Evidence map›Paper›PMID 36952108›Full record

ArticleInternational urology and nephrology2023

Identifying the main predictors of urine output in autosomal-dominant polycystic kidney disease (ADPKD) patients taking tolvaptan.

Francisco José Borrego Utiel, Ana Isabel Morales García, Aurora Polo Moyano, Francisco Roca Oporto, Enoc Merino García, Rafael Esteban de la Rosa

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In one paragraph

Article in International urology and nephrology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 31% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 4 institutions in 1 country.

Francisco José Borrego UtielUnidad de Gestión Clínica (UGC) de Nefrología, Hospital Universitario de Jaén, Jaén, Spain. fjborregou@yahoo.com.ORCID http://orcid.org/0000-0001-8861-3132
Ana Isabel Morales GarcíaServicio de Nefrología, Hospital Universitario Clínico San Cecilio, Granada, Spain.
Aurora Polo MoyanoUGC de Nefrología, Hospital Universitario Virgen de Las Nieves, Granada, Spain.
Francisco Roca OportoUGC de Nefrología, Hospital Universitario Virgen del Rocío, Seville, Spain.
Enoc Merino GarcíaUnidad de Gestión Clínica (UGC) de Nefrología, Hospital Universitario de Jaén, Jaén, Spain.
Rafael Esteban de la RosaUGC de Nefrología, Hospital Universitario Virgen de Las Nieves, Granada, Spain.
Complejo Hospitalario de Jaén · ESHospital Universitario Virgen de las Nieves · ESHospital Universitario Virgen del Rocío · ESInstituto de Investigación Biosanitaria de Granada · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundFew works have analyzed factors associated with urine output in ADPKD patients taking tolvaptan (TVP).

methodsWe selected 24-h urine samples from ADPKD patients treated with TVP. Urine osmolality/creatinine ratio was used as estimator of urinary osmolar load.

resultsWe included 127 urine samples from 61 patients. After TVP, urine output doubled with a parallel reduction in urine solute concentration. However, when expressed as urine solute/creatinine ratios, no significant changes were observed. Daily osmolar load and osmolality/creatinine ratio did not change significantly. Before TVP, urine output was positively correlated with body weight and urine osmolality/creatinine ratio and negatively with eGFR, urine morning osmolality, and 24-h urine-calculated osmolality. After TVP, urine output was positively correlated with body weight, eGFR and negatively with age. There was a poor correlation with urine-calculated osmolality. We constructed a predictor model using mixed-effects modeling and we found that urine output was related to lower age, higher body weight, higher eGFR, and greater doses of TVP. When body weight was removed, urine output was also related to male sex and a higher daily osmolar excretion. Equation of prediction was: Urine output (mL/day) = 2771-52.9 × Age (years) + 58.4 × Weight (kg) + 18.7 × eGFR (mL/min) + 870 (if TVP = 90/30 mg) + 517 (if TVP = 60/30 mg).

conclusionPatients taking TVP will undergo an increase about twice in urine production from baseline. Greater doses of TVP cause a progressive increase in urine production. GFR, age, and body weight are the main predictors of future urine output in patients taking TVP.

Indexed as

Polycystic Kidney, Autosomal DominantAntidiuretic Hormone Receptor AntagonistsBody WeightCreatinineGlomerular Filtration RateHumansKidneyMaleTolvaptanAntidiuretic Hormone Receptor AntagonistsCreatinineTolvaptanAutosomal polycystic kidney diseaseGlomerular filtration rateTolvaptanUrine osmolar loadUrine output

Identifiers

PMID36952108
OpenAlexW4360600887

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.