Evidence map›Paper›PMID 40771842›Full record

ArticleLaryngoscope investigative otolaryngology2025

Treatment Durability of Injection Augmentation of Vocal Fold Atrophy.

Anumitha Venkatraman, Ruth J Davis, Susan Thibeault

Abstract read
In one paragraph

Article in Laryngoscope investigative otolaryngology, 2025. 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
–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

2 citing papers in PubMed.

  1. Article
  2. Treatment Durability of Injection Augmentation of Vocal Fold Atrophy.Laryngoscope investigative otolaryngology · 2025
    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

3 authors.

Anumitha VenkatramanDepartment of Otolaryngology Head and Neck Surgery University of Wisconsin Madison USA.ORCID https://orcid.org/0000-0003-4341-9701
Ruth J DavisDepartment of Otolaryngology Head and Neck Surgery University of Wisconsin Madison USA.ORCID https://orcid.org/0000-0001-9592-932X
Susan ThibeaultDepartment of Otolaryngology Head and Neck Surgery University of Wisconsin Madison USA.ORCID https://orcid.org/0000-0002-9046-4356

Funding

University of Wisconsin Voice Research Training Program (T32)T32DC009401 · NIDCD · UNIVERSITY OF WISCONSIN-MADISON · PI Susan Lynn Thibeault · 2009 to 2026
$6.3M
NIDCD NIH HHS T32 DC009401
6 · The paper itself

Abstract

Objective: Injection augmentation (or injection laryngoplasty) is a common treatment for presbyphonia. As current injection materials are temporary, it is anticipated that patients injected for presbyphonia will either need a repeat injection or framework surgery to maintain glottal competence (or sufficient glottal closure). Despite the expected temporary nature of these injections, patients report variable durability of effect, and some do not require a repeat injection. The primary aim of this investigation was to identify factors that affect treatment durability of injection augmentation among patients with presbyphonia. Methods: Patients who underwent one or multiple injection augmentations for presbyphonia between May 2008 and September 2017 were extracted from the UW Madison Voice and Swallow Outcomes Database. Variables collected included demographics (age, sex), injection material, volume, duration between injections, date of first and last follow-up, voice therapy (yes/no, number of sessions), and pre- and post-injection voice measures (Maximum Phonation Time, Dysphonia Severity Index, Glottal Function Index score, Vocal Handicap Index Score) in an observational cohort design. For patients receiving one injection (TF group), duration between injection and last follow-up was taken as a durability measure termed "time to follow up." For patients receiving multiple injections (TR group), duration between injection treatments were termed "time to reinjection." Patients receiving one or more injections were compared separately and together (where treatment durability Results: Thirty-five patients with presbyphonia met inclusion criteria (mean age 74.3 years [SD 7.6], 78% male). Twenty patients received only one injection. Repeat injection augmentation was performed in 40% of patients ( Conclusion: Factors that affected treatment durability TF Level of Evidence: III, Retrospective cohort study.

Indexed as

dysphoniaglottal insufficiencyinadequate glottal closureinjection augmentationinjection laryngoplastyinjection materialpresbyphoniavoice therapy

Identifiers

PMID40771842
PMCPMC12326623

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.