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1.
Prog Urol ; 31(7): 422-429, 2021 Jun.
Artículo en Francés | MEDLINE | ID: mdl-33863637

RESUMEN

INTRODUCTION: The French Department of Health published on October 23, 2020 a decree governing acts associated with mid-urethral sling (MUS) operations. The aim of this study was to evaluate the changes in practice following this new legislation. METHODS: A cross-sectional study was carried out among French urologists and gynecologists using an online survey to collect changes in practices since the publication of the decree. RESULTS: From January to February 2021, 436 surgeons participated in the survey. Among these surgeons, 87% were aware of the new legislation and 56% of them considered the decree as useless. The order resulted in an increase in working time in 81% of cases. Among these surgeons, 66% of the surgeons worked in tertiary referral centers for the management of incontinence, of which 55% had a multidisciplinary meeting in urogynecology. Among the surgeons, 31% considered this meeting to be useful but 80% considered that it did not lead to any change in surgical indications, even though 33% of complications of BSU were discussed there. In conclusion, 61% of surgeons felt more reluctant to schedule a BSU placement with this new legislation. CONCLUSION: The majority of questioned surgeons considered the decree as useless. It generated few changes in practices which already respected the law on information, consultation, consent, experience and training. Most urologists and gynecologists are more reluctant to offer MUS after this new legislation. LEVEL OF EVIDENCE: 4.


Asunto(s)
Utilización de Equipos y Suministros/legislación & jurisprudencia , Utilización de Equipos y Suministros/tendencias , Ginecología , Pautas de la Práctica en Medicina , Cabestrillo Suburetral/tendencias , Urología , Estudios Transversales , Utilización de Equipos y Suministros/estadística & datos numéricos , Francia , Humanos , Cabestrillo Suburetral/estadística & datos numéricos
2.
Prog Urol ; 30(7): 402-410, 2020 Jun.
Artículo en Francés | MEDLINE | ID: mdl-32409239

RESUMEN

OBJECTIVES: To identify various clinical presentation leading to the diagnosis of mid-urethral sling (MUS) complications and to analyze the functional outcomes after surgical management of these complications. METHOD: Retrospective observational monocentric study of all patients treated by MUS section or removal, between December 2005 and October 2019, in a pelviperineology centre. RESULTS: During this study, 96 patients were included. MUS complications surgically managed were vaginal mesh exposure (48 %), urethral mesh exposure (17 %), bladder mesh exposure (10 %); dysuria (30 %), pain (6 %), and infection (3 %). The mean time to diagnosis was 2 years. This diagnosis delay was caused by a non-specific and heterogeneous symptomatology. Surgical management consisted in MUS partial removal (79 %) and MUS simple section (21 %) with low perioperative morbidity. At three months follow-up, 36 patients (53 %) had stress urinary incontinence (SUI), including 13 (19 %) de novo (meaning no SUI before MUS section/removal) and 19 (28 %) had overactive bladder, including 9 (13 %) de novo. Half of the patients with SUI after MUS section/removal were able to be treated by a second MUS with a success rate of 83 % at 3 years. CONCLUSION: Clinical presentation of MUS complications is heterogeneous. Surgical treatment was associated with low morbidity in our study. Post-operatively, half of the patients had SUI and a second MUS was a relevant treatment option after proper evaluation. LEVEL OF EVIDENCE: 4.


Asunto(s)
Complicaciones Posoperatorias/cirugía , Cabestrillo Suburetral/efectos adversos , Incontinencia Urinaria de Esfuerzo/cirugía , Anciano , Femenino , Humanos , Persona de Mediana Edad , Recuperación de la Función , Estudios Retrospectivos , Resultado del Tratamiento
3.
Clin Orthop Relat Res ; (343): 25-9, 1997 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-9345201

RESUMEN

From 1988 to 1966, 34 patients with advanced chronic hemophilic synovitis (25 Grade III and nine Grade IV) were treated with intraarticular injections of long acting dexamethasone (sodium phosphate of dexamethasone plus acetate of dexamethasone) in cycles of three injections with 3-week intervals between each injection with 6-month rest intervals between cycles for as many as three cycles, depending on the evolution of each case. All patients had chronic severe synovitis, axial deformity, muscular atrophy, and diminution of range of movement. There were 31 knees, two ankles, and two shoulders. Subjective and objective evaluations were done grouping the results in good, fair, and poor according to grade of patient satisfaction, presence of synovitis and pain, range of movement, and limitation of activities of daily living. In the subjective results there were 19 good results, 12 fair results, and four poor results, and in the objective evaluation there were 22 good results, nine fair results, and four poor results at an average followup of 1.5 years. The use of intraarticular dexamethasone as an alternative in the short to medium term for treatment of advanced chronic hemophilic synovitis with pain and limitation of function before doing an invasive surgical treatment is proposed.


Asunto(s)
Antiinflamatorios/uso terapéutico , Dexametasona/uso terapéutico , Glucocorticoides/uso terapéutico , Hemofilia A/complicaciones , Sinovitis/tratamiento farmacológico , Actividades Cotidianas , Adolescente , Adulto , Articulación del Tobillo/efectos de los fármacos , Antiinflamatorios/administración & dosificación , Artralgia/tratamiento farmacológico , Enfermedad Crónica , Dexametasona/administración & dosificación , Esquema de Medicación , Estudios de Seguimiento , Glucocorticoides/administración & dosificación , Hemartrosis/clasificación , Hemartrosis/tratamiento farmacológico , Hemartrosis/etiología , Hemofilia B/complicaciones , Humanos , Inyecciones Intraarticulares , Deformidades Adquiridas de la Articulación/etiología , Articulación de la Rodilla/efectos de los fármacos , Atrofia Muscular/etiología , Satisfacción del Paciente , Rango del Movimiento Articular , Articulación del Hombro/efectos de los fármacos , Sinovitis/clasificación , Sinovitis/etiología , Sinovitis/cirugía , Resultado del Tratamiento
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