por heparina (TIH) en un hospital de atención terciaria, basado en una revisión retrospectiva de 10 pacientes durante un período de dos años. El protocolo se centra principalmente en dos agentes inhibidores directos de la trombina etiquetados para la TIH —lepirudina y argatrobán— proporcionando orientación sobre dosificación, selección, monitorización y suspensión de la terapia. Si bien la lepirudina se identifica como un inhibidor directo de la trombina etiquetado para el manejo de la TIH dentro de este protocolo, el resumen no describe su origen, mecanismo de acción ni ninguna conexión con sanguijuelas o hirudoterapia. No puede establecerse ninguna conexión defendible con la sanguijuela a partir del resumen por sí solo; el artículo aborda el manejo del protocolo de TIH en la práctica hospitalaria.

Citación

Standardizing the management of heparin-induced thrombocytopenia.

Fugate S, Chiappe J · American journal of health-system pharmacy, 2008

Contexto clínico relacionado

Añadido a la biblioteca ASH: May 27, 2026 · Última actualización del sitio: 18 de junio de 2026

Este sitio web proporciona información educativa y no constituye consejo médico, diagnóstico ni recomendaciones de tratamiento. La terapia con sanguijuelas medicinales conlleva riesgos clínicamente significativos y debe ser realizada únicamente por profesionales calificados bajo protocolos aprobados institucionalmente. La autorización 510(k) de la FDA para sanguijuelas medicinales se limita a indicaciones específicas; las discusiones sobre uso investigativo y fuera de indicación se señalan correspondientemente. Para orientación médica específica, consulte a un profesional de salud calificado.