Long Term Clinical Outcomes of Treatment of In-Stent Restenosis With Drug Eluting Stents

Long Term Clinical Outcomes of Treatment of In-Stent Restenosis With Drug Eluting Stents

Abstracts 8 LONG TERM CLINICAL OUTCOMES OF TREATMENT OF IN-STENT RESTENOSIS WITH DRUG ELUTING STENTS S Cherian 1,∗ , C Devlin 2 Sebastian 2 , A Pur...

53KB Sizes 1 Downloads 40 Views

Abstracts

8 LONG TERM CLINICAL OUTCOMES OF TREATMENT OF IN-STENT RESTENOSIS WITH DRUG ELUTING STENTS S Cherian 1,∗ , C Devlin 2

Sebastian 2 , A

Puri 2 , M

Liang 2 , G

1 University 2 Waikato

of Adelaide, Adelaide, Australia Hospital, Hamilton, New Zealand

Background: Optimal treatment for instent restenosis (ISR) is an enigma, with drug eluting stents (DES) currently regarded as the treatment of choice. We report the clinical outcome of patients undergoing treatment of ISR with DES over a 5-year period among other treatment modalities. Method: Patients with symptomatic ISR (diameter stenosis of >50%) from January 2003 to January 2008 were analysed for long term clinical outcomes of Readmission MI and Death. Results: 215 ISR lesions were recorded in 207 patients. 199 (92.6%) were bare metal stent (BMS) ISR and 16 (7.4%) were DES ISR. The mean follow up was 30.6 ± 17.5 months. The ISR lesion classification was Type I in 67%; II in 16%; III in 8% and IV in 9%. Treatment of ISR was DES in 130 (60.5%), BMS in 12 (5.6%), Plain Balloon Angioplasty (POBA) in 27 (12.6%), CABG in 17 (7.9%) and medical in 29 (13.5%) patients. A total of 24 deaths occurred in the group. Treatment/ Outcomes

ReReMI restenosis admission

DES (n = 130) 13 (10%) BMS (n = 12) 2 (17%) POBA (n = 27) 5 (18%) CABG (n = 17) 0 Medical (n = 29) 3 (10%)

24 (19%) 4 (33%) 8 (30%) 2 (12%) 6 (21%)

10 (8%) 2 (17%) 3 (11%) 1 (6%) 4 (14%)

Death

Cardiac Death

Death, MI, Readmision

12 (9%) 4 (33%) 4 (15%) 2 (12%) 2 (7%)

5 (4%) 2 (17%) 3 (11%) 2 (12%) 2 (7%)

46 (35%) 10 (83%) 15 (56%) 5 (29%) 12 (41%)

Conclusion: Management of ISR remains problematic, with ongoing morbidity and mortality, regardless of treatment with DES. doi:10.1016/j.hlc.2009.04.011 9 NURSE-LED OUTPATIENT CHEST PAIN CLINIC: SAFETY AND EFFICACY KL Chow ∗ , L Ball, E Griner, C Edwards, G Armstrong North Shore Hospital, Auckland, New Zealand Background: We established an outpatient nurse-led chest pain clinic to assess chest pain referrals from GPs. The aim was to reduce waiting times and to decrease utilisation of resources and personnel. This novel approach was evaluated for safety and efficacy. Methods: Patients judged to be at low-medium risk of coronary disease filled out a questionnaire. The nurse then took a history, carried out a cardiovascular examination and undertook treadmill exercise ECG. This entire evaluation, together with the planning of subsequent management, was carried out by one nurse without assistance. A cardiologist was available for advice but did

S5

not routinely see the patients or discuss management. The first 149 patients seen at the clinic were followed up at 6 months by telephone and review of hospital records. Results: The nurse’s final diagnosis was non-cardiac chest symptoms in 60%, possible angina in 13%, probable angina in 22% and invalid entry in 5%. Final disposition was discharge in 55%, coronary angiography in 20%, echocardiography in 7%, stress imaging study in 8%, other test in 3%. At six-month follow-up, two patients had further unplanned medical attendances. Study Endpoints: There were no deaths, myocardial infarctions or positive stress imaging studies. Admission with angina occurred in 3% of patients, all of whom had been wait-listed for coronary angiography. Coronary stenosis >70% occurred in 11% of the total patients, i.e. 59% of those referred for coronary angiography. Conclusions: Nurse-led outpatient chest pain evaluation appears safe and efficacious at 6-month follow-up. doi:10.1016/j.hlc.2009.04.012 10 QUANTITATIVE EVALUATION OF AORTIC REGURGITATION IN ASYMPTOMATIC PATIENTS USING CARDIAC MRI PREDICTS LONG-TERM OUTCOME JP Christiansen ∗ , C Edwards, G Armstrong, H Patel, T Scott, HH Hart Cardiovascular Division, North Shore Hospital, Auckland, New Zealand Background: Aortic valve replacement (AVR) after LV decompensation may result in suboptimal outcomes. Timing of AVR in asymptomatic patients with aortic regurgitation (AR) is currently determined by LV dimensions. Cardiac MRI (CMR) measures ventricular volumes, regurgitant volume (Rvol ) and fraction (Rfr ) reproducibly. We assessed the value of quantitative CMR in predicting prognosis in significant AR. Methods: Twenty-seven asymptomatic patients with isolated moderate or greater AR were identified at initial CMR. Ventricular and regurgitant volumes were quantified. Clinical records were subsequently reviewed for up to 5 years follow-up. Death or AVR were the primary endpoint. CMR results were not used to determine timing of AVR. Results: Seven patients (26%) underwent AVR during follow-up, all for the development of important symptoms. There was one death in a patient who was declined surgery. Average follow-up was 3 years. Average Rvol was 39 ± 21 mL and Rfr 25 ± 10%. On ROC analysis, Rvol ≥ 45 mL and Rfr > 28% predicted the need for AVR with 78% sensitivity and 83% specificity (Area = 0.95). Rvol and Rfr (0.83) were more predictive of AVR than indexed LVEDV (0.81), LVESV (0.73) and EF% (0.51). Kaplan–Meier analysis demonstrates the significant long-term risk of AVR/death in patients with Rvol ≥ 45 mL (p < 0.05) (Graph shown).

ABSTRACTS

Heart, Lung and Circulation 2009;18S:S1–S31