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Christopher Cutts, BScGradClinDip, is
Quality Use of Medicines Advisor (Clinical Pharmacist), Queensland
Rural Medical Support Agency, and Lecturer, University of Queensland
School of Pharmacy.
Adam LaCaze, BPharmGradDipClinPharm, is Quality Use of
Medicines Advisor (Clinical Pharmacist) Queensland Rural Medical
Support Agency, and Associate Lecturer, University of Queensland
School of Pharmacy.
BACKGROUND: Nonsteroidal
anti-inflammatory drugs (NSAIDs) are associated with significant
morbidity and mortality. They remain widely prescribed.
AIM: To describe current prescribing of non-COX-2 inhibitor
NSAIDs.
METHODS: Audit of a convenience sample of general
practitioners. Individual and group results were fed back to
individual GPs.
RESULTS: Seventy-one GPs submitted 790 patient records. A wide
range of NSAIDs was used. NSAIDs with a higher risk of
gastrointestinal side effects were used in 30% of patients over 70
years. The most common risk factors for their use were age,
cardiovascular disease and concomitant ACE inhibitor prescribing. Over
85% of participating doctors stated that feedback of these data would
change their future use of NSAIDs.
CONCLUSION: Patients are often exposed to the potential risks
of NSAIDs.
Received 13 November 2001; accepted 2 May
2002
Nonsteroidal anti-inflammatory drugs (NSAIDs)
are widely prescribed in Australia for a range of inflammatory and
pain conditions in a wide variety of patient populations. They pose
significant risks, especially gastro-intestinal (GI) damage,
exacerbation of congestive heart failure, hypertension, platelet
dysfunction and exacerbation of asthma.[1–9]
Despite this being highlighted in recent years,[8]
there has been little decrease in NSAID prescribing.[10]
Recently, cyclo–oxygenase–2 (COX–2) inhibitors, with fewer
gastrointestinal adverse effects reported, were introduced.
We describe prescribing of NSAIDs, since the
introduction of COX–2 inhibitors, in a convenience sample of rural
general practitioners participating in a clinical audit as part of
their continuing medical education and quality assurance (CME/QA).[11,12]
Methods
An audit form was developed to document any
exposure to the potential risks of NSAID therapy. (The GPs were later
asked to reflect on their data in relation to key papers as part of
the CME/QA).
The volunteer rural GPs in Queensland were asked
to apply the audit to 20 patients selected either retrospectively or
prospectively at the GPs’ discretion between January and March 2001.
We present the use of non–COX–2 inhibitor NSAIDs.
Results
The records of 1417 patients recorded by 71 GPs
yielded 790 uses of non–COX–2 inhibitor NSAIDs for osteoarthritis
(45%); strains or sport injuries (20%); rheumatoid arthritis (6%);
chronic pain (8%); nonspecific back pain (14%); menstruation problems
(3%); gout (5.6%) and other miscellaneous musculoskeletal conditions
(14%). Some patients were receiving NSAIDs for more than one
therapeutic indication. Thirty percent of patients used NSAIDs
regularly. Low risk NSAIDs were used by 45% of patients (Table
1). Many patients used additional analgesia: 54% occasional
paracetamol; 8% regular paracetamol (4g per day); 5% opioid; and 11%
others.
Table 1. Nonsteroidal anti—inflammatory
drugs (NSAIDs) used, by risk of gastroenteritis side effects
| Risk of
gastrointestinal side effects[5]
|
NSAID |
Number of patients n (%) |
Number of patients over 70 years old n (%) |
| Low |
ibuprofen, diclofenac |
354
(45) |
63
(39) |
| Moderate |
aspirin, sulindac, naproxen, indomethacin |
212
(27) |
38
(24) |
| High |
ketoprofen, piroxicam |
185
(23) |
48
(30) |
| Risk data not
available |
tiaprofenic acid, diflusinal, tenoxicam, ketorolac, mefenamic acid |
30
(4) |
12
(7) |
| NSAID name not
recorded |
|
9
(1) |
1 |
| |
|
|
|
| Total |
|
790 |
162 |
Some patients also used gastric acid suppression
drugs: 11% histamine–2 antagonists; 4% proton pump inhibitors; 2%
antacids; and 0.4% misoprostol.
Three hundred and sixty-three (47%) patients had
risk factors with special risks for the use of NSAIDs (Table
2). The most common were age; hypertension; and taking concurrent
angiotensin converting enzyme (ACE) inhibitors. Thirty-three percent
used at least one additional drug with potential for interactions.
Table 2. Risk factors identified in patients
taking NSAID therapy
| Risk factor |
Number of patients n (%) |
Number of patients over 70 years old n (%) |
| Renal impairment |
27
(3) |
17
(11) |
| Heart failure |
39
(5) |
27
(17) |
| Hypertension |
232
(29) |
71
(44) |
| Aspirin allergy |
6
(1) |
10
(1) |
| Previous peptic
ulcer disease |
53
(7) |
15
(9) |
| Self purchase of
over the counter NSAID therapy (oral or topical) |
13
(2) |
2
(1) |
| Taking low dose
aspirin |
84
(11) |
37
(23) |
| Taking an ACE
inhibitor |
130
(17) |
40
(25) |
| Taking warfarin
|
11
(1) |
5
(3) |
| Taking diuretics
|
76
(10) |
37
(23) |
| Taking a SSRI |
37
(5) |
4
(3) |
| Taking a
corticosteroid |
37
(5) |
14
(9) |
| Taking cyclosporin
|
1
(0.1) |
0 |
| |
| Total |
790 |
162 |
Discussion
Generalisability of these data is limited
because doctors and patients were not selected randomly. Nevertheless,
these results highlight a number of issues surrounding NSAID
prescribing.
Osteoarthritis was the most common reason for
the prescription of an NSAID, even though NSAIDs are no better than
regular paracetamol for most arthritic patients.[14]
We found that although a large minority of
patients were prescribed NSAIDs of low gastrointestinal risk (eg.
diclofenac, ibuprofen), many elderly patients especially were
prescribed high risk NSAIDs (eg. ketoprofen, piroxicam), despite being
at considerably higher risk. Different NSAIDs have different
gastrointestinal risks.[5]
Few patients took gastro–protective agents.
NSAIDs were often used in patients with
significant co-existing risk factors, such as older age, heart failure
and concomitant use of ACE inhibitors. In these patients the benefits
and risks of NSAID therapy need to be acknowledged and the decision to
continue therapy needs to be assessed on a case-by-case basis with due
consideration of opportunities to reduce risk, such as use of regular
paracetamol, low GI risk NSAID and gastro–protective agents.
Acknowledgements
Thanks to Deborah Askew for editorial
assistance.
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This article appeared in the June 2002 edition
of Australian Family Physician, Volume 31, Number 6, pages 590-592. |