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Effects of esomeprazole treatment for gastroesophageal reflux disease on quality of life in 12- to 17-year-old adolescents: an international health outcomes study
BMC Gastroenterologyvolume 9, Article number: 84 (2009)
Although gastroesophageal reflux disease (GERD) is common in adolescents, the burden of GERD on health-related quality of life (HRQOL) in adolescents has not been previously evaluated. Therefore, the objective of the study was to examine the effect of GERD on HRQOL in adolescents.
This international, 31-site, 8-week safety study randomized adolescents, aged 12 to 17 years inclusive, with GERD to receive esomeprazole 20 or 40 mg once daily. The Quality of Life in Reflux and Dyspepsia questionnaire (QOLRAD), previously validated in adults, consists of 25 questions grouped into 5 domains: emotional distress, sleep disturbance, food/drink problems, physical/social functioning, and vitality. The QOLRAD was administered at the baseline and week-8 (final) visits.
Of the 149 patients randomized, 134 completed the QOLRAD at baseline and final visits and were eligible for analysis of their HRQOL data. Baseline QOLRAD scores indicated GERD had a negative effect on the HRQOL of these adolescents, especially in the domains of vitality and emotional distress, and problems with food/drink. At the final visit, mean scores for all 5 QOLRAD domains improved significantly (P < .0001); change of scores (ie, delta) for all domains met or exceeded the adult QOLRAD minimal clinically significant difference standard of 0.5 units.
GERD had a negative effect on QOL in adolescents. After esomeprazole treatment, statistically and clinically significant improvements occurred in all domains of the QOLRAD for these adolescents.
D9614C00098; ClinicalTrials.gov Identifier NCT00241501
Gastroesophageal reflux disease (GERD) is recognized increasingly as a common condition in adolescents . Recent surveys of high school students show that at least 21% had significant GERD symptoms occurring a minimum of 1 time per month [2–4]. A survey conducted in pediatric practices revealed that 5.2%, 5.0%, and 8.2% of children and adolescents aged 10 to 17 years reported experiencing heartburn, epigastric pain, and regurgitation, respectively, in the previous week . Moreover, in the same time period, 27.9% of children aged 10 to 17 years experienced abdominal pain, which may be a symptom of GERD .
Findings of numerous studies have shown the negative effect of GERD on health-related quality of life (HRQOL) in adults; however, few studies have assessed the effect of GERD on HRQOL in children and adolescents [6–15]. Although previously validated in adults , no data are available on the validity and performance of the Quality of Life in Reflux and Dyspepsia questionnaire (QOLRAD) in adolescent GERD patients or on the burden of GERD on HRQOL in adolescents.
Proton pump inhibitors (PPIs) have been recommended as the most effective acid suppression therapy for adults and children with GERD [17, 18]. PPIs have been shown to relieve or resolve GERD symptoms in most adult and pediatric patients [19–23]. In Gold et al, we reported the safety and efficacy of esomeprazole in treating the symptoms of GERD in adolescents . In the current article, we explore the effects of esomeprazole on QOL in the adolescent patients from the Gold et al  study.
This international, phase 3, randomized study double blinded for dose safety was conducted at 31 sites in Canada, France, Italy, and the United States (D9614C00098; ClinicalTrials.gov Identifier NCT00241501). The study was performed in accordance with the ethical principles that have their origin in the Declaration of Helsinki and that are consistent with ICH/Good Clinical Practice. The study protocol was approved by the institutional review boards, and all patients and their parents or guardians provided written informed consent and assent before any study procedure was conducted.
Patients were randomized 1:1 to receive esomeprazole (Nexium®; AstraZeneca LP, Wilmington, DE) 20 or 40 mg (no placebo control) orally once daily for 8 weeks. Esomeprazole was administered approximately 60 minutes before breakfast. For patients unable to swallow capsules, capsule contents could be mixed with 1 tablespoon of applesauce. Age-appropriate chewable antacid tablets were provided for use as rescue medication.
Adolescents aged 12 to 17 years with a clinical diagnosis of GERD based on medical history, physical examination, any laboratory test results, and/or information from any diagnostic testing (eg, pH monitoring, endoscopy, biopsy) were eligible to participate in the study. The study entry criteria were consistent with GERD diagnostic guidelines of the North American Society for Pediatric Gastroenterology, Hepatology, and Nutrition . Patients who were infected with Helicobacter pylori (as documented by the investigator using standard medical practice) but had no evidence of active ulceration or recent gastrointestinal bleeding were permitted at the discretion of the investigator. Postpubertal girls must have had a negative result on their urine pregnancy tests at the screening and week-4 and -8 visits. Patients who had any gastrointestinal pathology that required surgery, interfered with study participation, or potentially confounded study data were excluded. Patients who had an acute or chronic illness or condition (eg, pervasive developmental disorders, suspected abuse/neglect, recent trauma) that, in the opinion of the investigator, placed the patient at risk for not completing the study or for potentially confounding the study data were excluded. Patients could not have taken any PPI within 14 days or H2-receptor antagonist or prokinetic agent within 3 days of randomization. Patients also could not use any study-restricted medications (eg, antiemetics, bismuth-containing products, macrolide antibiotics, systemic steroids) on a continuous basis during the study.
The QOLRAD, previously validated in adults , generally can be completed in approximately 12 to 15 minutes and consists of 25 questions grouped into 5 domains: emotional distress, sleep disturbance, food/drink problems, vitality, and physical/social functioning . The QOLRAD also has been translated and cross-culturally validated into languages including French, German, Spanish, Italian, and French Canadian . The QOLRAD was administered at the randomization (baseline) and week-8 (final) visits. Responses were based on a 1-week recall period and scored using a 7-point Likert response scale (1 = all of the time/a great deal; 7 = none of the time/none at all); higher scores indicated better QOL. Administration of the QOLRAD was standardized, and procedures were used throughout the study to enhance patient compliance in correctly completing the QOLRAD, such as quiet, privacy, and administration before other examinations.
Data from patients in both treatment groups were pooled for analysis, and between-group comparisons were not made. Mean total scores and individual domain scores were calculated at baseline and final visits and compared using the paired t test. Mean change in score between baseline and the final visit was considered clinically significant if 0.5 or more units . This minimally clinically significant change was established based on findings from a previously conducted study assessing the reliability and responsiveness to change over time of QOLRAD . Missing item responses were replaced by the mean value of completed items in that domain if 50% or more items in that domain had been completed.
A post hoc assessment was conducted to compare baseline QOLRAD scores from adolescents in this study with those of adults in the previous QOLRAD validation study . Though the methods and primary results of the QOLRAD validation study were published previously, baseline scores had not been reported previously . Briefly, the adult study was an international, multicenter psychometric evaluation in which 759 adult patients with chronic or recurrent upper gastrointestinal symptoms completed the QOLRAD. In the analysis presented here, mean baseline QOLRAD scores from each of the 5 domains were calculated according to baseline heartburn severity (mild, moderate, severe). Differences in QOLRAD scores 0.5 or more units between adult and adolescent patients were considered to be clinically significant.
Of the 149 patients randomized, more were girls (59.7%) and white (83.2%) and the mean body mass index was 23.5 ± 4.9 kg/m2. Of these 149 patients, 134 completed the QOLRAD at the baseline and final visits.
Baseline QOLRAD mean total scores (Figure 1) and mean domain scores (Figure 2) indicated that GERD had a negative effect on the HRQOL of these patients compared with normal adults. The QOLRAD domains most negatively affected by GERD were vitality, emotional distress, and problems with food/drink (Figure 2).
QOLRAD mean total scores and mean domain scores were improved significantly from baseline values after 8 weeks of esomeprazole therapy (P < .001) (Figures 1 and 2). Mean changes from baseline values in the QOLRAD total and domain scores met or exceeded the established adult QOLRAD minimum clinically significant difference standard of 0.5 units (Table 1) .
At baseline, QOLRAD scores were similar in adolescents and adults with mild heartburn (Table 2). However, the differences in baseline QOLRAD scores in the domains of emotional stress, sleep disturbance, and vitality between adolescents and adults with moderate heartburn were clinically significant (scores varied by ≥0.5 units). In addition, differences in baseline scores for the sleep disturbance and vitality domains between adolescents and adults with severe heartburn were clinically significant (Table 2).
In this study, the burden of illness in adolescent patients with GERD was measured by a disease-specific HRQOL instrument, QOLRAD, previously validated in adults  and used for the first time here in adolescents. Our results demonstrated that GERD has a negative effect on HRQOL in adolescents. These results are consistent with those of a recent study by Tolia et al , which shows that, in children aged 2 to 18 years, GERD symptoms negatively affect the QOL of children and their parents.
Because no placebo control group existed in the study, it could not be determined how much of the change from baseline in QOLRAD scores was attributable directly to esomeprazole therapy. However, this study is the first to show an improvement from baseline in HRQOL in all QOLRAD domains (emotional distress, sleep disturbance, food/drink problems, vitality, and physical/social functioning) in adolescents after treatment with a PPI in a clinical trial. In addition, the trial was a safety study, and patients were randomized to different dose groups for this purpose; it was not designed to be a comparative dosing study of esomeprazole. Between-group assessments were not made, and pooling of the data allowed for a better estimate in comparison with QOLRAD data in adults. Despite these study limitations, the findings are consistent with improvement considered clinically significant (≥0.5 units)  and establish a benchmark for future QOL studies in children of different ages with GERD.
In adult patients, 4 weeks of treatment with the PPI esomeprazole has been shown to significantly improve QOLRAD scores from baseline [9, 11, 13, 14]. In the study reported by Talley et al , after 4 weeks of treatment with esomeprazole 20 mg, esomeprazole 40 mg, or omeprazole 20 mg daily, changes from baseline in QOLRAD domain scores ranged from 0.81 to 1.43. This unit change for adult QOL was higher slightly than the changes from baseline reported in this study in adolescents (Table 1) . Similarly, El-Dika et al  reported changes in domain scores after 4 weeks of treatment with esomeprazole ranging from 1.3 to 2.0. However, in a study reported by Pace et al , 4 weeks of treatment with esomeprazole 40 mg yielded domain changes ranging from 0.37 to 0.66, slightly lower than those observed in our study (Table 1). Moreover, studies in adults have shown that improved QOL is maintained with esomeprazole treatment through 6 months [11, 13].
QOLRAD scores from adults in other studies are difficult to compare with scores from this study of adolescents because the change from baseline in QOLRAD scores in sleep disturbance and food/drink problems has been shown to be associated with baseline symptom severity (none, mild, moderate, or severe); therefore, the largest changes in QOLRAD scores occur in patients with more severe symptoms at baseline . An appropriate comparison of the effect of GERD on QOL between adults and adolescents would be within the baseline level of symptom severity. Therefore, we compared baseline QOLRAD scores according to baseline heartburn severity from adolescents in this study with those from adults in a separate study . For patients with moderate or severe heartburn, clinically significantly greater scores were observed for adolescents compared with adults for the QOLRAD domains of emotional distress (moderate heartburn only), sleep disturbance, and vitality, indicating that moderate or severe heartburn has a more negative effect on HRQOL in adults than adolescents. However, the effect of mild heartburn on HRQOL in adolescents and adults is similar.
Clinically significant improvements in HRQOL from baseline values were observed in this 8-week trial of esomeprazole treatment for GERD, which suggests that esomeprazole treatment may reduce the negative effect of GERD on HRQOL, particularly in the domains of vitality, emotional distress, and problems with food/drink in adolescents.
Gold BD, Freston JW: Gastroesophageal reflux in children: pathogenesis, prevalence, diagnosis, and role of proton pump inhibitors in treatment. Pediatr Drugs. 2002, 4: 673-685.
Ramesh P, Santiago M, Schmidt K, Gunasekaran TS: Prevalence of gastroesophageal reflux disease (GERD) symptoms in an African American (AA) predominant adolescent high school population [abstract]. J Pediatr Gastroenterol Nutr. 2001, 33: 421-
Gunasekaran TS, Dahlberg M, Ramesh P, Namachivayam G: Prevalence and associated features of gastroesophageal reflux symptoms in a Caucasian-predominant adolescent school population. Dig Dis Sci. 2008, 53: 2373-2379. 10.1007/s10620-007-0150-5.
Asokan S, Ramesh P, Gunasekaran TS, Creech S: Prevalence of gastroesophageal reflux disease (GERD) symptoms in a Hispanic American adolescent [abstract]. J Pediatr Gastroenterol Nutr. 2003, 37: 337-
Nelson SP, Chen EH, Syniar GM, Christoffel KK, for Pediatric Practice Research Group: Prevalence of symptoms of gastroesophageal reflux during childhood. Arch Pediatr Adolesc Med. 2000, 154: 150-154.
Wiklund I: Review of the quality of life and burden of illness in gastroesophageal reflux disease. Dig Dis. 2004, 22: 108-114. 10.1159/000080308.
Havelund T, Lind T, Wiklund I, Glise H, Hernqvist H, Lauritsen K, Lundell L, Pedersen SA, Carlsson R, Junghard O, Stubberöd A, Anker-Hansen O: Quality of life in patients with heartburn but without esophagitis: effects of treatment with omeprazole. Am J Gastroenterol. 1999, 94: 1782-1789. 10.1111/j.1572-0241.1999.01206.x.
Revicki DA, Crawley JA, Zodet MW, Levine DS, Joelsson BO: Complete resolution of heartburn symptoms and health-related quality of life in patients with gastro-oesophageal reflux disease. Aliment Pharmacol Ther. 1999, 13: 1621-1630. 10.1046/j.1365-2036.1999.00669.x.
Talley NJ, Fullerton S, Junghard O, Wiklund I: Quality of life in patients with endoscopy-negative heartburn: reliability and sensitivity of disease-specific instruments. Am J Gastroenterol. 2001, 96: 1998-2004. 10.1111/j.1572-0241.2001.03932.x.
De La Loge C, Trudeau E, Marquis P, Revicki DA, Rentz AM, Stanghellini V, Talley NJ, Kahrilas P, Tack J, Dubois D: Responsiveness and interpretation of a quality of life questionnaire specific to upper gastrointestinal disorders. Clin Gastroenterol Hepatol. 2004, 2: 778-786. 10.1016/S1542-3565(04)00349-0.
Pace F, Negrini C, Wiklund I, Rossi C, Savarino V, for The Italian One Investigators Study Group: Quality of life in acute and maintenance treatment of non-erosive and mild erosive gastro-oesophageal reflux disease. Aliment Pharmacol Ther. 2005, 22: 349-356. 10.1111/j.1365-2036.2005.02558.x.
Madisch A, Kulich KR, Malfertheiner P, Ziegler K, Bayerdörffer E, Miehlke S, Labenz J, Carlsson J, Wiklund IK: Impact of reflux disease on general and disease-related quality of life—evidence from a recent comparative methodological study in Germany. Z Gastroenterol. 2003, 41: 1137-1143. 10.1055/s-2003-45277.
Hansen ÅN, Bergheim R, Fagertun H, Lund H, Wiklund I, Moum B: Long-term management of patients with symptoms of gastro-oesophageal reflux disease—a Norwegian randomized prospective study comparing the effects of esomeprazole and ranitidine treatment strategies on health-related quality of life in a general practitioners setting. Int J Clin Pract. 2006, 60: 15-22. 10.1111/j.1368-5031.2006.00768.x.
El-Dika S, Guyatt GH, Armstrong D, Degl'innocenti A, Wiklund I, Fallone CA, Tanser L, Veldhuyzen van Zanten S, Heels-Ansdell D, Wahlqvist P, Chiba N, Barkun AN, Austin P, Schünemann HJ: The impact of illness in patients with moderate to severe gastro-esophageal reflux disease. BMC Gastroenterol. 2005, 5: 23-30. 10.1186/1471-230X-5-23.
Tolia V, Essenbacher L, Boyer K, Ager J: Gastroesophageal reflux disease (GERD) questionnaire to assess quality of life (QOL) in patients and parents [abstract: poster session]. J Pediatr Gastroenterol Nutr. 2004, 39: S424-S425.
Wiklund IK, Junghard O, Grace E, Talley NJ, Kamm M, Veldhuyzen van Zanten S, Paré P, Chiba N, Leddin DS, Bigard MA, Colin R, Schoenfeld P: Quality of life in reflux and dyspepsia patients. Psychometric documentation of a new disease-specific questionnaire (QOLRAD). Eur J Surg Suppl. 1998, 583: 41-49.
Rudolph CD, Mazur LJ, Liptak GS, Baker RD, Boyle JT, Colletti RB, Gerson WT, Werlin SL: Guidelines for evaluation and treatment of gastroesophageal reflux in infants and children: recommendations of the North American Society for Pediatric Gastroenterology and Nutrition. J Pediatr Gastroenterol Nutr. 2001, 32 (suppl 2): S1-S31. 10.1097/00005176-200100002-00001.
DeVault KR, Castell DO: Updated guidelines for the diagnosis and treatment of gastroesophageal reflux disease. Am J Gastroenterol. 2005, 100: 190-200. 10.1111/j.1572-0241.2005.41217.x.
Richter JE, Kahrilas PJ, Johanson J, Maton P, Breiter JR, Hwang C, Marino V, Hamelin B, Levine JG, for Esomeprazole Study Investigators: Efficacy and safety of esomeprazole compared with omeprazole in GERD patients with erosive esophagitis: a randomized controlled trial. Am J Gastroenterol. 2001, 96: 656-665. 10.1111/j.1572-0241.2001.03600.x.
Johnson DA, Benjamin SB, Vakil NB, Goldstein JL, Lamet M, Whipple J, Damico D, Hamelin B: Esomeprazole once daily for 6 months is effective therapy for maintaining healed erosive esophagitis and for controlling gastroesophageal reflux disease symptoms: a randomized, double-blind, placebo-controlled study of efficacy and safety. Am J Gastroenterol. 2001, 96: 27-34. 10.1111/j.1572-0241.2001.03443.x.
Fiedorek S, Tolia V, Gold BD, Huang B, Stolle J, Lee C, Gremse D: Efficacy and safety of lansoprazole in adolescents with symptomatic erosive and non-erosive gastroesophageal reflux disease. J Pediatr Gastroenterol Nutr. 2005, 40: 319-327. 10.1097/01.MPG.0000155369.54464.41.
Hassall E, Israel D, Shepherd R, Radke M, Dalväg A, Sköld B, Junghard O, Lundborg P, for International Pediatric Omeprazole Study Group: Omeprazole for treatment of chronic erosive esophagitis in children: a multicenter study of efficacy, safety, tolerability and dose requirements. J Pediatr. 2000, 137: 800-807. 10.1067/mpd.2000.109607.
Gold BD, Gunasekaran T, Tolia V, Wetzler G, Conter H, Traxler B, Illueca M: Safety and symptom improvement with esomeprazole in adolescents with gastroesophageal reflux disease. J Pediatr Gastroenterol Nutr. 2007, 45: 520-529. 10.1097/MPG.0b013e318148c17c.
Kulich K, Wiklund I, Junghard O: Factor structure of the quality of life in reflux and dyspepsia (QOLRAD) questionnaire evaluated in patients with heartburn predominant reflux disease. Qual Life Res. 2003, 12: 699-708. 10.1023/A:1025192100450.
Junghard O, Wiklund IK: Effect of baseline symptom severity on patient-reported outcomes in gastroesophageal reflux disease. Eur J Gastroenterol Hepatol. 2007, 19: 555-560. 10.1097/MEG.0b013e328133f2d1.
The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-230X/9/84/prepub
This study was supported by AstraZeneca LP, Wilmington, Delaware.
Data from this manuscript were presented at the North American Society for Pediatric Gastroenterology, Hepatology & Nutrition (NASPGHAN) Annual Meeting, October 19-22, 2006, Orlando City, Florida. The authors thank Daniel Donahue and Libby Pethick (AstraZeneca LP) for study leadership and project management, respectively; Lisa M. Klumpp, PhD, and Judy E. Fallon, PharmD (Scientific Connexions, Newtown, PA), for medical writing services funded by AstraZeneca LP; Mary Wiggin (AstraZeneca LP) for editorial assistance; the patients and their parents; and the study-site staff members.
Joel Andres, MD (Orlando, FL); Ramalingam Arumugam, MD (St Paul, MN); Phyllis Bishop, MD (Jackson, MS); Jeffrey Blumer, MD, PhD (Cleveland, OH); Jeffrey Bornstein, MD (Orlando, FL); Jean-Pierre Cezard, MD, PhD (Paris, France); Salvatore Cucchiara, MD (Rome, Italy); David DeVoid, MD (Chattanooga, TN); Frederic Gottrand, MD (Lille, France); Ivor Hill, MD (Winston Salem, NC); Elizaveta Iofel, MD (New Hyde Park, NY); Vijay Kumar, MD (Sudbury, Ontario, Canada); Chris Liacouras, MD (Philadelphia, PA); Alberto Martini, MD (Genova, Italy); Grant Matheson, MD (Parkdale, Prince Edward Island, Canada); Chantal Maurage, MD (Tours, France); Adam Mezoff, MD (Dayton, OH); Bhanu Muram, MD (Mount Pearl, Newfoundland, Canada); Oluremi Ogundimu, MD (Sudbury, Ontario, Canada); Anthony Ottley, MD (Halifax, Nova Scotia, Canada); Rabin Persad, MD (Hamilton, Ontario, Canada); Yolanda Rivas, MD (Bronx, NY); Gregory Scagnelli, MD (Binghamton, NY); Stephen Shaffer, MD (Wilmington, DE); Eduardo Tron, MD (Buffalo, NY); John Tung, MD (Wilmington, DE); Dana Ursea, MD (Phoenix, AZ); Lauren Willis, MD (Norfolk, VA); and Harland Winter, MD, PhD (Boston, MA).
TG, VT, RBC, and BDG receive grant/research support from AstraZeneca; TG, VT, and BDG are consultants to AstraZeneca; BDG and VT are consultants to Wyeth; BDG is a consultant and speaker for TAP pharmaceuticals and on the Advisory Board of Santarus, Inc.; VT receives research support from GlaxoSmithKline and Wyeth; MI, BT, and JAC are employees of AstraZeneca LP.
TG was involved in the conception and design of the manuscript, revising the manuscript critically for intellectual content, and final approval of the version to be published. VT was involved in the conception and design of the manuscript, acquisition of data, analysis and interpretation of the data, drafting the manuscript, revising the manuscript critically for intellectual content, and final approval of the version to be published. RBC was involved in acquisition of data, revising the manuscript critically for important intellectual content, and final approval of the version to be submitted. BDG was involved in the conception and design of the manuscript, analysis and interpretation of the data, revising the manuscript critically for intellectual content, and final approval of the version to be published. BT was involved in the conception and design of the manuscript, analysis and interpretation of the data, drafting the manuscript, revising the manuscript critically for intellectual content, and final approval of the version to be published. MI was involved in the conception and design of the manuscript, acquisition of data, analysis and interpretation of the data, revising the manuscript critically for intellectual content, and final approval of the version to be published. JAC was involved in the conception and design of the manuscript, analysis and interpretation of the data, revising the manuscript critically for intellectual content, and final approval of the version to be published.