Evidence map›Paper›PMID 37323369›Full record

ReviewAnnals of thoracic medicine

Characteristics of pleural effusion due to amyloidosis.

Cristina Pou, Lucía Ferreiro, Juan Suárez-Antelo, Antonio Golpe, José M Álvarez-Dobaño, María Elena Toubes, Adriana Lama, Nuria Rodríguez-Núñez, Jorge Ricoy, Carlos Rábade and 2 more

Open access · diamondAbstract readReview
In one paragraph

Review in Annals of thoracic medicine. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
0.9field-weighted citation impact, top 25% 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, 1 synthesis or guideline pooled it, 6 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. 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

12 authors at 3 institutions in 1 country.

Cristina PouDepartment of Pulmonology, Álvaro Cunqueiro University Teaching Hospital, Vigo, Spain.
Lucía FerreiroDepartment of Pulmonology, University Clinical Hospital of Santiago de Compostela, Santiago de Compostela, Spain.
Juan Suárez-AnteloDepartment of Pulmonology, University Clinical Hospital of Santiago de Compostela, Santiago de Compostela, Spain.
Antonio GolpeDepartment of Pulmonology, University Clinical Hospital of Santiago de Compostela, Santiago de Compostela, Spain.
José M Álvarez-DobañoDepartment of Pulmonology, University Clinical Hospital of Santiago de Compostela, Santiago de Compostela, Spain.
María Elena ToubesDepartment of Pulmonology, University Clinical Hospital of Santiago de Compostela, Santiago de Compostela, Spain.
Adriana LamaDepartment of Pulmonology, University Clinical Hospital of Santiago de Compostela, Santiago de Compostela, Spain.
Nuria Rodríguez-NúñezDepartment of Pulmonology, University Clinical Hospital of Santiago de Compostela, Santiago de Compostela, Spain.
Jorge RicoyDepartment of Pulmonology, University Clinical Hospital of Santiago de Compostela, Santiago de Compostela, Spain.
Carlos RábadeDepartment of Pulmonology, University Clinical Hospital of Santiago de Compostela, Santiago de Compostela, Spain.
Tamara LouridoDepartment of Pulmonology, Álvaro Cunqueiro University Teaching Hospital, Vigo, Spain.
Luis ValdésDepartment of Pulmonology, University Clinical Hospital of Santiago de Compostela, Santiago de Compostela, Spain.
Universidade de Santiago de Compostela · ESInstituto de Investigación Sanitaria de Santiago · ESUniversity Hospital Complex Of Vigo · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The characteristics of patients with pleural amyloidosis (PA) are poorly known. A systematic review was performed of studies reporting clinical findings, pleural fluid (PF) characteristics, and the most effective treatment of PA. Case descriptions and retrospective studies were included. The review included 95 studies with a total sample of 196 patients. The mean age was 63 years, male/female ratio was 1.6:1, and 91.9% of patients were >50 years. The most common symptom was dyspnea (88 patients). PF was generally serious (63%), predominantly lymphocytic, and with the biochemical characteristics of transudates (43.4%) or exudates (42.6%). Pleural effusion was generally bilateral (55%) and <1/3 of the hemithorax (50%), although in 21% pleural effusion (PE) exceeded 2/3. Pleural biopsy was performed in 67 patients (yield: 83.6%; 56/67) and was positive in 54% of exudates and 62.5% of unilateral effusions. Of the 251 treatments prescribed, only 31 were effective (12.4%). The combination of chemotherapy and corticosteroids was effective in 29.6% of cases, whereas talc pleurodesis was effective in 21.4% and indwelling pleural catheter in 75% of patients (only four patients). PA is more frequent in adults from 50 years of age. PF is usually bilateral, serous, and indistinctly a transudate or exudate. A pleural biopsy can aid in diagnosis if effusion is unilateral or an exudate. Treatments are rarely effective and there may be definitive therapeutic options for PE in these patients.

Indexed as

Amyloidosispleural effusionpleural fluid

Identifiers

PMID37323369
PMCPMC10263077
OpenAlexW4367021256

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.