Evidence map›Paper›PMID 26978558›Full record

ReviewWomen's health (London, England)2016

Managing the female patient with hereditary angioedema.

Aleena Banerji, Marc Riedl

Abstract readReview
In one paragraph

Review in Women's health (London, England), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
–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

22 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Prevalence and Incidence of Hereditary Angioedema: A Systematic Literature Review.International archives of allergy and immunology · 2026
    Pooled it
  2. Review
  3. Article
  4. The International/Canadian hereditary angioedema guideline.Allergy, asthma, and clinical immunology : official journal of the Canadian Society of Allergy and Clinical Immunology · 2026
    Review
  5. Article
  6. Article
  7. Article
  8. The complexities of decision-making associated with on-demand treatment of hereditary angioedema (HAE) attacks.Allergy, asthma, and clinical immunology : official journal of the Canadian Society of Allergy and Clinical Immunology · 2024
    Article
  9. Article
  10. Article
  11. Observational
  12. Increased thromboinflammatory load in hereditary angioedema.Clinical and experimental immunology · 2023
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. High Estrogen States in Hereditary Angioedema: a Spectrum.Clinical reviews in allergy & immunology · 2021
    Review
  18. Article
  19. Article
  20. Review
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

2 authors.

Aleena BanerjiMassachusetts General Hospital, Cox 201, 55 Fruit Street, Boston, MA, USA.
Marc RiedlUniversity of California, San Diego, La Jolla, CA, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hereditary angioedema (HAE) is a rare disorder resulting from decreased functional levels of C1-inhibitor (C1-INH), which manifests as periodic episodes of localized edema which can be extremely painful, debilitating and even fatal if the swelling affects the larynx. HAE can complicate many aspects of obstetric/gynecologic care, and an awareness of the disease is critical for clinicians involved in the care of women because of potential HAE-related complications pertaining to pregnancy, labor and delivery, and other women's health issues. This article provides a review of published literature specific to HAE and its management in female patients, including important concerns regarding obstetric/gynecologic care. A growing body of relevant experience is presented to help guide the care of women with HAE.

Indexed as

Angioedemas, HereditaryAntifibrinolytic AgentsComplement C1 Inactivator ProteinsComplement C1 Inhibitor ProteinDisease ManagementFemaleHumansAntifibrinolytic AgentsComplement C1 Inactivator ProteinsComplement C1 Inhibitor ProteinSERPING1 protein, humanC1-inhibitorecallantidehereditary angioedemaicatibantwomen

Identifiers

PMID26978558
PMCPMC5384520

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.