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Clinical cardiology · 2021

Percutaneous coronary intervention and 30-day unplanned readmission with chest pain in the United States (Nationwide Readmissions Database).

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Sykes R, Mohamed MO, Kwok CS, Mamas MA, Berry C

Аннотация

Percutaneous coronary intervention (PCI) improves anginal chest pain in most, but not all, treated patients. PCI is associated with unplanned readmission for angina and non-specific chest pain within 30-days of index PCI. Patients with an index hospitalization for PCI between January-November in each of the years 2010-2014 were included from the United States Nationwide Readmissions Database. Of 2 723 455 included patients, the 30-day unplanned readmission rate was 7.2% (n = 196 581, 42.3% female). This included 9.8% (n = 19 183) with angina and 11.1% (n = 21 714) with non-specific chest pain. The unplanned readmission group were younger (62.2 vs 65.1 years; P < 0.001), more likely to be females (41.0% vs 34.2%; P < 0.001), from the lowest quartile of household income (32.9% vs 31.2%; P < 0.001), have higher prevalence of cardiovascular risk factors or have index PCI performed for non-acute coronary syndromes (ACS) (OR:3.46, 95%CI 3.39-3.54). Factors associated with angina readmissions included female sex (OR:1.28, 95%CI 1.25-1.32), history of ischemic heart disease (IHD) (OR:3.28, 95%CI 2.95-3.66), coronary artery bypass grafts (OR:1.79, 95%CI 1.72-2.86), anaemia (OR:1.16, 95%CI 1.11-1.21), hypertension (OR:1.13, 95%CI 1.09, 1.17), and dyslipidemia (OR:1.10, 95%CI 1.06-1.14). Non-specific chest pain compared with angina readmissions were younger (mean difference 1.25 years, 95% CI 0.99, 1.50), more likely to be females (RR:1.13, 95%CI 1.10, 1.15) and have undergone PCI for non-ACS (RR:2.17, 95%CI 2.13, 2.21). Indications for PCI other than ACS have a greater likelihood of readmission with angina or non-specific chest pain at 30-days. Readmissions are more common in patients with modifiable risk factors, previous history of IHD and anaemia.

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https://creativecommons.org/licenses/by/4.0/ This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

INTRODUCTION

Percutaneous coronary intervention (PCI) is indicated for acute coronary syndromes (ACS) or the relief of anginal symptoms secondary to myocardial ischemia, in patients with obstructive coronary artery disease (CAD). Around 3 million procedures are performed worldwide every year. The results of recent randomized, controlled trials of clinical strategies involving invasive management of CAD have not provided evidence of clear benefits for coronary revascularization over medical therapy in patients with chronic coronary syndromes (CCS). 1 , 2

In the ABSORB‐4 trial, which compared clinical outcomes in patients treated with either a bioresorbable scaffold or a 3rd generation drug eluting stent, the occurrence and time‐course of angina post‐PCI was similar in both groups, occurring in 11% of subjects by 30 days and 22% of patients by 1‐year. 3 The clinical characteristics associated with anginal chest pain at these time‐points and experience in less‐selected, real‐world populations are uncertain. Readmission within 30 days following PCI is not uncommon, with a broad spectrum of etiologies and degrees of severity. 4 Readmissions are commonly secondary to cardiac‐related disorders or PCI complications and it is reported that readmission is associated with a greater risk of mortality. 5 , 6 , 7 , 8

In this study, we accessed a large, national readmissions database to investigate the proportion of patients re‐admitted to hospital with chest pain attributed to angina or non‐specific chest pain within 30 days after PCI for ACS or CCS and the associated clinical characteristics. In addition, we evaluated the cost burden of chest pain readmissions compared with readmissions due to other causes.

METHODS

In the United States, the Healthcare Cost and Utilization Project (HCUP) Nationwide Readmissions Database (NRD) records, hospitalization and readmission data for all hospitalized patients within 21 States and is produced by the Agency for Healthcare Research and Quality. This study utilized deidentified data collected and distributed by HCUP and does not require consent from individual patients or an institutional board review (IRB) approval. The distribution of included municipalities is geographically diverse and represents 49.1% of all hospital inpatients, including patients with and without insurance. Admissions are linked by an individual identification number, which enables linkage between admissions independent of readmission location.

Patients were included if they are 18 years or older and underwent PCI at index admission (ICD‐9 Procedure code: 00.66, 36.06, 36.07) with discharge data from 2010 to 2014. Only the first admission with PCI within a calendar year was considered. Cases were excluded if they died during index admission, had duplicate data, were missing demographic or readmission data, or readmitted electively. Additionally, patients admitted in December are excluded as they lack 30 days of follow‐up. Patients who were readmitted with a primary chest pain diagnosis are defined by ICD‐9 codes ( Angina – ICD‐9: 413.0, 413.1, 413.9; non‐specific chest pain [ NSCP ] – ICD‐9: 786.5, 786.51) and clinic classification software codes ( stable coronary artery disease including angina – CCS: 101; Non‐specific chest pain – CCS: 102; see Table A1 ). Demographic, comorbidity at index admission and outcome data as well as detail of inpatient stay was captured through a combination of NRD coding, ICD‐9 and Elixhauser comorbidity codes. Cost‐to‐charge ratios were applied to total charges as recommended by HCUP in order to provide an estimate of inpatient cost.

The primary outcome of this analysis is 30‐day readmission with a primary diagnosis of chest pain post‐PCI, and variables associated with readmission. A sub‐group analysis of the characteristics of patients with a primary diagnosis of angina and non‐specific chest pain is also performed.

Statistical analysis was performed using IBM Statistics SPSS (version 24.0). Weighting is performed using sample discharge weights. Dichotomization of patients based on the presence or absence of readmission within 30 days and subsequent descriptive statistics are presented. Chi‐square or Independent Student‐T testing with 95% two‐tailed significance was utilized for comparing patient demographics. Multiple logistic regression analyses were performed to evaluate the association between these variables and readmission within 30‐days with angina, non‐specific chest pain and the combined population readmitted with angina or non‐specific chest pain. Furthermore, the relative risk (RR) of association with variables and readmission within 30‐days of angina versus non‐specific chest pain is also evaluated.

RESULTS

Of 3 700 737 identified as undergoing PCI in the United States in the years 2010–2014, 2 723 455 were included in the analysis. The reasons for exclusion are described in Figure 1 . Of note, 326 759 were excluded due to a December discharge date. In total, 104 696 patients were excluded from analysis due to missing demographic, discharge or mortality data.

FIGURE 1 Flow diagram
FIGURE 1 Flow diagram

Characteristics of patients readmitted for chest pain or angina within 30‐days post‐PCI

Within this post‐PCI cohort ( n = 2 723 455), 196 581 (7.2%) had an unplanned hospital readmission for any cause within 30‐days. Of these, 40 897 (20.8%) patients (1.5% of the whole post‐PCI cohort) were readmitted with a primary diagnosis of chest pain at 30 days, including 19 183 patients with angina and 21 714 with non‐specific chest pain. The demographics and medical history of the patients who were or were not readmitted during a 30‐day period are provided within Table 1 . Peak readmissions for chest pain, angina and non‐specific chest pain are observed within the first 48 h following discharge post‐PCI (Figure 2 ).

TABLE 1
Patient demographics and characteristics including co‐morbidities at index admission
Abbreviations: ACS, acute coronary syndromes; CABG, coronary artery bypass grafts; IHD, ischemic heart disease; NSCP, non‐specific chest pain; PCI, percutaneous coronary intervention.

VariableAll patientsAll chest painNSCPAngina
Control group No readmissionUnplanned readmissionUnplanned readmissionUnplanned readmission
( n = 2 723 455)( n = 2 682 557)( n = 40 897)( n = 21 714)( n = 19 183)
Age in years (SE)65.1(0.01)65.1(0.01)62.2(0.07)61.6(0.09)62.8(0.10)
Female934 57434.3%917 81434.2%16 76041.0%944843.5%731238.1%
Length of stay in days (SE)3.85(0.00)3.87(0.00)2.39(0.01)1.84(0.01)3.02(0.03)
Cost of inpatient stay (SE)$19 937(10.6)$20 133(10.7)$7083(48.7)$5064(24.7)$9368(97.3)
Quartile of median household income
0‐25th850 33331.2%836 86831.2%13 46532.9%703032.4%643533.5%
26th‐50th721 85426.5%711 17826.5%10 67726.1%570026.3%497725.9%
51st‐75th632 30323.2%622 98823.2%931522.8%509823.5%421722.0%
76th‐100th518 96419.1%511 52319.1%744118.2%388617.9%355518.5%
Smoker1 106 46040.6%1 091 32340.7%15 13837.0%787536.3%726337.9%
Obesity421 97115.5%416 40215.5%556913.6%291713.4%265213.8%
Chronic renal failure407 29415.0%401 71515.0%557913.6%273812.6%284114.8%
Family history of IHD296 63810.9%293 37410.9%32648.0%16197.5%16458.6%
Personal history of IHD2 565 06094.2%2 526 13194.2%38 93095.2%20 08692.5%18 84498.2%
Previous MI457 33516.8%447 47816.7%985624.1%523324.1%462324.1%
Dyslipidemia1 915 62670.3%1 886 21470.3%29 41271.9%15 30170.5%14 11173.6%
Hypertension2 032 12674.6%2 000 64774.6%31 47977.0%16 58676.4%14 89377.6%
Diabetes mellitus1 027 61237.7%1 011 49537.7%16 11839.4%849039.1%762839.8%
Heart failure101 5933.7%101 2413.8%3530.9%760.4%2771.4%
Valvular heart disease30 9231.1%30 8151.1%1080.3%180.1%900.5%
History of stroke/TIA161 9535.9%159 3055.9%26486.5%14516.7%11976.2%
Peripheral vascular disease316 55811.6%312 85011.7%37089.1%17027.8%200610.5%
Anaemia345 13312.7%340 07612.7%505812.4%242411.2%263413.7%
Atrial fibrillation349 32012.8%345 30312.9%40179.8%17998.3%221811.6%
Previous CABG251 4659.2%245 3279.1%613815.0%311314.3%302515.8%
Non‐ACS index PCI913 02633.5%887 49733.1%25 52962.4%17 20879.2%832143.4%
ACS index PCI1 810 42966.5%1 795 05966.9%15 36937.6%450620.8%10 86356.6%
STEMI565 26420.8%561 39420.9%38699.5%17338.0%213611.1%
NSTEMI/Unstable angina1 261 85646.3%1 249 66346.6%12 19329.8%279112.9%940249.0%
FIGURE 2 Distribution of readmissions with angina (A), non‐specific chest pain (B), all chest pain (C), all‐causes of readmission (D) within 30‐days ( X axis: days to readmission;…
FIGURE 2 Distribution of readmissions with angina (A), non‐specific chest pain (B), all chest pain (C), all‐causes of readmission (D) within 30‐days ( X axis: days to readmission; Y axis: frequency )

Multiple logistic regression models were created to examine the associations between clinical characteristics and co‐morbidities and the likelihood of readmission with a primary diagnosis of angina or non‐specific chest pain at 30 days after PCI. We found several characteristics that were strongly associated with readmission with chest pain at 30‐days (Table 2 ). The unplanned readmission group were younger (62.2 vs 65.1 years; P < 0.001), more likely to be females (41.0% vs 34.2%; P < 0.001) and within the lowest quartile of household income (32.9% vs 31.2%; P < 0.001). The readmission group also had a higher prevalence of previous ischemic heart disease (IHD), coronary artery bypass grafts (CABG), hypertension and dyslipidemia. Furthermore, they were more likely to have index PCI performed for non‐ACS (odds ratio [OR]: 3.46, 95% CI 3.39, 3.54) ( Supplementary Figure 1 ).

TABLE 2
Demographic and clinical characteristics associated with the likelihood of readmission at 30‐days with chest pain following PCI
Abbreviations: ACS, acute coronary syndromes; CABG, coronary artery bypass grafts; IHD, ischemic heart disease; NSCP, non‐specific chest pain; PCI, percutaneous coronary intervention.

VariableAll chest painNSCPAngina
( n = 40 897)( n = 21 714)( n = 19 183)
Odds Ratio (95% C.I.)P valueOdds Ratio (95% C.I.)P valueOdds Ratio (95% C.I.)P value
Female1.44 (1.41, 1.47)<0.00051.57 (1.53, 1.62)<0.00051.28 (1.25, 1.32)<0.0005
Age0.97 (0.97, 0.97)<0.00050.97 (0.97, 0.97)<0.00050.98 (0.98, 0.98)<0.0005
Smoker0.87 (0.85, 0.89)<0.00050.91 (0.89, 0.94)<0.00050.84 (0.81, 0.86)<0.0005
Obesity0.78 (0.76, 0.80)<0.00050.79 (0.76, 0.82)<0.00050.78 (0.75, 0.81)<0.0005
Q1 (0‐25th %)1.04 (1.01, 1.07)0.021.01 (0.97, 1.05)0.571.06 (1.02, 1.11)0.006
Q2 (26‐50th %)1.00 (0.97, 1.04(0.7871.02 (0.98, 1.06)0.410.99 (0.95, 1.03)0.653
Q3 (51‐75th %)1.01 (0.98, 1.04)0.7461.05 (1.01, 1.10)0.0240.96 (0.92, 1.00)0.06
Q4 (76‐100th %)0.97 (0.94, 0.99)0.020.99 (0.95, 1.03)0.5720.94 (0.91, 0.98)0.006
Chronic kidney disease0.94 (0.91, 0.97)<0.00050.88 (0.84, 0.92)<0.00051.00 (0.96, 1.04)0.916
Family history of IHD0.74 (0.71, 0.76)<0.00050.74 (0.70, 0.78)<0.00050.74 (0.71, 0.78)<0.0005
Personal history of IHD1.20 (1.15, 1.26)<0.00050.76 (0.70, 0.78)<0.00053.28 (2.95, 3.66)<0.0005
Previous MI1.36 (1.33, 1.39)<0.00051.28 (1.24, 1.32)<0.00051.44 (1.39, 1.49)<0.0005
Dyslipidemia1.08 (1.06, 1.11)<0.00051.07 (1.04, 1.10)<0.00051.10 (1.06, 1.14)<0.0005
Hypertension1.12 (1.09, 1.15)<0.00051.11 (1.07, 1.14)<0.00051.13 (1.09, 1.17)<0.0005
Diabetes Mellitus0.97 (0.95, 0.99)0.0090.96 (0.93, 0.98)0.0020.99 (0.96, 1.02)0.624
Heart Failure0.18 (0.17, 0.20)<0.00050.07 (0.05, 0.08)<0.00050.36 (0.32, 0.41)<0.0005
Valvular Heart Disease0.28 (0.23, 0.34)<0.00050.09 (0.06, 0.14)<0.00050.53 (0.43, 0.65)<0.0005
History of Stroke/TIA1.11 (1.07, 1.16)<0.00051.18 (1.11, 1.24)<0.00051.03 (0.97, 1.10)0.289
Peripheral Vascular Disease0.76 (0.73, 0.78)<0.00050.65 (0.62, 0.68)<0.00050.88 (0.84, 0.92)<0.0005
Anaemia1.04 (1.01, 1.08)0.0090.94 (0.89, 0.98)0.0031.16 (1.11, 1.21)<0.0005
Atrial Fibrillation0.84 (0.82, 0.87)<0.00050.70 (0.66, 0.73)<0.00051.01 (0.97, 1.06)0.663
Previous CABG1.67 (1.63, 1.72)<0.00051.54 (1.49, 1.61)<0.00051.79 (1.72, 1.86)<0.0005
Non‐ACS PCI on index adm.3.46 (3.39, 3.54)<0.00058.26 (7.99, 8.54)<0.00051.49 (1.45, 1.54)<0.0005
ACS PCI on index admission0.29 (0.28, 0.30)<0.00050.12 (0.12, 0.13)<0.00050.67 (0.65, 0.69)<0.0005

Characteristics of patients readmitted for angina within 30‐days post‐PCI

Patients readmitted with angina within 30‐days were more likely to be female (OR: 1.28, 95% CI 1.25, 1.32), younger (OR: 0.98, 95% CI 0.98, 0.98), associate with the 0–25% of median household income (OR: 1.06, 95% CI 1.02, 1.11), have history of IHD including previous myocardial infarction (OR: 1.44, 95% CI 1.39, 1.49) or coronary artery bypass grafting (OR: 1.79 95% CI 1.72, 1.86, dyslipidemia (OR: 1.10, 95% CI 1.02, 1.14), hypertension (OR: 1.13, 95% CI 1.09, 1.17) and anaemia (OR: 1.16, 95% CI 1.11, 1.21). These patients were also more likely to have undergone index PCI for indications other than ACS (OR: 1.49, 95% CI 1.45, 1.54). Smoking status at index admission, obesity, association with 76–100% of median household income, history of heart failure, valvular heart disease, peripheral vascular disease, and acute coronary syndrome on index PCI (OR = 0.67, 95% CI 0.65, 0.69) were less likely to be observed compared with those who were not readmitted within 30‐days (Figure 3 ).

FIGURE 3 Demographic and clinical characteristics associated with the likelihood of readmission at 30‐days with angina following PCI. PCI, Percutaneous coronary intervention
FIGURE 3 Demographic and clinical characteristics associated with the likelihood of readmission at 30‐days with angina following PCI. PCI, Percutaneous coronary intervention

Characteristics of patients readmitted for non‐specific chest pain within 30‐days post‐PCI

Of those readmitted with non‐specific chest pain within 30‐days, female gender (OR: 1.57, 95% CI 1.53, 1.62), younger age (OR: 0.97, 95% CI 0.97, 0.97), association with 51–75% of household income (OR: 1.05, 95% CI 1.01, 1.10), previous history of coronary artery bypass grafting (OR: 1.54, 95% CI 1.49, 1.61), myocardial infarction (OR: 1.28, 95% CI 1.24, 1.32), hypertension (OR: 1.11, 95% CI 1.07, 1.14), dyslipidemia (OR: 1.07, 95% CI 1.04, 1.10), and history of cerebrovascular events (OR: 1.18, 95% CI 1.11, 1.24) are more likely characteristics compared with patients who were not readmitted. Patients who underwent PCI for indications other than ACS at index admission were observed to have a greater likelihood of readmission at 30‐days (OR: 8.26, 95% CI 7.99, 8.54). Reduced likelihood is observed in those with a history of smoking, obesity, chronic kidney disease (stage 1–3), family or personal history of IHD, diabetes mellitus, atrial fibrillation, anaemia, peripheral vascular disease and valvular heart disease or history of heart failure prior to index PCI ( Supplementary Figure 2 ).

Comparisons of patients readmitted with angina versus non‐specific chest pain

Compared with patients readmitted within 30 days for nonspecific chest pain, patients who were readmitted with a diagnosis of angina within 30 days were older, more likely to be male, to associate with the 0–25% of household income, have a smoking history, family or personal history of IHD, chronic kidney disease (stage 1–3), dyslipidemia, history of heart failure or valvular heart disease, peripheral vascular disease, anaemia, atrial fibrillation, previous CABG and acute coronary syndrome on admission for index PCI ( Supplementary Table 3 ). Patients with angina readmissions within 30‐days had a higher inpatient mortality rate ( Supplementary Table 1 ). Total charges were greater in those readmitted with angina with longer average duration of admission compared with non‐specific chest pain.

Duration of admission and costs

Patients readmitted with angina or non‐specific chest pain had a shorter duration of readmission hospital stay (mean: 2.3, 95% CI 2.37, 2.42) compared with those readmitted for other causes within a 30‐day period (mean: 5.18 days, 95% CI 5.16, 1.21) ( P < 0.005). Angina or non‐specific chest pain readmissions were also associated with lower hospitalization costs ($7083) compared with other causes of readmission ($11 642) ( P < 0.005) ( Supplementary Table 2 ).

DISCUSSION

We have assessed unplanned readmission with a primary diagnosis of angina or non‐specific chest pain within 30‐days of PCI in a large, national database. We have found that early readmission with angina or non‐specific chest pain after PCI is uncommon. Only 1.5% of patients treated with PCI were readmitted with angina or non‐specific chest pain and affected patients had more cardiovascular risk factors and history of previous IHD. Nonetheless, since many patients undergo PCI, a readmission rate of 1–2% within 30 days equates to a considerable number of patients. Readmission after PCI was associated with an appreciable cost. Mortality during readmission is low in keeping with the coded diagnoses.

Causes of angina post‐PCI

PCI is indicated for patients with anginal symptoms despite guideline‐directed medical therapy to relieve symptoms of angina and may improve prognosis. 9 , 10 However, although PCI is routinely successful, angina may persist. 11 The causes of persisting or recurrent angina include incomplete revascularization, complications of PCI for example, side‐branch loss, or unusually, unsuccessful PCI. A further issue may be the underutilization of available secondary preventative therapy combinations, which may prevent the requirement to progress to invasive management in chronic coronary syndromes. 12 An under‐recognized problem is ischemia and no obstructive coronary artery disease (INOCA). This group of disorders includes microvascular angina, vasospastic angina or mixed microvascular/vasospastic angina, in the absence of obstructive (≥50% diameter stenosis) or flow‐limiting (fractional flow reserve ≤0.80; non‐hyperemic pressure ratio ≤ 0.89) CAD. 13 Patients with INOCA have a burden of anginal symptoms and typically poorer quality of life compared to patients with obstructive CAD. 14 Microvascular angina may be associated with obstructive CAD (Type 3 microvascular angina), or, alternatively, CAD may be falsely classified as obstructive when in fact the primary cause of angina is microvascular disease. Our analysis does not provide information on the etiology of the chest pain in this cohort out with diagnosis code however, it is observed that index acute coronary syndrome was significantly less common in angina and non‐specific chest pain readmissions at 30‐days compared with index population within this cohort. A limitation to this estimate is that readmissions from recurrent myocardial infarction are more likely to occur within an acute coronary syndrome subset rather than readmission with non‐specific or angina pain. Furthermore, identification of culprit arteries may be less clear in patients undergoing PCI for non‐ACS indications so as not, to provide symptomatic benefit for patients with angina, and therefore cause proportionately more readmissions. Further studies to investigate etiology within patients readmitted with chest pain including the success of revascularization, residual coronary disease burden and discharge medication are warranted.

Chest pain after PCI may be experienced in 36% to 42% of patients undergoing both elective and emergent PCI. 15 , 16 , 17 It is most commonly described in the first 24 h following PCI but is described as occurring within the first 3 weeks. 16 In addition to non‐cardiac causes it is important to distinguish patients with benign chest pain from critical chest pain after PCI due to acute stent thrombosis, incomplete revascularization, or disease progression affecting alternative coronary regions. However, risk stratification in these patients is challenging and may be influenced by the presence of persistently elevated cardiac enzymes or electrocardiograph evolution in the absence of new myocardial injury. 18 , 19 , 20 Benign chest pain and patients with stable angina post‐PCI pain in the absence of ACS, pulmonary or upper gastrointestinal pathologies is therefore understandably recorded in up to one third of overall PCI re‐admissions. 21 , 22 No standard nomenclature for the clinical phenomenon of chest pain post‐PCI currently exists due to differing opinions of etiology and there are no guidelines for a standardized approach to management. 23

A further entity may include the psychological burden associated with a diagnosis of non‐specific chest pain and it is estimated that anxiety disorders are prevalent in 30–50% of these patients. 24 Somatization disorders with chest pain symptoms may influence readmission, particularly in non‐ACS PCI indications.

Healthcare implications of hospital readmission post‐PCI

Readmissions are a significant source of burden both on the patient and the healthcare system, which is often used as a proxy‐marker for quality of care and penalty systems are implemented for providers with greater proportions of readmission. 25

Patients with chest pain constitute between 0.6 to 2.4% of unplanned presentations to emergency departments and up to one in four admissions to medical and cardiology wards. 26 , 27 , 28 , 29 In the United Kingdom, this represents a significant burden with non‐ACS chest pain equating to an average of 15.8 and 16.8 bed days per 1000 population for angina and non‐specific chest pain respectively with standalone 30‐day mortalities of 1.5% and 0.7%. 28 The incidence and demographical distribution of patients readmitted with chest pain syndromes has not previously been explored. Therefore, the burden on health services as well as mortality and major adverse cardiac event (MACE) rate for patients readmitted with chest pain post‐PCI is not clearly defined.

Our study involved a large sample that is likely to be reasonably representative of the US population undergoing PCI. The NRD has been utilized previously in patients with chest pain, which provides precedent for selection in this study. 30 Local audit and assessment of chest pain readmissions should be encouraged in order to establish local requirement for interventions, which may reduce readmissions with non‐specific chest pain and angina following PCI. This would ensure appropriate utilization of available resources and financial investment dependent on the localized burden of readmissions.

Associations with cardiovascular risk factors: implications for risk stratification

Demographic factors associated with higher likelihood of unplanned readmission in this sample are in keeping with known cardiovascular risk factors. However, smoking in this sample was not associated with increased readmission at 30 days. This is based on index smoking status and it is plausible that this may be subject to the smoking modification and cessation programmes, which are commonplace in the management of patients with coronary disease. Patients with heart failure, valvular heart disease and non‐cardiac vascular disease were observed to be less likely to be re‐admitted at 30‐days. This is in part due to the proportion undergoing PCI for ACS in whom ventricular dysfunction if present will be identified following PCI rather than as a co‐morbidity on index admission and may also be secondary to increased involvement of secondary care outpatient services in their management and treatment planning.

Optimization of modifiable risk factors prior to intervention is performed in surgical patients and the pre‐operative assessment is commonplace in order to improve surgical morbidity and mortality. 31 , 32 However, currently there are no similar formalized pathways for patients undergoing PCI which could be implemented in elective angiography patients to improve long‐term outcomes. Median household income was significantly associated with increased likelihood of readmission at 30‐days in patients with angina and those associating with the 76–100% had a lower likelihood of readmission with a primary diagnosis of angina. Chronic kidney disease in this population was not associated with increased likelihood of re‐admission however, the majority of patients included are of mild impairment as would be expected to undergo PCI with contrast. Female gender was more likely for patients readmitted within 30‐days with angina and non‐specific chest pain and it is previously observed that microvascular and vasospastic angina with INOCA or obstructive CAD is more common in female patients. 33 Male gender was observed in the majority of all groups in keeping with gender as a known risk factor of cardiovascular disease. Anaemia in this dataset is associated with increased readmission with a primary diagnosis of angina at 30‐days following PCI. Although discharge haemoglobin concentrations are not provided in the database, this may provide an area of potential modification for patients prior to being discharged following PCI.

One evidence‐based example of an intervention to reduce readmissions following PCI is a multimodal strategy as described by Tanguturi et al (2016). 34 This involved a risk assessment of readmission with the production of patient videos regarding subsequent chest pain or symptoms of heart failure. In addition, a formal clinic review with a cardiology fellow and a computerized alert system for re‐presentations facilitated early cardiologist review. This package of interventions reduced 30‐day hospital readmission from 9.6% to 5.3% over the 4‐year study period.

Limitations

Limitations included the composition of the database from separate yearly data, which prevents multi‐year follow‐up of these patients and excludes those admitted in December from 30‐day follow‐up. On the other hand, a longer follow‐up period for example at 6 months would necessitate the exclusion of the inverse proportion for that year and would have reduced the external validity of the analysis. The database is comprised of inpatient admissions and does not include discharges from emergency care, community data or patients managed in observation areas following PCI. In the United States approximately 7.6 million patients present with chest pain per annum, four out of five will not require admission. A further limitation is the lack of information on completeness of revascularization for included patients or their prescribed medications at the time of discharge. This would be of value in this cohort, particularly where subsequent angina diagnoses are coded on readmission in patients who have undergone PCI for indications other than ACS.

CONCLUSIONS

Our study provides insights into the prevalence, risk factors and health burden of readmission with angina or non‐specific chest pain following PCI. Secondary prevention measures to reduce cardiovascular risk such as correction of anaemia may help to optimize the clinical status of patients prior to undergoing PCI. PCI performed for an indication other than ACS is associated with a greater likelihood of readmission with angina or non‐specific chest pain at 30‐days within this cohort and further investigation of the etiology within these patients is required.

CONFLICT OF INTEREST

Professor Colin Berry is employed by the University of Glasgow, which holds consultancy and research agreements for his work with companies that have commercial interests in the diagnosis and treatment of angina. The companies include Abbott Vascular, Astra Zeneca, Boehringer Ingelheim, GSK, HeartFlow, Menarini, Novartis, and Siemens Healthcare. None of the other authors have any potential conflicts of interest.

Supporting information

Appendix S1 : Supporting information

Click here for additional data file.

ACKNOWLEDGMENTS

The authors would like to thank the Healthcare Cost and Utilization Project for access to the Nationwide Readmissions Database.

DATA AVAILABILITY STATEMENT

The data underlying this article were provided by the Healthcare Cost and Utilization Project under licence. Data will be shared on request to the corresponding author with permission of the Healthcare Cost and Utilization Project

REFERENCES

1 Sedlis SP , Hartigan PM , Teo KK , et al. The COURAGE trial Investigators. Effect of PCI on long‐term survival in patients with stable ischemic heart disease . N Engl J Med . 2015 ; 373 : 1937 ‐ 1946 . 26559572 10.1056/NEJMoa1505532 PMC5656049

2 Al‐Lamee R , Thompson D , Dehbi HM , et al. Percutaneous coronary intervention in stable angina (ORBITA): a double‐blind . Randomised Controlled Trial Lancet . 2018 ; 391 : 31 ‐ 40 . 29103656 10.1016/S0140-6736(17)32714-9

3 Stone GW , Ellis SG , Gori T , et al. Blinded outcomes and angina assessment of coronary bioresorbable scaffolds: 30‐day and 1‐year results from the ABSORB IV randomised trial . The Lance . 2018 ; 392 : 1530 ‐ 1540 . 10.1016/S0140-6736(18)32283-9 30266412

4 Kwok CS , Narain A , Pacha HM , et al. Readmissions to hospital after percutaneous coronary intervention: a systematic review and meta‐analysis of factors associated with readmissions . Cardiovascular Res Med . 2020 ; 21 : 375 ‐ 391 . 10.1016/j.carrev.2019.05.016 31196797

5 Kwok CS , Hulme W , Olier I , Holroyd E , Mamas MA . Review of early hospitalisation after percutaneous coronary intervention . Int J Cardiol . 2016 ; 227 : 370 ‐ 377 . 27839805 10.1016/j.ijcard.2016.11.050

6 Kwok CS , Potts J , Gulati M , et al. Effect of gender on unplanned readmissions after percutaneous coronary intervention (from the Nationwide readmissions database) . Am J Cardiol . 2018 ; 121 : 810 ‐ 817 . 29448978 10.1016/j.amjcard.2017.12.032

7 Kwok CS , Shah B , Al‐Suwaidi J , et al. Causes of unplanned readmissions after percutaneous coronary intervention: insights from the nationwide readmissions database . JACC Cardiovascular Intervention . 2019 ; 12 : 734 ‐ 748 . 10.1016/j.jcin.2019.02.007 PMC6843988 30928446

8 Kwok CS , Rao SV , Potts JE , et al. Burden of 30‐day readmissions after percutaneous coronary intervention in 833,344 patients in the United States: predictors, causes, and cost: insights from the Nationwide readmission database . JACC Cardiovascular Intervention . 2018 ; 11 : 665 ‐ 674 . 10.1016/j.jcin.2018.01.248 29622145

9 Neumann FJ , Sousa‐Uva M , Ahlsson A , et al. ESC Scientific Document Group. 2018 ESC/EACTS Guidelines on myocardial revascularization . Eur Heart J . 2019 ; 40 : 87 ‐ 165 .30165437

10 Patel MR , Calhoon JH , Dehmer GJ , et al. AATS/AHA/ASE/ASNC/SCAI/SCCT/STS 2016 appropriate use criteria for coronary revascularization in patients with acute coronary syndromes . J Am Coll Cardiol . 2017 ; 69 : 570 ‐ 591 . 28012615 10.1016/j.jacc.2016.10.034

11 Crea F , Bairey Merz CN , Beltrame JF , et al. Mechanisms and diagnostic evaluation of persistent or recurrent angina following percutaneous coronary revascularization . European Heart J . 2019 ; 40 ( 29 ): 2455 ‐ 2462 . 10.1093/eurheartj/ehy857 . 30608528

12 Mukherjee D . Coronary revascularization in the United States—patient characteristics and outcomes in 2020 . JAMA Netw Open . 2020 ; 3 ( 2 ): e1921322 . 32058547 10.1001/jamanetworkopen.2019.21322

13 Bairey Merz CN , Pepine CJ , Walsh MN , Fleg JL . Ischemia and no obstructive coronary artery disease (INOCA): developing evidence‐ based therapies and research agenda for the next decade . Circulation . 2017 ; 135 : 1075 ‐ 1092 . 28289007 10.1161/CIRCULATIONAHA.116.024534 PMC5385930

14 Ford TJ , Yii E , Sidik N , et al. Ischemia and no obstructive coronary artery disease prevalence and correlates of coronary Vasomotion disorders. Circulation: cardiovascular . Interventions . 2019 ; 12 : e008126 . 10.1161/CIRCINTERVENTIONS.119.008126 PMC6924940 31833416

15 Schüepp M , Ullmer E , Weinbacher M , et al. Chest pain early after percutaneous coronary intervention: incidence and relation to ECG changes, cardiac enzymes and follow‐up events . J Invasive Cardiol . 2001 ; 13 : 211 ‐ 216 . 11231646

16 Kini AS , Lee P , Mitre CA , Duffy ME , Sharma SK . Postprocedure chest pain after coronary stenting: implications on clinical restenosis . J Am Coll Cardiol . 2003 ; 41 : 33 ‐ 38 . 12570941 10.1016/s0735-1097(02)02617-7

17 Chang C , Chen Y , Ong E , et al. Chest pain after percutaneous coronary intervention in patients with stable angina . Clin Interv Aging . 2016 ; 11 : 1123 ‐ 1128 . 27574412 10.2147/CIA.S103605 PMC4993255

18 Garbarz E , Iung B , Lefevre G , et al. Frequency and prognostic value of cardiac troponin I elevation after coronary stenting . American J Cardiol . 1999 ; 84 : 515 ‐ 518 . 10.1016/s0002-9149(99)00369-0 10482147

19 La Vecchia L , Bedogni F , Finocchi G , et al. Troponin I and creatine kinase‐MB mass after elective coronary stenting . Coron Artery Dis . 1996 ; 7 : 535 ‐ 540 . 8913672 10.1097/00019501-199607000-00008

20 Selvanayagam JB , Porto I , Channon K , et al. Troponin elevation after percutaneous coronary intervention directly represents the extent of irreversible myocardial injury: insights from cardiovascular magnetic resonance imaging . Circulation . 2005 ; 111 : 1027 ‐ 1032 . 15723982 10.1161/01.CIR.0000156328.28485.AD

21 Vidula MK , McCarthy CP , Butala NM , et al. Causes and predictors of early readmission after percutaneous coronary intervention among patients discharged on oral anticoagulant therapy . PLoS One . 2018 ; 13 : e0205457 . 30379868 10.1371/journal.pone.0205457 PMC6209191

22 Tripathi A , Abbott JD , Fonarow GC , et al. Thirty‐day readmission rate and costs after percutaneous coronary intervention in the United States . Circulation: coronary interventions. 2017 ; 10 : e005925 . 10.1161/CIRCINTERVENTIONS.117.005925 29246918

23 Taha Y , Bhatt DL , Mukherjee D , et al. Early post‐percutaneous coronary intervention chest pain: a Nationwide survey on interventional Cardiologists' perspective . Cardiovasc Revasc Med . 2020 ; 21 ( 12 ): 1517 ‐ 1522 . 32563712 10.1016/j.carrev.2020.05.011

24 Demiryoguran NS , Karcioglu O , Topacoglu H , et al. Anxiety disorder in patients with non‐specific chest pain in the emergency setting . Emerg Med J . 2006 ; 23 : 99 ‐ 102 . 16439735 10.1136/emj.2005.025163 PMC2564064

25 McIIlvennan CK , Eapen ZJ , Allen LA . Hospital readmissions reduction program . Circulation . 2015 ; 131 : 1796 ‐ 1803 . 25986448 10.1161/CIRCULATIONAHA.114.010270 PMC4439931

26 Fothergill NJ , Hunt MT , Touquet R . Audit of patients with chest pain presenting to an accident and emergency department over a 6 month period . Arch Emerg Med . 1993 ; 10 : 155 ‐ 160 . 8216586 10.1136/emj.10.3.155 PMC1285980

27 Goodacre S , Cross E , Arnold J , Angelini K , Capewell S , Nicholl J . The healthcare burden of acute chest pain . Heart . 2005 ; 91 : 229 ‐ 230 . 15657244 10.1136/hrt.2003.027599 PMC1768669

28 Blatchford O , Capewell S , Murray S , Blatchford M . Emergency admissions in Glasgow: general practices vary despite adjustment for age, sex, and deprivation . British J General Practice . 1999 ; 49 : 551 ‐ 554 . PMC1313475 10621990

29 MacIntyre K , Murphy NF , Chalmers J , et al. Hospital burden of acute coronary syndromes: recent trends . Heart . 2006 ; 92 : 691 ‐ 692 . 16614290 10.1136/hrt.2005.068742 PMC1860941

30 Kwok CS , Parwani PJ , Fischman DL , et al. Nonspecific chest pain and 30‐day unplanned readmissions in the United States (from the Nationwide readmission database) . Am J Cardiol . 2019 ; 123 : 1343 ‐ 1350 . 30709600 10.1016/j.amjcard.2019.01.012

31 Muñoz M , Acheson AG , Auerbach M , et al. International consensus statement on the peri‐operative management of anaemia and iron deficiency . Anaesthesia . 2017 ; 72 : 233 ‐ 247 . 27996086 10.1111/anae.13773

32 Mjåland O , Høgevold HE , Buanes T . Standard preoperative assessment can improve outcome after cholecystectomy . Eur J Surg . 2001 ; 166 : 129 ‐ 135 . 10.1080/110241500750009474 10724490

33 Ford TJ , Stanley B , Good R , et al. Stratified medical therapy using invasive coronary function testing in angina: the CorMicA trial . J Am Coll Cardiol . 2018 ; 72 : 2841 ‐ 2855 . 30266608 10.1016/j.jacc.2018.09.006

34 Tanguturi VK , Temin E , Yeh RW , et al. Clinical interventions to reduce preventable hospital readmission after percutaneous coronary intervention . Circ Cardiovasc Qual Outcomes . 2016 ; 9 : 600 ‐ 604 . 27553598 10.1161/CIRCOUTCOMES.116.003086

TABLE A1
Classification of clinic classification software codes for readmissions causes

Causes of readmissionCCS codeDiagnosis
Respiratory127Chronic obstructive pulmonary disease and bronchiectasis
128Asthma
130Pleurisy, pneumothorax, pulmonary collapse
131Respiratory failure, insufficiency and arrest
132Lung disease due to external agents
133Other lower respiratory disease
134Other upper respiratory disease
221Respiratory distress syndrome
Infection1Tuberculosis
2Septicemia
3Bacterial infection
4Mycoses
5HIV infection
6Hepatitis
7Viral infection
8Other infection
9Sexually transmitted infection
76Meningitis
77Encephalitis
78Other CNS infection and poliomyelitis
90Inflammation or infection of eye
122Pneumonia
123Influenza
124Acute and chronic tonsillitis
125Acute bronchitis
126Other upper respiratory infections
129Aspiration pneumonitis
135Intestinal infection
197Skin and subcutaneous tissue infections
201Infective arthritis and osteomyelitis (except that caused by tuberculosis or sexually transmitted disease)
Bleeding60Acute posthaemorrhagic anaemia
153Gastrointestinal haemorrhage
182Haemorrhage during pregnancy; abrutio placenta; placenta previa
Peripheral vascular disease114Peripheral and visceral atherosclerosis
115Aortic, peripheral and visceral artery aneurysms
116Aortic and peripheral arterial embolism or thrombosis
117Other circulatory disease
118Phlebitis, thrombophlebitis and thromboembolism
119Varicose veins of lower extremities
Genitourinary159Urinary tract infection
160Calculus of the urinary tract
161Other diseases of kidney and ureters
162Other diseases of bladder and urethra
163Genitourinary symptoms and ill‐defined conditions
164Hyperplasia of prostate
165Inflammatory conditions of the male genital organs
166Other male genital disorders
170Prolapse of female genital organs
175Other female genital disorders
215Genitourinary congenital anomalies
Renal disease156Nephritis; nephrosis; renal sclerosis
157Acute and unspecified renal failure
158Chronic kidney disease
Gastrointestinal138Esophageal disorders
139Gastroduodenal ulcer (except haemorrhage)
140Gastritis and duodenitis
141Other disorders of stomach and duodenum
142Appendicitis and other appendiceal conditions
143Abdominal hernia
144Regional enteritis and ulcerative colitis
145Intestinal obstruction without hernia
146Diverticulosis and diverticulitis
147Anal and rectal conditions
148Peritonitis and intestinal abscess
149Biliary tract disease
150Liver disease; alcohol‐related
151Other liver diseases
152Pancreatic disorders (not diabetes)
154Noninfectious gastroenteritis
155Other gastrointestinal disorders
214Digestive congenital anomalies
222Haemolytic jaundice and perinatal jaundice
250Nausea and vomiting
251Abdominal pain
TIA/stroke109Acute cerebrovascular disease
110Occlusion of stenosis of precerebral arteries
111Other and ill‐defined cerebrovascular disease
112Transient cerebral ischemia
113Late effects of cerebrovascular disease
Trauma207Pathological fracture
225Joint disorders and dislocations; trauma‐related
226Fracture of neck of femur (hip)
227Spinal cord injury
228Skull and face fractures
229Fracture of upper limb
230Fracture of lower limb
231Other fractures
232Sprains and strains
233Intracranial injury
234Crushing injury or internal injury
235Open wounds of head; neck; and trunk
236Open wounds of extremities
239Superficial injury; contusion
244Other injuries and conditions due to external causes
260All (external causes of injury and poisoning)
Endocrine/metabolic48Thyroid disorders
49Diabetes mellitus without complication
50Diabetes mellitus with complication
51Other endocrine disorders
53Disorders of lipid metabolism
58Other nutritional and endocrine/metabolic disorders
186Diabetes or abnormal glucose tolerance complicating pregnancy; childbirth; or the puerperium
Neuropsychiatric650Adjustment disorders
651Anxiety disorders
652Attention‐deficit, conduct, and disruptive behavior disorders
653Delirium, dementia, and amnestic and other cognitive disorders
654Developmental disorders
655Disorders usually diagnosed in infancy and childhood or adolescence
656Impulse control disorders, NEC
657Mood disorders
658Personality disorders
659Schizophrenia and other psychotic disorders
660Alcohol‐related disorders
661Substance‐related disorders
662Suicide and intentional self‐inflicted injury
663Screening and history of mental health and substance abuse codes
670Miscellaneous mental health disorders
79Parkinson's disease
80Multiple sclerosis
81Other hereditary and degenerative nervous system conditions
82Paralysis
83Epilepsy, convulsions
84Headache including migraine
85Coma, stupor and brain damage
95Other nervous system disorders
216Nervous system congenital anomalies
650Adjustment disorders
651Anxiety disorders
652Attention‐deficit, conduct, and disruptive behavior disorders
653Delirium, dementia, and amnestic and other cognitive disorders
654Developmental disorders
655Disorders usually diagnosed in infancy and childhood or adolescence
656Impulse control disorders
657Mood disorders
658Personality disorders
659Schizophrenia and other psychotic disorders
660Alcohol‐related disorders
661Substance‐related disorders
662Suicide and intentional self‐inflicted injury
663Screening and history of mental health and substance abuse codes
670Miscellaneous mental health disorders
Hematological/neoplastic11Cancer of head and neck
12Cancer of esophagus
13Cancer of stomach
14Cancer of colon
15Cancer of rectum and anus
16Cancer of liver and intrahepatic bile ducts
17Cancer of pancreas
18Cancer of other gastrointestinal organs, peritoneum
19Cancer of bronchus, lung
20Cancer of other respiratory and intrathoracic
21Cancer of bone and connective tissue
22Melanoma of skin
23Other non‐epithelial cancer of skin
24Cancer of breast
25Cancer of uterus
26Cancer of cervix
27Cancer of ovary
28Cancer of other female genital organs
29Cancer of prostate
30Cancer of testis
31Cancer of other male genital organs
32Cancer of bladder
33Cancer of kidney and renal pelvis
34Cancer of other urinary organs
35Cancer of brain and nervous system
36Cancer of thyroid
37Hodgkin's disease
38Non‐Hodgkin's lymphoma
39Leukemias
40Multiple myeloma
41Cancer, other and unspecified primary
42Secondary malignancies
43Malignant neoplasm without specification of site
44Neoplasm of unspecified nature or uncertain behavior
46Benign neoplasm of uterus
47Other and unspecified benign neoplasm
59Deficiency and other anaemias
61Sickle cell anaemia
62Coagulation and haemorrhagic disorders
63Disease of white blood cells
64Other hematologic conditions
Rheumatology problem54Gout and other crystal arthropathies
Opthalmology problem86Cataract
87Retinal detachment defects, vascular occlusion and retinopathy
88Glaucoma
89Blindness and vision defects
91Other eye disorders
ENT problem92Otitis media and related conditions
93Conditions associate with dizziness or vertigo
94Other ear and sense organ disorder
Non‐specific chest pain102Non‐specific chest pain
Oral health problem136Disorders of teeth and jaw
137Diseases of mouth; excluding dental
Obstetric admission including pregnancy174Female infertility
176Contraceptive and procreative management
177Spontaneous abortion
178Induced abortion
179Postabortion complication
180Ectopic pregnancy
181Other complications of pregnancy
184Early or threatened labor
185Prolonged pregnancy
187Malposition; malpresentation
188Fetopelvic disproportion; obstruction
189Previous C‐section
190Fetal distress and abnormal forces of labor
191Polyhydramnios and other problems of amniotic cavity
192Umbilical cord complication
193OB‐related trauma to perineum and vulva
194Forceps delivery
195Other complications of birth; puerperium affecting management of mother
196Other pregnancy and deliver including normal
218Liveborn
219Short gestation; low birth weight; and fetal growth retardation
220Intrauterine hypoxia and birth asphyxia
223Birth trauma
224Other perinatal conditions
Dermatology problem198Other inflammatory condition of skin
199Chronic ulcer of skin
200Other skin disorders
Poisoning241Poisoning by psychotrophic agents
242Poisoning by other medication and drugs
243Poisoning by nonmedical substances
Syncope245Syncope
Other non‐cardiac10Immunization and screening for infectious disease
45Maintenance chemotherapy, radiotherapy
52Nutritional deficiencies
55Fluid and electrolyte disorders
56Cystic fibrosis
57Immunity disorder
120Hemorrhoids
121Other diseases of veins and lymphatics
167Nonmalignant breast conditions
168Inflammatory disease of female pelvic organs
169Endometriosis
172Ovarian cyst
173Menopausal disorders
202Rheumatoid arthritis and related disease
203Osteoarthritis
204Other non‐traumatic joint disorders
205Spondylosis; intervertebral disc disorders; other back problems
206Osteoporosis
208Acquired foot deformities
209Other acquired deformities
210Systemic lupus erythematosus and connective tissue disorders
211Other connective tissue disease
212Other bone disease and musculoskeletal deformities
217Other congenital anomalies
237Complication of device; implant or graft
238Complications of surgical procedure or medical care
240Burns
246Fever of unknown origin
247Lymphadenitis
248Gangrene
252Malaise and fatigue
253Allergic reactions
254Rehabilitation care; fitting of prostheses; and adjustment of devices
255Administrative/social admission
256Medical examination/evaluation
257Other aftercare
258Other screening for suspected conditions (not mental disorders or infectious disease)
259Residual codes; unclassified
Heart failure108Congestive heart failure non‐hypertensive
Arrhythmia106Cardiac dysrhythmias
107Cardiac arrest and ventricular fibrillation
Conduction disorder105Conduction disorders
Valve disorders96Heart valve disorder
Hyper/hypotension98Essential hypertension
99Hypertension with complications and secondary hypertension
183Hypertension complicating pregnancy; childbirth and the puerperium
249Shock
Pericarditis97Peri‐, endo‐ and myocarditis, cardiomyopathy
Coronary artery disease including angina101Coronary atherosclerosis and other heart disease includes angina
Acute myocardial infarction100Acute myocardial infarction
Others (cardiac)103Pulmonary heart disease
104Other and ill‐defined heart disease
213Cardiac and circulatory congenital anomalies

ИП Урсолов Владлен Сергеевич

ИНН 500118482352 · ОГРНИП 314500117700049

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