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Socioeconomic Status, Secondary Prevention Activities and Recurrence After a Myocardial Infarction

Secondary Prevention Treatments and Activities Post Myocardial Infarction Underlying the Risk of Recurrent Hard Cardiovascular Outcomes Associated With Socioeconomic Status

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04199663
Enrollment
30191
Registered
2019-12-16
Start date
2006-01-01
Completion date
Unknown
Last updated
2020-02-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiovascular Disease, Myocardial Infarction, Secondary Prevention, Socioeconomic Status, Stroke

Brief summary

This is a nationwide cohort study on real-world patients (n≈30,000) surviving a first myocardial infarction (MI) 2006-2013 and alive to attend a routine 1-year follow-up. Associations between Socioeconomic Status (SES) and secondary preventive actions (SPAs) throughout the first year is studied and assessed as possible mechanisms underlying the increased risk of a first recurrent hard cardiocvascular (CV) outcome, recurrent atherosclerotic cardiovascular disease (rASCVD), in patients with low Socioeconomic Status during long-term follow-up (2006-2018).

Interventions

None listed

Sponsors

Karolinska Institutet
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 76 Years

Inclusion criteria

* Swedish resident * Alive and registered in The Swedish Websystem for Enhancement and Development of Evidence based care in Heart disease Evaluated According to Recommended Therapies (SWEDEHEART)'s secondary prevention subregistry between 1 January 2006 and 31 December 2013 at the 1-year-revisit

Exclusion criteria

* Age \>76 years at baseline * Missing data for disposable household income * History of MI, stroke, coronary artery bypass graft (CABG), or percutaneous coronary intervention (PCI) prior to the index MI * Not present in initial care registry (RiksHIA) * Date of index MI before 2004 or missing * revisit outside 13±2 month window post-MI

Design outcomes

Primary

MeasureTime frameDescription
first recurrent atherosclerotic cardiovascular disease event (rASCVD)from date of 1-year visit post-MI (baseline) until date of outcome, censoring or study end (2018)composite outcome including non-fatal MI (I210-I214, I219, I220, I221, I228 or I229) or coronary heart disease death (CHD) (I210-I214, I219, I220, I221, I228, I229, I461 or I469) or fatal or non-fatal ischemic stroke (I630-I635, I638 or I639) according to the International Classification of Diseases 10th edition (ICD-10)

Other

MeasureTime frameDescription
Goal: LDL-C goalat 1-year revisitattained LDL-C level below treatment target
Goal: Blood pressure goalat 1-year revisitattained blood pressure levels below treatment target
Goal: smoking cessationat 1-year revisitPatients being current smokers at their initial care who successfully quit smoking.
Goal: physical activityat 1-year revisitreported \>30 minutes of physical activity ≥5 times a week
Goal: statin treatmentat 1-year revisiton statin treatment 1 year after the index MI
Goal: Renin-angiotensin-aldosteron system (RAAS)-inhibitionat 1-year revisitPatients with congestive heart failure, diabetes or hypertension at the index Mi on treatment with angiotensin converting enzyme inhibitor or angiotensin receptor blocker.
Goal: HbA1c goalat 1-year revisitPatients with diabetes with attained HbA1c treatment target
SPA: cardiac rehabilitation programduring 1st year after initial careparticipation in structured program after the index MI
SPA: diet courseduring 1st year after initial careparticipation in course after the index MI
SPA: statin intensity increase2 months or 1 year after initial carestatin intensity increase decided at routine revisits (Dosages categorized into high (Rosuvastatin 20-40 mg or Atorvastatin 40-80 mg), moderate (Rosuvastatin 5-10 mg, Atorvastatin 10-20 mg, or Simvastatin 20-40 mg) and low (Simvastatin 10 mg))
Goal: physical training programat 1-year revisitparticipated in organized physical training program after the initial care
SPA: LDL-C reduction2 months and 1 year after initial careLDL-C reduction between routine revisits
SPA: lipid monitoring2 months or 1 year after initial careBlood lipid panel measured
SPA: type of follow-up2 month revisitdecided follow-up by office revisit or by phone
SPA: reperfusioninitial caretype of reperfusion treatment chosen in STEMI and NSTEMI
SPA: revascularizedinitial careachieved complete revascularization in STEMI and NSTEMI
SPA: staged procedureinitial careDecision on continued invasive procedures at a later stage
SPA: smoking cessation counseling2 months or 1 year after initial carereceived through cessation program or counseling
SPA: HbA1c monitoringduring initial care, at 2 months and 1 year after initial carePatients with diabetes at initial care having their HbA1c measured at least twice
SPA: Anti-stress program1 year after initial carePatients reporting anxiety or sadness participating in anti-stress program
SPA: counter-metabolic syndrome actions2 months or 1 year after initial carePatients with the metabolic syndrome participating in physical training and diet course or in cardiac rehabilitation program
SPA: high intensity statinsat 1-year revisiton high intensity statin treatment (Rosuvastatin 20-40 mg or Atorvastatin 40-80 mg)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026