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Obstructive uropathy following aortofemoral graft surgery
M Gil-Salom1, J Martinez-León, L Maldonado
1Service of Urology, Hospital Clínico Universitario, University of Valencia, Spain.
Urologia Internationalis
|January 1, 1991
Summary
Hydronephrosis is rare after aortoiliac or aortofemoral bypass surgery. Postoperative ultrasound screening and follow-up beyond one year are recommended to detect this complication in patients with arteriosclerotic obliteration.
Area of Science:
- Vascular Surgery
- Nephrology
- Diagnostic Imaging
Background:
- Aortoiliac arteriosclerotic obliteration is a serious condition requiring surgical intervention.
- Aortoiliac or aortofemoral bypass grafting using Dacron prostheses is a common treatment.
- Potential complications, such as hydronephrosis, require careful monitoring.
Purpose of the Study:
- To evaluate the incidence of hydronephrosis in patients following aortoiliac or aortofemoral bypass surgery.
- To assess the utility of ultrasound in detecting post-surgical hydronephrosis.
- To discuss pathogenic mechanisms and therapeutic strategies for hydronephrosis in this patient cohort.
Main Methods:
- Real-time sectorial ultrasound examination was performed on fifty patients.
- Patients had previously undergone aortoiliac or aortofemoral bypass with a bifurcated Dacron graft.
- Follow-up assessments were conducted, with a minimum of one year post-surgery.
Main Results:
- Hydronephrosis was detected in only one out of fifty patients (2% incidence).
- The low observed incidence may be attributed to spontaneous resolution of early-stage hydronephrosis within the first postoperative year.
- Ultrasound proved to be an effective screening tool for hydronephrosis.
Conclusions:
- The incidence of hydronephrosis after aortoiliac or aortofemoral bypass surgery is low.
- Preoperative and postoperative ultrasound screening, with follow-up extending beyond one year, is strongly recommended for patients undergoing aortoiliac or aortofemoral reconstructive surgery.
- Understanding potential pathogenic mechanisms and therapeutic options is crucial for managing this complication.