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1.
Ann Surg ; 248(2): 166-79, 2008 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-18650625

RESUMEN

OBJECTIVE: To determine whether skills acquired by simulation-based training transfer to the operative setting. SUMMARY BACKGROUND DATA: The fundamental assumption of simulation-based training is that skills acquired in simulated settings are directly transferable to the operating room, yet little evidence has focused on correlating simulated performance with actual surgical performance. METHODS: A systematic search strategy was used to retrieve relevant studies. Inclusion of articles was determined using a predetermined protocol, independent assessment by 2 reviewers, and a final consensus decision. Only studies that reported on the use of simulation-based training for surgical skills training, and the transferability of these skills to the operative setting, were included. RESULTS: Ten randomized controlled trials and 1 nonrandomized comparative study were included in this review. In most cases, simulation-based training was in addition to normal training programs. Only 1 study compared simulation-based training with patient-based training. For laparoscopic cholecystectomy and colonoscopy/sigmoidoscopy, participants who received simulation-based training before undergoing patient-based assessment performed better than their counterparts who did not receive previous simulation training, but improvement was not demonstrated for all measured parameters. CONCLUSIONS: Skills acquired by simulation-based training seem to be transferable to the operative setting. The studies included in this review were of variable quality and did not use comparable simulation-based training methodologies, which limited the strength of the conclusions. More studies are required to strengthen the evidence base and to provide the evidence needed to determine the extent to which simulation should become a part of surgical training programs.


Asunto(s)
Competencia Clínica , Simulación por Computador , Cirugía General/educación , Transferencia de Experiencia en Psicología , Colecistectomía Laparoscópica/educación , Colonoscopía/métodos , Educación Médica/métodos , Medicina Basada en la Evidencia , Femenino , Humanos , Masculino , Ensayos Clínicos Controlados Aleatorios como Asunto , Sensibilidad y Especificidad , Procedimientos Quirúrgicos Operativos/educación , Procedimientos Quirúrgicos Operativos/métodos
2.
ANZ J Surg ; 81(1-2): 9-17, 2011 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-21299793

RESUMEN

BACKGROUND: Dermal fillers are gaining popularity for rapid aesthetic improvement. Long-term efficacy and safety have not been well documented. The aim of this systematic review was to assess the safety and efficacy of injectable dermal fillers compared with other facial augmentation techniques for the management of age-related lines and wrinkles. METHODS: Studies including patients receiving injectable semi-permanent or permanent dermal fillers for age-related lines and wrinkles were included in this review. Efficacy outcomes (including changes in skin thickness and patient satisfaction) and safety outcomes (including mortality, lumps and infections) were examined. RESULTS: Three randomized control trials and six case series were included. Permanent and semi-permanent dermal fillers improved subjective ratings of appearance and resulted in higher patient satisfaction than temporary fillers. Long-term efficacy appeared good in the few studies that reported it. Short-term safety appeared favourable. Lumps were reported in all but one study but received little follow-up. Long-term safety data were limited. CONCLUSIONS: The treatment of age-related lines and wrinkles with permanent and semi-permanent dermal fillers is more efficacious compared with temporary fillers in those studies that compared them. Case series evidence suggests that these fillers achieve their objective, which is to decrease the visible effects of age-related changes. These fillers appear at least as safe as temporary fillers in the short term in those studies that compared them. Long-term safety could not be determined.


Asunto(s)
Materiales Biocompatibles/uso terapéutico , Mesoterapia/métodos , Polímeros/uso terapéutico , Envejecimiento de la Piel , Materiales Biocompatibles/efectos adversos , Colágeno/efectos adversos , Colágeno/uso terapéutico , Durapatita/efectos adversos , Durapatita/uso terapéutico , Etanolaminas/efectos adversos , Etanolaminas/uso terapéutico , Humanos , Ácido Hialurónico/efectos adversos , Ácido Hialurónico/análogos & derivados , Ácido Hialurónico/uso terapéutico , Mesoterapia/efectos adversos , Satisfacción del Paciente , Polímeros/efectos adversos , Siliconas/efectos adversos , Siliconas/uso terapéutico , Resultado del Tratamiento
3.
AIDS Patient Care STDS ; 23(9): 699-714, 2009 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-19673594

RESUMEN

The objective of this study was to assess the safety and efficacy of injectable semipermanent and permanent dermal fillers, compared to other facial augmentation techniques, for the management of facial lipoatrophy as a result of highly active antiretroviral therapy (HAART) for HIV infection through a systematic review of the literature. A systematic search strategy was used to retrieve relevant studies. Inclusion of articles was by the application of a predetermined protocol, independent assessment by two reviewers, and a final consensus decision. One randomized controlled trial (RCT), one pseudo-RCT, two nonrandomized comparative studies, and seven case series were included for review. Injections with permanent and semipermanent dermal fillers improved subjective ratings of appearance and resulted in high patient satisfaction. Although short-term safety appeared favorable, of the seven studies that reported lumps, three studies reported these events in more than 40% of patients. Long-term safety data were lacking. Evidence suggests that permanent and semipermanent dermal fillers achieve their objective, which is to decrease the visible effects of HIV-associated facial lipoatrophy, with high patient satisfaction. Safety appears favorable in the short term, but further studies are required to determine long-term outcomes.


Asunto(s)
Materiales Biocompatibles/uso terapéutico , Técnicas Cosméticas , Síndrome de Lipodistrofia Asociada a VIH/terapia , Polímeros/uso terapéutico , Terapia Antirretroviral Altamente Activa/efectos adversos , Cara , Infecciones por VIH/tratamiento farmacológico , VIH-1 , Síndrome de Lipodistrofia Asociada a VIH/inducido químicamente , Humanos , Inyecciones Intradérmicas , Inyecciones Subcutáneas
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