The Incidence of Antihypertensive Drug-induced Side Eects in Patients
ORIGINAL ARTICLE doi: 10.5455/medarh.2014.68.372-375
Med Arh. 2014 Dec; 68(6): 372-375 Received: October 15th 2014 | Accepted: December 05th 2014
AVICENA 2014
The Incidence of Antihypertensive Drug-induced Side Eects in Patients with Diabetes Mellitus Type 2 and Hypertension
Svjetlana Loga-Zec1, Mensura Asceric2, Natasa Loga-Andrijic3, Berina Kapetanovic4, Enver Zerem5
Institute of Pharmacology, Clinical Pharmacology and Toxicology, Faculty of Medicine, University of Sarajevo, Bosnia and Herzegovina1Institute of Pharmacology, Clinical Pharmacology and Toxicology, Faculty of Medicine, University of Tuzla, Bosnia and Herzegovina2Department of Neurology, Clinical Center University of Sarajevo, Bosnia and Herzegovina3Department of Internal Medicine, Clinical Center University of Sarajevo, Bosnia and Herzegovina4Department of Internal Medicine, University Clinical Center Tuzla, Bosnia and Herzegovina5
Corresponding author: prof. Enver Zerem, MD, PhD. University Clinical Center Tuzla, Trnovac bb, 75000 Tuzla. Bosnia and Herzegovina. Phone: +38762344293, E-mail: [email protected]
ABSTRACT
Objective: To determine types and frequency of side eects of antihypertensive drugs in patients with diabetes mellitus (DM) type 2 and hypertension. Subjects and Methods: We performed a prospective study of 79 patients with DM type 2 and hypertension, randomly selected by systematic sampling, who were followed over a period of six months. Patients were assessed at baseline and once a month measuring following parameters: types of used antihypertensive drugs and frequency of side eects, the values
(mmHg) of systolic (SBP) and diastolic blood pressure (DBP). Results: Out of 79 patients, 48/79 (60.8%) were males and 31/79 (39.2%) were females. The median age in males was 53 years (IQR=48 to 55 years), in females 53 years (IQR=49 to 56 years). There was no statistically signicant dierence in median age between males and females (P=0.368). There is a statistically signicant dierence in the values
of SBP [2(5)=312.296, P<0.001] and DBP [2(5)=216.051, P<0.001] over a period of six months follow-up. The drug side eects were noted in 9/79 (11.4%) patients between 1-2 months, in 6/79 (7.6%) between 2-3 months, in 1/79 (1,3%) between 3-4 months. The most common side eect was cough (11/79 or 13.9%) associated with the combination of ACE inhibitor and thiazide diuretics. In 5/79 (6.3%) patients there were reports of: ushing, palpitations, headache, dizziness and leg edema associated with Ca blockers. Conclusion: The most common side eect of antihypertensive treatment was cough (13.9%) associated with the combination of ACE inhibitor and thiazide diuretic.
Key words: diabetes mellitus type 2, hypertension, antihypertensive drugs, side eects
1. INTRODUCTION
Hypertension is a common comorbidity of diabetes mellitus (DM) and it occurs in 20-60% of people with DM (1).The application of combined antihypertensive treatment proved to be necessary in diabetics, kidney patients and patients at high risk, and generally whenever a lower blood pressure (BP) value is desired (2). In view of the increasing number of available antihypertensive agents, clinicians are faced with the need to become familiar with the potential side eects of these drugs. In order to minimize the incidence of drug-induced side eects, several facts need to be remembered: (a) the most important side eect of diuretics is hypokalemia, which can cause cardiac arrhythmias and may be dangerous in patients who are taking digitalis, ones with chronic arrhythmias and acute myocardial infarction; (b) -blockers (-B) can induce bronchoconstriction, peripheral vasoconstriction, glycogenolysis, inhibition of insulin secretion and sometimes induce severe bradycardia. They can also cause cold
limbs, faster fatigue, nightmares, insomnia and depression; (c) calcium channel blockers (CaB) of the rst generation, particularly nifedipine, a representative of dihydropyridine, causes a number of side eects: sudden drop in blood pressure (BP) value, sympathetic activation and reex tachycardia, especially dangerous in coronary patients, facial ushing and headache; (d) angiotensin-convertin enzyme (ACE) inhibitors side eects are rare and the two of them are specic: cough andangio neurotic edema. They are associated with the action on the brady-kinin system (3).
Unfortunately, adverse antihypertensive drugs reactions cannot always be predicted from the pharmacological prole and only prolonged clinical experience will reveal theirs adverse eects.
In this study, we evaluated the incidence of adverse effects of antihypertensive drugs in patients with diabetes mellitus type 2 and hypertension.
372 Med Arh. 2014 Dec; 68(6): 372-375
Figure 1
Figure 1. The frequency of use of antihypertensive drugs over a six-months follow-up period (ACEIangiotensin-converting enzyme (ACE) inhibitors; TDthiazide diuretics; CaBcalcium channel blockers; ARBangiotensin receptor antagonists;-B-Blockers; Ddiuretics)
Figure 2
The Incidence of Antihypertensive Drug-induced Side Eects in Patients
2. PATIENTS AND METHODS
A clinical, prospective study was conducted at the Department of Internal Medicine, Clinical Center University of Sarajevo (CCUS) during 2012-2013. Th e study was conducted with the consent of the Ethical Committee of the CCUS.
2.1. Patients
Th e study included 79 patients with DM type 2 and hypertension, randomly selected by systematic sampling who were followed over a period of six months. Th e inclusion criteria were: patients with DM type 2 and arterial hypertension (blood pressure measured in the sitting position after at least 5 minutes rest, average of three readings at the last run-in-visit, should range from 140 to 179 mmHg systolic or from 90 to 109 mmHg diastolicgrades 1 or 2 of hypertension; women or men with uncomplicated hypertension within the age range from 40 to 60 years old, because of the lesser likelihood of the existence of any vascular incidents as a complication of DM. Th e exclusion criteria were: a history of cardiovascular disease; secondary hypertension; renal dysfunction; recent treatment with two or more antihypertensive drugs or a contraindication to discontinue blood pressure lowering agents; severe non-cardiovascular disease; known contra-indications for the rst-line study medications, pregnant and lactating women. All participants signed informed consents for participation in this study.
2.2. Methods
Patients were assessed at baseline and once a month by measuring following parameters: types of used antihypertensive drugs and frequency of side eects, the values (mmHg) of systolic (SBP) and diastolic blood pressure (DBP). Th e incidence rate of adverse eects was the primary outcome variable calculated according to the formula: the number of new cases with side eects that occurred during a specied period of time/the total number of treated patients during that period of time expressed as a percentage. Sitting SBP and DBP (average of three readings) were secondary outcome variables.
2.3. Statistical analysis
Th e KolmogorovSmirnov statistic Test with a Lilliefors signicance level was used for testing normality. In case of categorical variables, counts and percentages were reported. A P-value <0.05 was considered as signicant. Th e Friedman Test is used to test dierences between dierent periods. Post-hoc analysis with Wilcoxon Signed-Rank Tests was conducted applying Bonferroni correction, resulting in a signicance level set at P<0.003. Statistical analysis was performed by using the Statistical Package for the Social Sciences (SPSS Release 21.0; SPSS Inc., Chicago, Illinois, United States of America) software.
3. RESULTS
Out of 79 patients, 48/79 (60.8%) were males and 31/79 (39.2%) were females (2(1)=3.658; P=0.056). Th e median age in males was 53 years (IQR=48 to 55 years) and in females was 53 years (IQR=49 to 56 years). Th ere was no statistically signicant dierence in median age between males and females (P=0.368).
Th e most commonly proscribed therapy was the combination of three antihypertensive drugs (35.4%), followed
with the combination of four antihypertensive drugs (31.9%), two antihypertensive drugs (15.7%) and ve antihypertensive drugs (9.1%). Th e monotherapy is used in 5.1% and the combination of six antihypertensive drugs in 2.8%.
Th e drug side eects were noted in 9/79 (11,4%) patients between 1- 2 months, where eight subjects 8/79 (10.1%) were reported with cough associated with ACEI
Figure 2
Figure 2. The monthly dierence of systolic blood pressure in patients with diabetes mellitus type 2 and hypertension (n=79) treated with antihypertensive drugs over a period of six months (All P-values< .001, between 5-6 months P> .05).
Figure 3
Figure 3. The monthly dierence of diastolic blood pressure in patients with diabetes mellitus type 2 and hypertension (n=79) treated with antihypertensive drugs over a period of six months (All P-values< .001, between 1-2 months and 5-6 months P> .05).
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The Incidence of Antihypertensive Drug-induced Side Eects in Patients
+ TD, while one patient 1/79 (1.3%) experienced dizziness and ushing associated with Cab. Between 2-3 month, the drug side eects were noted in 6/79 (7,6%), where three patients 3/79 (3.8%) were reported with cough, associated with ACEI + TD, while the other three patients, 3/79 (3.8%) experienced side eects associated with CaB: allergies, headache, ushing and leg edema.
Dizziness and palpitations associated with CaB appeared between 3-4 months in one patient 1/79 (1.3%). Th e drug side eects were not recorded during 4-5 and 5-6 months periods.
At the beginning of the study, the median value of SBP was 150 mmHg (IQR=150 to160 mmHg), and after six-month treatment was 125 mmHg (IQR=120 to130 mmHg), which represents a reduction of SBP for 25 mmHg. Th ere was a statistically signicant dierence in the SBP values over the six-month use of the antihypertensive therapy (2 (5) =312.296; P<.001).
At the beginning of the study, the median value of DBP was 100 mmHg (IQR=90 to100mmHg), and after six months of treatment was 80 mmHg (IQR=80 to 85mmHg), which represents a reduction of DBP for 20mmHg. Th e DBP value in patients (n=79) signicantly changed during the six months of therapy with antihypertensive drugs (n=79) (2 (5) =216.051; P <.001).
4. DISCUSSION
In this prospective study, we found that the most common side eect of antihypertensive treatment was cough (13.9%) associated with the combination of ACEI + TD used between 1-2 months and 2-3 months of follow-up. Between 3-6 month these antihypertensive drugs were used in 15.6%16.9% of patients and there were no adverse eects associated with them during this period. A dry cough occurs in 10-15% of patients treated with ACE inhibitors, due to the accumulation of bradykinin, substance P and/or prostaglandin in the lungs (3), which coincides with our results. Th iazide diuretics are one of the cheapest and most commonly used antihypertensive drugs worldwide. Thiazides, however, have signicant tside-eect prole and often, as monotherapy, are insuffi -cient to normalize blood pressure value. Ng Lp et al. were conducted a retrospective study to identify patients who discontinued the use of ACE inhibitors and they found that 30.4% of patients discontinued the use of ACE inhibitors due to cough (4). Caldeira et al. conducted systematic review and meta-analysis to evaluate the tolerability of ARBs in patients with intolerance to ACE inhibitors and they found that ARBs had fewer cough events versus ACE inhibitors (5). In our study, the incidence of adverse reactions to CaB was 6.3%. Out of the total number of patients with adverse eects to CaB (n=5), two of them were females who experienced ushing. Kajiwara et al. study revealed that vasodilation-related adverse symptoms to dihydropyridine calcium channel blockers occurred signicantly more often in females than in males (OR 1.87, 95% CI 1.28-2.71, p=0.001) and furthermore, exclusively among females. Th e younger age group (<50years) complained more frequently of vasodilation-related symptoms (OR 2.39, 95% CI 1.02-5.59, p=0.045) (6). Peripheral edema, particularly of the lower limbs, is one of the
most common adverse eects of dihydropyridine calcium channel blockers and may result in the need of dose reduction or drug withdrawal, both of which can adversely aect antihypertensive effi cacy (7). In our study, one patient had leg edema associated with CaB. In the study conducted by Luis MR, side eects such as: headaches and dizziness were more frequent in the group of olmesartan/hydrochlorothiazide compared to olmesartan group, hydrochlorothiazide group and the placebo group (8). Barrios et al. found that the treatment with medoksomilolmesartan, 40 mg/per day, was associated with a lower frequency of side eects compared to the combinational therapy of olmesartan medoksomil/hydrochlorothiazide (21.5% vs. 28.3%) (9). In the study conducted by Pool J Let al., 1.346 patients were randomized into eight groups: valsartan (VAL) 160 and 320mg; hydrochlorothiazide (HCTZ) 12.5 and 25mg; VAL/HCTZ160/12,5;320/12,5; 320/25mg and placebo groups (10). Each of these combinations was associated with a signicant reduction in SBP values and DBP values compared to monotherapy and placebo groups (all P<.001). Th e incidence of hypokalemia was lower in the combination of valsartan/hydrochlorothiazide (1.8%-6.1%) compared to monotherapy with hydrochlorothiazide (7.1%-13.3%). Th e study by Bangalore S et al. (11) quested whether the therapy with the targeted normal SBP value (<120 mm Hg) reduces the incidence of the large cardiovascular incidents in patients with type 2 diabetes and cardiovascular disease or additional risk factors. Th e total number of 4.733 patients with type 2 diabetes (10-year median), aged 40-88 years (mean 62 year), were randomized to intensive or standard therapy for achieving SBP<120 mmHg and<140 mmHg, respectively. Serious side eects, which are attributed to antihypertensive treatment, appeared in 77(3.3%) subjects with intensive therapy and in 30 (1.3%) patients with a standard therapy (P < .0001).
5. CONCLUSION
Th e most common side eect of antihypertensive treatment was cough (13.9%) associated with the combination of ACE inhibitor and thiazide diuretic. Th e optimal choice and antihypertensive drug dosage should be done in accordance with the guidelines, by taking into consideration all patients characteristics.
CONFLICT OF INTEREST: NONE DECLARED.
REFERENCES
1. Arauz-Pacheco C, Parrott MA, Raskin P. Treatment of hypertension in adults with diabetes. Diabetes Care. 2003; 26: S80-S82.
2. National Kidney Foundation Guideline. K/DOQI clinical practice guidelines for chronic kidney disease: Evaluation, classication, and stratication. Kidney Disease Outcome Quality Initiative. Am J Kidney Dis. 2002; 39: S1-246.
3. Holmes RL,Fadden CT. Evaluation of the patient with chronic cough. Am Fam Physician.2004; 69: 2159-2166.
4. Ng LP, Goh PS. Incidence of discontinuation of angiotensin-converting enzyme inhibitors due to cough, in a primary healthcare centre in Singapore. Singapore Med J. 2014; 55: 146-149.
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5. Caldeira D, David C, Sampaio C. Tolerability of angiotensin-receptor blockers in patients with intolerance to angiotensin-converting enzyme inhibitors: a systematic review and meta-analysis. Am J Cardiovasc Drugs. 2012; 12: 263-277.
6. Kajiwara A, Saruwatari J, Kita A, Oniki K, Yamamura M, Murase M, Koda H, Hirota S, Ishizuka T, Nakagawa K. Younger females are at greater risk of vasodilation-related adverse symptoms caused by dihydropyridine calcium channel blockers: results of a study of 11,918 Japanese patients. Clin Drug Investig.2014; 34: 431-435.
7. Weir MR. Incidence of pedal edema formation with dihydropyridine calcium channel blockers: issues and practical significance. J Clin Hypertens (Greenwich). 2003; 5: 330-335.
8. Luis MR. Clinical effi cacy and safety of olmesartan/hydro-chlorothiazide combination therapy in patients with essential hypertension. Vasc Health Risk Manag. 2008; 4: 1237-1248.
9. Barrios V, Boccanelli A, Ewald S, Girerd X, Heagerty A, Krzesinski JM, Lins R, Rodicio J, Stefenelli T, Woittiez A, et al. Efcacy and tolerability of olmesartan medoxomil in patients with mild to moderate essential hypertension: the OLMEBEST Study. Clin Drug Investig. 2007; 27: 545-558.
10. Pool JL, Glazer R, Weinberger M, Alvarado R, Huang J, GraA. Comparison of valsartan/hydrochlorothiazide combination therapy at doses up to 320/25 mg versus monotherapy: a double-blind, placebo-controlled study followed by long-term combination therapy in hypertensive adults. Clin Th er. 2007; 29: 61-73.11. Bangalore S, Kumar S, Lobach I, Messerli FH. Blood pressuretargets in subjects withtype 2 diabetes mellitus/impaired fasting glucose: observations from traditional and bayesian random-eects meta-analyses of randomized trials. Circulation. 2011; 123: 2799.
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Copyright Academy of Medical Sciences of Bosnia and Herzegovina 2014
Abstract
Objective: To determine types and frequency of side effects of antihypertensive drugs in patients with diabetes mellitus (DM) type 2 and hypertension. Subjects and Methods: We performed a prospective study of 79 patients with DM type 2 and hypertension, randomly selected by systematic sampling, who were followed over a period of six months. Patients were assessed at baseline and once a month measuring following parameters: types of used antihypertensive drugs and frequency of side effects, the values (mmHg) of systolic (SBP) and diastolic blood pressure (DBP). Results: Out of 79 patients, 48/79 (60.8%) were males and 31/79 (39.2%) were females. The median age in males was 53 years (IQR=48 to 55 years), in females 53 years (IQR=49 to 56 years). There was no statistically significant difference in median age between males and females (P=0.368). There is a statistically significant difference in the values of SBP [x2(5)=312.296, P<0.001] and DBP [x2(5)=216.051, P<0.001] over a period of six months follow-up. The drug side effects were noted in 9/79 (11.4%) patients between 1-2 months, in 6/79 (7.6%) between 2-3 months, in 1/79 (1,3%) between 3-4 months. The most common side effect was cough (11/79 or 13.9%) associated with the combination of ACE inhibitor and thiazide diuretics. In 5/79 (6.3%) patients there were reports of: flushing, palpitations, headache, dizziness and leg edema associated with Ca blockers. Conclusion: The most common side effect of antihypertensive treatment was cough (13.9%) associated with the combination of ACE inhibitor and thiazide diuretic.
You have requested "on-the-fly" machine translation of selected content from our databases. This functionality is provided solely for your convenience and is in no way intended to replace human translation. Show full disclaimer
Neither ProQuest nor its licensors make any representations or warranties with respect to the translations. The translations are automatically generated "AS IS" and "AS AVAILABLE" and are not retained in our systems. PROQUEST AND ITS LICENSORS SPECIFICALLY DISCLAIM ANY AND ALL EXPRESS OR IMPLIED WARRANTIES, INCLUDING WITHOUT LIMITATION, ANY WARRANTIES FOR AVAILABILITY, ACCURACY, TIMELINESS, COMPLETENESS, NON-INFRINGMENT, MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. Your use of the translations is subject to all use restrictions contained in your Electronic Products License Agreement and by using the translation functionality you agree to forgo any and all claims against ProQuest or its licensors for your use of the translation functionality and any output derived there from. Hide full disclaimer