Increased Risk of Peripheral Arterial Disease
After Hip
Replacement: An 11-Year Retrospective
Population-Based
Cohort Study
Tzu-Yi Chou, Ta-Wei Su, Herng-Jeng Jou, Pei-Yu Yang, Hsuan-Ju Chen,
Chih-Hsin Muo, and Chia-Hung Kao
INTRODUCTION
H
ip replacement (Hip-Rep), also called total hip arthroplasty, is a common and efficacious surgical procedure.1,2The number of Hip-Reps rapidly increased over the past decade.3 Kurtz et al reported a significant increase in the
primary total Hip-Rep rate in the United States from 47/100,000 in 1990 to 69/100,000 in 2002 (an increase of 22/100,000 in 12 years).4 A Taiwan-based cohort study revealed
that the rate of primary total Hip-Reps and primary partial Hip-Reps increased from 37/100,000 in 1996 to 55/100,000 in 2004 (an increase of 18/100,000 in 8 years).5
Peripheral arterial disease (PAD) is a manifestation of systemic atherosclerosis and is highly related to the risk of ischemic stroke (IS), myocardial infarction, and fatal vascular events. Even without previous myocardial infarction or IS, patients with PAD exhibit an almost equal relative risk of death from cardiovascular causes as do patients with a history of coronary or cerebrovascular disease.6–8 The worldwide prevalence
rate of PAD ranges from 3% to 12%.9,10 Regensteiner and
Hiatt reported that nearly 20% of adults older than 70 years have PAD.11 Claudication, atypical leg discomfort, and rest pain are
common symptoms ofPAD; however,most critically, asmany as 50% of patients with PAD are asymptomatic.10,12 The reported
risk factors for developing PAD include aging, diabetes mellitus (DM), smoking, hypertension (HTN), and hyperlipidemia.6,9 In
this article, ‘‘PAD’’ denotes vascular diseases including atherosclerosis of the abdominal aorta, iliac, and extremity arteries;
extremity artery bypass graft; arterial embolisms and thrombosis; and unspecified disorders of the arteries and arterioles.
Several studies have reported that Hip-Rep is associated with an increased risk of PAD;2,13–15 however, no research has
investigated this association in an Asian context. Thus, we conducted a nationwide retrospective cohort study to examine the risk of developing PAD in patients who received a Hip-Rep, hypothesizing that the procedure might increase the risk of developing PAD.
METHODS
Data Source
This retrospective cohort study used data from the Longitudinal
Health Insurance Database (LHID). The LHID is a subset of the National Health Insurance Research Database
(NHIRD) program, which was established by the Taiwan Bureau of NHI (BNHI). The NHI program, inaugurated in 1995, covers approximately 99% of the more than 23 million people in Taiwan.
By the end of 2010, the BNHI had contracts with all
hospitals and 92% of clinics nationwide. Each person covered by the NHI receives a unique identification number. All NHI
data sets can be interlinked using these anonymized identification numbers. Comprehensive information on insured
patients, including demographic data, clinic visit dates, disease diagnoses, and prescription details, is included in the LHID. The diagnostic codes used were those in the International Classification of Diseases, Ninth Revision, Clinical Modification
(ICD-9-CM). This study was approved by the institutional review board of China Medical University and Hospital, Taiwan (CMU-REC-101–012).
Study Population
This national population-based cohort study included 2 groups. We identified 5284 patients who received a Hip-Rep (ICD-9-CM codes 815.1 and 815.2) but had no history of PAD
(ICD-9-CM codes 440.0, 440.2, 440.3, 440.8, 440.9, 443, 444.0, 444.22, 444.8, 447.8, and 447.9) from 2000 to 2011. The date of Hip-Rep was used as the index date. A control group was
randomly selected from insured people with no Hip-Rep or history of PAD and was matched with the Hip-Rep group at a ratio of approximately 4:1 according to sex, age, and year of Hip-Rep. The index dates of the control cohort were assigned according to days and months randomly, and the index years were the same year as those of the matched cases. In total, 5284 patients were included in the Hip-Rep group and 21,124 patients comprised the control group.
Covariates and Main Outcome
Demographic factors included sex and age (in groups ages <50, 50–64, 65–79, and >80 years). Patients with HTN (ICD-9-CM codes 401–405), hyperlipidemia (ICD-(ICD-9-CM code 272), DM (ICD-9-CM code 250), ischemic stroke (IS, ICD-9-CM codes 433–438), ischemic heart disease (IHD, ICD-9-CM codes 410–414), chronic obstructive pulmonary disease (COPD, ICD-9-CM codes 490, 491, 495, and 496), or chronic kidney disease (CKD, ICD-9-CM code 585) diagnosed before the index date were considered to have a comorbidity. We identified a significant outcome of PAD development (ICD-9-CM codes 440.0, 440.2, 440.3, 440.8, 440.9, 443, 444.0, 444.22, 444.8, 447.8, and 447.9). Patients were followed from the index date until either December 2011, onset of PAD, death, or withdrawal from the NHI.
Statistical Analysis
The distribution of sex, age, and comorbidities (HTN, hyperlipidemia, DM, IS, IHD, COPD, and CKD) between
the Hip-Rep and the control groups were compared. Differences were examined using the chi-square tests for categorical variables and the Student t test for continuous variables. Follow-up
time in person-years was calculated for each person from the index date until PAD development. The incidence rate was calculated by dividing the number of PAD diagnoses by the number of person-years. The cumulative incidence of PAD was computed using the Kaplan–Meier method, and the difference in cumulative incidence between the groups was tested using a
log-rank test. Hazard ratios (HRs) and 95% confidence intervals (CIs) were calculated using Cox proportional hazards models to assess the association between Hip-Rep and PAD, with sex, age, and comorbidities adjusted for. All analyses were performed using SAS Version 9.3 (SAS Institute, Cary, NC). The significance level was set at less than.05 for the 2-sided P value.
RESULTS
A total of 5284 patients who had received a Hip-Rep
between 2000 and 2011 was frequency-matched according to sex, age, and year of Hip-Rep with 21,124 patients who had not received a Hip-Rep. The Hip-Rep group had a mean age of 67.2 years (standard deviation [SD]¼16.2 years) and a slight female predominance (52.5%). Compared with the control group, the Hip-Rep group exhibited a significantly higher prevalence of HTN (58.5% vs 51.1%), DM (22.1% vs 17.4%), IS (27.7% vs 19.9%), IHD (30.0% vs 26.9%), COPD (32.6% vs 28.1%), and CKD (5.2% vs 2.6%) (Table 1). The results of Kaplan–Meier analysis revealed that the Hip-Rep group had a higher cumulative incidence rate of PAD than did the control group (log-rank test, p¼0.001) (Figure 1). During the follow-up period, the incidence rates of PAD for the Hip-Rep and control groups were 7.79 and 5.79 per 1000 person-years, respectively. After adjustments for sex, age, and comorbidities, patients who received a Hip-Rep exhibited an increased risk of PAD compared with those in the control group (adjusted HR¼1.24, 95% CI¼1.05–1.48) (Table 2). Compared with patients ages 50 years and younger, the adjusted HR of PAD was 3.46-fold higher among those ages 50–64 years, 4.61-fold higher among those ages 65–79 years, and 4.87-fold higher among those ages 80 years and older. Multivariate Cox proportional hazards analysis revealed that PAD was independently associated with HTN (adjusted HR¼1.35, 95% CI¼1.12–1.63), DM (adjusted HR¼1.58, 95% CI¼1.34–1.86), IHD (adjusted HR¼1.70, 95% CI¼1.44–1.99), and CKD (adjusted HR¼1.75, 95%
CI¼1.29–2.37). Stratified by sex, the incidence rates of PAD in women and men who received a Hip-Rep were 9.34 and 9.17 per 1000
men in the control cohort (6.54 and 5.01 per 1000 person-years, respectively). In addition, women who received a Hip-Rep exhibited a 1.29-fold (95% CI¼1.03–1.61) higher risk of developing PAD than did women who did not receive a Hip-Rep. Among the age groups, a significantly higher HR of PAD was observed among patients who received a Hip-Rep while ages 65 years or younger (adjusted HR¼1.67, 95% CI¼1.18– 2.36). Stratified by follow-up year, the Hip-Rep group exhibited a significantly higher risk than did the comparison group of developing PAD within 0.5 years and 0.5–1 years (adjusted HR¼1.69, 95% CI¼1.03–2.78 and adjusted HR¼1.63, 95% CI¼1.01–2.63, respectively) (Table 3).
Compared with patients without the examined diseases and Hip-Rep treatment, patients received Hip-Rep without any comorbidity had a 2.45-fold risk for PAD (95% CI¼1.54– 3.89). Patients with only DM exhibited the highest risk of developing PAD (adjusted HR¼3.66, 95% CI¼1.67–7.99), followed by those with only IS (adjusted HR¼3.64, 95% CI¼1.80–7.35) and those with only IHD (adjusted
HR¼3.44, 95% CI¼1.71–6.94) compared to people with no comorbidity. Among patients who received a Hip-Rep, those
with four or more comorbidities exhibited a significantly increased risk of PAD (adjusted HR¼6.00, 95% CI¼4.16– 8.67), followed by those with any three comorbidities (adjusted HR¼4.32, 95% CI¼2.84–6.59), those with any two comorbidities (adjusted HR¼3.49, 95% CI¼2.25–5.43), and those
with one comorbidity (adjusted HR¼2.80, 95% CI¼1.74– 4.49) (Table 4).
DISCUSSION
We conducted this nationwide population-based retrospective cohort study to elucidate the relationship between Hip-Rep and the risk of developing PAD. After adjustments for sex, age, HTN, DM, IS, IHD, COPD, and CKD, patients who received a Hip-Rep exhibited a 1.24-fold higher risk of developing PAD than did patients in the control group. Age, HTN, DM, IHD, COPD, and CKD were also significantly associated with PAD. Most notably, a significantly higher risk of developing PAD was noted among women who received a Hip-Rep, patients who
received a Hip-Rep while ages 65 years or younger, and patients who received a Hip-Rep within the first follow-up year.
Our data revealed that advanced age, rather than sex, influenced the risk of developing PAD. This outcome was consistent with those in previous studies.6,10 However, this
study did not demonstrate that patients with only hyperlipidemia were at increased risk of developing PAD (compared with
patients without the examined diseases), as previous studies
have shown. Using more cases or longer study periods might reveal the positive association between hyperlipidemia and the
risk of developing PAD.
This study revealed that patients who received a Hip-Rep had more comorbidities (HTN, DM, and CKD) than did patients in the control group. Moreover, HTN, DM, and CKD are
associated with PAD.6,16,17 Accordingly, one possible reason
for the increased risk of PAD in the Hip-Rep group is that the patients in the group had a significantly higher prevalence of comorbidities. We did not have sufficient data on the prevalence of comorbidities in Asian patients who received a Hip-Rep. However, a 1990–2004 National Hospital Discharge Surveybased statistical analysis in the United States reported that
patients who received a Hip-Rep had an increased likelihood of developing DM, HTN, hypercholesterolemia, obesity, pulmonary disease, or CAD.18
Alternatively, the population of patients with PAD identified in this study might have been underestimated because PAD is frequently underdiagnosed.10,19 Thus, the number of patients
with PAD was likely greater than that diagnosed and enrolled; therefore, the impact of Hip-Rep on the risk of developing PAD might have been underestimated.
Limitations were also caused by incomplete data. First, the diagnoses recorded in the National Health Insurance Research Database (NHIRD) are primarily for administrative billing purposes and were not validated for academic purposes. Second, data on symptoms of PAD, family medical history, lifestyle, smoking habit, BMI status, laboratory data, and imaging findings, which are all potentially relevant to this study, are not included in the NHIRD. Third, the evidence
derived from a retrospective cohort study is generally of lower methodological quality than that of prospectively randomized trials because a retrospective cohort study design is subject to numerous biases related to adjustments for confounding factors. Despite our meticulous study design with the adequate control of confounding factors, a key limitation was that bias could have existed because of possible unmeasured or unknown confounders. Thus, a bias such as PAD patients with a mistaken
diagnosis of arthrosis might occur. Fourth, causality could not be established beyond doubt in this observational study. We could not verify the exact temporal relationship between Hip-Rep and PAD by using the NHIRD data.
Our findings have clinical importance. First, the results indicated that Hip-Rep independently increases the risk of developing PAD. Because Hip-Rep has been reported as being associated with an increased risk of atherosclerosis and unspecified cardiovascular disease2 and arterial thrombosis,13 few
studies have examined the specific relationship between Hip-Rep and PAD or considered Hip-Hip-Rep an independent risk factor for developing PAD. Some reports suggested a positive association between Hip-Rep and risk of developing PAD. For
example, Islam and Blake reported a total infrarenal aortic
occlusion condition after primary Hip-Rep, and that an aortobifemoral bypass resolved the problem.20 Hemodynamic
change, or vascular compromise, was proposed as a potential factor or an aggravated factor for developing PAD.15,21 However,
future prospective, large-scale research; systematic reviews; or meta-analyses might validate this finding. The second clinically notable aspect of this study is that the more comorbidities in the Hip-Rep group, the more risk of PAD and related morbidity and mortality; physicians should consider these conditions and treat patients accordingly.
This study has several strengths. First, this study is the first to examine the relationship between Hip-Rep and the risk of developing PAD in an Asian country. Second, we conducted this retrospective cohort research using nationwide population data from the NHIRD, which covers a highly representative
policy is universal and operated only by the government. Moreover, all insurance claims are scrutinized by peer
review and medical reimbursement specialists. PAD was accurately diagnosed and coded (ICD-9 codes) by the specialists
according to the standard diagnosed criteria including typical symptoms/signs, laboratory data, and imaging findings. In addition, if the doctors or hospitals make the wrong codes or diagnoses, the National Health Insurance Administration will punish them with a lot of penalty. Therefore, the diagnoses of PAD in this study were highly reliable. Third, the joint effect of Hip-Rep and different numbers of comorbidities are discussed, possibly elucidating the risk of PAD among patients with multiple comorbidities.
In conclusion, patients who received a Hip-Rep might have an increased risk of developing PAD. Age, HTN, DM, IHD, and CKD are also crucial risk factors for developing PAD. Patients who receive a Hip-Rep and have the aforementioned comorbidities are at an even higher risk of developing PAD. An
increased risk of developing PAD was present among women who received a Hip-Rep, patients who received a Hip-Rep while ages 65 years or younger, and patients who received a Hip-Rep within the first follow-up year in our study period. Although Hip-Rep is an orthopedic procedure, it might influence the vascular system profoundly. We suggest that further research involving larger samples and a more rigorous methodology be conducted.
