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1.
Phlebology ; 30(1 Suppl): 73-80, 2015 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-25729071

RESUMO

Chronic pelvic pain accounts for approximately 10% of outpatient gynecologic visits and among the varied causes, pelvic congestion syndrome is second only to endometriosis in frequency. Manifestations may include pelvic pain, dyspareunia, dysuria, and dysmenorrhea as well as external varices and a number of psychosocial symptoms. Although a variety of treatments have been proposed-including pharmacologic ovarian suppression, hysterectomy with or without oophorectomy, and ovarian vein resection-transcatheter embolization is the least invasive and most efficacious management option. Complete or partial symptom improvement has been reported in 68.2-100% of patients and there has been a consistent reduction in visual analog pain scores after treatment. Based upon these results, recommendation of either pharmacotherapy or other surgical procedures is difficult to justify. However, it is also clear that 6-31.8% of patients do not get substantial relief from pelvic venous embolization. Potential explanations for an inadequate response to treatment include patient variability, procedural variability, and inadequate outcome measures. The latter are particularly important and future investigation should focus on the development of disease-specific quality of life measures as well as identifying those aspects of the procedure, such as choice of embolic agents and extent of embolization, associated with the best clinical outcomes.


Assuntos
Embolização Terapêutica , Hiperemia/terapia , Dor Pélvica/terapia , Insuficiência Venosa/veterinária , Feminino , Humanos , Hiperemia/patologia , Hiperemia/fisiopatologia , Hiperemia/psicologia , Dor Pélvica/patologia , Dor Pélvica/fisiopatologia , Dor Pélvica/psicologia , Síndrome , Insuficiência Venosa/patologia , Insuficiência Venosa/fisiopatologia , Insuficiência Venosa/psicologia
2.
J Vet Cardiol ; 11(2): 141-5, 2009 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-19703798

RESUMO

Inferior vena cava obstruction, a rare but serious complication of transvenous pacemaker lead placement in humans, has not been reported in dogs. We describe this complication in a dog that developed ascites 8 months after pacemaker implantation. Radiography disclosed a loop of redundant lead within the caudal vena cava (CVC), and angiography demonstrated obstruction to blood flow. Withdrawal of the loop from the CVC did not restore blood flow. Persistent obstruction was suspected secondary to fibrosis resulting from vascular damage caused by the loop of lead. Angioplasty of the CVC obstruction restored blood flow and resolved the dog's clinical signs.


Assuntos
Doenças do Cão/etiologia , Marca-Passo Artificial/veterinária , Veia Cava Inferior , Insuficiência Venosa/veterinária , Animais , Doenças do Cão/diagnóstico , Cães , Feminino , Marca-Passo Artificial/efeitos adversos , Radiografia , Veia Cava Inferior/diagnóstico por imagem , Insuficiência Venosa/diagnóstico , Insuficiência Venosa/etiologia
3.
Angiology ; 51(8 Pt 2): S33-8, 2000 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-10959509

RESUMO

Expanded polytetrafluoroethylene (ePTFE) external valve support devices (EVS) have been used successfully in patients to restore valve function in leg veins with incompetent valves when incompetence is due to dilatation of the vein walls or elongation of the valve leaflet edges. To assess tissue response to these devices, the authors implanted 12 of them in dogs, wrapping the devices around veins in the head and neck. The dogs recovered from the implantation procedure uneventfully, and the veins remained patent on color flow Doppler scanning. Gross and histologic evaluations of vein segments and attached EVS devices after sacrifice of the dogs 30 days postoperatively showed that the ePTFE devices did not affect vein patency or the cellular composition or architecture of vein walls. There were no adverse tissue reactions to the EVS and no thrombus formation in the veins to which the EVS had been applied. Tissue attachment to the EVS was apparent in all specimens. These histologic results support clinical experiences indicating that the ePTFE EVS device is safe to use in external valvuloplasty for the treatment of venous incompetence.


Assuntos
Politetrafluoretileno/uso terapêutico , Procedimentos Cirúrgicos Vasculares/instrumentação , Insuficiência Venosa/cirurgia , Animais , Cães , Feminino , Perna (Membro)/irrigação sanguínea , Masculino , Desenho de Prótese , Falha de Prótese , Implantação de Prótese , Procedimentos Cirúrgicos Vasculares/métodos , Veias/ultraestrutura , Insuficiência Venosa/veterinária
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