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Randomized, double-blind, placebo-controlled, crossover trial of oral doxycycline for epistaxis in hereditary hemorrhagic telangiectasia.

Publication ,  Journal Article
Thompson, KP; Sykes, J; Chandakkar, P; Marambaud, P; Vozoris, NT; Marchuk, DA; Faughnan, ME
Published in: Orphanet J Rare Dis
November 7, 2022

BACKGROUND: Vascular malformations in hereditary hemorrhagic telangiectasia (HHT) lead to chronic recurrent bleeding, hemorrhage, stroke, heart failure, and liver disease. There is great interest in identifying novel therapies for epistaxis in HHT given its associated morbidity and impact on quality of life. We aimed to measure the effectiveness of oral doxycycline for the treatment of epistaxis and explore mechanisms of action on angiogenic, inflammatory and pathway markers in HHT using a randomized controlled trial. METHODS: 13 HHT patients with epistaxis were recruited from the Toronto HHT Center at St. Michael's Hospital. Recruitment was stopped early due to COVID-19-related limitations. The study duration was 24 months. Patients were randomly assigned to the treatment-first or placebo-first study arm. We compared the change in weekly epistaxis duration and frequency, biomarkers, blood measurements, and intravenous iron infusion and blood transfusion requirements between treatment and placebo. RESULTS: There was no significant difference in the change in weekly epistaxis duration (p = 0.136) or frequency (p = 0.261) between treatment and placebo. There was no significant difference in the levels of MMP-9, VEGF, ANG-2, IL-6 or ENG with treatment. Hemoglobin levels were significantly higher (p = 0.0499) during treatment. Ferritin levels were not significantly different between treatment and placebo. There was no significant difference in RBC transfusions between treatment periods (p = 0.299). CONCLUSION: Overall, our study did not demonstrate effectiveness of doxycycline as a treatment for epistaxis in patients with HHT, though the study was underpowered. Secondary analyses provided new observations which may help guide future trials in HHT. Trial Registration ClinicalTrials.gov, NCT03397004. Registered 11 January 2018 - Prospectively registered, https://clinicaltrials.gov/ct2/show/NCT03397004.

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Published In

Orphanet J Rare Dis

DOI

EISSN

1750-1172

Publication Date

November 7, 2022

Volume

17

Issue

1

Start / End Page

405

Location

England

Related Subject Headings

  • Treatment Outcome
  • Telangiectasia, Hereditary Hemorrhagic
  • Quality of Life
  • Humans
  • Genetics & Heredity
  • Epistaxis
  • Doxycycline
  • Cross-Over Studies
  • COVID-19
  • 3202 Clinical sciences
 

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Thompson, K. P., Sykes, J., Chandakkar, P., Marambaud, P., Vozoris, N. T., Marchuk, D. A., & Faughnan, M. E. (2022). Randomized, double-blind, placebo-controlled, crossover trial of oral doxycycline for epistaxis in hereditary hemorrhagic telangiectasia. Orphanet J Rare Dis, 17(1), 405. https://doi.org/10.1186/s13023-022-02539-8
Thompson, K. P., J. Sykes, P. Chandakkar, P. Marambaud, N. T. Vozoris, D. A. Marchuk, and M. E. Faughnan. “Randomized, double-blind, placebo-controlled, crossover trial of oral doxycycline for epistaxis in hereditary hemorrhagic telangiectasia.Orphanet J Rare Dis 17, no. 1 (November 7, 2022): 405. https://doi.org/10.1186/s13023-022-02539-8.
Thompson KP, Sykes J, Chandakkar P, Marambaud P, Vozoris NT, Marchuk DA, et al. Randomized, double-blind, placebo-controlled, crossover trial of oral doxycycline for epistaxis in hereditary hemorrhagic telangiectasia. Orphanet J Rare Dis. 2022 Nov 7;17(1):405.
Thompson, K. P., et al. “Randomized, double-blind, placebo-controlled, crossover trial of oral doxycycline for epistaxis in hereditary hemorrhagic telangiectasia.Orphanet J Rare Dis, vol. 17, no. 1, Nov. 2022, p. 405. Pubmed, doi:10.1186/s13023-022-02539-8.
Thompson KP, Sykes J, Chandakkar P, Marambaud P, Vozoris NT, Marchuk DA, Faughnan ME. Randomized, double-blind, placebo-controlled, crossover trial of oral doxycycline for epistaxis in hereditary hemorrhagic telangiectasia. Orphanet J Rare Dis. 2022 Nov 7;17(1):405.
Journal cover image

Published In

Orphanet J Rare Dis

DOI

EISSN

1750-1172

Publication Date

November 7, 2022

Volume

17

Issue

1

Start / End Page

405

Location

England

Related Subject Headings

  • Treatment Outcome
  • Telangiectasia, Hereditary Hemorrhagic
  • Quality of Life
  • Humans
  • Genetics & Heredity
  • Epistaxis
  • Doxycycline
  • Cross-Over Studies
  • COVID-19
  • 3202 Clinical sciences