A Retrospective Study on the Effects of Kinesiology Taping on Edema of the Lower Limb in 14 Patients Following Intramedullary Nailing for Femoral Shaft Fracture.

BACKGROUND Kinesiology tape indications of use include pain mitigation, neurosensory input, and promotion of circulation. Current evidence suggests that residual functional limitations following intramedullary nailing of the femoral shaft may be due to soft tissue injury and compromise. This retrospective study from a single center aimed to compare the effects of kinesiology taping on edema of the lower limb in 14 patients following intramedullary nailing for femoral shaft fracture. MATERIAL AND METHODS The randomized control trial design consisting of 2 groups totaling 14 patients. The intervention group (n=7) received standard therapy and kinesiology tape decompression/fan application. The control group (n=7) received standard therapy with no kinesiology tape. Outcome measures included limb girth tape measurements, Visual Analog Scale (VAS) for pain, involved knee ROM goniometry, and Timed Up and Go (TUG). RESULTS Results of this study showed there was a decrease in limb volume in the control group and an increase in limb volume in the intervention group. Both groups had improvements in TUG scores. The only statistically significant finding was among the control group, which had a decrease of 1.6 in mean VAS score before and after IM nailing (P=0.010). CONCLUSIONS In this study from a single center, kinesiology tape in patients with intramedullary nailing for femoral shaft fracture did not significantly reduce the volume of the lower limb, reduce pain, or improve postoperative mobility. The only significant improvement from the use of kinesiology tape was improved active knee extension due to improvement in quadriceps force.

Síndrome de Sheehan: descripción de un caso clínico y revisión de la literatura / Sheehan’s syndrome: a case report and literature review

Introducción: la necrosis hipofisaria posparto o síndrome de Sheehan se presenta secundaria a una hemorragia obstétrica, ocasionando un colapso circulatorio intenso el cual, a su vez, predispone a la isquemia de la hipófisis aumentada de tamaño. Objetivo: presentar un caso clínico de una paciente quien consultó por manifestaciones tardías de este síndrome y hacer una revisión de la literatura. Metodología: se buscó información en la bases de datos de PubMed/MEDLINE, Cochrane y SciELO; así como en referencias de artículos de revista y textos principalmente de los últimos cinco años. Seguidamente, se tomaron los siete artículos más relevantes según la calificación de la revista en donde fueron publicados. Resultados: la característica clínica del síndrome de Sheehan que se manifiesta con mayor frecuencia es la incapacidad para lactar debido a una producción insuficiente de prolactina. Otras manifestaciones tardías incluyen: secreción inadecuada de la hormona antidiurética y deficiencias en la secreción de cortisol, de hormona tiroidea y de gonadotrofinas. Es importante que el obstetra y el médico general sepan reconocer este síndrome, ya que la pérdida aguda del funcionamiento de la adenohipófisis puede ser de mal pronóstico si no se realiza un reemplazo hormonal adecuado. Además, el buen control hormonal evita o disminuye las complicaciones metabólicas y cardiovasculares. Conclusión: el síndrome de Sheehan es una enfermedad poco frecuente, la cual es difícil de diagnosticar tempranamente. Asimismo, requiere una terapia de reemplazo hormonal con controles permanentes clínicos y paraclínicos.

Introduction: postpartum pituitary necrosis, or Sheehan’s syndrome, occurs following obstetric haemorrhage which causes intense circulatory collapse, thereby predisposing pituitary ischemia leading to this organ becoming enlarged (the posterior pituitary is generally affected). This document presents a clinical case of a patient who consulted due to late manifestations of this syndrome. A literature review is also made. Objective: presenting the case of a patient who consulted for late manifestations of Sheehan’s syndrome and reviewing the pertinent literature. Methodology: information was sought in the PubMed / Medline, Cochrane, SciELO databases and references from articles in journals and texts (mainly from the last five years) were also taken into account. The seven most relevant articles were taken according to the impact of the journal in which they were published. Results: the most frequently found clinical characteristic was an inability to lactate due to insufficient prolactin production. The most common clinical feature found was an inability to breastfeed due to insufficient prolactin production. Other manifestations included inappropriate antidiuretic hormone secretion and cortisol, thyroid hormone and gonadotropin secretion deficiencies. Obstetricians and GPs should be able to recognise this syndrome and know about its management as the acute loss of adenohypophysis functioning may have a poor prognosis without timely and suitable hormone replacement. Good hormone control prevents or decreases metabolic and cardiovascular complications. Conclusion: this is a rare syndrome in which early diagnosis is difficult and requires hormone replacement therapy with ongoing clinical and laboratory controls.