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Chlamydia Service Training For Support Staff - A Success! UK
Posted by: admin in Pharmacy Drugs on November 07th, 2009
On 14 October 2009, two half-day training sessions were held for support staff involved in the London commissioned chlamydia service. The training was run by the NPA Pharmacy Services team with support from the Terence Higgins Trust.
The main purpose of the training was to increase activity in the service by ensuring participants:
- Understood how the pharmacy chlamydia screen and treat service operates
- Understood how their role can support provision of the service in their pharmacy
- Would know how to approach young people in a pro-active, non-judgemental manner.
A total of 22 support staff attended from across the three PCTs commissioning the service: Westminster; Hammersmith and Fulham; and Kensington and Chelsea. 100% of delegates rated the overall usefulness of the training as excellent or very good.
Helen Rhodes, NPA Pharmacy Services Implementation Manager said: “The training covered how the pharmacy team can support provision of the service and how to approach young people. Pharmacy support staff can be essential to the success of a service like this ??” they are often the first person who the patient or public sees.”
“The skills that were developed on the day can also be used to approach patients and the public about any new pharmacy service. Most new pharmacy services are dependent upon the pharmacist and their team pro-actively engaging with patients and the public, for example, MURs, Health Checks and Weight Management. Where we see new pharmacy services operating well it usually also involves the drive and enthusiasm of the support staff.”
Source
National Pharmacy Association
IDSA: Old Drug Back in Favor but Resistance Growing (CME/CE)
Posted by: admin in Pharmacy Drugs on November 07th, 2009
- Explain to interested patients that polymyxin B, an antibiotic developed in the 1960s but long ignored, is regaining popularity because it works against infections that are resistant to more modern drugs.
- Note that this study was published as an abstract and presented at a conference. These data and conclusions should be considered preliminary until published in a peer-reviewed journal.
PHILADELPHIA — An old antibiotic — one of the last drugs still active against many bacteria — is facing rapidly developing resistance, a researcher said here.
Polymyxin B, which fell out of favor because of toxicity after it was developed in the 1960s, is becoming the treatment of last resort for some drug-resistant Gram-negative bacteria, according to Jason Kessler, MD, of Columbia University in New York.
But a retrospective analysis of clinical isolates tested at his institution showed that resistance to polymyxin B, while still low, increased 50% between 2006 and 2008, he said at the annual meeting of the Infectious Diseases Society of America.
The drug is an injectable agent and member of a class called polymyxins that also includes colistin, Kessler told reporters. They were left on the shelf because of kidney toxicity.
“Our clinical experience has been that the drug is relatively well-tolerated,” Kessler said, perhaps because several decades of progress have made it easier to manage the kidney issues.
Precisely because it has not been widely used, polymixin B is often still potent against bacteria, such as Klebsiella pneumoniae and Pseudomonas aeruginosa — that are resistant to many other classes of antibiotics. This has led to wider use of the old antibiotic, Kessler said.
In an attempt to measure that use, Kessler and colleagues checked to see how often clinical isolates were tested for resistance to polymyxin B at Columbia University Medical Center from 2005 through 2008.
Such testing, he said, could be considered a proxy for actual use, which is harder to measure. But it also offers information about the change in resistance over time, he said.
In 2005, Kessler said, the hospital tested 239 isolates from 99 patients and found that the vast majority of samples — 223 — were sensitive to the drug.
But in the following years, while the number of patients grew steadily, the proportion of resistant strains also grew sharply:
- In 2006, 937 isolates from 319 patients were tested, and 66 were resistant.
- In 2007, 1,210 isolates were tested from 382 patients and 138 were resistant.
- In 2008, 1,248 were tested, from 416 patients, and 122 were resistant.
Over the study period, Kessler and colleagues reported, 74% of the isolates tested for polymyxin susceptibility were resistant to at least three other classes of drugs and 32% to five classes.
The increasing use of polymyxin is not an isolated phenomenon, according to Neil Fishman, MD, of the University of Pennsylvania, who was not part of the study but who moderated a news conference at which it was discussed.
Fishman said his medical training in the 1980s included almost no mention of the drugs, except for the warning: “they’re toxic and you’ll never have to use them.”
“Starting two years ago, I did have to use them,” he said, adding that he and colleagues are still trying to learn how to use the drugs and to manage the toxicity.
An additional issue, he said, is that some of the drugs are in short supply. “Because they are old antibiotics, there aren’t a lot of companies making them and their use in increasing,” he said, “and it has become increasingly difficult to obtain some of the polymyxins for clinical use.”
The researchers did not report any external support or any conflicts.
Primary source: Infectious Diseases Society of America
Source reference:
Kessler J, et al “Changes in susceptibility to polymyxin B amongst clinical specimens in a New York hospital, 2005-2008″ IDSA 2009; Abstract 903.
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FDA Okays Diabetes Drug for First-Line Use, Adds Warning
Posted by: admin in Pharmacy Drugs on November 07th, 2009
WASHINGTON — The FDA has expanded the indication and prescribing language for the type 2 diabetes drug exenatide (Byetta), extending its approval to use as monotherapy for glycemic control in adults.
The updated warning label includes a pancreatitis caution, including nonfatal hemorrhagic or necrotizing pancreatitis, and an expansion of an existing warning for patients with renal impairment.
The new indication was based on a clinical study of 232 patients unable to achieve glycemic control through diet and exercise alone.
Those enrolled reduced blood sugar over three months by 0.7% and 0.9%. with the 5 mcg and 10 mcg dosages respectively versus placebo. Patients lost an average of around 6 pounds between exenatide groups.
Although the updated label warns of pancreatitis, a recent study found the disease was not more common in exenatide than in other type 2 diabetes drugs. (See EASD: No Extra Risk of Acute Pancreatitis Seen with Exenatide)
Additional side effects include severe allergic reactions, nausea, vomiting, diarrhea, dizziness, headache, jitters, and acidic stomach.
The injectable drug was the first GLP-1 receptor agonist for improved blood sugar after food intake for patients with type 2 diabetes. Exenatide was first marketed in 2005 by drug manufacturers Amylin Pharmaceuticals and Lilly.
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