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Effect of tranexamic acid administration on bleeding in primary total hip arthroplasty. / Efecto de dosis única intravenosa de ácido tranexámico sobre el sangrado en artroplastia total de cadera. Estudio prospectivo, controlado y aleatorizado.
Fernández-Cortiñas, A B; Quintáns-Vázquez, J M; Gómez-Suárez, F; Murillo, O Simón; Sánchez-López, B R; Pena-Gracía, J M.
Affiliation
  • Fernández-Cortiñas AB; Servicio de Cirugía Ortopédica y Traumatología, Hospital COSAGA, Ourense, España. Electronic address: anabelen6k@gmail.com.
  • Quintáns-Vázquez JM; Servicio de Cirugía Ortopédica y Traumatología, Hospital COSAGA, Ourense, España.
  • Gómez-Suárez F; Servicio de Cirugía Ortopédica y Traumatología, Hospital COSAGA, Ourense, España.
  • Murillo OS; Servicio de Cirugía Ortopédica y Traumatología, Hospital COSAGA, Ourense, España.
  • Sánchez-López BR; Servicio de Calidad y Estadística, Hospital COSAGA, Ourense, España.
  • Pena-Gracía JM; Servicio de Cirugía Ortopédica y Traumatología, Hospital COSAGA, Ourense, España.
Rev Esp Cir Ortop Traumatol ; 61(5): 289-295, 2017.
Article in En, Es | MEDLINE | ID: mdl-28689785
ABSTRACT

OBJECTIVE:

To study the efficacy of tranexamic acid to decrease perioperative bleeding in patients who have undergone a total hip arthroplasty operation and to evaluate drug safety. MATERIAL AND

METHODS:

Observational, prospective, controlled and randomized study on the efficacy of tranexamic acid as a method to reduce bleeding in primary hip replacement surgery. We included 134 patients operated during 2014 in our centre, who were divided into 2 groups according to whether or not they had received tranexamic acid. The main study variables were haemoglobin and haematocrit levels, the amount of blood collected from the post-operative drain in the first 12, 24 and 48hours and transfusion requirements.

RESULTS:

Post-operative haemoglobin and haematocrit levels were statistically higher (P<.001) in the group with treatment. During the first 48hours bleeding values from the group that did not receive TAX were higher compared to patients treated with tranexamic acid. Statistically significant differences (P=.001) were found as to the need for transfusion according to group, more transfusions were performed in the cohort that had not received tranexamic acid 25.37% compared to 4.48% for the group with tranexamic acid. No adverse events related to administration of tranexamic acid were recorded.

CONCLUSIONS:

Administration of tranexamic acid has proved to be an effective and safe method to reduce peri-operative bleeding in patients who underwent total hip arthroplasty and avoids allogenic blood transfusion. Therefore, tranexamic acid treatment could entail a financial saving for the healthcare system and expose the patient to less risk.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Tranexamic Acid / Postoperative Hemorrhage / Arthroplasty, Replacement, Hip / Antifibrinolytic Agents Type of study: Clinical_trials / Diagnostic_studies / Observational_studies / Risk_factors_studies Limits: Aged / Aged80 / Female / Humans / Male Language: En / Es Journal: Rev Esp Cir Ortop Traumatol Year: 2017 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Tranexamic Acid / Postoperative Hemorrhage / Arthroplasty, Replacement, Hip / Antifibrinolytic Agents Type of study: Clinical_trials / Diagnostic_studies / Observational_studies / Risk_factors_studies Limits: Aged / Aged80 / Female / Humans / Male Language: En / Es Journal: Rev Esp Cir Ortop Traumatol Year: 2017 Document type: Article