The effectiveness of hyaluronic acid in reducing adverse effects associated with inhaled hypertonic saline therapy in patients with cystic fibrosis: A systematic review and meta-analysis

Author:

Arshid Sana1ORCID,Ullah *Saad Ehsan1ORCID,Imran Junaid2ORCID,Syed Meeran Asher3ORCID,Choradia Aakash4ORCID,Gousy Nicole5ORCID,Boparai Sukhman6ORCID,Shoaib Mudassir7ORCID,Shah Bidhan Bikram8ORCID,Netha Aadarsh9ORCID

Affiliation:

1. Shaikh Zayed Hospital

2. Khyber Medical College

3. Fauji Foundation Hospital

4. Tribhuwan University

5. American University of Antigua

6. Acharya Shri Chander College of Medical Sciences and Hospital

7. Jinnah Medical & Dental College

8. Kathmandu Medical College

9. Melmaruvathur Adhiparasakthi Institute of Medical Sciences and Research

Abstract

Background Inhaled hypertonic saline (HS) is an effective mucolytic agent in patients with cystic fibrosis (CF). However, adverse events can impair the clinical utility of hypertonic saline (HS) in this patient population. In this study, we aimed to investigate the effectiveness of hyaluronic acid (HA) in reducing these adverse events. Methods A literature search was conducted across three electronic databases (Medline, Cochrane Central, and EMBASE) from inception through February 2023. Randomized controlled trials (RCTs) assessing the impact of hyaluronic acid (HA) in reducing adverse events in patients taking hypertonic saline (HS) for CF were included in the analysis. Outcomes of interest included cough, throat irritation, unpleasant taste, and FEV1. Evaluations were reported as risk ratios (RRs) and mean differences (MDs) with 95% confidence intervals (CI). The Cochrane Risk of Bias Tool (CRBT) was employed to assess the quality of RCTs. The New Castle Ottawa Scale was used to assess the quality of observational studies. Results From the 1960 articles retrieved from the initial search, five relevant studies (n=236 patients) were included in the final analysis. Compared with patients only on HS, patients with HS and HA were significantly less likely to experience cough (RR: 0.45; 95% CI, 0.28–0.72, p=0.001), throat irritation (RR: 0.43; 95% CI, 0.22–0.81, p= 0.009), and unpleasant smell (RR: 0.43; 95% CI, 0.23 – 0.80, p=0.09). In addition, patients with HS with HA had significantly less forced expiratory volume (FEV1) (MD: -2.97; 95% CI, -3.79—2.15, p=0.52) compared to patients only on HS. Discussion The addition of HA to HS was linked to a better tolerability profile. When HS was coupled with HA, there was a reduction in all side effects. This may permit tolerance of the medication in otherwise difficult patients, improve adherence to patients receiving frequent inhalations, and improve therapeutic outcomes. Conclusion The addition of HA is advantageous in CF patients who require continuous HS therapy and have previously shown poor tolerance to therapy.

Publisher

Canadian Society of Respiratory Therapists

Subject

Pulmonary and Respiratory Medicine,Health Professions (miscellaneous)

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