Evidence map›Paper›PMID 41416018›Full record

ReviewCureus2025

Woakes' Syndrome: A Systematic Review of Reported Cases.

Badrun Shurovi, Benjamin Samra

Abstract readReview
In one paragraph

Review in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Badrun ShuroviOtolaryngology, Royal London Hospital, London, GBR.
Benjamin SamraGeneral Surgery, Queen Elizabeth Hospital Birmingham, Birmingham, GBR.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Woakes' syndrome is a rare form of chronic rhinosinusitis with nasal polyps (CRSwNP) characterized by the progressive expansion of the nasal framework. We aimed to systematically review the literature on Woakes' syndrome to characterize its clinical features, comorbidities, management strategies, and outcomes. A literature search was conducted in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines. A systematic search of several databases (PubMed, Embase, Cochrane Library, etc.) was conducted for all reports of Woakes' syndrome. All study types (case reports, case series) were included if they provided clinical data on Woakes' syndrome. Non-English-language papers were excluded. Data on patient demographics, comorbidities (e.g., asthma, aspirin-exacerbated respiratory disease), treatments, and outcomes were extracted and synthesized descriptively. Twenty-three studies met the inclusion criteria, comprising 39 unique patients (mean age 39.5 years; range 5-81; 65% male). Both paediatric and adult-onset cases were identified. Common comorbidities included Samter's triad (seven cases) and bronchiectasis or sinobronchial disease (two cases). All patients underwent surgical treatment, most commonly functional endoscopic sinus surgery, with adjunctive procedures including digital nasal bone compression (six cases) and formal rhinoplasty or septorhinoplasty (seven cases). Pre- and postoperative steroid therapy was variably reported with most prescribed topical or systemic corticosteroids. Follow-up data were inconsistently reported; where available, the mean follow-up was approximately 12.5 months, with seven documented recurrences (six despite nasal steroid therapy). Woakes' syndrome is an extremely rare but distinct clinical entity in rhinology, representing an aggressive phenotype of CRSwNP that causes facial deformity. Both paediatric and adult-onset cases occur, frequently associated with underlying conditions such as aspirin-exacerbated respiratory disease in adults. Management requires a combination of aggressive surgical polyp removal and prolonged treatment with steroids to maintain remission. Long-term disease control remains challenging, and emerging treatments such as biological therapies to target chronic inflammation may provide benefit in the most refractory cases.

Indexed as

crswnpnasal deformitynasal polypssystematic reviewwoakes' syndrome

Identifiers

PMID41416018
PMCPMC12709414

What OpenQuestion holds

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Registered trials

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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.