Literature DB >> 10150160

Translating safety, efficacy and compliance into economic value for controlled release dosage forms.

M P Cramer1, S R Saks.   

Abstract

Advanced controlled release (CR) dosage forms are relative newcomers to pharmaceutical markets, and few studies relate their efficacy, safety or compliance benefits to economic value. This literature review was undertaken to assess the cost effectiveness of CR dosage forms using such measures as purchase costs, total treatment costs, and economic value of improved therapeutic outcomes compared with those with non-CR dosage forms. Three therapeutic areas were examined: cardiovascular therapy, pain management and estrogen replacement therapy. In cardiovascular therapy, prescription costs of sustained release (SR) verapamil were significantly higher than for conventional release verapamil. However, these were more than offset by lower physician, hospital and laboratory expenditures for the SR group, in whom compliance was superior. Similarly, patients receiving SR diltiazem had better prescription refill compliance than those using a conventional formulation of the drug, as well as significantly lower aggregate healthcare costs during a 1-year study period. These lower costs with both SR verapamil and diltiazem may relate to better compliance. CR nifedipine has lower daily acquisition costs than the conventional form, simplifies the dosage regimen to once daily, extends the indications of the drug to hypertension as well as angina, and reduces vasodilatory adverse effects by reducing peak plasma drug concentrations and the postdose rate of increase in concentration. Compared with oral clonidine given twice daily, transdermal clonidine, given once weekly, had higher purchase costs, but was associated with improved compliance, reduced adverse effects (due to control of plasma concentrations), and lower nondrug health costs, such as physician, hospital and laboratory costs. Lower costs were also found for once daily oral formulations of various antihypertensives, suggesting that the economics of both types of CR dosage forms related to compliance. CR metoprolol 50 or 100mg and conventional release atenolol 50mg, each given once daily, provided effective beta1-adrenoceptor blockade. The conventional formulation caused deterioration in the sense of well-being that was temporally associated with sharp peaking of its plasma concentrations. Such peaking did not occur with either dose of CR metoprolol, nor did any deterioration in the sense of well-being. Transdermal nitroglycerin (glyceryl trinitrate), compared with long-acting oral nitrates, improved quality of life (QOL) {despite a higher incidence of some adverse effects, such as headache, dizziness and skin irritation}. Furthermore, in some studies, this formulation reduced angina attacks, sublingual nitroglycerin use, and hospitalisation or emergency room use. Cost comparisons between transdermal products favoured those that have superior adhesion.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1994        PMID: 10150160     DOI: 10.2165/00019053-199405060-00005

Source DB:  PubMed          Journal:  Pharmacoeconomics        ISSN: 1170-7690            Impact factor:   4.981


  94 in total

1.  Potential cost-avoidance with oral extended-release morphine sulfate tablets versus morphine sulfate solution.

Authors:  B R Goughnour; W W Arkinstall
Journal:  Am J Hosp Pharm       Date:  1991-01

2.  Biologic effects of transdermal estradiol.

Authors:  R J Chetkowski; D R Meldrum; K A Steingold; D Randle; J K Lu; P Eggena; J M Hershman; N K Alkjaersig; A P Fletcher; H L Judd
Journal:  N Engl J Med       Date:  1986-06-19       Impact factor: 91.245

3.  Transdermal estradiol in the treatment of postmenopausal bone loss.

Authors:  S Adami; R Suppi; F Bertoldo; M Rossini; M Residori; V Maresca; V Lo Cascio
Journal:  Bone Miner       Date:  1989-08

4.  Controlled release morphine tablets: a double-blind trial in patients with advanced cancer.

Authors:  G W Hanks; R G Twycross; J M Bliss
Journal:  Anaesthesia       Date:  1987-08       Impact factor: 6.955

Review 5.  Sustained release nifedipine formulations. An appraisal of their current uses and prospective roles in the treatment of hypertension, ischaemic heart disease and peripheral vascular disorders.

Authors:  D Murdoch; R N Brogden
Journal:  Drugs       Date:  1991-05       Impact factor: 9.546

6.  Transdermal fentanyl for pain control in patients with cancer.

Authors:  Angela W Miser; Prem K Narang; Judith A Dothage; Robert C Young; William Sindelar; James S Miser
Journal:  Pain       Date:  1989-04       Impact factor: 6.961

7.  Transdermal fentanyl for chronic cancer pain: detailed case reports and the influence of confounding factors.

Authors:  R B Patt; L A Hogan
Journal:  J Pain Symptom Manage       Date:  1992-04       Impact factor: 3.612

8.  Effects of low doses of transdermal 17 beta-estradiol on carbohydrate metabolism in postmenopausal women.

Authors:  A Cagnacci; R Soldani; P L Carriero; A M Paoletti; P Fioretti; G B Melis
Journal:  J Clin Endocrinol Metab       Date:  1992-06       Impact factor: 5.958

9.  Carbohydrate metabolism during hormonal substitution therapy.

Authors:  K De Cleyn; P Buytaert; M Coppens
Journal:  Maturitas       Date:  1989-09       Impact factor: 4.342

10.  Compliance with hormone therapy.

Authors:  V A Ravnikar
Journal:  Am J Obstet Gynecol       Date:  1987-05       Impact factor: 8.661

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  17 in total

Review 1.  Current status of sustained release formulations in the treatment of hypertension. An overview.

Authors:  E Mutschler; H Knauf
Journal:  Clin Pharmacokinet       Date:  1999       Impact factor: 6.447

Review 2.  Noncompliance with antihypertensive therapy. Economic consequences.

Authors:  T L Skaer; D A Sclar; L M Robison
Journal:  Pharmacoeconomics       Date:  1996-01       Impact factor: 4.981

Review 3.  Controlled release dosage forms: from ground to space.

Authors:  P Colombo; R Bettini; M T Peracchia; P Santi
Journal:  Eur J Drug Metab Pharmacokinet       Date:  1996 Apr-Jun       Impact factor: 2.441

Review 4.  Pharmacoeconomics: where is the link with pharmacokinetics and biopharmaceutics?

Authors:  F Peys
Journal:  Eur J Drug Metab Pharmacokinet       Date:  1996 Apr-Jun       Impact factor: 2.441

Review 5.  Pharmacoeconomics: where is the link with pharmacokinetics and biopharmaceutics?

Authors:  F Peys
Journal:  Pharm World Sci       Date:  1997-04

Review 6.  Controlled release drug delivery systems to improve post-operative pharmacotherapy.

Authors:  Prabhat Bhusal; Jeff Harrison; Manisha Sharma; David S Jones; Andrew G Hill; Darren Svirskis
Journal:  Drug Deliv Transl Res       Date:  2016-10       Impact factor: 4.617

7.  Extended release drug delivery strategies in psychiatry: theory to practice.

Authors:  Steven J Siegel
Journal:  Psychiatry (Edgmont)       Date:  2005-06

8.  Single-dose pharmacokinetics of once-daily cyclobenzaprine extended release 30 mg versus cyclobenzaprine immediate release 10 mg three times daily in healthy young adults : a randomized, open-label, two-period crossover, single-centre study.

Authors:  Mona Darwish; Edward T Hellriegel; Fang Xie
Journal:  Clin Drug Investig       Date:  2008       Impact factor: 2.859

9.  Replenishable drug depot to combat post-resection cancer recurrence.

Authors:  Yevgeny Brudno; Matthew J Pezone; Tracy K Snyder; Oktay Uzun; Christopher T Moody; Michael Aizenberg; David J Mooney
Journal:  Biomaterials       Date:  2018-05-06       Impact factor: 12.479

10.  Effect of food on the pharmacokinetics of once-daily cyclobenzaprine extended-release 30 mg: a randomized, open-label, crossover, single-centre study.

Authors:  Mona Darwish; Fang Xie
Journal:  Clin Drug Investig       Date:  2009       Impact factor: 2.859

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