Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 3 de 3
Filtrar
Más filtros

Medicinas Complementárias
Bases de datos
País/Región como asunto
Tipo del documento
País de afiliación
Intervalo de año de publicación
1.
J Pediatr Orthop B ; 32(6): 599-603, 2023 Nov 01.
Artículo en Inglés | MEDLINE | ID: mdl-36912098

RESUMEN

Trigger thumb surgery can be performed through open surgery or percutaneous release. Open surgery often requires hospitalization, an operating room, a surgical incision, and postoperative wound care; however, percutaneous release does not require hospitalization or surgery, and is relatively easier and faster. We aimed to assess the results of percutaneous A-1 pulley release using local anesthesia without hospitalization for the treatment of pediatric trigger thumb. In this retrospective study, we included patients operated on between March 2013 and August 2020 with the diagnosis of trigger thumb. The percutaneous release under local anesthesia was applied to all the children by one orthopedic surgeon. All percutaneous release procedures were performed in outpatient clinic conditions. There were 183 children (218 thumbs) who were enrolled in the clinic. Eighty-seven patients were male (47.5%) and 96 were female (52.5%). The average follow-up duration was 5 years (1-8.5 years). Among the 218 trigger thumb cases, 211 were satisfactory (successful result rate 96.8%). Relapse was seen in only 3 thumbs in the early postoperative period. No patient experienced neurovascular deficit or infection. The percutaneous surgical release in pediatric trigger thumb treatment is a simple, minimally invasive procedure that can be done in an outpatient setting under local anesthesia. In addition, the procedure duration is short and has minimal complication rates and maximum patient satisfaction. Level of Evidence III.


Asunto(s)
Procedimientos Ortopédicos , Trastorno del Dedo en Gatillo , Humanos , Niño , Masculino , Femenino , Trastorno del Dedo en Gatillo/cirugía , Resultado del Tratamiento , Estudios Retrospectivos , Anestesia Local , Procedimientos Ortopédicos/efectos adversos , Procedimientos Ortopédicos/métodos
2.
Jt Dis Relat Surg ; 31(3): 582-588, 2020.
Artículo en Inglés | MEDLINE | ID: mdl-32962592

RESUMEN

OBJECTIVES: This study aims to evaluate the quality, accuracy, and readability of Turkish online resources for platelet-rich plasma (PRP) injections for orthopedic therapy. PATIENTS AND METHODS: In this retrospective study, online searches using Google, Yandex, and Yahoo search engines were performed on 21-22-23 May 2019, respectively. "Platelet-rich plasma", "platelet-rich plasma treatment", "PRP", and "PRP treatment" were entered in Turkish into these three search engines. The first 50 websites from each search were collected. The quality and accuracy of online information related to PRP injections for orthopedic therapy were evaluated by three reviewers with the use of scoring criteria specific to PRP. The Flesch-Kincaid (FK) score was used to determine readability. RESULTS: Eighty-six unique websites were evaluated. The average quality and accuracy scores of all websites were 7.1±4.3 out of a maximum of 25 points and 7.3±2 out of a maximum of 12 points, respectively. The average FK score of all websites was 10.8±2.2. Only 27 websites (31.4%) had a FK score that was at or below the eighth-grade level. There were no significant differences among the mean scores of websites categorized by search terms, search results ranking, owners or reading level for both quality and accuracy scores. CONCLUSION: The information regarding PRP usage in orthopedic conditions provided by Turkish online resources has low quality and low accuracy ratings and is also difficult to read.


Asunto(s)
Información de Salud al Consumidor/normas , Internet , Enfermedades Musculoesqueléticas/terapia , Plasma Rico en Plaquetas , Terapia Biológica , Comprensión , Humanos , Inyecciones , Lectura , Estudios Retrospectivos , Turquía
3.
Acta Orthop Belg ; 70(5): 401-5, 2004 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-15587026

RESUMEN

The aim of this study was to evaluate the clinical effectiveness of distal forearm intravenous regional anaesthesia (IVRA) with the tourniquet applied 3 cm above the wrist. One hundred and twenty patients undergoing out-patient hand surgery were operated for 13 different hand problems under distal forearm IVRA, using 10 ml of a solution containing 1.5 mg/kg prilocaine. Sensory block onset time was 4.5 minutes (3.5-6.5 min.). Mean tourniquet time was 17.6 minutes (range, 7-27.5 min). Mean tourniquet pressure was 240 mmHg (range, 220-270 mm Hg). The mean VAS score for tourniquet pain was 3.8 (range, 2-10). No local or systemic side effects related to the IVRA were observed. The study showed that distal forearm IVRA using 10 ml of a solution containing 1.5 mg/kg prilocaine provides safe, rapid and effective anaesthesia for patients undergoing outpatient hand surgery.


Asunto(s)
Anestesia Local/métodos , Anestésicos Locales/uso terapéutico , Mano/cirugía , Prilocaína/uso terapéutico , Torniquetes , Adolescente , Adulto , Anciano , Procedimientos Quirúrgicos Ambulatorios/métodos , Anestesia Intravenosa , Femenino , Mano/fisiopatología , Humanos , Masculino , Persona de Mediana Edad , Procedimientos Ortopédicos/métodos , Dolor Postoperatorio , Estudios Prospectivos , Medición de Riesgo , Sensibilidad y Especificidad , Resultado del Tratamiento
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA