Rational use of Metoprolol: The Relationship of Its Blood Concentration to Patient Compliance, Poor Quality Medicines and Side Effects

Authors

  • Methaq A.H.Husain
  • Layth Jabbar
  • Abdullah M. Jawad

Keywords:

Metoprolol, Plasma concentrations, Adverse effects, Brand products, Proper use

Abstract

Background: Patients with cardiovascular diseases might be poorly educated regarding the rational use of their drug treatment, such as dealing with missing doses, relationship to food, and potential side effects. In addition, many poor quality medications are available in our drug market that might differ in their efficacy and safety profiles.

Aim: Metoprolol, a commonly used drug in our local medical practice, is to be investigated through measuring its blood concentration at one point of time after achieving the steady state, and to correlate blood concentration with compliance, side effects and the quality of brand products they are using.

Methods: Measurement of levels of metoprolol (by scanning spectrometry) in blood samples taken from patients at their visits to the consultation clinics in Thi-Qar during the period October 2014 to April 2015 was made. Their blood concentrations was correlated with compliance, side effects and the quality of the drugs they were using. A questionnaire containing patient demographic information, type disease, type of drugs, trade names, and a check-list of potential side effects, was used.

Results: Out of the 56 patients who were treated with different preparations and dosage regimens of metoprolol, 53 patients were within the reported therapeutic range of metoprolol plasma concentration (0.035-0.5µg/ml). The two brand metoprolol products used were found interchangeable with no significant difference in their achieved plasma concentration. The most frequent adverse effects associated with the use of metoprolol were tiredness followed by dyspnea and bradycardia. There is no difference between the two brand products of metoprolol in relation to the frequency of side effects. Around 90% of patients using metoprolol were not aware of the proper action to be taken when they miss a dose. 23.2% of patients who reported missing one or more doses did not take any action till the next dose.

Conclusion: Availability of more than one brand product of metoprolol and other drugs need to be investigated in terms of their blood levels and occurrence of adverse effects especially when these drugs are used for long duration to test their interchangeability. Patient awareness of the proper use of drugs is necessary in order to increase effectiveness of their treatment and decrease potential side effects.

References

Campbell TJ, Williams KM. Therapeutic drug monitoring: antiarrhythmic drugs. British Journal of Clinical Pharmacology 2001; 52: 21-34.

Follath F, Ganzinger U,Scheutz E. Reliability of antiarrhythmic drug plasma concentration monitoring. Clinical Pharmacokinetic 1983; 8:63-82.

Edvardsson N, Olsson SB. Clinical value of plasma concentrations of antiarrhythmic drugs. European Heart Journal 1987; 8:83-90.

Woosley RL. Role of plasma concentration monitoring in the evaluation of response to antiarrhythmic drugs. The American Journal of Cardiology 1988; 62: 9-17.

Wolf M, Köpp A, Dörfelt A, Haen E. Beta-blockers in psychiatry: Pharmacokinetic interactions of antipsychotics with CYP2D6- HPLC as a quantitative method for analysis in TDM. Pharmacopsychiatry 2012;45:27.

Wanzhu Tu, Andrew B, Morris, Jingjin Li, Jingwei Wu, James Yo, et al. Association between adherence measurements of metoprolol and Health care utilization in older patients with heart failure. Clinical Pharmacology and Therapeutics 2005; 77: 189–201.

Badulescu M, Balalau D,Cacovean I, Ilie M, Baconi DL. UV-VIS spectrophotometric assay of metoprolol. Farmacia 2008; 4: 363-370.

Hope CJ, Wu J, Tu W, Young J, Murray MD. Association of medication adherence, knowledge, and skills with emergency department visits by adults 50 years or older with congestive heart failure. American Journal Health -System Pharmacy 2004; 61:2043-2052.

Bengtsson C, Johnsson G, Regardh CG. Plasma levels and effects of metoprolol on blood pressure and heart rate in hypertensive patients after an acute dose and between two doses during long term treatment. Clinical Pharmacology and Therapeutics 1975; 17:400-408.

Wormke M, Puzik A, Pochic I, Sterns T, Wiedmann M, Wedel C, et al. A comparative bioequivalence study of two prolonged-release metoprolol preparations. Geriatria 2012; 6: 34-40.

Maldonado C; Mello N; Fagiolino P; Vázquez M. Safe use of a daily 20 mg dose of omeprazole in order to avoid hypomagnesaemia. International Journal of Pharmacy 2015; 5: 315-321.

Zlott D A and Byrne M. Mechanisms by which pharmacologic agents may contribute to fatigue. PM&R Journal 2010; 2: 451-455.

Kardas P. Compliance, clinical outcome, and quality of life of patients with stable angina pectoris receiving once-daily betaxolol versus twice daily metoprolol: a randomized controlled trial. Vascular Health and Risk Management 2007; 3: 235–242.

Spiers MV, Kutzik DM, Lamar M. Variation in medication understanding among the elderly. American Journal of Health System Pharmacy 2004; 15: 373-380.

Stone VE, Hogan JW, Schuman P, Rompalo AM, Howard AA, Korkontzelou C, et al. Antiretroviral regimen complexity, self-reported adherence, and HIV patients understanding of their regimens: survey of women in the HER study. Journal of Acquired Immune Deficiency Syndromes 2001; 28: 124-132.

Abu Hussein NB, Eissa IM, Abdel-Kader AA. Analysis of factors affecting patients’ compliance to topical antiglaucoma medications in Egypt as a developing country model. Journal of Ophthalmology 2015; 15:1-7.

Gaude GS, Hattiholi J, Chaudhury A. Role of health education and self-action plan in improving the drug compliance in bronchial asthma. Journal of Family Medicne and Primary Care 2014; 3: 33–38.

Kumar V, Sharma A, SANDEEP Arora S, Dhillon V. Use of simple spectrophotometric method for estimation of theophylline (TH) in saliva and urine of healthy volunteer. International Journal of Pharma and Bio Sciences 2011; 2: 36-41.

Gujral R S, Haque S M, Shanker P. Development and Validation of Pregabalin in Bulk, Pharmaceutical Formulations and in Human Urine Samples by UV Spectrophotometry. International journal of biomedical science 2009; 5: 175-180.

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Published

2019-04-26

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