Quantifying the Impact of NSAID-Associated Adverse Events

Published Online: November 20, 2013
Michael Fine, MD
Nonsteroidal anti-inflammatory drugs (NSAIDs) are widely used among patients experiencing many different types of pain, including inflammatory, acute pain (eg, injury, low back pain, headache, postoperative pain), and chronic pain (eg, rheumatoid arthritis, osteoarthritis). However, both traditional NSAIDs and second-generation NSAIDs (cyclooxygenase-2 inhibitors) can lead to very expensive and serious adverse events. Gastrointestinal, cardiovascular, and renal complications associated with NSAIDs have been shown to be dose-dependent. In 2005, to help minimize these risks, the US Food and Drug Administration issued a public health advisory stating that “NSAIDs should be administered at the lowest effective dose for the shortest duration consistent with individual patient treatment goals.” This article reviews the undue clinical and economic burden associated with NSAID-related serious adverse events.

Am J Manag Care. 2013;19(16 suppl):S267-S272
Nonsteroidal anti-inflammatory drugs (NSAIDs) are the cornerstone of pain management in patients who have inflammatory, acute pain (eg, headache, postoperative pain, and orthopedic fractures), and chronic pain (eg, rheumatoid arthritis, osteoarthritis, and gout).1,2 Approximately 70% of people 65 years or older use NSAIDs at least once per week, with half of them taking at least 7 doses per week. In 2000, more than 111 million prescriptions were written for NSAIDs in the United States, at an approximate cost of $4.8 billion.3 The use of NSAIDs is likely to increase even more as the US population continues to age and experience painful conditions that are more common among older adults.4

Both traditional NSAIDs and the second generation cyclooxygenase- 2 (COX-2) inhibitors offer superior efficacy compared with acetaminophen, but also carry significant risk for serious gastrointestinal (GI), cardiovascular (CV), and renal adverse events.1,5-7 A systematic review of 17 prospective observational studies found that 11% of preventable drug-related hospital admissions could be attributed to NSAIDs.8 Studies have documented that the risk of adverse events associated with NSAIDs are both dose-dependent and duration dependent.1,7,9

In 2005, the US Food and Drug Administration (FDA) issued a public health advisory warning of an increased risk for serious CV events with NSAID use.10 In 2007, the FDA published a medication guide for NSAIDs that recommended using the lowest dose possible for treatment. The guide listed myocardial infarction (MI), stroke, kidney problems, and GI bleeding as some of the serious potential side effects. Despite the emerging evidence, few studies have been conducted to help quantify the true burden of these side effects, especially when NSAIDs are used for acute pain.

The Impact of Pain Management

Acute pain is typically associated with an event, such as an injury or surgery, and usually resolves when the underlying event is treated or healed. Examples include headache, postoperative pain, fractures, low back pain, and neck pain.11,12 Approximately 40% of patient visits to primary care providers are due to mild to moderate acute pain.2 More than 70% of emergency department (ED) visits are for acute pain, making it the most common reason why patients seek treatment. Among the over 115 million ED visits annually in the United States, headache alone accounts for 2.1 million.11,13 Considering that the average cost of a visit to the ED is $1349, the costs associated with acute pain are substantial.14

Acute pain can also occur in the presence of chronic pain conditions such as osteoarthritis and low back pain; this type of pain is referred to as breakthrough pain. Both osteoarthritis and low back pain have placed significant economic burden on the US healthcare system.12,15 Data from the National Health Interview Survey show that in 2011, 28.4% of American adults reported experiencing low back pain within the previous 3 months.16 Buurma et al (2012) estimated that in 2011, there were 116.5 million cases of acute low back and neck pain in the United States. By 2021, the number is expected to reach 128.5 million cases (or, a 10% growth over the next decade).17

Similarly, the number of Americans with osteoarthritis is rising. Researchers estimate that the prevalence of arthritis in the United States among patients over 40 years of age grew from 10.1% in 1999 to 12.8% in 2008 (P = .011).18 Data from the Medical Expenditure Panel Survey (MEPS) showed that osteoarthritis was among the 5 most commonly treated conditions in 2009, totaling $29.5 billion. MEPS data showed that 17.4 million adults between the ages of 40 and 64 years were treated for osteoarthritis in 2009.19

NSAIDs: The Hidden Costs

The cost of treating acute and chronic pain conditions is well documented. What is less well understood is the price tag attached to the side effects associated with their treatment. Some estimates suggest that each year more than 100,000 patients are hospitalized for NSAID-related GI complications alone, with direct costs ranging from $1800 to $8500 per patient per hospitalization. Moreover, it has been reported that 16,500 persons die annually from these complications. In the elderly, the medical costs of adverse GI events associated with NSAID use likely exceed $4 billion per year.20

NSAID use is also associated with costly adverse events impacting the CV and renal systems. For example, NSAID use has been associated with increased risk for hospitalization due to MI as well as for heart failure (HF). According to recent data from the Agency for Healthcare Research and Quality, the average hospitalizations for acute MI and congestive HF cost $18,500 and $10,500, respectively. Likewise, acute renal failure, which is also associated with NSAID use, can ultimately lead to expensive dialysis treatment. Although direct cost data specific to NSAID adverse events are limited, several studies have examined healthcare utilization that results from the morbidity and mortality associated with these adverse events.

Gastrointestinal Adverse Events

A meta-analysis published in 2012 examined the relative risk (RR) of upper GI complications (upper GI bleeding and/or perforation, or peptic ulcer) for both traditional NSAIDs and COX-2 inhibitors using pooled data from 28 observational studies published between 1980 and May 2011. Researchers found an increased risk for upper GI complications across all 16 of the NSAIDs studied. Data showed that the risk was lowest for aceclofenac and celecoxib (RR, 1.4 and 1.5, respectively) and highest for ketorolac and azapropazone (RR, 11.5 and 18.5, respectively). Most of the NSAIDs were associated with an RR for upper GI complications between approximately 2 and 4. Researchers also found that the risk was dose-dependent. The use of high daily doses was associated with an approximately 2- to 3-fold increase in RR compared with low to medium doses for all NSAIDs except celecoxib, for which the effect was not dose-dependent.1

One of the more recent studies conducted regarding the GI side effects associated with NSAIDs was a 2013 metaanalysis by the Coxib and traditional NSAID Trialists’ (CNT) Collaboration of 280 studies (124,514 participants). The study examined the relationship between the use of NSAIDs and upper GI complications, such as peptic ulcer perforations, obstructions, and bleeding. Data for naproxen, ibuprofen, and diclofenac, as well as for the COX-2 inhibitors rofecoxib, etoricoxib, lumiracoxib, valdecoxib, and GW403681, were analyzed. CNT researchers found an elevated risk for upper GI complications across all of the medications studied. The RR was nearly twice as high for ibuprofen and naproxen compared with diclofenac and COX-2 inhibitors (Figure 1).6

A similar increased risk was found in a study among Quebec residents. Patients using NSAIDs had a risk of developing GI adverse events that was 2.5 times (95% confidence interval [CI], 2.04-3.00) that of patients not taking NSAIDs. In addition, researchers estimated that the average cost for GI adverse events added an average of 66% to the cost of care. In patients over the age of 85 years with more than 5 physician claims, the costs of management of adverse events associated with NSAIDs increased the cost of each prescription by a factor of 7.5.21

Cardiovascular Risks

The CNT study described above also examined the vascular risk associated with NSAIDs. The primary outcome was major vascular events, defined as nonfatal MI, nonfatal stroke, or death from a vascular cause. The study also measured the risk for major coronary events, stroke, hospitalization for HF, and death.

As shown in Figure 1, there was an elevated risk for major vascular events, HF, and cause-specific mortality for the COX-2 inhibitors. Diclofenac use at higher doses was associated with an increased risk for major vascular events and HF. Ibuprofen and naproxen use carried an increased risk for HF.6

A separate prospective study following 7636 individuals without a previous history of stroke examined the risk of stroke associated with traditional NSAIDs and COX-2 inhibitors. After adjusting for baseline body mass index, blood pressure, cholesterol level, and smoking status, researchers found that the risk of stroke increased by 1.58 for nonselective NSAID use and 2.40 for COX-2 selective NSAID use.22 A study among patients 30 years or older with a history of HF from the Danish National Patient Registry examined the link between NSAID prescription claims after hospital discharge and subsequent death, hospitalization due to HF, and hospitalization due to MI. Researchers included data for rofecoxib, celecoxib, ibuprofen, diclofenac, naproxen, and other NSAIDs. Data showed an increase in risk of death, hospitalization due to HF, and hospitalization due to MI across all NSAIDs. Researchers also found that for most of the NSAIDs studied, there was a clear, dose-dependent risk across all 3 end points. For example, high-dose diclofenac was associated with an increased risk for hospitalization due to MI at 100 mg per day (hazard ratio [HR], 2.43; P <.001), but had a nonsignificant increase at daily doses below 100 mg (HR, 1.14; P = .26).23

Renal Adverse Events

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