Single versus multiple instillation of povidone iodine and urographin in the treatment of chyluria: A prospective randomised study
نویسندگان
چکیده
OBJECTIVE To compare the safety, efficacy and complications of single vs multiple instillations of povidone iodine (PI) and urographin as a sclerosing agent in the treatment of chyluria. PATIENTS AND METHODS The study included 58 patients diagnosed with chyluria between March 2006 and January 2013. The inclusion criteria were either severe attacks of chyluria or patients with mild-to-moderate chyluria who had failed conservative treatment. The patients were randomly allocated to one of two groups: those in Group A had a single instillation of a combination of PI 0.2% plus the contrast-agent urographin 76%, while those in Group B had multiple instillations of the same combination twice daily for 3 successive days. RESULTS The mean (SD) age of the patients in Groups A and B was 38.22 (10.67) and 37.9 (10.86) years, respectively. Chyluria was severe in eight patients (14.8%), moderate in 25 (46.3%) and mild in 21 (38.9%). The success rate in Group A (single instillation) was 85.2% and in Group B (multiple instillation) was 88.9%. The recurrence rate in Group A was 14.8% with a disease-free duration (DFD) of 4-15 weeks, while in group B it was 11.1% with a DFD of 6-18 weeks. CONCLUSION There was no significant difference between a single instillation of a combination of PI 0.2% and urographin 76% as a sclerosing agent in the treatment of chyluria and multiple instillations. However, the single instillation protocol is more cost effective with a shorter hospital stay.
منابع مشابه
Sclerotherapy for Chyluria Using Single Dose 0.2%Povidone- Iodine: A Prospective Study
Aim:-To assess the efficacy of single dose 0.2% povidone -iodine instillation in the management of chyluria. Materials & method: Forty-five patients who presented with chyluria to surgical out-patient department at Dr RML Combined hospital, Lucknow from JUNE 2014 to FEBRUARY 2015. There were 27 males and 18 females, between age groups 25 to 48 years. After taking informed consent for the study ...
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