Abstract:How Often Do You Fail to Take All of Your Medication?T o the Editor: We read with interest the article by Prieto-Jimenez et al (1); however, the conclusion overlooks the problem of adherence to treatment. A success rate of 44% has never been reported since dual therapies were introduced or in more recent pediatric trials. Compliance is the most important factor predicting treatment success (2), and eradication rates of 20% were reported in those taking <60% of pills (3).In the El Paso children, several indicat… Show more
“…Visruthan et al 13 reported a case of a 12-year-old Chinese male patient who was started on a 14-day course of triple therapy for eradication of Helicobacter pylori . Treatment included omeprazole 20 mg twice daily, amoxicillin 500 mg twice daily, and clarithromycin 500 mg twice daily.…”
Section: Literature Reviewmentioning
confidence: 99%
“…The authors conclude that PPIs should be recognized as having the potential for this rare adverse effect, especially in children reciving triple therapy with concomitant use of clarithromycin. 13…”
Section: Literature Reviewmentioning
confidence: 99%
“…Additionally, the author concluded that omeprazole therapy may cause subtle biochemical changes at the subcellular level because no major side effects were seen in prior short-term studies. 12 Visruthan et al 13 reported a case of a 12-year-old Chinese male patient who was started on a 14-day course of triple therapy for eradication of Helicobacter pylori. Treatment included omeprazole 20 mg twice daily, amoxicillin 500 mg twice daily, and clarithromycin 500 mg twice daily.…”
A limited body of published data suggests that PPI use has been associated with myopathy-like symptoms without long-term effects following discontinuation. Although myopathy is a rare adverse effect observed with PPIs, it can be a serious side effect to be considered when starting a patient on acid suppression therapy.
“…Visruthan et al 13 reported a case of a 12-year-old Chinese male patient who was started on a 14-day course of triple therapy for eradication of Helicobacter pylori . Treatment included omeprazole 20 mg twice daily, amoxicillin 500 mg twice daily, and clarithromycin 500 mg twice daily.…”
Section: Literature Reviewmentioning
confidence: 99%
“…The authors conclude that PPIs should be recognized as having the potential for this rare adverse effect, especially in children reciving triple therapy with concomitant use of clarithromycin. 13…”
Section: Literature Reviewmentioning
confidence: 99%
“…Additionally, the author concluded that omeprazole therapy may cause subtle biochemical changes at the subcellular level because no major side effects were seen in prior short-term studies. 12 Visruthan et al 13 reported a case of a 12-year-old Chinese male patient who was started on a 14-day course of triple therapy for eradication of Helicobacter pylori. Treatment included omeprazole 20 mg twice daily, amoxicillin 500 mg twice daily, and clarithromycin 500 mg twice daily.…”
A limited body of published data suggests that PPI use has been associated with myopathy-like symptoms without long-term effects following discontinuation. Although myopathy is a rare adverse effect observed with PPIs, it can be a serious side effect to be considered when starting a patient on acid suppression therapy.
“…The drugs that the patient had been exposed to before the onset of myositis were reviewed and myositis might also be related to daptomycin, omeprazole or allopurinol. [6][7][8] While their participation cannot be definitively excluded, the three of them usually present with elevated CK levels, with or without muscle symptoms while our patient presented with serum CK within normal range despite muscle pain and swelling. In addition, our patient had previously been exposed to omeprazole without having observed any side effects.…”
A 47-year-old man, newly diagnosed with acute promyelocytic leukemia was treated with all-trans retinoic acid (ATRA) and idarrubicin. On day +24, he presented with fever and swelling in the left lower limb. The US and MRI were compatible with a myositis of tibialis anterior, later confirmed by muscle biopsy. ATRA-induced myositis was suspected. On day +29, ATRA was discontinued and the patient treated with dexamethasone. The patient improved promptly and ATRA was administered thereafter without any myositis relapse. The Naranjo scale indicated a probable relationship between ATRA and myositis. We herein review the published cases. Re-exposition to the drug seems to be safe for the patient.
“…From this evidences omeprazole is the primary candidate that induced myopathy. In addition, there were 16 case reports in the literature and summarized in a case series that associate the use of omeprazole with myopathy . Among these 16 cases, two were identified as Asians, but race was not reported among the other cases.…”
Polypharmacy increases the risk of drug-drug interactions (DDIs). Combining epidemiological studies with pharmacokinetic modeling, we detected and evaluated high-dimensional DDIs among 30 frequent drugs. Multidrug combinations that increased the risk of myopathy were identified in the US Food and Drug Administration Adverse Event Reporting System (FAERS) and electronic medical record (EMR) databases by a mixture drug-count response model. CYP450 inhibition was estimated among the 30 drugs in the presence of 1 to 4 inhibitors using in vitro / in vivo extrapolation. Twenty-eight three-way and 43 four-way DDIs had significant myopathy risk in both databases and predicted increases in the area under the concentration-time curve ratio (AUCR) >2-fold. The high-dimensional DDI of omeprazole, fluconazole, and clonidine was associated with a 6.41-fold (FAERS) and 18.46-fold (EMR) increased risk of myopathy local false discovery rate (<0.005); the AUCR of omeprazole in this combination was 9.35. The combination of health record informatics and pharmacokinetic modeling is a powerful translational approach to detect high-dimensional DDIs.
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