The management of cystic fibrosis chronic rhinosinusitis: An evidenced-based review with recommendations

Research output: Contribution to journalReviewResearchpeer-review

Standard

The management of cystic fibrosis chronic rhinosinusitis : An evidenced-based review with recommendations. / Spielman, Daniel B.; Beswick, Daniel M.; Kimple, Adam J.; Senior, Brent A.; Aanaes, Kasper; Woodworth, Bradford A.; Schlosser, Rodney J.; Lee, Stella; Cho, Do Yeon; Adappa, Nithin D.; DiMango, Emily; Gudis, David A.

In: International Forum of Allergy and Rhinology, Vol. 12, No. 9, 2022, p. 1148-1183.

Research output: Contribution to journalReviewResearchpeer-review

Harvard

Spielman, DB, Beswick, DM, Kimple, AJ, Senior, BA, Aanaes, K, Woodworth, BA, Schlosser, RJ, Lee, S, Cho, DY, Adappa, ND, DiMango, E & Gudis, DA 2022, 'The management of cystic fibrosis chronic rhinosinusitis: An evidenced-based review with recommendations', International Forum of Allergy and Rhinology, vol. 12, no. 9, pp. 1148-1183. https://doi.org/10.1002/alr.22953

APA

Spielman, D. B., Beswick, D. M., Kimple, A. J., Senior, B. A., Aanaes, K., Woodworth, B. A., Schlosser, R. J., Lee, S., Cho, D. Y., Adappa, N. D., DiMango, E., & Gudis, D. A. (2022). The management of cystic fibrosis chronic rhinosinusitis: An evidenced-based review with recommendations. International Forum of Allergy and Rhinology, 12(9), 1148-1183. https://doi.org/10.1002/alr.22953

Vancouver

Spielman DB, Beswick DM, Kimple AJ, Senior BA, Aanaes K, Woodworth BA et al. The management of cystic fibrosis chronic rhinosinusitis: An evidenced-based review with recommendations. International Forum of Allergy and Rhinology. 2022;12(9):1148-1183. https://doi.org/10.1002/alr.22953

Author

Spielman, Daniel B. ; Beswick, Daniel M. ; Kimple, Adam J. ; Senior, Brent A. ; Aanaes, Kasper ; Woodworth, Bradford A. ; Schlosser, Rodney J. ; Lee, Stella ; Cho, Do Yeon ; Adappa, Nithin D. ; DiMango, Emily ; Gudis, David A. / The management of cystic fibrosis chronic rhinosinusitis : An evidenced-based review with recommendations. In: International Forum of Allergy and Rhinology. 2022 ; Vol. 12, No. 9. pp. 1148-1183.

Bibtex

@article{8544dc59ec214bd69e97b0e3fb737a76,
title = "The management of cystic fibrosis chronic rhinosinusitis: An evidenced-based review with recommendations",
abstract = "Background: Cystic fibrosis (CF) chronic rhinosinusitis (CRS) has emerged as a distinct diagnostic entity, unique from other endotypes of CRS in its presentation, pathophysiology, diagnosis, treatment, and outcomes. As the sinonasal health of this patient population may have broad effects on pulmonary health and quality of life, a comprehensive understanding of the diagnostic and therapeutic approach to CF CRS is essential. In recognizing recent scientific advances and unique treatment modalities specific to this challenging patient population, in this review we systematically evaluate the scientific literature and provide an evidenced-based review with recommendations (EBRR) for fundamental management principles of CF CRS. Methods: A systematic review of the literature was performed. Studies evaluating interventions for the management of CF CRS were included. An iterative review process was implemented in accordance with EBRR guidelines. A treatment recommendation was generated based on an assessment of the benefits, harms, and the overall grade of evidence. Results: We evaluated the published literature on 5 unique topics. Each of the following therapeutic categories was investigated explicitly for treatment outcomes in patients with CF CRS: (1) nasal saline; (2) intranasal corticosteroids (INCS); (3) topical antibiotics; (4) cystic fibrosis transmembrane conductance regulator (CFTR) modulator therapy; and (5) endoscopic sinus surgery (ESS). Conclusion: Based on the currently available evidence, nasal saline, ESS, and CFTR modulators are recommended in the management of CF CRS when appropriate. INCS and topical antibiotics are options. Clinical judgment and experience are essential in caring for patients with this uniquely challenging disorder.",
author = "Spielman, {Daniel B.} and Beswick, {Daniel M.} and Kimple, {Adam J.} and Senior, {Brent A.} and Kasper Aanaes and Woodworth, {Bradford A.} and Schlosser, {Rodney J.} and Stella Lee and Cho, {Do Yeon} and Adappa, {Nithin D.} and Emily DiMango and Gudis, {David A.}",
note = "Publisher Copyright: {\textcopyright} 2021 ARS-AAOA, LLC",
year = "2022",
doi = "10.1002/alr.22953",
language = "English",
volume = "12",
pages = "1148--1183",
journal = "International Forum of Allergy and Rhinology",
issn = "2042-6976",
publisher = "JohnWiley & Sons, Inc.",
number = "9",

}

RIS

TY - JOUR

T1 - The management of cystic fibrosis chronic rhinosinusitis

T2 - An evidenced-based review with recommendations

AU - Spielman, Daniel B.

AU - Beswick, Daniel M.

AU - Kimple, Adam J.

AU - Senior, Brent A.

AU - Aanaes, Kasper

AU - Woodworth, Bradford A.

AU - Schlosser, Rodney J.

AU - Lee, Stella

AU - Cho, Do Yeon

AU - Adappa, Nithin D.

AU - DiMango, Emily

AU - Gudis, David A.

N1 - Publisher Copyright: © 2021 ARS-AAOA, LLC

PY - 2022

Y1 - 2022

N2 - Background: Cystic fibrosis (CF) chronic rhinosinusitis (CRS) has emerged as a distinct diagnostic entity, unique from other endotypes of CRS in its presentation, pathophysiology, diagnosis, treatment, and outcomes. As the sinonasal health of this patient population may have broad effects on pulmonary health and quality of life, a comprehensive understanding of the diagnostic and therapeutic approach to CF CRS is essential. In recognizing recent scientific advances and unique treatment modalities specific to this challenging patient population, in this review we systematically evaluate the scientific literature and provide an evidenced-based review with recommendations (EBRR) for fundamental management principles of CF CRS. Methods: A systematic review of the literature was performed. Studies evaluating interventions for the management of CF CRS were included. An iterative review process was implemented in accordance with EBRR guidelines. A treatment recommendation was generated based on an assessment of the benefits, harms, and the overall grade of evidence. Results: We evaluated the published literature on 5 unique topics. Each of the following therapeutic categories was investigated explicitly for treatment outcomes in patients with CF CRS: (1) nasal saline; (2) intranasal corticosteroids (INCS); (3) topical antibiotics; (4) cystic fibrosis transmembrane conductance regulator (CFTR) modulator therapy; and (5) endoscopic sinus surgery (ESS). Conclusion: Based on the currently available evidence, nasal saline, ESS, and CFTR modulators are recommended in the management of CF CRS when appropriate. INCS and topical antibiotics are options. Clinical judgment and experience are essential in caring for patients with this uniquely challenging disorder.

AB - Background: Cystic fibrosis (CF) chronic rhinosinusitis (CRS) has emerged as a distinct diagnostic entity, unique from other endotypes of CRS in its presentation, pathophysiology, diagnosis, treatment, and outcomes. As the sinonasal health of this patient population may have broad effects on pulmonary health and quality of life, a comprehensive understanding of the diagnostic and therapeutic approach to CF CRS is essential. In recognizing recent scientific advances and unique treatment modalities specific to this challenging patient population, in this review we systematically evaluate the scientific literature and provide an evidenced-based review with recommendations (EBRR) for fundamental management principles of CF CRS. Methods: A systematic review of the literature was performed. Studies evaluating interventions for the management of CF CRS were included. An iterative review process was implemented in accordance with EBRR guidelines. A treatment recommendation was generated based on an assessment of the benefits, harms, and the overall grade of evidence. Results: We evaluated the published literature on 5 unique topics. Each of the following therapeutic categories was investigated explicitly for treatment outcomes in patients with CF CRS: (1) nasal saline; (2) intranasal corticosteroids (INCS); (3) topical antibiotics; (4) cystic fibrosis transmembrane conductance regulator (CFTR) modulator therapy; and (5) endoscopic sinus surgery (ESS). Conclusion: Based on the currently available evidence, nasal saline, ESS, and CFTR modulators are recommended in the management of CF CRS when appropriate. INCS and topical antibiotics are options. Clinical judgment and experience are essential in caring for patients with this uniquely challenging disorder.

U2 - 10.1002/alr.22953

DO - 10.1002/alr.22953

M3 - Review

C2 - 34933415

AN - SCOPUS:85122671437

VL - 12

SP - 1148

EP - 1183

JO - International Forum of Allergy and Rhinology

JF - International Forum of Allergy and Rhinology

SN - 2042-6976

IS - 9

ER -

ID: 305691563