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These studies suggest that blood pressure drugs can have side effects such as increased blood pressure, skin diseases, and treatment discontinuations due to adverse events.
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Blood pressure (BP) medications are essential for managing hypertension, but they come with a range of potential side effects. Understanding these side effects is crucial for both patients and healthcare providers to ensure effective and safe treatment.
Nonsteroidal anti-inflammatory drugs (NSAIDs) are commonly used to relieve pain and inflammation but can significantly impact blood pressure. Studies have shown that NSAIDs, including both nonselective and selective types, can increase BP, particularly in patients with pre-existing hypertension . Indomethacin, a nonselective NSAID, has been observed to raise BP and lower pulse rates in patients taking enalapril, an ACE inhibitor, but had little effect on those taking amlodipine, a calcium channel blocker. This suggests that the choice of antihypertensive medication can influence the extent of BP changes induced by NSAIDs.
The primary mechanism by which NSAIDs increase BP is through sodium retention, which leads to elevated blood volume and pressure. This effect is more pronounced in patients taking ACE inhibitors, as the inhibition of prostaglandin synthesis by NSAIDs reduces the effectiveness of these drugs .
Bisphosphonates (BPs) are widely used for treating osteoporosis but are associated with gastrointestinal (GI) side effects, such as esophagitis and esophageal ulcers . Despite these concerns, a meta-analysis has shown that BPs do not significantly increase the risk of severe GI adverse events compared to placebo. However, non-severe GI side effects are more common and can affect patient adherence to treatment.
To mitigate these side effects, novel drug delivery systems (DDSs) such as nanoparticles, liposomes, and transdermal systems are being explored. These advanced DDSs have shown promise in reducing GI side effects and improving the bioavailability of BPs.
Different classes of antihypertensive drugs have varying rates of discontinuation due to adverse events. A meta-analysis of randomized controlled trials (RCTs) revealed that all classes of BP-lowering drugs, except angiotensin receptor blockers (ARBs), significantly increase the risk of treatment discontinuation due to adverse events. Diuretics, beta-blockers, calcium antagonists, and ACE inhibitors were all associated with higher discontinuation rates compared to placebo.
Despite these discontinuation rates, antihypertensive drugs are effective in lowering BP over the long term. An individual-level data meta-analysis of large-scale RCTs demonstrated that BP-lowering pharmacotherapy remains effective for up to four years, with sustained reductions in BP across various patient demographics.
Recombinant human erythropoietin (rHuEPO), used to treat anemia in chronic renal failure, is known to increase BP in about one-third of patients. This side effect often necessitates the initiation or intensification of antihypertensive therapy. The mechanism behind this increase is not fully understood but is thought to involve increased blood viscosity and systemic vascular resistance.
Blood pressure medications, while essential for managing hypertension, come with a range of potential side effects that can impact patient adherence and overall treatment efficacy. NSAIDs can significantly raise BP, particularly in patients on ACE inhibitors, while bisphosphonates are associated with GI side effects that novel DDSs aim to mitigate. Understanding these side effects and their mechanisms is crucial for optimizing treatment strategies and ensuring patient safety.
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