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Андрология и генитальная хирургия. 2014; 15: 6-14

Медикаментозное лечение симптомов нижних мочевых путей у мужчин. Роль уроселективности в выборе препарата

Аляев Ю. Г., Гаджиева Заида Камалудиновна, Рапопорт Л. М., Казилов Ю. Б.

https://doi.org/10.17650/2070-9781-2014-1-6-14

Аннотация

У большинства пациентов расстройства мочеиспускания обусловлены как механическим, так и функциональным факторами. Своевременное выявление характера уродинамических нарушений, в первую очередь инфравезикальной обструкции и гиперактивности детрузора, у больных доброкачественной гиперплазией предстательной железы имеет важное практическое значение, так как без учета этого фактора существенно ухудшаются функциональные результаты хирургического лечения. α1-адреноблокаторы являются первой линией терапии для мужчин с симптомами нижних мочевых путей (СНМП). Они должны быть предложены пациентам с умеренными и тяжелыми СНМП. Выбор α1-адреноблокатора должен склоняться к более селективным представителям класса.

Селективность α-адреноблокатора обеспечивает наряду с высокой эффективностью низкий процент побочных реакций, особенно со стороны сердечно-сосудистой системы.

Так же как и α-адреноблокаторы, М-холиноблокаторы различаются по степени селективности в отношении воздействия именно на мочевой пузырь. Солифенацин более селективен в отношении мочевого пузыря, чем толтеродин и осибутинин. Селективность данного препарата по отношению к мочевому пузырю выражается относительно низкой частотой возникновения побочных эффектов, особенно сухости во рту, при его применении, а также возможностью длительной терапии. Комбинированное лечение α1-адреноблокатором с М-холиноблокатором может рассматриваться у пациентов с умеренными и тяжелыми СНМП с преобладанием симптомов наполнения, особенно если монотерапия не привела к облегчению симптомов.

Список литературы

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44. coexisting benign prostatic obstruction: a prospective, randomized, controlled multicenter study. J Urol 2005;174:1334–8.

45. Kaplan S. A., Roehrborn C. G., Rovner E. S. et al. Tolterodine and tamsulosin for treatment of men with lower urinary tract symptoms and overactive bladder: a randomized controlled trial. JAMA 2006;296 (19):2319–28.

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47. Drake M., Chapple C., van Kerrebroeck P. et al. Efficacy of combination therapy with tamsulosin OCAS and solifenacin in NEPTUNE: Results from a randomised, phase 3 trial in men with LUTS. Eur Urol 2012; EAU abstracts #746H.

Andrology and Genital Surgery. 2014; 15: 6-14

Drug treatment of lower urinary tract symptoms in males. Role uroselectivity in the choice of drug

Alyaev Yu. G., Gadzhieva Z. K., Rapoport L. M., Kazilov Yu. B.

https://doi.org/10.17650/2070-9781-2014-1-6-14

Abstract

Most patients lower urinary tract symptoms (LUTS) caused both mechanical and functional factors. Timely identification of the nature of urodynamics, primarily of bladder outlet obstruction and detrusor overactivity, in patients with benign prostatic hyperplasia is of practical importance, since without this factor significantly worse functional outcome of surgical treatment. α1-adrenoblockers are the first line therapy for men with bothersome LUTS. They should be offered to patients with moderate to severe LUTS. Choosing α1-adrenoblocker should lean toward more selective class representatives. Selectivity α1-adrenoblocker provides high efficiency along with a low percentage of adverse effects, especially for cardiovascular system.

As well as α-adrenoblockers, M-cholinobloсkers varying degrees of selectivity of the impact is on the bladder. Solifenacin is more selective for the bladder than tolterodine and oxybutynin. The selectivity of the drug with respect to the bladder is reflected in the relatively low frequency of adverse effects, especially occurrence of dry mouth in its application, as well as the possibility of long term therapy. Combined treatment with α1-adrenoreceptor antagonist with M-cholinergic antagonists may be considered in patients with moderate to severe LUTS with a predominance of filling symptoms, especially if monotherapy led to relief of symptoms.

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6. Van Dijk M. M., de la Rosette J. J., Michel M. C. Tamsulosin – modified-release and oral controlled absorption system formulation in the treatment of benign prostatic hyperplasia. Therapy 2006;3:237–46.

7. Nickel J. C., Sander S., Moon T. D. A meta-analysis of the vascular-related safety profile and efficacy of alpha-adrenergic blockers for symptoms related to benign prostatic hyperplasia. Int J Clin Pract 2008;62:1547–59.

8. Michel M. C., Vrydag W. Alpha1-, alpha2- and beta-adrenoceptors in the urinary bladder, urethra and prostate. Br J Pharmacol 2006;147(Suppl 2):S88–119.

9. Guimaraes S., Moura D. Vascular adrenoceptors: an update. Pharmacol Rev 2001;53:319–56.

10. Rudner X. L., Berkowitz B. A., Booth J. V. et al. Subtype specific regulation of human vascular α1-adrenergic receptors by vessel bed and age. Circulation 1999;100:2336–43.

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41. Athanasopoulos A., Gyftopoulos K., Giannitsas K. et al. Combination treatment with an α-blocker plus an anticholinergic for bladder outlet obstruction: a prospective, randomized, controlled study. J Urol 2003;169:2253–6.

42. Lee K. S., Kim D. Y., Kim J. C. et al. Combination treatment with propiverine hydrochloride plus doxazosin gits in men with overactive bladder coexisting benign prostatic obstruction: a prospective, randomized, controlled, multicenter study. ICS annual meeting, 2004 (abstr. 207).

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44. coexisting benign prostatic obstruction: a prospective, randomized, controlled multicenter study. J Urol 2005;174:1334–8.

45. Kaplan S. A., Roehrborn C. G., Rovner E. S. et al. Tolterodine and tamsulosin for treatment of men with lower urinary tract symptoms and overactive bladder: a randomized controlled trial. JAMA 2006;296 (19):2319–28.

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