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Prescrire Int [JOURNAL]

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Asthma. A summary of first-choice treatments.

Prescrire Int · 2016 Mar · PMID 27152404

First identify and avoid factors that trigger or aggravate asthma attacks First-line treatment for asthma is inhaled salbutamol: used on demand to relieve respiratory discomfort or to prevent attacks due to a known trigg... First identify and avoid factors that trigger or aggravate asthma attacks First-line treatment for asthma is inhaled salbutamol: used on demand to relieve respiratory discomfort or to prevent attacks due to a known trigger; or on a daily basis if necessary, in combination with an inhaled corticosteroid such as beclometasone, for patients with persistent asthma. Treatment of severe persistent asthma is based on daily use of a high-dose inhaled corticosteroid, or possibly an oral corticosteroid, for as short a period as possible. To limit adverse effects and drug interactions, the dose should be reduced, or the treatment gradually withdrawn, once asthma is under control.

Drug-induced non-immune-mediated angioedema.

Prescrire Int · 2016 Mar · PMID 27152403

Combinations of drugs that increase vascular permeability increase the risk of angioedema. Combinations of drugs that increase vascular permeability increase the risk of angioedema.

Imatinib: muscle pain suggestive of a withdrawal syndrome.

Prescrire Int · 2016 Mar · PMID 27152402

Muscle pain after stopping imatinib that resolves on reintroduction of the drug. Muscle pain after stopping imatinib that resolves on reintroduction of the drug.

Epidural corticosteroid injections: serious neurological disorders.

Prescrire Int · 2016 Mar · PMID 27152401

The harm-benefit balance of epidural corticosteroid injections for low back pain with sciatica is unfavourable. The harm-benefit balance of epidural corticosteroid injections for low back pain with sciatica is unfavourable.

Extravasation of infused drugs: tissue damage, and not only with cancer drugs.

Prescrire Int · 2016 Mar · PMID 27152400

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Gliflozins: ketoacidosis.

Prescrire Int · 2016 Mar · PMID 27152399

Metabolic acidosis with elevated levels of ketones in patients with type 2 diabetes. Metabolic acidosis with elevated levels of ketones in patients with type 2 diabetes.

Quetiapine: misuse and abuse.

Prescrire Int · 2016 Mar · PMID 27152398

Prescribers and pharmacists should be aware of the problem. Prescribers and pharmacists should be aware of the problem.

Botulinum toxin type A (Botox) and idiopathic overactive bladder. For some severely affected patients.

Prescrire Int · 2016 Mar · PMID 27152397

In two clinical trials, botulinum toxin injected during cystoscopy transiently prevented urinary incontinence in 1 in 5 patients but sometimes provoked urine retention and urinary tract infections. In two clinical trials, botulinum toxin injected during cystoscopy transiently prevented urinary incontinence in 1 in 5 patients but sometimes provoked urine retention and urinary tract infections.

COMMON STEM-lisib.

Prescrire Int · 2016 Mar · PMID 27152396

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Ketoconazole and endogenous Cushing's syndrome. Effective but tricky to use.

Prescrire Int · 2016 Mar · PMID 27152395

Endogenous Cushing's syndrome is a rare but serious disease. Ketoconazole was effective in over 50% of cases in non-comparative series in a total of 800 patients. However, ketoconazole is hepatotoxic and interacts with m... Endogenous Cushing's syndrome is a rare but serious disease. Ketoconazole was effective in over 50% of cases in non-comparative series in a total of 800 patients. However, ketoconazole is hepatotoxic and interacts with many other drugs.

Siltuximab (Sylvant). Castleman's disease: good symptomatic efficacy in some patients.

Prescrire Int · 2016 Mar · PMID 27152394

Multicentric Castleman's disease is a rare lymphoproliferative disorder characterised by disseminated lymphadenopathy. Symptoms and outcomes differ widely from one patient to another. The median survival time is about 2.... Multicentric Castleman's disease is a rare lymphoproliferative disorder characterised by disseminated lymphadenopathy. Symptoms and outcomes differ widely from one patient to another. The median survival time is about 2.5 years. There is no consensus on treatment. Siltuximab, a monoclonal antibody that antagonises interleukin-6, has been authorised in the European Union for patients with multicentric Castleman's disease who are not infected with HIV or HHV-8. In a randomised, double-blind trial in 79 patients, most of whom had mild or moderate symptoms, the estimated one-year survival rate was 100% in the siltuximab group versus 92% in the placebo group after a median follow-up of 60 weeks. However, half of the patients in the placebo group received siltuximab after disease progression. Symptoms disappeared for at least 18 weeks in one-quarter of patients in the siltuximab group versus none of those in the placebo group; the median symptom-free period in the siltuximab group was about 16 months. The known adverse effects of siltuximab are related to its immunosuppressive effect. They include frequent infections, neutropenia and thrombocytopenia. Reactions can occur during the infusion, and mouth sores have been reported. Other adverse events that appear to be more frequent with siltuximab include cutaneous disorders, oedema, renal and cardiac disorders, and peripheral neuropathy. Cases of gastrointestinal perforation have been reported in trials in other clinical settings. Siltuximab can mask the signs and symptoms of acute inflammation, in particular by suppressing fever and acute-phase markers such as C-reactive protein. Interleukin-6 is a cytochrome P450 inhibitor. Siltuximab activates its isoenzymes and can thus reduce the effectiveness of the numerous drugs that are substrates of this enzyme system. This risk of interactions is likely to persist up to several weeks after siltuximab withdrawal, because of its long plasma elimination half-life (about 16 days). In practice, the only available trial suggests that siltuximab has a marked impact on the symptoms of mild or moderate multicentric Castleman's disease in patients who are not infected with HIV or HHV-8. Siltuximab seems to be a reasonable option in this setting, despite its numerous adverse effects, provided patients are fully informed of the many unknowns and are closely monitored.

No more denial.

Prescrire Int · 2016 Mar · PMID 27152393

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Oseltamivir for influenza, from birth: no more useful than in adults.

Prescrire Int · 2016 Feb · PMID 27073818

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Tramadol: hyponatraemia.

Prescrire Int · 2016 Feb · PMID 27073817

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Tramadol: hypoglycaemia.

Prescrire Int · 2016 Feb · PMID 27073816

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Tramadol: respiratory depression in a child.

Prescrire Int · 2016 Feb · PMID 27073815

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Oseltamivir: over 15 years of data retention and systematic stonewalling.

Prescrire Int · 2016 Feb · PMID 27042737

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Oseltamivir and influenza: still no robust data.

Prescrire Int · 2016 Feb · PMID 27042736

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Influenza vaccination during pregnancy.

Prescrire Int · 2016 Feb · PMID 27042735

In a randomised, double-blind trial in pregnant women, a seasonal inactivated influenza vaccine without a lipid adjuvant and covering strain A/H1N1v was partially effective: the incidence of influenza in the mothers and... In a randomised, double-blind trial in pregnant women, a seasonal inactivated influenza vaccine without a lipid adjuvant and covering strain A/H1N1v was partially effective: the incidence of influenza in the mothers and their infants was about 1.8% with the vaccine versus 3.6% with placebo. No noteworthy adverse reactions were reported.

Pregnancy: morphine, or sometimes buprenorphine, when paracetamol is ineffective.

Prescrire Int · 2016 Feb · PMID 27042734

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