Cardiogenic shock primary prevention: Difference between revisions
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==Overview== | ==Overview== | ||
The most common causes of [[cardiogenic shock]] remain [[MI]]. The [[American College of Cardiology]] and [[American Heart Association]], in collaboration with the [[Canadian Cardiovascular Society]], have issued an update of the 2004 guideline for the management of patients with [[ST-segment elevation myocardial infarction]]. The [[American Academy of Family Physicians]] endorses and accepts this guideline as its policy. Early recognition and prompt initiation of [[reperfusion therapy]] remains the cornerstone of management of [[ST-segment elevation myocardial infarction]]. [[Aspirin]] should be given to symptomatic patients. [[Beta blockers]] should be used cautiously in the acute setting because they may increase the risk of [[cardiogenic shock]] and [[death]]. The combination of [[clopidogrel]] and [[aspirin]] is indicated in patients who have had [[ST-segment elevation myocardial infarction]]. A stepped care approach to analgesia for [[musculoskeletal]] [[pain]] in patients with [[coronary heart disease]] is provided. [[Cyclooxygenase inhibitors]] and [[nonsteroidal anti-inflammatory drugs]] increase [[mortality]] risk and should be avoided. Primary prevention is important to reduce the burden of heart disease. Secondary prevention interventions are critically important to prevent recurrent events in patients who survive. Available data indicate that the development of shock after hospital admission with acute MI is as common as [[cardiogenic shock]] on presentation. Because of the > 50% [[mortality]] associated with both of these conditions, the most favorable means of making an impact on [[shock]] [[mortality]] is to prevent its development. Therefore, effective therapy for shock must include a [[prevention]] strategy. In the [[GUSTO study]], 70% of patients who developed [[cardiogenic shock]] after admission were Killip class I on admission, and of the remaining patients most were in Killip class II with only mild heart failure. For this reason, other clinical clues must be used to recognize patients at high risk for developing shock. The development of [[tachycardia]] or [[evidence]] of [[peripheral]] [[vasoconstriction]] are early clinical signs ofthe [["preshock"]] state. Data from the [[Secondary Prevention Reinfarction Israel Nifedipine Trial]] ([[SPRINT]]) study") suggest that the presence of [[diabetes]], history of [[angina]], [[peripheral vascular]] or [[cerebrovascular disease]], prior [[MI]], and [[female]] [[gender]] are all risks for development of shock in Killip class I patients with acute infarction. These investigators estimated a 35% probability of developing shock if all six of these factors were present on admission. In addition to these clinical factors obtained from the history and physical examination, diagnostic studies such as early two-dimensional [[echocardiography]] may be helpful in evaluating selected patients. In a consecutive series of over 80 patients, Gibson etnl. stratified patients with acute [[MI]] into two groups: those with [[asynergy]] in the [[infarct zone]] only and those with [[asynergy]] in the [[infarct]] zone plus a remote zone. They found that the latter group had a significantly higher incidence of [[cardiogenic shock]] (34 vs. 8%, p = 0.01), as well as higher rates of [[death]], [[reinfarction]], and Killip class progression than patients with [[asynergy]] in the [[infarct]] zone only. It is likely that all of the above information is helpful in identifying patients with [[triple-vessel]] [[coronary artery disease]] in an otherwise low-risk clinical group (i.e., patients without [[heart failure]] on admission). | |||
==Primary prevention== | ==Primary prevention== | ||
Attending to the definition of [[primary prevention]], namely the group of measures that aim to avoid the development of a disease state (preventive measures) and considering the fact that [[left ventricular failure]] following [[acute MI]] is the most common cause of cardiogenic shock, these patients should undergo [[primary prevention]] of [[myocardial infarction]].<ref name="pmid24222015">{{cite journal| author=Eckel RH, Jakicic JM, Ard JD, Hubbard VS, de Jesus JM, Lee IM et al.| title=2013 AHA/ACC Guideline on Lifestyle Management to Reduce Cardiovascular Risk: A Report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines. | journal=Circulation | year= 2013 | volume= | issue= | pages= | pmid=24222015 | doi=10.1161/01.cir.0000437740.48606.d1 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=24222015 }} </ref> | Attending to the definition of [[primary prevention]], namely the group of measures that aim to avoid the development of a disease state (preventive measures) and considering the fact that [[left ventricular failure]] following [[acute MI]] is the most common cause of cardiogenic shock, these patients should undergo [[primary prevention]] of [[myocardial infarction]].<ref name="pmid24222015">{{cite journal| author=Eckel RH, Jakicic JM, Ard JD, Hubbard VS, de Jesus JM, Lee IM et al.| title=2013 AHA/ACC Guideline on Lifestyle Management to Reduce Cardiovascular Risk: A Report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines. | journal=Circulation | year= 2013 | volume= | issue= | pages= | pmid=24222015 | doi=10.1161/01.cir.0000437740.48606.d1 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=24222015 }} </ref>The ACC/AHA guideline stresses the importance of primary prevention. The consensus opinion is that a risk factor assessment for CHD should be performed every three to five years in all patients. Risk factors include smoking, diabetes, hypercholesterolemia, hypertension, family history, age, and sex. In patients with two or more major risk factors, calculation of a 10-year coronary artery disease risk score is recommended to assess the need for primary prevention.3 The risk score can also be an effective tool to start a dialogue with patients about lifestyle change.The American College of Cardiology (ACC) and American Heart Association (AHA) have updated their 2004 guideline1 for the management of patients with ST-segment elevation myocardial infarction (STEMI). The updated guideline was developed in collaboration with the Canadian Cardiovascular Society and published in 2008. The American Academy of Family Physicians endorses and accepts this guideline as its policy. This review summarizes the key recommendations as they apply to the prevention of coronary heart disease (CHD), acute management of STEMI, and secondary prevention of recurrent events. | ||
==References== | ==References== | ||
Latest revision as of 18:37, 8 January 2020
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: João André Alves Silva, M.D. [2] Syed Musadiq Ali M.B.B.S.[3]
Overview
The most common causes of cardiogenic shock remain MI. The American College of Cardiology and American Heart Association, in collaboration with the Canadian Cardiovascular Society, have issued an update of the 2004 guideline for the management of patients with ST-segment elevation myocardial infarction. The American Academy of Family Physicians endorses and accepts this guideline as its policy. Early recognition and prompt initiation of reperfusion therapy remains the cornerstone of management of ST-segment elevation myocardial infarction. Aspirin should be given to symptomatic patients. Beta blockers should be used cautiously in the acute setting because they may increase the risk of cardiogenic shock and death. The combination of clopidogrel and aspirin is indicated in patients who have had ST-segment elevation myocardial infarction. A stepped care approach to analgesia for musculoskeletal pain in patients with coronary heart disease is provided. Cyclooxygenase inhibitors and nonsteroidal anti-inflammatory drugs increase mortality risk and should be avoided. Primary prevention is important to reduce the burden of heart disease. Secondary prevention interventions are critically important to prevent recurrent events in patients who survive. Available data indicate that the development of shock after hospital admission with acute MI is as common as cardiogenic shock on presentation. Because of the > 50% mortality associated with both of these conditions, the most favorable means of making an impact on shock mortality is to prevent its development. Therefore, effective therapy for shock must include a prevention strategy. In the GUSTO study, 70% of patients who developed cardiogenic shock after admission were Killip class I on admission, and of the remaining patients most were in Killip class II with only mild heart failure. For this reason, other clinical clues must be used to recognize patients at high risk for developing shock. The development of tachycardia or evidence of peripheral vasoconstriction are early clinical signs ofthe "preshock" state. Data from the Secondary Prevention Reinfarction Israel Nifedipine Trial (SPRINT) study") suggest that the presence of diabetes, history of angina, peripheral vascular or cerebrovascular disease, prior MI, and female gender are all risks for development of shock in Killip class I patients with acute infarction. These investigators estimated a 35% probability of developing shock if all six of these factors were present on admission. In addition to these clinical factors obtained from the history and physical examination, diagnostic studies such as early two-dimensional echocardiography may be helpful in evaluating selected patients. In a consecutive series of over 80 patients, Gibson etnl. stratified patients with acute MI into two groups: those with asynergy in the infarct zone only and those with asynergy in the infarct zone plus a remote zone. They found that the latter group had a significantly higher incidence of cardiogenic shock (34 vs. 8%, p = 0.01), as well as higher rates of death, reinfarction, and Killip class progression than patients with asynergy in the infarct zone only. It is likely that all of the above information is helpful in identifying patients with triple-vessel coronary artery disease in an otherwise low-risk clinical group (i.e., patients without heart failure on admission).
Primary prevention
Attending to the definition of primary prevention, namely the group of measures that aim to avoid the development of a disease state (preventive measures) and considering the fact that left ventricular failure following acute MI is the most common cause of cardiogenic shock, these patients should undergo primary prevention of myocardial infarction.[1]The ACC/AHA guideline stresses the importance of primary prevention. The consensus opinion is that a risk factor assessment for CHD should be performed every three to five years in all patients. Risk factors include smoking, diabetes, hypercholesterolemia, hypertension, family history, age, and sex. In patients with two or more major risk factors, calculation of a 10-year coronary artery disease risk score is recommended to assess the need for primary prevention.3 The risk score can also be an effective tool to start a dialogue with patients about lifestyle change.The American College of Cardiology (ACC) and American Heart Association (AHA) have updated their 2004 guideline1 for the management of patients with ST-segment elevation myocardial infarction (STEMI). The updated guideline was developed in collaboration with the Canadian Cardiovascular Society and published in 2008. The American Academy of Family Physicians endorses and accepts this guideline as its policy. This review summarizes the key recommendations as they apply to the prevention of coronary heart disease (CHD), acute management of STEMI, and secondary prevention of recurrent events.
References
- ↑ Eckel RH, Jakicic JM, Ard JD, Hubbard VS, de Jesus JM, Lee IM; et al. (2013). "2013 AHA/ACC Guideline on Lifestyle Management to Reduce Cardiovascular Risk: A Report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines". Circulation. doi:10.1161/01.cir.0000437740.48606.d1. PMID 24222015.