[Polyuria, pollakiuria, and nocturia in children: diagnostic and therapeutic approach]

S Martini1, J P Guignard

  • 1Service de pédiatrie, Unité de néphrologie, CHUV, Lausanne. stephan.martini@chuv.hospvd.ch

Revue Medicale De La Suisse Romande
|May 11, 2001
PubMed

Insights

Polyuria involves excessive diluted urine due to concentration issues, stemming from issues like cranial or nephrogenic diabetes insipidus. Diagnosis and treatment focus on identifying the cause and managing symptoms to prevent dehydration.

Area of Science:

  • Nephrology
  • Endocrinology
  • Urology

Context:

  • Polyuria, characterized by large volumes of diluted urine, arises from impaired urine concentration.
  • Underlying causes include cranial diabetes insipidus, nephrogenic diabetes insipidus, primary polydipsia, osmotic diuresis, electrolyte disorders, or drug effects.

Purpose:

  • To differentiate causes of polyuria and pollakiuria.
  • To outline diagnostic approaches, including fluid deprivation tests and vasopressin administration.
  • To detail therapeutic strategies for various polyuria etiologies.

Summary:

  • Polyuria results from deficient vasopressin (cranial DI) or renal resistance (nephrogenic DI).
  • Diagnostic tools like fluid deprivation tests and exogenous vasopressin aid in clarifying mechanisms.
  • Treatment is causal or symptomatic, with vasopressin for cranial DI and salt restriction/diuretics for nephrogenic DI.

Impact:

  • Provides a framework for diagnosing and managing polyuria and related urinary disorders.
  • Highlights the importance of identifying underlying causes for effective treatment.
  • Offers specific therapeutic recommendations for cranial and nephrogenic diabetes insipidus.

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