Evidence map›Paper›PMID 34362426›Full record

SynthesisItalian journal of pediatrics2021

Hypertonic saline in people with cystic fibrosis: review of comparative studies and clinical practice.

Vito Terlizzi, Eleonora Masi, Michela Francalanci, Giovanni Taccetti, Diletta Innocenti

Open access · goldAbstract readSystematic Review
In one paragraph

Synthesis in Italian journal of pediatrics, 2021. 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
1.8field-weighted citation impact, top 14% 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

9 citing papers in PubMed, 15 citations in OpenAlex.

  1. Review
  2. Article
  3. Phenazine-1 carboxylic acid ofAntimicrobial agents and chemotherapy · 2024
    Article
  4. Article
  5. Article
  6. Review
  7. Review
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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

5 authors at 1 institution in 1 country.

Vito TerlizziDepartment of Paediatric Medicine, Cystic Fibrosis Regional Reference Center, Anna Meyer Children's Hospital, Viale Gaetano Pieraccini 24, 50139, Florence, Italy. vito.terlizzi@meyer.it.ORCID http://orcid.org/0000-0003-1106-4424
Eleonora MasiRehabilitation Unit, Anna Meyer Children's Hospital, Florence, Italy.
Michela FrancalanciDepartment of Paediatric Medicine, Cystic Fibrosis Regional Reference Center, Anna Meyer Children's Hospital, Viale Gaetano Pieraccini 24, 50139, Florence, Italy.
Giovanni TaccettiDepartment of Paediatric Medicine, Cystic Fibrosis Regional Reference Center, Anna Meyer Children's Hospital, Viale Gaetano Pieraccini 24, 50139, Florence, Italy.
Diletta InnocentiRehabilitation Unit, Anna Meyer Children's Hospital, Florence, Italy.
Meyer Children's Hospital · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cystic fibrosis (CF) is a multisystem disorder, caused by mutations in the CF transmembrane conductance regulator (CFTR) gene. These cause a reduced secretion of chloride, a marked absorption of sodium and, therefore, of water, through the epithelium, resulting in the formation of thickened secretions in organs such as lung or pancreas. These viscous secretions lead to airway obstruction, chronic infection and inflammation resulting in progressive lung damage, bronchiectasis and eventual respiratory failure. Although the average life expectancy has increased over the last 30 years, lung disease is the most common cause of death in people with CF. For these reasons, the improvement of sputum clearance is a major therapeutic aim in CF and early initiation of airway clearance is widely recommended and implemented. Symptomatic mucolytic therapy today is mainly based on inhalation of DNase, hypertonic saline or mannitol, in combination with physiotherapy. Mucolytic agents break down the gel structure of mucus and therefore decrease its elasticity and viscosity, reducing the pulmonary exacerbation frequency and to improve and stabilize lung function. Nevertheless, high quality studies comparing these mucolytic drugs are still few, and the individual experiences of patients and caregivers explain the high variability of their use globally. This review will summarize the current knowledge on hypertonic saline in the treatment of CF lung disease. Furthermore, we report the real-world prescription of inhaled mucolytic agents in CF.

Indexed as

Administration, InhalationCystic FibrosisExpectorantsHumansHyaluronic AcidNebulizers and VaporizersSaline Solution, HypertonicExpectorantsHyaluronic AcidSaline Solution, HypertonicDornase alfaMannitolMucolytic agentsPhysiotherapy

Identifiers

PMID34362426
PMCPMC8343926
OpenAlexW3190124885

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.