Literature DB >> 33774753

Pretreatment morning urine osmolality and oral desmopressin lyophilisate treatment outcome in patients with primary monosymptomatic enuresis.

S Abdovic1, M Cuk2, I Hizar2, M Milosevic3, A Jerkovic2, M Saraga4,5.   

Abstract

PURPOSE: To determine the association between urine osmolality (Uosm) in patients with primary monosymptomatic enuresis (PMNE) and response to desmopressin (dDAVP) lyophilisate.
METHODS: This was a prospective cohort study that included 419 children with enuresis seen in outpatient clinic between October 2017 and October 2019. Patient workup included symptom checklist, 48 h frequency/volume chart, kidney and bladder ultrasound, uroflow, urinalysis and culture, spot urine Ca/creatinine, and first-morning Uosm. Patients < 5 years, with secondary enuresis, or loss of follow-up were excluded. Oral dDAVP lyophilisate was recommended to all with PMNE and normal bladder capacity. After 1 month of therapy, initial success was assessed according to ICCS. Significant predictor variables for complete response were identified and analyzed using correlation coefficients and binary logistic regression.
RESULTS: There were 48 patients with PMNE who received dDAVP and were followed for treatment success. Partial and complete responses were achieved for 14 (29.2%) and 20 cases (41.7%), respectively. Older age and lower Uosm were found to be significantly in favor of complete response to dDAVP lyophilisate, P = 0.007 and 0.033, respectively. ROC analysis determined the Uosm of ≤ 814 mOsm/kg as a cut-off value for complete success (sensitivity 65% and specificity 75%, AUC = 68.2%). The odds ratio for complete success for selected cut-off value was 5.57 (95% CI 1.588-19.551, P = 0.007).
CONCLUSION: High pretreatment morning Uosm (> 814 mOsm/kg) might be suggestive of an alternative treatment to dDAVP lyophilisate in PMNE because of the higher risk of treatment failure.
© 2021. The Author(s), under exclusive licence to Springer Nature B.V.

Entities:  

Keywords:  Child; Desmopressin; Nocturnal enuresis; Treatment outcome; Urine osmolality

Mesh:

Substances:

Year:  2021        PMID: 33774753     DOI: 10.1007/s11255-021-02843-5

Source DB:  PubMed          Journal:  Int Urol Nephrol        ISSN: 0301-1623            Impact factor:   2.370


  26 in total

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Authors:  Patrina H Y Caldwell; Aniruddh V Deshpande; Alexander Von Gontard
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2.  The role of urine osmolality and ions in the pathogenesis of primary enuresis nocturna and in the prediction of responses to desmopressin and conditioning therapies.

Authors:  Tolga Unüvar; Ferah Sönmez
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Review 3.  Comparison of desmopressin, alarm, desmopressin plus alarm, and desmopressin plus anticholinergic agents in the management of paediatric monosymptomatic nocturnal enuresis: a network meta-analysis.

Authors:  Pan Song; Chuiguo Huang; Yan Wang; Qingwei Wang; Wen Zhu; Yiwei Yue; Wancong Wang; Jinjin Feng; Xiangfei He; Lingang Cui; Tingxiang Wan; Jianguo Wen
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6.  Transcutaneous parasacral electrical neural stimulation in children with primary monosymptomatic enuresis: a prospective randomized clinical trial.

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Journal:  J Urol       Date:  2013-03-29       Impact factor: 7.450

7.  The standardization of terminology of lower urinary tract function in children and adolescents: Update report from the standardization committee of the International Children's Continence Society.

Authors:  Paul F Austin; Stuart B Bauer; Wendy Bower; Janet Chase; Israel Franco; Piet Hoebeke; Søren Rittig; Johan Vande Walle; Alexander von Gontard; Anne Wright; Stephen S Yang; Tryggve Nevéus
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8.  Characteristics of primary nocturnal enuresis in adults: an epidemiological study.

Authors:  C K Yeung; J D Y Sihoe; F K Y Sit; W Bower; B Sreedhar; J Lau
Journal:  BJU Int       Date:  2004-02       Impact factor: 5.588

9.  Practical consensus guidelines for the management of enuresis.

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10.  Desmopressin, Imipramine, and Oxybutynin in the Treatment of Primary Nocturnal Enuresis: A Randomized Clinical Trial.

Authors:  Maryam Seyfhashemi; Raheb Ghorbani; Abbas Zolfaghari
Journal:  Iran Red Crescent Med J       Date:  2015-07-01       Impact factor: 0.611

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