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Impact of renal insufficiency on mortality in patients with ST-segment elevation myocardial infarction treated with primary percutaneous coronary intervention
© Sabroe et al.; licensee BioMed Central Ltd. 2014
Received: 7 July 2013
Accepted: 28 January 2014
Published: 7 February 2014
Chronic kidney disease is associated with increased risk of mortality. We examined the impact of moderate and severe renal insufficiency (RI) on short- and long-term mortality among unselected patients with ST-segment elevation myocardial infarction (STEMI) treated with primary percutaneous coronary intervention (PCI).
From January 1, 2002 to December 31, 2010 all patients with STEMI treated with primary PCI were identified. The hazard ratio (HR) for death was estimated using a Cox regression model, controlling for potential confounders. RI was defined as creatinine clearance (CrCl) < 60 mL/min (moderate RI: CrCl ≤30 < 60 mL/min and severe RI: CrCl < 30 mL/min).
The study cohort consisted of 4,116 patients of whom 898 (21.8%) had RI and 3,218 (78.2%) had a CrCl ≥ 60 mL/min. Compared to patients without RI, patients with RI were older, more often female and more likely to have diabetes mellitus, hypertension and to present with a higher Killip class.
Among patients with a preserved kidney function and patients with RI, 30-day all-cause mortality was 3.5% vs. 20.9% (log-rank p < 0.001); 1-year all-cause mortality was 5.7% vs. 29.4% (log-rank p < 0.001); 5-year all-cause mortality was 13.4% vs. 47.4% (log-rank p < 0.001). Moderate and severe RI were associated with higher 1-year mortality compared to patients with a preserved renal function (CrCl ≤30 < 60 mL/min: adjusted HR 2.71 [95% CI 2.09-3.51], p < 0.001), and (CrCl < 30 mL/min: adjusted HR 7.09 [4.82-10.44], p < 0.001).
In unselected STEMI patients treated with primary PCI, moderate and severe RI were associated with increased risk of mortality.
Cardiovascular disease (CVD) is a leading cause of death in the western countries . Studies have shown that impaired renal function is to be considered a risk factor in relation to CVD and patients suffering from renal disease have a higher risk of CVD [2–4]. Also, chronic kidney disease (CKD) is found to be strongly associated with an increased risk of myocardial infarction (MI) and CVD mortality [5, 6]. Furthermore, CKD is found to affect patients on a global scale and with an increasing incidence and prevalence . After ST-segment elevation MI (STEMI) and non-STEMI the mortality has been reported to be significantly higher among patients with renal disease compared to patients with preserved renal function [8–10]. Today primary PCI is the recommended reperfusion strategy when treating patients with STEMI, which also applies to STEMI patients with renal dysfunction . Limited data are available on the outcome after primary PCI in STEMI patients with RI, because they have been underrepresented in randomized trials, as renal failure is a commonly used exclusion criterion .
In our study, data from the Western Denmark Heart Registry (WDHR) were used in order to assess the impact of moderate and severe renal insufficiency (RI) on short- and long-term mortality among unselected STEMI patients treated with primary PCI. Primary PCI has been the recommended treatment for STEMI after publication of the results of the DANish trial in Acute Myocardial Infarction-2 (DANAMI-2) in 2003 .
Setting and design
The study was conducted using WDHR for patients treated at Odense University Hospital. A detailed description of the databases has been reported previously . The study was a registry study and ethical approval was not required.
Patients and procedures
To be eligible for primary PCI, patients must meet the following criteria: 1) symptoms present less than 12 hours from onset of pain to time of catheterization, and 2) ST-segment elevation (at least 0.1 mV in two or more standard leads or at least 0.2 mV in two or more contiguous pre-cordial leads) or a new left bundle-branch block (LBBB). Patient with cardiogenic shock were not excluded. We used the WDHR to identify all primary PCIs performed from January 1, 2002 through December 31, 2010. Drug eluting stent (DES), bare metal stent (BMS), glycoprotein IIb/IIIa receptor blocker, and intra-aortic balloon pump was administered at the operator’s discretion. All patients received antiplatelet regimen including a bolus of 10,000 IU heparin, lifelong acetylsalicylic acid (75–150 mg once daily), and clopidogrel with a loading dose of 300 mg followed by maintenance with 75 mg daily. The recommended duration of clopidogrel treatment was 3 to 12 months until November 2002 and 12 months thereafter.
Blood samples were taken from the arterial sheath before the first contrast injection and serum creatinine - concentration was assessed in the hospital laboratory. Estimation of renal function is commonly based on estimated creatinine clearance (CrCl). Different methods are available. Studies have shown that The Modification of Diet in Renal Disease (MDRD) formula gives a reliable estimated CrCl [15–17], representing estimated glomerular filtration ratio (eGFR). Therefore the MDRD formula was used in this study: eGFR = estimated CrCl = 186 × standardized S-Cr-1.154 × age-0.203 × 0.742 [if female] . The unit of this equation is expressed as mL/min per 1.73 m2 body surface area. An eGFR less than 60 mL/min per 1.73 m2 was considered equivalent to RI. Based on eGFR the study population was divided into three groups, a group with eGFR ≥ 60 mL/min per 1.73 m2, a group with moderate RI: CrCl ≤30 < 60 mL/min per 1.73 m2, and a group with severe RI: CreaCl < 30 mL/min per 1.73 m2. This classification of patients into different stages of CKD is identical with those universally endorsed and based on the National Kidney Foundation data  where patients with an eGFR ≥ 60 mL/min per 1.73 m2 is STAGE I/II, patients with 30 ≤ eGFR < 60 mL/min per 1.73 m2 are in STAGE III, and patients with eGFR < 30 mL/min per 1.73 m2 are in STAGE IV/V.
Primary end-point of the study was all cause-mortality rate. Data on mortality were obtained from the Danish Civil Registration System [19, 20], which has kept electronic records on the gender, date of birth, changes in address, date of emigration, and changes in vital status of the entire Danish population since 1968.
Continuous variables were presented as medians with inter quartile range (IQR 25th, 75th) or mean ± 1 standard deviations (SD). Medians were compared using the Mann–Whitney U test, and means were compared using the unpaired t test. Categorical variables were presented as numbers and percentages. Distributions of categorical variables were compared using the Chi-square test.
We counted end-point events that occurred during the follow-up period and compared rates for the two groups (CrCl ≥60 mL/min per 1.73 m2 vs. CrCl <60 mL/min per 1.73 m2). Follow-up began on the date of primary PCI procedure and continued until date of death, December 31, 2010 or after 5 years follow-up (to ensure at least 10% of the study population at risk), whichever came first. Kaplan-Meier curves for all-cause mortality according to kidney function (CrCl ≥ 60 mL/min per 1.73 m2, CrCl ≤30 < 60 mL/min per 1.73 m2 and CrCl <30 mL/min per 1.73 m2) were obtained.
Cox proportional hazards regression analysis was used to estimate the hazard ratio (HR) mortality. Crude and adjusted hazard ratios (HRs) with 95% confidence intervals (CIs) were computed. Potential confounders associated with time to death in the univariable Cox regression analysis were included in the multivariable Cox regression model. Thus, in the final model, we adjusted for RI, age diabetes mellitus, hypertension, previous myocardial infarction, treatment with glycoprotein IIb/IIIa receptor blocker, Killip class and duration of procedure. All data analyses were carried out using SPSS software version 20. A two-sided P value <0.05 was considered significant.
Baseline clinical characteristics according to kidney function
CrCl ≥ 60
CrCl < 60
Pvalue (CrCl ≥ 60 vs. CrCl < 60)
CrCl ≤30 < 60
CrCl < 30
Pvalue (CrCl < 30 vs. CrCl ≤30 < 60)
Number of patients - no.
Male gender - no. (%)
Age – (year)
61.5 ± 12.1
73.5 ± 11.0
73.5 ± 10.8
72.8 ± 12.8
Family history - no. (%)
Smoking - no. (%)
Body Mass Index – (kg/m2)
Diabetes - no. (%)
Hypertension - no. (%)
Previous coronary artery bypass grafting - no. (%)
Previous percutaneous coronary intervention - no. (%)
Previous myocardial infarction - no. (%)
Lipid lowering therapy - no. (%)
Glycoprotein IIb/IIIa receptor blocker – no. (%)
Systolic blood pressure - (mmHg)
Diastolic blood pressure - (mmHg)
66.0 ± 15.1
66.4 ± 15.1
62.3 ± 15.9
Angiographic and procedural characteristics according to kidney function
CrCl ≥ 60
CrCl < 60
Pvalue (CreaCl ≥ 60 vs. CreaCl < 60)
CrCl ≤30 < 60
CrCl < 30
Pvalue (CrCl < 30 vs. CrCl ≤30 < 60)
Number of patients - no.
Multivessel disease no. (%)
Infarct related artery –no. (%)
Left anterior descending artery - no. (%)
Left circumflex artery - no. (%)
Right coronary artery - no. (%)
Left main - no. (%)
Anterior STEMI or LBBB – no. (%)
Killip class – no. (%)
Preintervention TIMI flow – no. (%)
Final TIMI flow - no. (%)
Lesion length – mm median (IQR)
Reference segment – mm median (IQR)
Minimum lumen diameter – mm median (IQR)
Sapheneous vein graft – no. (%)
Lesion type B2/C
Stent length – mm median (IQR)
Stent number - no. (%)
Drug-eluting stent – no. (%)
Max balloon pressure – atm median (IQR)
Max balloon diameter – mm median (IQR)
Duration of procedure - minutes median (IQR)
Flouro time - minutes median (IQR)
Contrast – ml median (IQR)
crude and adjusted hazard ratio of covariates associated with 1-year mortality in Cox regression analysis
Crude hazard ratio (95% CI)
Adjusted hazard ratio (95% CI)
Creatinine clearance ≥ 60 mL/min
Creatinine clearance ≤30 < 60 mL/min
Creatinie clearance < 30 mL/min
Age – years
Previous myocardial infarction
Glycoprotein IIb/IIIa receptor blocker
Infarct related artery
Right coronary artery
Left anterior descending artery
Left circumflex artery
Duration of procedure - minutes
After adjustment for potential confounders (Table 3) we found CrCl, diabetes, age, hypertension and Killip class to be associated with increased 1-year mortality. After adjustment for covariates associated with mortality, RI was associated with increased mortality at 30-day (adjusted HR 2.38, 95% CI 1.34-4.21), 1-year (adjusted HR 2.29, 95% CI 1.50-3.50) and 5-year mortality (adjusted HR 2.02, 95% CI 1.50-2.72) compared to patients with preserved kidney function.
Based on an unselected cohort of STEMI patients this study aimed to explore the impact of renal disease on all-cause mortality among 4,116 STEMI patients treated with primary PCI. In this real-world setting we found, that RI was associated with increased short- and long-term mortality. The strength of the present study is that the patients are unselected, all-comer and consecutive. Today guidelines suggest, that patients with STEMI and renal dysfunction is treated in the same way as other STEMI patients with the exception of administration of contrast dye and some medications . However, as primary PCI in STEMI patients is an emergent therapy; neither the kidney function nor the creatinine clearance level will be known in these patients at the time of the primary PCI. In our registry, most of the patients were diagnosed prehospital in the ambulance and referred directly to the catheterization laboratory, where the first blood sample was collected from the arterial sheath before contrast injection. In a recent study Fox et al.  showed from the Acute Coronary Treatment and Intervention Outcome Network (ACTION) registry, that one third of patients with STEMI had an eGFR < 60 mL/min per 1.73 m2. This is a higher number than the 22% of patients with RI we found in our study, which may be related to the patient population, as patients in the ACTION registry had a different comorbidity risk, as the rate of diabetes mellitus and hypertension were 2 to 3 times higher in the ACTION registry compared to our registry data. In contrast to our study, Fox et al. described that information about kidney function were available to the treating physicians when therapeutic decisions were made, and only 90% of patients with STEMI received reperfusion therapy (80% as primary PCI and 10% were treated with fibrinolysis). In our study patients with RI were more likely to receive primary PCI without stent implantation and less likely to receive treatment with glycoprotein IIb/IIIa receptor blocker compared to patients without RI. Among 2,597 STEMI and non-STEMI patients Medi et al.  found, that patients with RI and comorbidity were less likely to undergo coronary angiography, despite having the same frequency of primary PCI treatment as non-RI patients after angiography.
In our real-world setting registry we found, that RI was associated with increased short- and long-term mortality. This is in accordance with previous studies where RI also has been found to be associated with a higher 30-days mortality and long term mortality [22–25]. Seyfarth et al.  found an increase in adjusted hazard ratio after one year follow-up of 1.20 per 10-mL/min decrease in eGFR. In a study of Morel et al.  STEMI and non-STEMI patients were found to have a higher 9-month all-cause mortality when diagnosed with renal disease. Sadeghi et al.  studied 1,933 patients from the “Controlled Abciximab and Device Investigation to Lower Late Angioplasty Complications (CADILLAC)” trial, where baseline creatinine levels were obtained before angiography, including 350 patients with RI defined as CrCl < 60 mL/min per 1.73 m2. In our registry cohort, both short-term and 1-year mortality rate was more than twice as high as in the study from Sadeghi et al. . This difference is probably caused by (1) an increased mortality risk in non-randomized and all-comer patients compared to results from a randomized controlled study and (2) that patients with cardiogenic shock were not excluded in our study. Bertomeu-Gonzales et al.  studied the relationship between Killip class and impact of renal disease on mortality and found, that renal disease was stronger associated with mortality in STEMI patients with Killip I compared to patients with a higher Killip class. In our study, patients with RI were more likely to be older and female and they were more likely to have diabetes, hyperlipidemia, and hypertension. The finding of women representing a large proportion of STEMI patients with RI is consistent with findings from other studies [10, 28, 30, 31]. RI was found to be an independent predictor of 1-year mortality whereas we did not find gender to be an independent risk factor for 1-year mortality when adjusted for confounders. Similar findings have been made by Damman et al.  where 3-year mortality was found to be associated with a decrease in renal function, whereas gender difference was not proven to be a predictor of mortality after adjustment for confounders.
The validity of our findings depends on data quality and the ability to control for potential confounding. Like all observational studies, our study is prone to biases related to unmeasured factors. Bias due to unknown variables cannot be eliminated. Patients with cardiogenic shock were not excluded from the present study. We did not have systematically access to creatinine values taken in the following days after the primary PCI or information about contrast-induced nephropathy. Patients with RI were more often treated with balloon dilatation without stent implantation or bare metal stent. One explanation for this treatment strategy may be related to the more common finding of severely calcified lesions, which are known to limit complete DES expansion. We also lacked data on causes of mortality, however, in a previous STEMI cohort from Western Denmark Heart Registry, we found that especially the early causes of death was caused by a cardiac reason: the 1-year mortality reason was cardiac in 75% of the patients, whereas the 3-year mortality reason is cardiac death in 60% of the patients .
In unselected STEMI patients treated with primary PCI, RI was associated with increased short- and long-term mortality compared to patients with a preserved kidney function.
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