Evidence map›Paper›PMID 32714439›Full record

ArticleObstetric medicine2020

Granulomatosis with polyangiitis and pregnancy: A case report and review of the literature.

A Daher, G Sauvetre, N Girszyn, E Verspyck, H Levesque, M Le Besnerais

Open access · greenAbstract read
In one paragraph

Article in Obstetric medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 36% 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

2 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. 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 1 institution in 1 country.

A DaherInternal Medicine Department, CHU de Rouen, Rouen, France.ORCID https://orcid.org/0000-0002-5240-5160
G SauvetreInternal Medicine Department, CHU de Rouen, Rouen, France.
N GirszynInternal Medicine Department, CHU de Rouen, Rouen, France.
E VerspyckObstetric and Gynecology Department, CHU de Rouen, Rouen, France.
H LevesqueInternal Medicine Department, CHU de Rouen, Rouen, France.
M Le BesneraisInternal Medicine Department, CHU de Rouen, Rouen, France.
Centre Hospitalier Universitaire de Rouen · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The association of granulomatosis with polyangiitis and pregnancy is rare and therapeutic options are limited by the risk of teratogenicity and fetotoxicity. There is a paucity of published literature to guide clinical decision-making in these cases. We report the case of a 26-year-old woman with no medical history who presented at 21 weeks of gestation with a bilateral sudden loss of hearing and erosive rhinitis. The diagnosis of granulomatosis with polyangiitis was confirmed radiologically and biologically. Corticosteroids were not enough to stabilize the disease and she received intravenous immunoglobulins with remission. A successful delivery of a healthy male newborn was done at 36 weeks. A review of all published literature on granulomatosis with polyangiitis in pregnancy between 1970 and 2017 is presented.

Indexed as

ANCA-associated vasculitisGranulomatosis with polyangiitisWegener’s granulomatosis

Identifiers

PMID32714439
PMCPMC7359661
OpenAlexW2921367416

What OpenQuestion holds

Textmetadata
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.