Literature DB >> 8671906

Cyst sclerotherapy with minocycline hydrochloride in patients with autosomal dominant polycystic kidney disease.

J Uemasu1, M Fujihara, C Munemura, E Nakamura, H Kawasaki.   

Abstract

BACKGROUND: The enlarged cysts in autosomal dominant polycystic kidney disease (ADPKD) frequently cause abdominal discomfort. Cyst sclerotherapy with minocycline hydrochloride was performed to relieve this symptom.
METHODS: Ten symptomatic ADPKD cases were recruited. As a sclerosant, minocycline hydrochloride solution (10 mg/dl) was used. This solution was instilled into the cysts under ultrasonographic control. Renal volume was calculated before therapy and at 6-month intervals thereafter. Renal function and blood pressure were regularly monitored. The effect of sclerotherapy on symptoms was also assessed at 6-month intervals.
RESULTS: At 6 months, renal volume was statistically lower than the presclerotherapy, and was associated with improvement in chronic symptoms. However, such ameliorating effects were blunted at 12 months. Renal volume reduction at 6 and 12 months showed a significant positive correlation with the dose of minocycline injected. No significant influence in renal function and blood pressure was observed.
CONCLUSIONS: These results suggest that cyst sclerotherapy with minocycline hydrochloride is a valid treatment regime for the relief of chronic symptoms in ADPKD cases, although repeated application of this approach may be required to obtain a more long-term effect.

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Year:  1996        PMID: 8671906     DOI: 10.1093/oxfordjournals.ndt.a027410

Source DB:  PubMed          Journal:  Nephrol Dial Transplant        ISSN: 0931-0509            Impact factor:   5.992


  7 in total

1.  Long-term functional results of aspiration and sclerotherapy with ethanol in patients with autosomal dominant polycystic kidney disease: a non-randomized pilot clinical study.

Authors:  Eyüp Veli Küçük; Ahmet Tahra; Ahmet Bindayi; Ferhat Yakup Suçeken; Fikret Fatih Önol; Uğur Boylu
Journal:  Int Urol Nephrol       Date:  2016-01-12       Impact factor: 2.370

Review 2.  Evaluation and management of pain in autosomal dominant polycystic kidney disease.

Authors:  Marie C Hogan; Suzanne M Norby
Journal:  Adv Chronic Kidney Dis       Date:  2010-05       Impact factor: 3.620

3.  Cyst ablation using a mixture of N-butyl cyanoacrylate and iodized oil in patients with autosomal dominant polycystic kidney disease: the long-term results.

Authors:  See Hyung Kim; Seung Hyup Kim; Jeong Yeon Cho
Journal:  Korean J Radiol       Date:  2009-06-25       Impact factor: 3.500

4.  Ablation of symptomatic cysts using absolute ethanol in 11 patients with autosomal-dominant polycystic kidney disease.

Authors:  Young Rae Lee; Kyu-Beck Lee
Journal:  Korean J Radiol       Date:  2003 Oct-Dec       Impact factor: 3.500

Review 5.  A stepwise approach for effective management of chronic pain in autosomal-dominant polycystic kidney disease.

Authors:  Niek F Casteleijn; Folkert W Visser; Joost P H Drenth; Tom J G Gevers; Gerbrand J Groen; Marie C Hogan; Ron T Gansevoort
Journal:  Nephrol Dial Transplant       Date:  2014-09       Impact factor: 5.992

6.  Collagen-driven remodeling of the intrahepatic duct wall in the PCK rat model of polycystic kidney disease-Caroli syndrome.

Authors:  Rithika Narayan; Jingsong Li; Anthony J Pellicano; Itzhak D Goldberg
Journal:  Clin Exp Hepatol       Date:  2020-05-21

7.  Foam Sclerotherapy for Cyst Volume Reduction in Autosomal Dominant Polycystic Kidney Disease: A Prospective Cohort Study.

Authors:  Ioan-Andrei Iliuta; Beili Shi; Marina Pourafkari; Pedram Akbari; Giancarlo Bruni; Ralph Hsiao; Steffan F Stella; Korosh Khalili; Eran Shlomovitz; York Pei
Journal:  Kidney Med       Date:  2019-10-18
  7 in total

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