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CARDIOVASCULAR JOURNAL OF AFRICA • Volume 32, No 1, January/February 2021

4

AFRICA

Trust the

!

Original

S3 ISMO-20 R/7.1.4/136. Isosorbide-5-mononitrate 20 mg/tablet.

For full prescribing information, please refer to package insert.

Pharmaco Distribution (Pty) Ltd. 3 Sandown Valley Crescent, South Tower, 1st Floor, Sandton, 2196; PO Box 786522, Sandton, 2146, South Africa. Tel: + 27 11 784 0077.

Website:

www.pharmaco.co.za

1

Long-term prophylaxis and management of

Angina Pectoris

2,3

=

100%

bioavailability

No first-pass metabolism

4

Twice daily

dosage regimen shown

to avoid withdrawal and tolerance

References: 1.

South African approved ISMO package insert.

2.

Ismo 20 Product Monograph (2015).

3.

Abshagen, U., 1992. Pharmacokinetics of isosorbide mononitrate.

The American Journal of Cardiology,

[online] 70(17), pp.G61-G66.

4.

Thadani U, Maranda CR, Amsterdam E, et al. Lack of Pharmacological Tolerance and Rebound

Angina Pectoris during Twice-daily Therapy with Isosorbide-5-Mononitrate.

Annals of Internal Medicine.

1994; 120:353-359. IS_0120.

indicating that the approach is achievable. Bleeding was avoided

despite the high risk, but it is important that if bleeding were

to occur, there was the option to discontinue DAPT without

incurring major risk.

Both studies included appropriate cases and had a high rate of

procedural success. Outcomes of the procedures were good and

in line with literature published in other geographical regions. It

is important that local datasets confirm the ability to replicate

published outcomes in our region and the authors are to be

commended for these efforts. Both studies are limited by their

observational nature and small numbers, but the publications are

nonetheless of value.

Bleeding avoidance is a major focus of current cardiovascular

research. Newer anticoagulant drugs with lower bleeding risk and

a change in antiplatelet monotherapy to non-aspirin alternatives

are the focus of current investigations. These, together with

procedural enhancements, such as seen in these two publications,

will hopefully successfully reduce bleeding risk going forward,

while continuing to prevent stroke and myocardial infarction.

References

1.

Kinnaird TD, Stabile E, Mintz GS, Lee CW, Canos DA, Gevorkian N,

et al

. Incidence, predictors, and prognostic implications of bleeding and

blood transfusion following percutaneous coronary interventions.

Am J

Cardiol

2003;

92

: 930–935.

2.

Doyle BJ, Rihal CS, Gastineau DA, Holmes DR Jr. Bleeding, blood

transfusion, and increased mortality after percutaneous coronary

intervention: implications for contemporary practice.

J Am Coll Cardiol

2009;

53

: 2019–2027.

3.

Larson E, German DM, Shatzel J, DeLoughery TG. Anticoagulation in

the cardiac patient: A concise review.

Eur J Haematol

2019;

102

: 3–19.

4.

Ducrocq G, Wallace JS, Baron G, Ravaud P, Alberts MJ, Wilson PWF,

et al

. Risk score to predict serious bleeding in stable outpatients with or

at risk of atherothrombosis.

Eur Heart J

2010;

31

: 1257–1265.

5.

Abelson M, Phillips A, Middlemost S. Nine-year, single-centre experi-

ence of left atrial appendage occlusion: patient characteristics, procedur-

al outcomes and long-term follow up.

Cardiovasc J Afr

2021;

32

: 33–36.

6.

Vachiat A, Ntsekhe M, Hellig F. Hybrid rotablation and drug-eluting

balloon strategy.

Cardiovasc J Afr

2021;

32

: 28–32.

7.

Connolly SJ, Eikelboom J, Joyner C, Diener H-C, Hart R, Golitsyn S,

et al

. Apixaban in patients with atrial fibrillation.

N Engl J Med

2011;

364

: 806–817.

8.

Windecker S, Latib A, Kedhi E, Kirtane AJ, Kandzari DE, Mehran R,

et al

. Polymer-based or polymer-free stents in patients at high bleeding

risk.

N Engl J Med

2020;

382

(13): 1208–1218.