Meta AnalysisID 4696

口服尿素补充治疗住院成人低钠血症:一项系统评价和Meta分析

CRD42019127987

1. Primary: Among hospitalized adults with hyponatremia (P), how does oral urea supplementation (I) affect serum sodium levels (O)? 2. Secondary: Among hospitalized adults with hyponatremia (P), is oral urea supplementat

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Record Fields

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Meta Analysis Id
4696
Evidence Id
13254
Core Evidence Id
13254
Source Meta Analysis Id
4663
Herb2 Meta Analysis Id
HBMA004663
Crd Id
CRD42019127987
Title
Oral urea supplementation in the treatment of hyponatremia among hospitalized adults: a systematic review and meta-analysis
Review Question
1. Primary: Among hospitalized adults with hyponatremia (P), how does oral urea supplementation (I) affect serum sodium levels (O)? 2. Secondary: Among hospitalized adults with hyponatremia (P), is oral urea supplementation (I) safe and well-tolerated (O)?
Study Type Included
Randomized clinical trials, cohort studies will be included; reviews, meta-analyses, case reports will be excluded.
Condition Being Studied
Acute, non-hypovolemic hyponatremia among hospitalized adults
Participant
Hospitalized adults (>17 years old) with acute hyponatremia (any severity, symptomatic & asymptomatic).
Animal
Human Disease Modelled
Intervention
Oral urea supplementation: Powdered supplemental urea taken by mouth or by enteral feeding tube; it is used for the correction of hyponatremia by promoting electrolyte-free water excretion. Recommended dosing for oral urea supplementation is 0.25-0.50 g/kg per day, and duration varies based upon patient response (may be provided for days, weeks, or months). For the purposes of this study, oral urea supplementation will be considered the predictor variable; any dosing regimen will be included, and studies utilizing intravenous urea will be excluded.
Comparator Control
None.
Main Outcome
Serum sodium levels: Also referred to as plasma sodium, serum sodium, or sodium concentrations in clinical practice and in the literature. Serum sodium levels may be identified using indirect (plasma) or direct (whole blood) measurements, and practices vary between studies and institutions. It is recommended that when monitoring serum sodium levels in the treatment of hyponatremia, either method is acceptable, but utilizing one method (rather than assessing both plasma and whole blood measurements) provides the best estimate of correction trajectories. Normal serum sodium levels range from 135 mEq/L to 145 mEq/L. For the purposes of this study, baseline serum sodium level will be considered that reported at the time of oral urea initiation, and change in serum sodium from baseline (in mEq/L) will be the primary outcome of interest. Measures of effect None
Outcome Measure
Additional Outcome
Safety: For the purposes of this study, safety will be reported using the measures of mortality (both hospital and ICU mortality), LOS, and incidence of ODS. Tolerability: For the purposes of this study, tolerability will be assessed using measures of gastrointestinal side effects (nausea, dysgeusia, gastroesophageal reflux, diarrhea, or vomiting) reported within the reviewed studies. Measures of effect None
Study Method
Narrative synthesis, Systematic review
Keyword
Adult; Humans; Hyponatremia; Urea
Contact
Emily Schwartz [email protected]
Organisational Affiliation
Rutgers University / Compass Group
Funding Source
Other Selection Criteria
Final Publication
Same Topic Review
Published Protocol
Review Type
Language
English
Country
United States of America
Review Stage
Review Completed not published
First Submission Date
2019-03-08
Registration Date
2019-04-09
Anticipated Start Date
2018-11-12
Anticipated Completion Date
2019-11-30
Title Cn
口服尿素补充治疗住院成人低钠血症:一项系统评价和Meta分析
Title En
Oral urea supplementation in the treatment of hyponatremia among hospitalized adults: a systematic review and meta-analysis
Bilingual Status
complete