Allergic rhinitis (AR) is one of the most common chronic respiratory diseases observed in the pediatric population, producing a significant morbidity, and an economic burden due to direct medical costs and indirect costs. Despite the high prevalence of AR in children and the importance of the use of topical intranasal corticosteroids for its treatment, comparative analyses of alternative treatments in pediatric patients, in terms of both cost and effectiveness are lacking.
Methods
A decision-analysis model was developed to estimate the cost-effectiveness of mometasone furoate nasal spray (MFNS) compared to beclomethasone dipropionate nasal spray (BDNS) for treating pediatric patients with AR over a 12-month period. Effectiveness parameters were obtained from a published study in which authors performed a systematic review of the literature. Cost data were obtained from a hospital´s bills and from the national manual of drug prices. The study assumed the perspective of the national healthcare in Colombia. The outcomes were three effectiveness measures summarized in a therapeutic index (TIX).
Results
For the base-case analysis, the model showed that compared to BDNS, therapy with MFNS was associated with lower costs (US$229.78 vs. 289.74 average cost per patient over 12 months) and a greater improvement in TIX score (0.9724 vs. 0.8712 score points on average per patient over 12 months), thus leading to dominance.
Conclusion
The present analysis shows that in Colombia, compared with BDNS, therapy with MFNS for treating pediatric patients with AR is a dominant strategy because it showed a greater improvement in a TIX reflecting both efficacy and safety, at lower total treatment costs.
The online version of this article (doi:10.1007/s12325-015-0192-6) contains supplementary material, which is available to authorized users.
Introduction
Allergic rhinitis (AR) is a global health problem and one of the most common chronic respiratory diseases observed in the pediatric and adult population, with an estimated prevalence of approximately 20–40 million in the US population [1]. In Colombia a prevalence of AR symptoms has been reported ranging from 29.5% to 33.9% for the whole population, and from 25.9% to 53.8% for the pediatric population [2, 3]. Despite the fact that AR is not directly associated with a high rate of mortality or a high rate of hospitalization, the disease produces a significant morbidity. This condition has a major impact on the quality of life, sleeping habits, academic performance, daily activities, and concentration of sufferers [4]. Furthermore, in pediatric patients, improperly managed AR may contribute to the worsening of comorbid conditions, including asthma, rhino sinusitis, and otitis media [5]. The aforementioned factors lead to significant economic burden due to direct medical costs such as prescriptions and ambulatory care visits, and indirect costs such as absenteeism from school and work [6, 7].
Although there are many therapeutic options for the treatment of AR, topical intranasal corticosteroids (INS) are considered the most effective medication class for controlling symptoms of the disease [1]. INS have shown to reduce nasal congestion, rhinorrhea, sneezing, pruritus, and can also relieve ocular symptoms [8]. In Colombia, beclomethasone dipropionate nasal spray (BDNS) and mometasone furoate nasal spray (MFNS) are the two most commonly prescribed and the leading INS by market share in the country [9]; however, currently BDNS is the only INS included in Colombia’s compulsory health insurance plan.
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Despite the high prevalence of AR in children and the importance of the use of INS for the treatment of AR, comparative analyses of alternative treatments in pediatric patients, in terms of both cost and effectiveness are lacking. These comparative analyses are important because differences in cost of acquisition, efficacy, side effects, and therapeutic adherence between alternative treatments for AR could have a considerable impact on the control and in the tremendous economic burden of the disease. Cost-effectiveness analysis (CEA) provides a tool with which to incorporate both cost and effectiveness of alternative treatments.
The aim of the present study was to compare the cost-effectiveness of MFNS compared to BDNS for treating pediatric patients with AR in Colombia.
Methods
Structure of the Model
A decision-analysis model was developed to estimate the cost-effectiveness of MFNS compared to BDNS for treating pediatric patients with AR. Although combination therapy with INS and antihistamines is occasionally used to treat the symptoms of AR, patients included in the model were only those treated with a single prescription therapy of INS for symptom relief of AR. We chose BDNS because it is currently the only INS included in Colombia’s compulsory health insurance plan. Additionally, MFNS, marketed by Merck Sharp & Dohme (MSD) under the brand-name Nasonex®, is—along with BDNS—the most commonly prescribed and the leading INS by market share in the country. For each of the two comparators, the model starts with a patient aged between 2 and 18 years who presents with AR and there is a probability (probability node) of improvement of symptoms. For patients whose symptoms improved, the model incorporates the probability that this improvement of symptoms has been due to improvement of nasal symptoms, ocular symptoms, or global assessment. Thereafter, the model incorporates the probability of treatment-related adverse events, and if these adverse events comprised epistaxis or not. For patients whose symptoms do not improve, the model incorporates the option (decision node) to continue treatment with a more effective INS or to send the patient for additional diagnostic and therapeutic procedures (Fig. 1). The model assumed that there would be complete compliance with either treatment measure throughout the entire year of follow-up. Although as determined by the natural history of AR it could be more appropriate to use a Markov model instead of a simple decision tree, we used the latter because we considered that using a simple decision tree it was possible to include the most important clinical events resulting from each of the two therapeutic options without unrealistic simplifying assumptions.
Fig. 1
Diagram of cost-effectiveness model for each treatment option. Asterisk For patients whose symptoms do not improve and the decision is to continue treatment with a more effective topical intranasal corticosteroid, the model follows as it is depicted for beclomethasone dipropionate nasal spray
×
The model compared the one-year direct medical costs (including medical consultations, imagenology studies, and other diagnostic and therapeutic procedures for patients with no improvement of symptoms on therapy with INS, or for patients who presented treatment-related adverse events such as epistaxis or increased intraocular pressure) and disease outcomes from the perspective of the national healthcare system in Colombia.
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Three effectiveness measures were chosen as the basis for this model: a composite total nasal symptom score (TNSS), defined as the average effect size for each of the two comparators for nasal symptoms, a composite total ocular symptom score (TOSS), defined as the average size for ocular symptoms, and a patient (or physician) global assessment (PGA).
Sources of Data
Disease Outcomes and Clinical Parameters
Assumptions regarding the probability of improvement of nasal symptoms, ocular symptoms and global assessment, the probability of treatment-related adverse events, and if these adverse events comprised epistaxis or not, were derived from the literature. Specifically, we identified a published study in which authors performed a systematic review of the literature (1966 to June 2009) to identify potentially relevant studies on efficacy and safety of several INS, including BDNS and MFNS [10]. In this study, the authors aimed to develop a therapeutic index (TIX) reflecting both efficacy and safety of these substances in a combined assessment. To develop this TIX, the authors performed meta-analyses for each single INS and for the parameters TNSS, TOSS, PGA, and epistaxis. The meta-analyses results for the different INS and the parameter TNSS, TOSS, PGA, and epistaxis were ordered and then categorized into scores from 0 to 3 using quartiles. The scores of long-term side effects and systemic ocular side effects were based on the highest level of evidence reflected by the study type of available studies and its results. The score points for the three efficacies and the three safety parameters were then summarized for each INS resulting in individual summation scores of ‘sum efficacy’ (ES) and ‘sum side effects’ (AES), which could range between a minimum of 0 and maximum of 9 points. A high ES would indicate a high efficacy and a high AES a high potential for side effects. The final TIX score was then calculated as the ratio of ES and AES with a theoretical maximum of 9 points indicating an optimal balance of a maximum efficacy and a minor potential of side effects [10]. Table 1 presents the summation scores of each parameter as well as the final TIX score for BDNS, MFNS, and for budesonide aqueous nasal spray (BANS). We included the data of BANS because, for patients whose symptoms do not improve, the model incorporates the possibility (decision node) to continue treatment with a more effective INS. Based on the summation scores of ES, the model assumed that MFNS is the next most effective INS for BDNS, and BANS is the next most effective INS for MFNS (Table 1). Probabilities of efficacy parameters were obtained based on the efficacy scores summarized in the TIX. The probability of improvement of symptoms with each one of the INS was calculated as the proportion of the maximum score for efficacy parameters with respect to the maximum possible score for efficacy parameters, and the probability of side effects with each one of the INS was calculated as the proportion of the maximum score for side effects parameters with respect to the maximum possible score for side effects parameters. Likewise, probabilities of efficacy parameters for TNSS, TOSS, and PGA were calculated as the proportion of the TIX scores for each parameter with respect to the maximum score for efficacy parameters, and probability of epistaxis was calculated as the proportion of the TIX score for epistaxis with respect to the maximum score for side effects.
Table 1
TIX scores for each parameter, subscales and final ratio by topical intranasal corticosteroid
AES sum side effects, BANS budesonide aqueous nasal spray, BDNS beclomethasone dipropionate nasal spray, ES sum efficacy, MFNS mometasone furoate spray nasal, TIX therapeutic index, TNSS total nasal symptom score, TOSS total ocular symptom score, PGA patient (or physicians) global assessment
Resource Utilization and Costs
As mentioned, the CEA was conducted from the perspective of the national healthcare system in Colombia and hence only direct costs were included in the analysis. In particular, the costs of medical consultations (pediatrician, otolaryngologists, allergologist, endocrinologist, and ophthalmologist), imagenologic studies (computed tomography scan of the paranasal sinuses, radiography of the paranasal sinuses, and lateral airway radiography to determine the adenoid size), as well as additional diagnostic and therapeutic procedures for patients with no improvement of symptoms on therapy with INS (Immunoglobulin E, skin prick testing, immunotherapy, impedance audiometry, endoscopic nasopharyngoscopy, adenoidectomy, septoplasty, tympanostomy tube placement, and turbinoplasty), were taken account of. Additional resources used for treatment-related adverse events (cauterization, anterior nasal packing, analgesic, topical antibiotics, and intraocular pressure measurement) were also included. All costs gathered were as close to reimbursement or true costs as possible.
Calculation of the daily therapy with INS was based on the estimated average daily dose appropriate for treating pediatric patients with AR, according to current international AR guidelines [11, 12], and the relative use of available concentrations for each medication according to current market research. The starting doses used in the present model were 2 sprays per nostril 2 times a day (400 µg total dose) for BDNS, 1 spray per nostril every day (100 µg total dose) for MFNS, and 1 spray per nostril 2 times a day (128 µg total dose) for BANS.
To determine the utilization rates of health resources and events for patients with no improvement of symptoms on therapy with INS and for patients with treatment-related adverse events, we performed a review of the literature, a consensus of experts consisting of a panel of three local pediatric otolaryngologists using the Delphi technique [13], and verified the results with a review of randomly selected medical records of 37 pediatric patients attended in the Fundacion Hospital La Misericordia with a principal diagnosis of AR (ICD-10 codes J30.1, J30.2, J30.3, and J30.4) between January 1 and December 31, 2013. The Fundacion Hospital La Misericordia is a referral hospital located in the metropolitan area of Bogota that receives patients from the most representative medical insurance companies in the city. The data number collected on health utilization were: the number of medical consultations per year (pediatrician, otolaryngologists, allergologist, endocrinologist, and ophthalmologist), the percent of patients requiring imagenologic studies (computed tomography scan of the paranasal sinuses, radiography of the paranasal sinuses, and lateral airway radiography to determine the adenoid size), the percent of patients requiring additional diagnostic and therapeutic procedures (immunoglobulin E, skin prick testing, immunotherapy, impedance audiometry, endoscopic nasopharyngoscopy, adenoidectomy, septoplasty, tympanostomy tube placement, and turbinoplasty), and the percent of patients requiring additional resources used for treatment-related adverse events (cauterization, anterior nasal packing, analgesic, and topical antibiotics).
Unit costs of all medications were taken from the Drug Price Information System (SISMED, 2013) [9], an official database provided by the Colombian Ministry of Health and Social Protection, which represents an important primary source of medication prices in the country. Costs of INS for the model were calculated as the expected days of therapy per year multiplied by their daily cost, dosed at their recommended starting doses.
Costs were calculated in Colombian Pesos (COP) and converted to Dollars (US$) based on the average exchange rate for 2013 (1 US$ = 1868.90 COP) [14]. All the costs were adjusted to 2013 COPs before converting them to US$s. Given that the model duration was 1 year, costs and effects were not discounted. The study protocol was approved by the local ethics board. The analysis in this article is based on previously conducted studies, and does not involve any new studies of human or animal subjects performed by any of the authors.
Sensitivity Analyses
A series of one-way, two-way, and multi-way sensitivity analyses (using a tornado diagram) and the effect of alternative model specifications were examined. Data ranges in sensitivity analyses were derived from various sources: for unit costs of resources, data ranges were plus or minus 25% of the base value, because it was considered that this range represents a reasonable one for these unit costs. For the rates of resource utilization for patients with no improvement of AR symptoms and for patients with treatment-related adverse events with INS, data ranges in sensitivity analyses were derived from 95% confidence intervals (CI) from the review of the literature, the values reported in the consensus of experts, and the review of the medical records. Finally, for unit costs of all medications, data ranges in sensitivity analyses were established from the low and high values reported from SISMED (an official database provided by the Colombian Ministry of Health). In addition, a probabilistic sensitivity analysis using second-order Monte Carlo simulation was conducted to account for the uncertainties associated with the model parameters using a cohort of 10,000 trial simulations for both alternatives. This probabilistic sensitivity analysis allowed us to generate 95% uncertainty intervals (UI) around costs and effects. These were presented graphically on a cost-effectiveness plane to show the estimated joint distribution of incremental costs against incremental effects and evaluated using net benefit analysis [15]. Subsequently, a cost-effectiveness acceptability curve (CEAC) was derived from these data [16] to identify which alternative would be the most cost-effective at various thresholds of willingness-to-pay (WTP) for TIX score point. All analyses were performed with software (TreeAgePro 2012, TreeAge Software, Williamstown, MA, USA).
Results
Base-Case Analysis
With respect to single INS the value of both the unit cost and the cost of daily treatment with BDNS were lower than those costs of MFNS, whereas the efficacy of MFNS was greater than the efficacy of BDNS. Likewise, the potential for side effects was higher for BDNS compared to MFNS (Table 2).
Table 2
Probability parameters (baseline value, low value and high value) used in decision tree model
Variable
Baseline value
Low value
High value
Treatment with beclomethasone dipropionate nasal spray
Improvement of symptoms
44.0
40.0
48.0
Improvement of nasal symptoms
50.0
45.0
50.0
Improvement of ocular symptoms
25.0
23.0
28.0
Side effects
77.0
69.0
85.0
Epistaxis
28.0
25.0
31.0
Treatment with mometasone furoate nasal spray
Improvement of symptoms
77.0
69.0
85.0
Improvement of nasal symptoms
43.0
39.0
47.0
Improvement of ocular symptoms
28.0
25.0
31.0
Side effects
11.0
10.0
12.0
Epistaxis
100.0
0.0
0.0
Treatment with budesonide aquous nasal spray
Improvement of symptoms
88.0
79.2
96.8
Improvement of nasal symptoms
25.0
23.0
28.0
Improvement of ocular symptoms
37.0
33.0
41.0
Side effects
44.0
40.0
48.0
Epistaxis
44.0
40.0
48.0
Probability calculations based on three efficacy and three safety parameters summarized in a therapeutic index [10]
While the anterior nasal packing was the resource with the greatest unit cost for patients with drug-related adverse events with INS use, septoplasty was the resource with the greatest unit cost for patients whose symptoms did not improve with the use of INS (Table 3). Likewise, while cauterization was the resource with the greatest rate of utilization for patients with drug-related adverse events with INS, immunotherapy, and endoscopic nasopharyngoscopy were the resources with the greatest rate of utilization for patients whose symptoms did not improve with the use of INS (Table 4).
Table 3
Unit costs of resources for pediatric allergic rhinitis (US$, 2013)
Cost item
Baseline value
Low value
High value
Drug-related adverse events with topical intranasal corticosteroids
Cauterization
17.81
13.36
22.26
Anterior nasal packing
28.56
21.42
35.70
Topical antibiotic
3.21
2.41
4.01
Analgesic
3.47
2.60
4.33
Seric cortisol
26.75
20.06
33.44
Diagnostic and/or therapeutic proceduresa
Immunoglobulin E
32.41
24.30
40.51
Skin prick testing
80.26
60.20
100.33
Immunotherapyb
62.02
46.51
77.52
Lateral airway radiography
18.43
13.82
23.04
CT scan of the paranasal sinuses
193.61
145.21
242.01
Impedance audiometry
6.02
4.51
7.52
Endoscopic nasopharyngoscopy
474.73
356.05
593.41
Tympanostomy tube placement
200.12
150.09
250.15
Turbinoplasty
433.26
324.95
541.58
Adenoidectomy
333.47
250.10
416.84
Septoplasty
824.84
618.63
1,031.05
Medical consultationsc
24.08
18.06
30.10
Topical intranasal corticosteroids
Beclomethasone dipropionate nasal sprayd
2.34
2.29
2.76
Mometasone furoate nasal spraye
13.29
9.13
14.25
Budesonide aquous nasal sprayf
43.62
37.59
46.22
CT computed tomography
aDiagnostic and/or therapeutic procedures for patients whose symptoms did not improve
bComplete monthly cost of immunotherapy
cUnit cost of medical consultations (pediatrician, otolaryngologist, allergologist, endocrinologist, and ophthalmologist)
dUnit cost of beclomethasone dipropionate nasal spray, 200 doses
eUnit cost of mometasone furoate nasal spray, 140 doses
fUnit cost of budesonide aqueous nasal spray, 120 doses
Table 4
Rates of resource utilization for patients with no improvement of allergic rhinitis symptoms and for patients with treatment-related adverse events with topical INS
Resources
Rate of resource utilization
Range
Patients with no improvement of allergic rhinitis symptoms
Immunoglobulin Ea
3.7%
1.7–5.7%
Skin prick testinga
46.7%
40.0–51.7%
Immunotherapya
50.0%
38.3–58.3%
Lateral airway radiographya
34.4%
31.0–37.3%
CT scan of the paranasal sinusesa
41.7%
37.3–46.0%
Impedance audiometrya
3.3%
1.7–6.7%
Endoscopic nasopharyngoscopya
50.0%
44.0–55.0%
Tympanostomy tube placementa
0.7%
0.0–2.0%
Turbinoplastya
25.0%
20.0–30.0%
Adenoidectomya
7.7%
3.3–13.3%
Septoplastya
2.3%
1.0–6.3%
Pediatric consultationb
4.3
4.0–5.0
Otolaryngologist consultationb
4.3
4.0–5.0
Allergologist consultationb
3.0
2.0–4.0
Patients with treatment-related adverse events with INS
Epistaxis
Cauterizationa
4.7%
2.3–9.7%
Anterior nasal packinga
0.7%
0.3–2.7%
Topical antibiotica
3.7%
2–7.3%
Analgesica
1.3%
0.3–3%
Pediatric consultationb
3.6
3.0–4.0
Otolaryngologist consultationb
2.6
2.0–3.0
Treatment-related adverse event other than epistaxis
Pediatric consultationb
3.0
2.0–4.0
Endocrinologic consultationb
2.0
1.0–3.0
Ophthalmologist consultationb
2.0
1.0–3.0
Seric cortisol measurementc
2.0
1.0–3.0
CT computed tomography, INS intranasal corticosteroids
aAverage percentage of patients that require the diagnostic/therapeutic procedure
bAverage number of consultations per year
cAverage number of measurements per year
Using the base-case assumptions, the model showed that compared to BDNS, therapy with MFNS was associated with lower costs (US$229.78 vs. US$289.74 average cost per patient over 12 months) and a greater improvement in TIX score (0.9724 vs. 0.8712 score points on average per patient over 12 months), thus leading to dominance. A position of dominance negates the need to calculate an incremental cost-effectiveness ratio (Table 5).
Table 5
Base-case cost-effectiveness analysis of MFNS versus BDNS for pediatric allergic rhinitis treatment
One-way, two-way, and multi-way deterministic sensitivity analyses (using a tornado diagram) showed that the cost of pediatric consultation and the cost of MFNS have the highest impact on the model outcome. However, MFNS was the dominant strategy over all the ranges of the cost of pediatric consultations and the cost of MFNS analyzed. Parameter distributions used in the probabilistic sensitivity analysis are presented in Table 6. The results of the probabilistic sensitivity analysis are graphically represented as a scatter plot in Fig. 2. This scatter plot shows that MFNS tends to be associated with lower costs and a greater improvement in TIX score. Based on the results from this simulation, the 95% UI for cost per patient treated with MFNS and BDNS were US$186.87 to US$282.22 and US$238.20 to US$348.60, respectively. Likewise, these 95% UI for TIX scores were 0.9464–0.9897 and 0.8240–0.9131 score points, respectively. In 97.6% of the iterations, MFNS was associated with a greater improvement in TIX score and lower costs compared to therapy with BDNS. The CEAC shows that the probability that daily therapy provides a cost-effective use of resources compared to intermittent therapy exceeds 99% for all WTP thresholds (Fig. 3).
Table 6
Parameter distributions used in the probabilistic sensitivity analysis
Scatter plot of each iteration’s cost and effectiveness values for each strategy in pediatric allergic rhinitis. The x-axis shows effectiveness measured as efficacy and safety parameters summarized in a therapeutic index; the y-axis shows costs measured in dollars (US$, 2013). Each point represents one of the 10,000 trial simulations, where each input was assigned a random value according to its probability density function
Fig. 3
Cost-effectiveness acceptability curve with MFNS versus BDNS for pediatric allergic rhinitis. The cost-effectiveness acceptability curve shows the probability of MFNS being cost-effective compared to BDNS over a wide range of WTP thresholds. This probability exceeds 99% for all WTP thresholds. BDNS beclomethasone dipropionate nasal spray, MFNS mometasone furoate nasal spray, WTP willingness-to-pay
×
×
Discussion
The present study shows that compared to BDNS, therapy with MFNS for treating pediatric patients with AR is a dominant strategy because it showed a greater improvement in a TIX reflecting both efficacy and safety, at lower total treatment costs. Although the variables that exhibited a significant effect on these results were the cost of pediatric consultation and the cost of MFNS, therapy with MFNS was the dominant strategy over all the ranges of the cost of pediatric consultations and the cost of MFNS analyzed. It is worth mentioning that, to the best of our knowledge, this is the first study to compare MFNS and BDNS for treating pediatric patients with AR, in terms of both cost and effectiveness.
The findings of the present study support the use of MFNS as the most efficient therapy in pediatric patients with AR diagnosis in Colombia and probably in other similar low- and middle-income countries (LMIC), at least when it is compared exclusively with BDNS. These results are important because although MFNS has a higher cost of acquisition relative to BDNS, it is associated with lower total treatment costs and better health outcomes in pediatric patients with AR. These findings should help to support the daily clinical decision-making process of choosing between a range of options for these patients. When choosing the most efficient therapy for treating pediatric AR, it is possible to impact on the significant morbidity and economic burden associated with the disease. Although traditionally it has been assumed that safety and efficacy is proven for all available INS, and that they are all equally effective in controlling symptoms of AR, our results do not support this previous assumption. Although there is no single trial which directly compares all the available INS, and our model did not include all INS currently licensed in Colombia for use in children with AR, the systematic aggregation and analysis of both efficacy and cost data in our study suggests that the choice among the different treatments available can have a great impact on the health outcomes and costs of the disease.
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Our results agree with those published by Portnoy et al. [17] who found, using an evidence-based medicine approach to assess efficacy and safety in a combined parameter comparing different INS, the best safety/efficacy ratio for MFNS. This study, however, considered only one parameter each for safety and efficacy, did not include BDNS in the analyses, and did not incorporate costs of alternative treatments. Likewise, in agreement with our findings, there are reports that support the difference in the proportion of costs for a daily dose of BDNS compared to a daily dose of MFNS [18]. Reissman et al. [19] determined the physician prescribing patterns of the leading INS from the National Disease and Therapeutic Index database in the US, and compared economic differences resulting from these prescribing behaviors. The authors of this study concluded that BANS offers more days of treatment at a lower cost per day than other leading INS. However, unlike our study, this study did not include BDNS in the analyses, did not consider parameters for safety or efficacy of alternative treatments, and did not take into account that starting dosage of INS is different in pediatric patients compared to adult patients. For the reasons mentioned above, it is difficult to more accurately compare our results with those published in the literature.
Our model also has some limitations. First, the base-case analysis was run for 12 months instead of a complete lifetime. However, we judged a 12-month period to be enough for determining the major health and economic consequences of the use of INS in pediatric AR. Second, we did not take into account the effect of incomplete and failing adherence to therapy that typically occurs when treating chronic diseases such as AR. However, this is a conservative approach, since fewer prescribed daily doses are likely an important component of adherence to AR therapy and improved long-term outcomes [20], and there are differences in dosing regimens between MFNS and BDNS (once daily vs. twice daily, respectively). In fact, published studies have reported a significantly greater level of adherence in patients with AR treated with MFNS compared to those treated with BDNS [21]. Third, although we assumed that differences in the results of the efficacy and safety parameters summarized in the TIX have a similar clinical significance, it’s unclear whether this assumption is actually true. This is mainly because there has not been a direct comparison of all INS with regard to the efficacy and safety outcomes analyzed in the present study. Fourth, assumptions regarding the probability of improvement of nasal symptoms, ocular symptoms and global assessment, the probability of treatment-related adverse events, and if these adverse events comprised epistaxis or not, were derived from a published study in which authors only included studies up to 2009, so it is probable that this study does not reflect the current state of scientific knowledge. However, in this study, authors performed a systematic review of the literature and developed a TIX reflecting both efficacy and safety of these substances in a combined assessment. Although this fact increase the confidence in obtaining unbiased results, it would be important that future studies determine the cost-effectiveness of different INS based on more recent literature. Finally, cost data were obtained from a single clinical center and may not be representative of the whole country. However, these data were obtained from a pediatric clinic that receives patients from the most important and representative medical insurance companies in the city. Moreover, costs were subject to wide sensitivity analyses.
Conclusions
The present analysis shows that in Colombia, compared with BDNS, therapy with MFNS for treating pediatric patients with AR is a dominant strategy because it showed a greater improvement in a TIX reflecting both efficacy and safety, at lower total treatment costs. Although it is difficult to assess the clinical relevance of differences in efficacy and safety parameters summarized in the TIX, these results may help to support clinical decision making until more robust evidence is available.
Acknowledgments
The study was partially funded by Merck Sharp & Dohme (MSD) Colombia. The article processing charges for this publication were funded by MSD Colombia. However, the authors had complete independence over the conduct, integrity, and publication of the study. The authors thank Mr. Charlie Barrett for his editorial assistance. All named authors meet the International Committee of Medical Journal Editors (ICMJE) criteria for authorship for this manuscript, take responsibility for the integrity of the work as a whole, and have given final approval for the version to be published. All authors had full access to all of the data in this study and take complete responsibility for the integrity of the data and accuracy of the data analysis.
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Conflict of interest
Carlos E. Rodriguez-Martinez and Monica P. Sossa-Briceño declare that they have no conflict of interest. Elkin Vladimir Lemos is an outcomes research manager in MSD Colombia.
Compliance with ethics guidelines
The analysis in this article is based on previously conducted studies, and does not involve any new studies of human or animal subjects performed by any of the authors.
Open Access
This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0), which permits use, duplication, adaptation, distribution, and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
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