Evidence map›Paper›PMID 38262422›Full record

ArticleKlinische Padiatrie2024

Ten-year experience of whole lung lavage in pediatric Pulmonary Alveolar Proteinosis.

Katja Nickel, Katharina Schütz, Julia Carlens, Simon Grewendorf, Martin Wetzke, Oliver Keil, Nils Dennhardt, Vanessa Rigterink, Harald Köditz, Michael Sasse and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Klinische Padiatrie, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.3field-weighted citation impact, top 22% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Outcomes and outcome measures in studies of pulmonary alveolar proteinosis: a scoping review.European respiratory review : an official journal of the European Respiratory Society · 2026
    Review
  2. Article
  3. Autoimmune Pulmonary Alveolar Proteinosis: A Rare Diagnosis in Pediatric Age.Journal of investigative medicine high impact case reports
    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

13 authors at 2 institutions in 1 country.

Katja NickelClinic of Anesthesiology and Intensive Care Medicine, Hannover Medical School, Hannover, Germany.
Katharina SchützDepartment of Pediatric Pneumology, Allergology and Neonatology, Hannover Medical School, Hannover, Germany.
Julia CarlensDepartment of Pediatric Pneumology, Allergology and Neonatology, Hannover Medical School, Hannover, Germany.
Simon GrewendorfDepartment of Pediatric Pneumology, Allergology and Neonatology, Hannover Medical School, Hannover, Germany.
Martin WetzkeDepartment of Pediatric Pneumology, Allergology and Neonatology, Hannover Medical School, Hannover, Germany.
Oliver KeilClinic of Anesthesiology and Intensive Care Medicine, Hannover Medical School, Hannover, Germany.
Nils DennhardtClinic of Anesthesiology and Intensive Care Medicine, Hannover Medical School, Hannover, Germany.
Vanessa RigterinkClinic of Anesthesiology and Intensive Care Medicine, Hannover Medical School, Hannover, Germany.
Harald KöditzDepartment of Pediatric Cardiology and Intensive Medicine, Hannover Medical School, Hannover, Germany.
Michael SasseDepartment of Pediatric Cardiology and Intensive Medicine, Hannover Medical School, Hannover, Germany.
Christine HappleDepartment of Pediatric Pneumology, Allergology and Neonatology, Hannover Medical School, Hannover, Germany.
Christiane E BeckClinic of Anesthesiology and Intensive Care Medicine, Hannover Medical School, Hannover, Germany.
Nicolaus SchwerkDepartment of Pediatric Pneumology, Allergology and Neonatology, Hannover Medical School, Hannover, Germany.
Medizinische Hochschule Hannover · DEGerman Center for Lung Research · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPulmonary Alveolar Proteinosis (PAP) is extremely rare and can be caused by hereditary dysfunction of the granulocyte macrophage colony-stimulating factor receptor (GM-CSF) receptor, autoantibodies against GM-CSF, or other diseases leading to alveolar macrophage (AM) dysfunction. This leads to protein accumulation in the lung and severe dyspnea and hypoxemia. Whole lung lavage (WLL) is the first line treatment strategy.

methodsHere, we present data from more than ten years of WLL practice in pediatric PAP. WLL performed by the use of a single lumen or double lumen tube (SLT vs. DLT) were compared for technical features, procedure time, and adverse events.

resultsA total of n=57 procedures in six PAP patients between 3.5 and 14.3 years of age were performed. SLT based WLL in smaller children was associated with comparable rates of adverse events but with longer intervention times and postprocedural intensive care treatment when compared to DLT based procedures. DISCUSSION: Our data shows that WLL is feasible even in small children. DLT based WLL seems to be more effective, and our data supports the notion that it should be considered as early as possible in pediatric PAP.

conclusionWLL lavage is possible in small PAP patients but should performed in close interdisciplinary cooperation and with age appropriate protocols.

Indexed as

Pulmonary Alveolar ProteinosisAutoantibodiesBronchoalveolar LavageChildGranulocyte-Macrophage Colony-Stimulating FactorHumansLungAutoantibodiesGranulocyte-Macrophage Colony-Stimulating Factor

Identifiers

PMID38262422
PMCPMC10883753
OpenAlexW4391126639

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.