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Incidence and cost of treatment-emergent comorbid events in insured patients with chronic hepatitis C virus infection: a retrospective cohort study
© Sapra et al.; licensee BioMed Central Ltd. 2014
- Received: 14 March 2014
- Accepted: 11 September 2014
- Published: 24 September 2014
Treatment-emergent comorbid events (TECs) are common In patients initiating treatment with pegylated interferon alpha (PEG-IFN-alfa) and ribavirin for chronic hepatitis C virus (HCV) infection. The purpose of this study was to estimate the incidence and incremental cost of these events.
In a retrospective cohort analysis of healthcare claims, we studied patients with HCV who were newly treated with PEG-IFN-alfa/ribavirin between 2006 and 2008. TECs were defined by new medical/pharmacy claims for predefined conditions in the 12 months after treatment initiation. The net incremental cost of the TECs was the difference between baseline and follow-up costs for these comorbidities and their treatment, excluding PEG-IFN-alfa/ribavirin costs.
Of 3,795 newly treated patients, 1,269 (mean age 50.2, 36.2% female) met the selection criteria. New TECs were common, with 61.6% of patients having ≥1 event. Anemia was identified in 29.2% of patients, fatigue in 16.4%, depression in 11.5%, and neutropenia in 11.0%. The mean incremental cost for the predefined TEC in the postindex period was $6,377 ($2,782 for medical and $3,595 for pharmacy claims).
In an insured US cohort with chronic HCV infection, TECs with PEG-IFN-alfa/ribavirin were common and increased costs by approximately $6,000 per treated patient. This estimate may be conservative because it excludes indirect costs. Costs might increase with new regimens that include a protease inhibitor because additional TECs may be expected. Better-tolerated therapies that reduce the financial burden on the healthcare system and improve patient experience are needed.
Chronic hepatitis C virus (HCV) infection, with a worldwide prevalence of 2%-3% , causes substantial loss of life and reduces quality of life in those who are infected . Although the screening of blood products has reduced the incidence of HCV infection in developed countries, there is a long latency period before the disease becomes symptomatic and thus large numbers of new cases will continue to be identified over the coming years. Estimates suggest that about half of the 3.1 million US patients infected with HCV are unaware of their infection and only a small fraction have been treated [3–5].
Under optimal conditions, treatment of chronic HCV infection with pegylated interferon alpha (PEG-IFN-alfa) and ribavirin dual therapy produces sustained virologic response (SVR) of above 50% in patients with HCV infection [6, 7]. For patients with the most common HCV genotype (GT) in the US, GT-1, 48 weeks of PEG-IFN-alfa/ribavirin results in an SVR in 45%-50%, whereas in patients with GT-2 and GT-3, 24 weeks of PEG-IFN-alfa/ribavirin results in an SVR in 80%. Nearly all patients who achieve a SVR are cured of infection  and have a reduced risk of hepatocellular carcinoma and death . However, treatment with PEG-IFN-alfa/ribavirin causes numerous adverse events including fatigue, flulike symptoms, gastrointestinal disturbances, psychological symptoms, and hematologic abnormalities . These adverse events lead to decreased adherence, dose reduction, and early discontinuation. Patients who are able to maintain at least 80% adherence to their drug regimen have the highest likelihood of achieving a SVR, but treatment-emergent comorbid events (TECs) commonly limit adherence [10–12].
In the initial treatment of HCV infection, the addition of a protease inhibitor (telaprevir or boceprevir) to PEG-IFN-alfa/ribavirin (triple therapy) significantly improved SVR [13, 14]. However, adverse events were reported at higher rates among users of triple therapy than among users of PEG-IFN-alfa/ribavirin [13, 14]. Although a small subset of patients receiving triple therapy who have a rapid response can receive a shorter course of treatment, the 47%-77% premature discontinuation rates of PEG-IFN-alfa/ribavirin reported in clinical care settings [15, 16] would likely be similar with triple therapy.
Premature discontinuation of treatment and nonadherence may cause viral resistance and increase costs. Although combination therapies to treat HCV may cost between $23,000 and $78,000 per year (depending on GT, patient weight, and drug selected) , treatment with PEG-IFN-alfa/ribavirin has been shown to be cost effective when patients are cured . In addition, nonadherent patients have higher HCV-related medical (i.e., excluding medication) costs than adherent patients . However, despite their frequency and effect on treatment success, little is known about the cost associated with adverse events due to treatment with PEG-IFN-alfa/ribavirin itself . The objective of this study was to estimate the incidence of TECs and the incremental costs of treating these events in insured patients initiating PEG-IFN-alfa/ribavirin treatment for chronic HCV infection. Secondary objectives were to explore, in a managed care population, the rate of discontinuation of PEG-IFN-alfa/ribavirin therapy and the temporal pattern of the costs of these TECs.
Study design and data source
This study was a retrospective cohort analysis that used data from the i3 Ingenix LabRx database spanning the 4-year period from 7/1/05 to 6/30/09. This database is a Health Insurance Portability and Accountability Act (HIPAA)-compliant administrative claims database of 8–10 million covered lives, representing all major regions of the US. The database contains deidentified adjudicated pharmacy and medical claims submitted for payment by providers, healthcare facilities, and pharmacies and includes information on physician visits, medical procedures, hospitalizations, drugs dispensed, and tests performed. Healthcare charges are reported (medical, inpatient, and pharmacy) in this database, but paid claims and costs are not. Also available are member enrollment and benefit information as well as limited patient, provider, and hospital demographic information. Since the study did not involve direct contact with human subjects, did not involve an intervention, and did not involve collection of any identifiable patient information, Institutional Review Board (IRB) approval was not required.
The study included treatment-naive patients with HCV infection who began treatment with PEG-IFN-alfa/ribavirin during a 2-year period between 7/1/06 and 06/30/08. PEG-IFN-alfa and ribavirin were identified using National Drug Codes. The date of the first medication fill for PEG-IFN-alfa/ribavirin within this period was defined as the index date. The 24-month study period included 12 months before and 12 months after the index date. Treatment-naive HCV-infected patients were defined as those who did not fill any prescriptions for PEG-IFN-alfa prescription for at least 12 months before the first such fill. HCV infection was defined by the presence of at least 1 medical claim with an ICD-9-CM (International Classification of Diseases, 9th Revision, Clinical Modification) code for HCV (070.41x, 070.44, 070.51, 070.54, 070.7x) during the preindex period.
Patients were excluded if they were <18 years of age or if they were not continuously enrolled during the 24-month study period. We also excluded individuals who initiated therapy at a dose not recommended by the manufacturer [21–24]. Finally, we excluded patients with certain medical claims during the preindex period, including those with an ICD-9-CM code for hepatitis B (070.2x, 070.3x),or hematologic malignancies for which interferon may have been indicated [leukemia (204.xx-208.xx), Hodgkin’s lymphoma (201.xx), non-Hodgkin’s lymphoma (200, 202.0-202.2, 202.8), multiple myeloma (203.0-203.1, 238.6), acute lymphocytic leukemia (204.0), chronic lymphocytic leukemia (204.1), acute nonlymphocytic leukemia including acute myeloid leukemia (205.0), acute monocytic leukemia (206.0), chronic myeloid leukemia (205.1), or other leukemias (204.2, 204.8-204.9, 205.2, 205.8-205.9, 206.1-206.2, 206.8-206.9, 207.8, 208.0-208.2, 208.8-208.9)].
The primary outcome variable was net incremental cost, which was calculated as the difference between preindex and postindex cost for a prespecified list of TECs (see following paragraph) and their treatments, excluding the cost of PEG-IFN-alfa/ribavirin therapy. Charges for TECs were taken from medical claims consistent with one of these events or pharmacy claims with National Drug Codes for medications to treat the events. Charges for visits lacking a code for one of the listed TECs were not included. New TECs were defined by a medical or pharmacy claim in the postindex period that was not present in the preindex period.
TECs were grouped as blood disorders (anemia, neutropenia, thrombocytopenia), gastrointestinal disorders (nausea/vomiting, diarrhea), endocrine disorders (diabetes, hyperthyroidism, hypothyroidism), psychiatric disorders (depression, anxiety disorders, bipolar disorders, insomnia), skin and subcutaneous disorders (alopecia, skin rash), and other disorders (dyspnea, fatigue, headache). Medications used to treat TECs were grouped similarly and included those to treat blood disorders (epoetin alfa, darbepoetin, filgastrim, and eltrombopag), endocrine disorders (antidiabetes medications and thyroid agents), psychiatric disorders (anxiolytics, antidepressants, antipsychotics/antimanics, and hypnotics), skin disorders (topical steroids), and other (antimigraine).
Secondary outcomes included the incidence of new TECs, timing of such TECs, and the rate of discontinuation of PEG-IFN-alfa/ribavirin therapy. PEG-IFN-alfa/ribavirin therapy was considered to be discontinued if there were no prescription fills for both medications for at least 60 days. The date of discontinuation was defined as the last day the patient had both PEG-IFN-alfa and ribavirin available, based on the days of supply as reported in the pharmacy claims. If PEG-IFN-alfa and ribavirin were discontinued on different dates, the earlier date was used.
Other measures included patient age, gender, race, geographic region, and the presence of human immunodeficiency virus (HIV) infection/acquired immune deficiency syndrome (AIDS). Because physician specialty may impact cost and resource use, we identified the specialty of each patient’s usual care physician using a validated method. The specialty of the physician prescribing therapy was not directly identifiable in the claims database. Instead, the method counts all claims for evaluation and management services and identifies the physician specialty with the largest plurality of such claims . Physician specialty was assigned using claims from the preindex period.
The recommended PEG-IFN-alfa/ribavirin treatment duration is either 24 or 48 weeks, depending on HCV GT. Claims data are used to process payments and generally do not contain clinical information such as test results. However, GT data were available for a small subset of study subjects and we thus explored discontinuation rates for this subset in a sensitivity analysis. In another sensitivity analysis, we restricted the group of patients analyzed to those who were treated beyond 28 weeks of PEG-IFN-alfa/ribavirin treatment, under the assumption that they had GT-1 infection.
For descriptive analysis, percentages, medians, means, and standard deviations were calculated for all baseline variables. We reported the percentage of patients with any new TEC as well as the percentage with a new event for each TEC. We reported the mean and standard deviations for TEC charges in both the pre- and postindex periods and for net incremental TEC charges. Treatment discontinuation was reported as the proportion of patients who no longer had PEG-IFN-alfa/ribavirin available at successive 4-week intervals. Charges for TECs were also stratified by duration of therapy. All data transformations and statistical analyses were performed using SAS version 9.2 (SAS Institute, Cary, NC).
Characteristics of insured patients initiating PEG-IFN-alfa and ribavirin treatment for chronic HCV infection
No. (%) of insured patients (n = 1269)
Age, mean (SD), y
Age group (y)
Type of health benefits
Frequency of various treatment-emergent comorbid events a in insured patients initiating PEG-IFN-alfa and ribavirin treatment for chronic HCV infection
No. (%) with treatment-emergent comorbid event in the preindex period
No. (%) with treatment-emergent comorbid event in the postindex period
No. (%) diagnosed with a new treatment-emergent comorbid event in the postindex periodb
(n = 1269)
(n = 1269)
(n = 1269)
Any treatment-related comorbid event
Skin and subcutaneous
Duration and discontinuation of PEG-IFN-alfa/ribavirin therapy in insured patients receiving treatment for chronic HCV infection
Duration of PEG-IFN-alfa/ribavirin therapy (days)
Discontinue before 12 wk
Discontinue before 24 wk
Discontinue before 48 wk
No. of patients
Patients with known GT
Patients treated >28 weeksa
In an insured US cohort with chronic HCV infection who were treated with PEG-IFN-alfa/ribavirin, most patients experienced one or more TEC. The most commonly identified TECs were anemia, fatigue, depression, and neutropenia. Anemia was identified in 29.2% of patients in this study, compared with in 22% of patients in clinical trials. Rates of several adverse events including fatigue (16%), insomnia (9%), and depression (12%) were lower than those observed in clinical trials (54%, 37%, 22%, respectively) . This may be expected since patients in clinical practice are typically monitored less aggressively than those in clinical trials. We used ICD-9-CM codes to identify TECs, and thus we only identified events that warranted an interaction with the healthcare system in the form of an office visit, hospitalization, or prescription. In addition, even when identified clinically, ICD-9-CM codes may not be recorded for less-severe events. As a result, the frequency and cost of TECs we report may be underestimated.
Despite this likely downward bias, we estimated that TECs increased direct treatment costs by 25% ($6,377), with just over half of charges from prescription medications and the rest from office visits, hospitalizations, and other nonprescription charges. Although we did not assess indirect costs in this study, several of the TECs (e.g., anemia, depression, and insomnia) experienced by patients who receive PEG-IFN-alfa/ribavirin therapy have associated indirect costs. For example, in studies of patients with anemia due to chronic kidney disease, hemoglobin values were positively correlated with days worked [26, 27]. In a study that reviewed healthcare claims from employees at a major US corporation, nearly 20% of the costs of depressive illness were related to disability, and this study did not take into account lost productivity or sick leave . Depressed individuals took significantly more time off work than those with diabetes, heart disease, or back problems . In addition, absenteeism and disability expenditures were higher in individuals with insomnia than those without it . Together these studies suggest that indirect costs of these TECs are likely to be significant.
Shortened treatment duration was not associated with a reduced cost of treating TECs. Nonprescription costs accounted for most of the total costs in patients who stopped treatment by 12 weeks and between 24 and 48 weeks, suggesting that these groups of patients frequently experience TECs. The lowest cost of treating TECs was for patients who stopped treatment between 13 and 24 weeks; most of these patients probably discontinued treatment because they completed treatment for GT 2/3 infection rather than because of TECs. Patients who completed therapy at 48 weeks had the lowest nonprescription costs but high prescription costs, possibly indicating stable management of TECs such as anemia or neutropenia with costly growth factors.
Although comparisons to other studies are difficult because of differences in methodology, the mean treatment duration of 215 days is consistent with estimates from other studies of 172–240 days [15, 16, 19, 30]. In a retrospective cohort study of Veterans Affairs patients, two of the most common TECs we identified, anemia and neutropenia, were associated with lower persistence with PEG-IFN-alfa/ribavirin treatment (mean 172 days) . Similar to patients in our study, the investigators identified patients with anemia and neutropenia through both ICD-9-CM codes and by identifying medication use (specifically the use of growth factors). Growth factors may improve treatment tolerability and thus enhance persistence. Dissimilarities in data sources, clinical care settings, data analysis techniques, and patient characteristics may explain some of the differences in the treatment discontinuation estimates. Although we could not distinguish between patients who discontinued therapy because of adverse events and those who discontinued therapy because of lack of virologic response, our findings support the concept that adverse events lead to high rates of therapy discontinuation.
Limitations of this study include those common to claims analysis. A commercially insured population may not be representative of the entire US population nor of treatment patterns in other countries. Lack of clinical data can confound interpretation. In particular, HCV treatment duration is dictated by GT, which was unavailable for most patients in this study. HCV GT was available for a subset of 238 patients. In this subset, 81% had GT 1/4/6, which is similar to other US cohorts, suggesting that our data are representative of the US population [31, 32]. According to standard treatment recommendations, these patients with predominately GT-1 would be expected to complete 48 weeks of treatment . This subset of patients had discontinuation rates that were similar to the overall group, which suggests that our assumption that treatment duration was indicative of GT was reasonable. Furthermore, response guided therapy would lead some patients to have treatment recommended beyond 48 weeks. If these patients continued treatment up to 48 weeks, they might be clinically discontinuing therapy prematurely, whereas in our analysis they would not be considered to have done so. Conversely, discontinuation of therapy may be recommended when virologic response is poor, and we could not distinguish between this and TECs as a cause of discontinuation. This study was intended to examine only one aspect of cost, not total treatment costs or cost effectiveness. HCV treatment with PEG-IFN-alfa/ribavirin costs between $23,000 and $78,000 per year, and newer treatments are substantially more expensive . Given the timing of this study, none of the patients were treated with newer direct acting antivirals.
In an additional sensitivity analysis of the patients who stopped therapy after 28 weeks and were thus presumed to have GT 1/4/6, 40% stopped before completing the recommended duration of therapy. Patients treated over 12 weeks with GT-1 would be expected to have had a virologic response  and thus discontinuations after 24 weeks would most likely be due to adverse events in those with GT-1. Overall, these sensitivity analyses further support the idea that discontinuation rates in patients treated with PEG-IFN-alfa/ribavirin are high and frequently due to TECs.
Additional limitations include miscoding or undercoding of claims, which may affect the accuracy of cost estimates. Finally, although we were only able to study patients who were receiving double therapy, the cost of TECs may rise with the use of triple therapy (PEG-IFN-alfa/ribavirin plus a protease inhibitor) because gastrointestinal events, skin rash, and anemia are more common with triple therapy than with PEG-IFN-alfa/ribavirin alone [10, 14, 34].
Treatment of chronic HCV infection with PEG-IFN-alfa/ribavirin led to frequent TECs and that these events were associated with significant costs. Furthermore, nearly half of treated patients discontinued therapy. It is likely that adding a protease inhibitor to the PEG-IFN-alfa/ribavirin treatment discussed in this study will result in similar or increased TECs. Thus, better-tolerated therapies associated with fewer TECs that reduce healthcare system costs and improve patient continuation rates are needed.
This study was funded by Bristol-Myers Squibb Company. Partnership for Health Analytic Research, LLC (PHAR, LLC) was paid by Bristol-Myers Squibb Company to conduct the research described in this manuscript.
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