Clin Exp Otorhinolaryngol.  2012 Mar;5(1):28-33.

Open-Label Observational Study for Evaluating the Short-term Benefits of Rabeprazole Medication on Laryngopharyngeal Reflux

Affiliations
  • 1Department of Social & Preventive Medicine, Sungkyunkwan University School of Medicine, Suwon, Korea.
  • 2Department of Otolaryngology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.
  • 3Department of Otolaryngology-Head & Neck Surgery, The Catholic University of Korea School of Medicine, Seoul, Korea.
  • 4Department of Otorhinolaryngology-Head & Neck Surgery, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea. yison@skku.edu

Abstract


OBJECTIVES
The aims of this study were to determine the benefits of short-term empirical proton pump inhibitor (PPI) medication on laryngopharyngeal reflux (LPR) and to determine whether scores on the reflux symptom index (RSI) and the reflux finding score (RFS) could be combined to identify subgroups of patients that will more likely to improve with this medication.
METHODS
Fifty-one Korean Otolaryngology Board-certified specialists joined this prospective, multi-center, and open-label observational study. A total of 1,142 adult patients with LPR was enrolled for 12 weeks of rabeprazol medication. According to pre-treatment scores on RSI and RFS, patients were divided into 4 subgroups. RFS and RSI were measured repeatedly with a month interval along the treatment period. Changes of RSI and RFS were analyzed in an overall study cohort as well as in each subgroup.
RESULTS
Approximately 40% (n=455) of enrolled patients were followed up until 12 weeks of PPI treatment. Significant improvement in RSI was obtained in 29%, 58%, and 75% of patients after 4, 8, and 12 weeks of PPI medication. RFS was improved in 16%, 42%, and 57% of the patients with 4, 8, and 12 weeks of PPI medication. All subgroups showed improvement regardless of their pre-treatment scores on the RSI and RFS.
CONCLUSION
Even though RSI and RFS may be used as a general guideline for LPR management, pre-treatment RSI and RFS are not useful in predicting the patients' response to short-term PPI medication in the usual pattern of practice for LPR, which is mostly based on the physical evaluation and history taking.

Keyword

Laryngopharyngeal reflux; Proton pump inhibitors; Rabeprazole; Short-term therapy; Predictors of response

MeSH Terms

2-Pyridinylmethylsulfinylbenzimidazoles
Adult
Cohort Studies
Humans
Laryngopharyngeal Reflux
Otolaryngology
Prospective Studies
Proton Pump Inhibitors
Proton Pumps
Specialization
2-Pyridinylmethylsulfinylbenzimidazoles
Proton Pump Inhibitors
Proton Pumps

Figure

  • Fig. 1 Changes of reflux symptom index (RSI) in each subgroup with short-term rabeprazole medication. According to initial scores of total RSI and reflux finding score (RFS), patients were divided into 4 subgroups. Changes of score on RSI were plotted along the 12 weeks period of rabeprazole medication in both a total patient cohort and each subgroup. All of the 4 subgroups as well as the total patient cohort showed a tendency toward improvement in RSI along the treatment period (P<0.0001).

  • Fig. 2 Changes of reflux finding scores (RFS) in each subgroup with short-term rabeprazole medication. According to initial scores of total reflux symptom index (RSI) and RFS, patients were divided into 4 subgroups. Changes of score on RFS were plotted along the 12 weeks period of rabeprazole medication in both a total patient cohort and each subgroup. All of the 4 subgroups as well as the total patient cohort showed a tendency toward improvement in RFS along the treatment period (P<0.0001).


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