Evidence map›Paper›PMID 26438039›Full record

ArticlePediatric nephrology (Berlin, Germany)2016

Long-term hemodialysis therapy in neonates and infants with end-stage renal disease: a 16-year experience and outcome.

Shirley Pollack, Israel Eisenstein, Mahdi Tarabeih, Hadas Shasha-Lavski, Daniella Magen, Israel Zelikovic

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Article in Pediatric nephrology (Berlin, Germany), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
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

9 citing papers in PubMed.

  1. Article
  2. Article
  3. Chronic haemodialysis in infants and children less than 15 kg.Pediatric nephrology (Berlin, Germany) · 2021
    Article
  4. Review
  5. End-stage kidney disease in infancy: an educational review.Pediatric nephrology (Berlin, Germany) · 2020
    Review
  6. Article
  7. Article
  8. Survival in children requiring chronic renal replacement therapy.Pediatric nephrology (Berlin, Germany) · 2018
    Review
  9. 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.

Shirley PollackDivision of Pediatric Nephrology, Ruth Rappaport Children's Hospital, Rambam Health Care Campus, P.O. Box 9602, Haifa, 3109601, Israel.
Israel EisensteinDivision of Pediatric Nephrology, Ruth Rappaport Children's Hospital, Rambam Health Care Campus, P.O. Box 9602, Haifa, 3109601, Israel.
Mahdi TarabeihDivision of Pediatric Nephrology, Ruth Rappaport Children's Hospital, Rambam Health Care Campus, P.O. Box 9602, Haifa, 3109601, Israel.
Hadas Shasha-LavskiDivision of Pediatric Nephrology, Ruth Rappaport Children's Hospital, Rambam Health Care Campus, P.O. Box 9602, Haifa, 3109601, Israel.
Daniella MagenDivision of Pediatric Nephrology, Ruth Rappaport Children's Hospital, Rambam Health Care Campus, P.O. Box 9602, Haifa, 3109601, Israel.
Israel ZelikovicDivision of Pediatric Nephrology, Ruth Rappaport Children's Hospital, Rambam Health Care Campus, P.O. Box 9602, Haifa, 3109601, Israel. israelz@tx.technion.ac.il.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPeritoneal dialysis is the preferred mode of renal replacement therapy in infants with end-stage renal disease (ESRD). Hemodialysis (HD) is seldom used in neonates and infants due to the risk of major complications in the very young.

methodsDemographic, clinical, laboratory, and imaging data on all infants younger than 12 months with ESRD who received HD in our Pediatric Dialysis Unit between January 1997 and June 2013 were analyzed.

resultsEighteen infants (n = 6 male) with ESRD (median age 3 months; median weight 4.06 kg) received HD through a central venous catheter (CVC) for a total of 543 months (median duration per infant 16 months). Seven of the infants (39%) were neonates, and five (28%) had serious comorbidities. There were five episodes of CVC infection, which is a rate of 0.3/1000 CVC days. Median catheter survival time was 320 days. Most infants had good oral intake, and only four (22%) required a gastric tube; 14 (78%) infants displayed normal growth. Fourteen (78%) infants had hypertension, of whom four (22%) had severe cardiac complications; eight (44%) showed delayed psychomotor development. Eleven (61%) of the infants, including six (86%) of the neonates, survived. Five (28%) infants underwent renal transplantation; 10-year graft survival was 80%.

conclusionsBased on these results, long-term HD in neonates and infants with ESRD is technically feasible, can be implemented without major complications, carries a very low rate of CVC infection and malfunction, and results in adequate nutrition, good growth, as well as good kidney graft and patient survivals. Future efforts should aim to prevent hypertension and its cardiac sequelae, improve neurodevelopmental outcome, and lower mortality rate in these infants.

Indexed as

Catheterization, Central VenousCatheter-Related InfectionsCentral Venous CathetersFemaleHumansInfantInfant, NewbornKidney Failure, ChronicMaleRenal DialysisSurvival RateTreatment OutcomeCentral venous catheterGrowthNeurodevelopmental outcomeRenal replacement therapyRenal transplantationSurvival

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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.