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1.
Aust N Z J Obstet Gynaecol ; 64(2): 95-103, 2024 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-37737451

RESUMEN

BACKGROUND: Persistent pelvic pain (PPP) is a complex and often debilitating condition. While widely accepted to be multifactorial in nature, the precise aetiology of PPP remains elusive. In many cases, women who undergo laparoscopy for PPP will have no visible pathology identified (a 'negative' laparoscopy). Currently, there are no consensus guidelines which outline the recommended management following a negative laparoscopy, and the woman's experiences and outcomes are not widely known. AIMS: This review aims to identify and summarise the literature surrounding the experiences of women with PPP who have a negative laparoscopy; specifically, their outcomes of pain, quality of life (QoL), satisfaction with care, and their overall management. MATERIALS AND METHODS: A systematic search of the electronic databases Ovid Medline, PubMed and Embase was performed. Studies in English exploring the outcomes of women with PPP following a negative laparoscopy were included. RESULTS: Four studies consisting of a total of 200 women were included. Results were inconsistent. Three studies concluded that the majority of women with PPP had persistent pain following a negative laparoscopy. A single study found that pain significantly improved after negative laparoscopy. QoL outcomes varied, with two studies reporting a positive impact and two studies reporting a deleterious impact on QoL following a negative laparoscopy. CONCLUSIONS: The impact on pain outcomes and QoL following a laparoscopy that does not diagnose pathology remains unknown, and the available evidence is insufficient to guide evidence-based practice. This review highlights a significant gap in our understanding of surgical management for PPP.


Asunto(s)
Endometriosis , Laparoscopía , Humanos , Femenino , Calidad de Vida , Laparoscopía/efectos adversos , Laparoscopía/métodos , Dolor Pélvico/etiología , Dolor Pélvico/cirugía , Endometriosis/complicaciones
2.
BMJ Case Rep ; 20132013 Jun 24.
Artículo en Inglés | MEDLINE | ID: mdl-23814000

RESUMEN

Poliomyelitis, once a worldwide epidemic, is becoming increasingly rare owing to the introduction of the polio vaccine in the 1950s. It is estimated that the number of cases of polio has reduced by 99% since the Global Polio Eradication Initiative (GPEI) started in 1988. Amyotrophic lateral sclerosis (ALS) is another relatively uncommon condition which also affects anterior horn cells with debilitating neurological, and deadly, consequences. An unusual case of an aggressive form of ALS developing in a 72-year-old patient with paralytic poliomyelitis in childhood is presented. Her initial presentation was puzzling, and our approach to the diagnostic dilemma is discussed.


Asunto(s)
Esclerosis Amiotrófica Lateral/diagnóstico , Poliomielitis/diagnóstico , Anciano , Esclerosis Amiotrófica Lateral/complicaciones , Esclerosis Amiotrófica Lateral/tratamiento farmacológico , Esclerosis Amiotrófica Lateral/fisiopatología , Diagnóstico Diferencial , Resultado Fatal , Femenino , Humanos , Fármacos Neuroprotectores/uso terapéutico , Poliomielitis/complicaciones , Poliomielitis/fisiopatología , Riluzol/uso terapéutico
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