Int J Angiol 2014; 23(04): 275-280
DOI: 10.1055/s-0033-1349163
Case Report
Thieme Medical Publishers 333 Seventh Avenue, New York, NY 10001, USA.

Spontaneous Coronary Artery Dissection and Hemodynamic Instability: Can Emergent PCI Be Life Saving? Report of Two Cases and Literature Review

Abdel Rahman A. Al Emam
1   Department of Internal Medicine, University Of Texas Medical Branch, Galveston, Texas
,
Ahmed Almomani
1   Department of Internal Medicine, University Of Texas Medical Branch, Galveston, Texas
,
Syed A. Gilani
2   Division of Cardiology, University Of Texas Medical Branch, Galveston, Texas
› Author Affiliations
Further Information

Publication History

Publication Date:
17 February 2014 (online)

Abstract

Spontaneous coronary artery dissection (SCAD) is a rare cause of acute coronary syndrome. It occurs predominantly among younger females and typically in the absence of atherosclerotic coronary artery disease. It is associated with peripartum period, connective tissue disorders, vasculitides, and extreme exertion. Presentations vary greatly, and this condition can be fatal. Given its rarity, there are no guidelines for management of SCAD. We present the cases of two female patients, with no coronary artery disease risk factors or recent pregnancy, who were presented with non-ST elevation myocardial infarction (NSTEMI) and ST elevation myocardial infarction (STEMI), respectively, secondary to SCAD. Both had excellent outcome after emergent percutaneous intervention. Our first patient was presented with NSTEMI with ongoing chest pain and dynamic electrocardiogram (ECG). Emergent left heart catheterization was significant for first obtuse marginal (OM1) dissection, confirmed by optical coherence tomography. Percutaneous coronary intervention (PCI) with two bare metal stents was performed with resolution of symptoms and ECG changes. The second patient is known to have syndrome, presented with STEMI and emergent coronary angiography showed left anterior descending dissection with intramural hematoma confirmed by intravascular ultrasound and treated with a drug-eluting stent with resolution of symptoms and ST changes. Her hospital course was complicated by post–myocardial infarction pericarditis that was improved with colchicine. Both the patients were observed in the coronary care unit for 24 hours. Both remained asymptomatic at 6-month follow-up. SCAD is a rare cause of acute coronary syndrome. In patients with early presentation, limited disease, and ongoing symptoms, emergent cardiac catheterization with percutaneous intervention has excellent outcome. More studies are needed to establish evidence-based management guidelines.

 
  • References

  • 1 Pretty HC. Dissecting aneurysm of coronary artery in a woman aged 42. BMJ 1931; 1: 667
  • 2 Verma PK, Sandhu MS, Mittal BR , et al. Large spontaneous coronary artery dissections-a study of three cases, literature review, and possible therapeutic strategies. Angiology 2004; 55 (3) 309-318
  • 3 Azzarelli S, Fiscella D, Amico F, Giacoppo M, Argentino V, Fiscella A. Multivessel spontaneous coronary artery dissection in a postpartum woman treated with multiple drug-eluting stents. J Cardiovasc Med (Hagerstown) 2009; 10 (4) 340-343
  • 4 Sherrid MV, Mieres J, Mogtader A, Menezes N, Steinberg G. Onset during exercise of spontaneous coronary artery dissection and sudden death. Occurrence in a trained athlete: case report and review of prior cases. Chest 1995; 108 (1) 284-287
  • 5 Tweet MS, Hayes SN, Pitta SR , et al. Clinical features, management, and prognosis of spontaneous coronary artery dissection. Circulation 2012; 126 (5) 579-588
  • 6 Auer J, Punzengruber C, Berent R , et al. Spontaneous coronary artery dissection involving the left main stem: assessment by intravascular ultrasound. Heart 2004; 90 (7) e39
  • 7 Jorgensen MB, Aharonian V, Mansukhani P, Mahrer PR. Spontaneous coronary dissection: a cluster of cases with this rare finding. Am Heart J 1994; 127 (5) 1382-1387
  • 8 Butler R, Webster MWI, Davies G , et al. Spontaneous dissection of native coronary arteries. Heart 2005; 91 (2) 223-224
  • 9 Klein J. Hakimian j, Makaryus A. Spontaneous Right Coronary Artery dissection. Tex Heart Inst J 2012; 39 (1) 95-98
  • 10 Cheung S, Mithani V, Watson RM. Healing of spontaneous coronary dissection in the context of glycoprotein IIB/IIIA inhibitor therapy: a case report. Catheter Cardiovasc Interv 2000; 51 (1) 95-100
  • 11 Schmid J, Auer J. Spontaneous coronary artery dissection in a young man - case report. J Cardiothorac Surg 2011; 6: 22
  • 12 Juszczyk M, Marnejon T, Hoffman DA. Spontaneous coronary artery dissection postpartum. J Invasive Cardiol 2004; 16 (9) 524-526
  • 13 Wain-Hobson J, Roule V, Dahdouh Z, Sabatier R, Lognoné T, Grollier G. Spontaneous coronary artery dissection: one entity with several therapeutic options. Cardiovasc Revasc Med 2012; 13 (3) e1-e4
  • 14 Missouris CG, Ring A, Ward D. A young woman with chest pain. Heart 2000; 84 (6) E12
  • 15 Roig S, Gómez JA, Fiol M , et al. Spontaneous coronary artery dissection causing acute coronary syndrome: an early diagnosis implies a good prognosis. Am J Emerg Med 2003; 21 (7) 549-551