Literature DB >> 35635649

Management of epistaxis in hereditary haemorrhagic telangiectasia (HHT) patients using pulsed dye laser and the effect of withholding treatment during the COVID pandemic.

Yuchen Jiang1, Simon C Dennis1, Mark P Brewin2.   

Abstract

Using a patient survey, pulsed dye laser (PDL) treatment of epistaxis for hereditary haemorrhagic telangiectasia (HHT) patients was evaluated after initial referral. Subsequently, due to the COVID pandemic, a natural experimental set-up allowed assessment of an enforced withdrawal of treatment. A total of 34 subjects were identified as undergoing PDL for HHT-related epistaxis. They were surveyed to look at the effectiveness of PDL treatment after initial referral and at the effect of delay to treatment during COVID on epistaxis and the associated quality of life. The survey also examined the comparison to other available treatments. Retrospective pre-COVID Epistaxis Severity Scores (ESS) were compared to post-COVID data to assess the effect of treatment withdrawal. The patients were then followed up after resumption of their treatment to assess the ensuing change in ESS. After initial referral, frequency and severity of epistaxis decreased. Fifty-six percent of patients experienced several bleeds per day before treatment, compared to 12% after. 88% of patients had episodes of epistaxis longer than 5 min, which was halved to 44% after treatment. Average ESS pre-COVID was 4.42 compared to 5.43 post-COVID delay, with a significant statistical difference (p = 0.02). On resumption of treatment, average ESS reduced to below pre-COVID levels at 4.39 after only 2 sessions. Seventy-six percent of patients found that withdrawal of PDL during COVID diminished their quality of life. PDL treatment of nasal mucosal telangiectasia reduces the frequency and duration of epistaxis. The ESS is reduced following treatment with PDL and quality of life subjectively improved.
© 2022. Crown.

Entities:  

Keywords:  COVID; Epistaxis; Hereditary haemorrhagic telangiectasia (HHT); Osler-Weber-Rendu disease; Pulsed dye laser (PDL)

Mesh:

Year:  2022        PMID: 35635649     DOI: 10.1007/s10103-022-03580-6

Source DB:  PubMed          Journal:  Lasers Med Sci        ISSN: 0268-8921            Impact factor:   2.555


  12 in total

1.  Permanent control of nosebleeds in patients with hereditary hemorrhagic telangiectasia.

Authors:  W H SAUNDERS
Journal:  Ann Intern Med       Date:  1960-07       Impact factor: 25.391

2.  Hereditary hemorrhagic teleangiectasia--argon laser.

Authors:  R Haye; J Austad
Journal:  Rhinology       Date:  1991-03       Impact factor: 3.681

3.  A laser end piece for the treatment of Epistaxis using the Pulsed Dye Laser.

Authors:  J C R Corlett; P G Shakespeare; P A Wright; P J Taylor
Journal:  Clin Otolaryngol       Date:  2008-02       Impact factor: 2.597

4.  Complications and mortality in hereditary hemorrhagic telangiectasia: A population-based study.

Authors:  James W Donaldson; Tricia M McKeever; Ian P Hall; Richard B Hubbard; Andrew W Fogarty
Journal:  Neurology       Date:  2015-04-10       Impact factor: 9.910

5.  Treatment of hereditary haemorrhagic telangiectasia by the pulsed dye laser.

Authors:  P G Harries; M J Brockbank; P G Shakespeare; J A Carruth
Journal:  J Laryngol Otol       Date:  1997-11       Impact factor: 1.469

6.  The natural history of epistaxis in hereditary hemorrhagic telangiectasia.

Authors:  O S AAssar; C M Friedman; R I White
Journal:  Laryngoscope       Date:  1991-09       Impact factor: 3.325

7.  Treatment of hereditary hemorrhagic telangiectasia by Nd-YAG laser photocoagulation.

Authors:  S M Shapshay; P Oliver
Journal:  Laryngoscope       Date:  1984-12       Impact factor: 3.325

8.  Hereditary haemorrhagic telangiectasia: a questionnaire based study to delineate the different phenotypes caused by endoglin and ALK1 mutations.

Authors:  J Berg; M Porteous; D Reinhardt; C Gallione; S Holloway; T Umasunthar; A Lux; W McKinnon; D Marchuk; A Guttmacher
Journal:  J Med Genet       Date:  2003-08       Impact factor: 6.318

Review 9.  Hereditary haemorrhagic telangiectasia: a clinical and scientific review.

Authors:  Fatima S Govani; Claire L Shovlin
Journal:  Eur J Hum Genet       Date:  2009-04-01       Impact factor: 4.246

10.  The UK prevalence of hereditary haemorrhagic telangiectasia and its association with sex, socioeconomic status and region of residence: a population-based study.

Authors:  J W Donaldson; T M McKeever; I P Hall; R B Hubbard; A W Fogarty
Journal:  Thorax       Date:  2013-11-04       Impact factor: 9.139

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