Failure of monotherapy in primary monosymptomatic enuresis: a combined desmopressin and propiverine treatment regimen improves efficacy outcomes

OBJECTIVE To evaluate, in a prospective study, the combination of the antimuscarinic propiverine and the antidiuretic hormone‐agonist desmopressin in children and adolescents not responsive to previous monotherapy, as in primary monosymptomatic enuresis (PME), combined treatments are considered a se...

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Veröffentlicht in:BJU international 2009-06, Vol.103 (12), p.1706-1712
Hauptverfasser: Alloussi, Saladin Helmut, Mürtz, Gerd, Gitzhofer, Silvia, Eichel, Robert, Lang, Christoph, Madersbacher, Helmut, Strugala, Gerhard, Alloussi, Schahnaz
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container_end_page 1712
container_issue 12
container_start_page 1706
container_title BJU international
container_volume 103
creator Alloussi, Saladin Helmut
Mürtz, Gerd
Gitzhofer, Silvia
Eichel, Robert
Lang, Christoph
Madersbacher, Helmut
Strugala, Gerhard
Alloussi, Schahnaz
description OBJECTIVE To evaluate, in a prospective study, the combination of the antimuscarinic propiverine and the antidiuretic hormone‐agonist desmopressin in children and adolescents not responsive to previous monotherapy, as in primary monosymptomatic enuresis (PME), combined treatments are considered a second‐line approach after the failure of monotherapy. PATIENTS AND METHODS The study included 122 children and adolescents (mean age 10.8 years, range 5–21) with PME and so far unresponsive to single or multiple monotherapy. Propiverine (body weight
doi_str_mv 10.1111/j.1464-410X.2008.08285.x
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PATIENTS AND METHODS The study included 122 children and adolescents (mean age 10.8 years, range 5–21) with PME and so far unresponsive to single or multiple monotherapy. Propiverine (body weight &lt;30 kg, 15 mg/day; ≥30 kg, 20 mg/day) and desmopressin (0.4 mg/night) were administered over 3 months, followed by successive structured withdrawal programmes for propiverine and desmopressin, depending on the amount of loss of urine at night before treatment. RESULTS The re‐evaluation of unresponsive patients, incorporating video‐urodynamics, showed neurogenic detrusor overactivity, isolated detrusor sphincter dyssynergia and vesicorenal reflux in 12.3% (15/122) of patients, so far falsely treated as enuresis. In 107 of 122 patients the diagnosis of PME was confirmed. The primary efficacy outcome, continence at night, was achieved in 104 of 107 patients (97.2%). During the individual follow‐up periods (3–12 months), 23 of 107 (21.5%) patients relapsed after withdrawal of both medications. Adverse events of moderate intensity were rare (3.7%). CONCLUSION Re‐evaluation of patients after monotherapy has failed is justified, because other entities can be discovered in patients so far treated unsuccessfully for enuresis. The combination of propiverine and desmopressin is highly effective in children with PME. Our results support the case for further optimizing the inaugurated treatment algorithm of PME for treatment duration, dose‐titration and structured withdrawal programmes, thus possibly further decreasing relapse rates.</description><identifier>ISSN: 1464-4096</identifier><identifier>EISSN: 1464-410X</identifier><identifier>DOI: 10.1111/j.1464-410X.2008.08285.x</identifier><identifier>PMID: 19154456</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Adolescent ; Adult ; Antidiuretic Agents - therapeutic use ; antimuscarinics ; Benzilates - therapeutic use ; Biological and medical sciences ; Child ; Child, Preschool ; combined treatment ; Deamino Arginine Vasopressin - therapeutic use ; desmopressin ; Drug Therapy, Combination ; Humans ; Medical sciences ; Muscarinic Antagonists - therapeutic use ; Nephrology. Urinary tract diseases ; Nocturnal Enuresis - drug therapy ; primary monosymptomatic enuresis ; propiverine ; Prospective Studies ; Secondary Prevention ; structured withdrawal programme ; treatment failures ; Treatment Outcome ; Urinary system involvement in other diseases. Miscellaneous ; Urinary tract. Prostate gland ; Young Adult</subject><ispartof>BJU international, 2009-06, Vol.103 (12), p.1706-1712</ispartof><rights>2008 THE AUTHORS. 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PATIENTS AND METHODS The study included 122 children and adolescents (mean age 10.8 years, range 5–21) with PME and so far unresponsive to single or multiple monotherapy. Propiverine (body weight &lt;30 kg, 15 mg/day; ≥30 kg, 20 mg/day) and desmopressin (0.4 mg/night) were administered over 3 months, followed by successive structured withdrawal programmes for propiverine and desmopressin, depending on the amount of loss of urine at night before treatment. RESULTS The re‐evaluation of unresponsive patients, incorporating video‐urodynamics, showed neurogenic detrusor overactivity, isolated detrusor sphincter dyssynergia and vesicorenal reflux in 12.3% (15/122) of patients, so far falsely treated as enuresis. In 107 of 122 patients the diagnosis of PME was confirmed. The primary efficacy outcome, continence at night, was achieved in 104 of 107 patients (97.2%). During the individual follow‐up periods (3–12 months), 23 of 107 (21.5%) patients relapsed after withdrawal of both medications. Adverse events of moderate intensity were rare (3.7%). CONCLUSION Re‐evaluation of patients after monotherapy has failed is justified, because other entities can be discovered in patients so far treated unsuccessfully for enuresis. The combination of propiverine and desmopressin is highly effective in children with PME. Our results support the case for further optimizing the inaugurated treatment algorithm of PME for treatment duration, dose‐titration and structured withdrawal programmes, thus possibly further decreasing relapse rates.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Antidiuretic Agents - therapeutic use</subject><subject>antimuscarinics</subject><subject>Benzilates - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>combined treatment</subject><subject>Deamino Arginine Vasopressin - therapeutic use</subject><subject>desmopressin</subject><subject>Drug Therapy, Combination</subject><subject>Humans</subject><subject>Medical sciences</subject><subject>Muscarinic Antagonists - therapeutic use</subject><subject>Nephrology. Urinary tract diseases</subject><subject>Nocturnal Enuresis - drug therapy</subject><subject>primary monosymptomatic enuresis</subject><subject>propiverine</subject><subject>Prospective Studies</subject><subject>Secondary Prevention</subject><subject>structured withdrawal programme</subject><subject>treatment failures</subject><subject>Treatment Outcome</subject><subject>Urinary system involvement in other diseases. Miscellaneous</subject><subject>Urinary tract. Prostate gland</subject><subject>Young Adult</subject><issn>1464-4096</issn><issn>1464-410X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkc1u1TAQhS1ERUvhFZA3sLvBju38ILGAirZUldhQiZ3l2GPwVRwHOynNW_DIOL2h3dYbj2e-Mx6dQQhTUtB83u8Lyiu-45T8KEpCmoI0ZSOKu2fo5KHw_H9M2uoYvUxpT0hOVOIFOqYtFZyL6gT9PVeunyPgYLEPQ5h-QVTjgt2Ax-i8ist9Oi1-nIJXk9MYhswnlz5ghXXwnRvAYAPJhzHnU1aqwWR1GN0txFzFUwQ1eRgmHOGnywF2PtdvIWGw1mmlFxzmKTeD9AodWdUneL3dp-jm_Mv3s8vd9beLr2efrneatbXY2RJMS9qOac2M0pbzlnS1ssxYIKJWuqVly0vRGWF4memmYbqutCacsDY_TtG7Q988yO8Z0iS9Sxr6Xg0Q5iSrmpOmFiKDzQHUMaQUwcrNGEmJXLch93I1Wq6my3Ub8n4b8i5L32x_zJ0H8yjc7M_A2w1QSaveRjVolx64kgrGKr4O-_HA_XE9LE8eQH6-ulkj9g8x2KsK</recordid><startdate>200906</startdate><enddate>200906</enddate><creator>Alloussi, Saladin Helmut</creator><creator>Mürtz, Gerd</creator><creator>Gitzhofer, Silvia</creator><creator>Eichel, Robert</creator><creator>Lang, Christoph</creator><creator>Madersbacher, Helmut</creator><creator>Strugala, Gerhard</creator><creator>Alloussi, Schahnaz</creator><general>Blackwell Publishing Ltd</general><general>Wiley-Blackwell</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>200906</creationdate><title>Failure of monotherapy in primary monosymptomatic enuresis: a combined desmopressin and propiverine treatment regimen improves efficacy outcomes</title><author>Alloussi, Saladin Helmut ; Mürtz, Gerd ; Gitzhofer, Silvia ; Eichel, Robert ; Lang, Christoph ; Madersbacher, Helmut ; Strugala, Gerhard ; Alloussi, Schahnaz</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3975-f2ed909b3cc3dacf4490b7af3dfe057ac9129425bd5d42f2e883c76cc04039883</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Antidiuretic Agents - therapeutic use</topic><topic>antimuscarinics</topic><topic>Benzilates - therapeutic use</topic><topic>Biological and medical sciences</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>combined treatment</topic><topic>Deamino Arginine Vasopressin - therapeutic use</topic><topic>desmopressin</topic><topic>Drug Therapy, Combination</topic><topic>Humans</topic><topic>Medical sciences</topic><topic>Muscarinic Antagonists - therapeutic use</topic><topic>Nephrology. Urinary tract diseases</topic><topic>Nocturnal Enuresis - drug therapy</topic><topic>primary monosymptomatic enuresis</topic><topic>propiverine</topic><topic>Prospective Studies</topic><topic>Secondary Prevention</topic><topic>structured withdrawal programme</topic><topic>treatment failures</topic><topic>Treatment Outcome</topic><topic>Urinary system involvement in other diseases. Miscellaneous</topic><topic>Urinary tract. Prostate gland</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Alloussi, Saladin Helmut</creatorcontrib><creatorcontrib>Mürtz, Gerd</creatorcontrib><creatorcontrib>Gitzhofer, Silvia</creatorcontrib><creatorcontrib>Eichel, Robert</creatorcontrib><creatorcontrib>Lang, Christoph</creatorcontrib><creatorcontrib>Madersbacher, Helmut</creatorcontrib><creatorcontrib>Strugala, Gerhard</creatorcontrib><creatorcontrib>Alloussi, Schahnaz</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>BJU international</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Alloussi, Saladin Helmut</au><au>Mürtz, Gerd</au><au>Gitzhofer, Silvia</au><au>Eichel, Robert</au><au>Lang, Christoph</au><au>Madersbacher, Helmut</au><au>Strugala, Gerhard</au><au>Alloussi, Schahnaz</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Failure of monotherapy in primary monosymptomatic enuresis: a combined desmopressin and propiverine treatment regimen improves efficacy outcomes</atitle><jtitle>BJU international</jtitle><addtitle>BJU Int</addtitle><date>2009-06</date><risdate>2009</risdate><volume>103</volume><issue>12</issue><spage>1706</spage><epage>1712</epage><pages>1706-1712</pages><issn>1464-4096</issn><eissn>1464-410X</eissn><abstract>OBJECTIVE To evaluate, in a prospective study, the combination of the antimuscarinic propiverine and the antidiuretic hormone‐agonist desmopressin in children and adolescents not responsive to previous monotherapy, as in primary monosymptomatic enuresis (PME), combined treatments are considered a second‐line approach after the failure of monotherapy. PATIENTS AND METHODS The study included 122 children and adolescents (mean age 10.8 years, range 5–21) with PME and so far unresponsive to single or multiple monotherapy. Propiverine (body weight &lt;30 kg, 15 mg/day; ≥30 kg, 20 mg/day) and desmopressin (0.4 mg/night) were administered over 3 months, followed by successive structured withdrawal programmes for propiverine and desmopressin, depending on the amount of loss of urine at night before treatment. RESULTS The re‐evaluation of unresponsive patients, incorporating video‐urodynamics, showed neurogenic detrusor overactivity, isolated detrusor sphincter dyssynergia and vesicorenal reflux in 12.3% (15/122) of patients, so far falsely treated as enuresis. In 107 of 122 patients the diagnosis of PME was confirmed. The primary efficacy outcome, continence at night, was achieved in 104 of 107 patients (97.2%). During the individual follow‐up periods (3–12 months), 23 of 107 (21.5%) patients relapsed after withdrawal of both medications. Adverse events of moderate intensity were rare (3.7%). CONCLUSION Re‐evaluation of patients after monotherapy has failed is justified, because other entities can be discovered in patients so far treated unsuccessfully for enuresis. The combination of propiverine and desmopressin is highly effective in children with PME. Our results support the case for further optimizing the inaugurated treatment algorithm of PME for treatment duration, dose‐titration and structured withdrawal programmes, thus possibly further decreasing relapse rates.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>19154456</pmid><doi>10.1111/j.1464-410X.2008.08285.x</doi><tpages>7</tpages></addata></record>
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subjects Adolescent
Adult
Antidiuretic Agents - therapeutic use
antimuscarinics
Benzilates - therapeutic use
Biological and medical sciences
Child
Child, Preschool
combined treatment
Deamino Arginine Vasopressin - therapeutic use
desmopressin
Drug Therapy, Combination
Humans
Medical sciences
Muscarinic Antagonists - therapeutic use
Nephrology. Urinary tract diseases
Nocturnal Enuresis - drug therapy
primary monosymptomatic enuresis
propiverine
Prospective Studies
Secondary Prevention
structured withdrawal programme
treatment failures
Treatment Outcome
Urinary system involvement in other diseases. Miscellaneous
Urinary tract. Prostate gland
Young Adult
title Failure of monotherapy in primary monosymptomatic enuresis: a combined desmopressin and propiverine treatment regimen improves efficacy outcomes
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