Archive for the ‘Scott Gavura’ Category

Guest Blog: Adherence: The difference between what is, and what ought to be

Scott Gavura
Friday, March 16th, 2012

Scott Gavura, BScPhm, MBA, RPh, works in the Ontario cancer system and has a professional interest in improving the cost-effective use of drugs at the population level, primarily focusing on evaluating new drugs.  He is a registered pharmacist in Ontario. He blogs on the Science-Based Pharmacy blog which he describes as “Turning an eye on the profession, separating fact from fiction on both sides of the counter”. This post originally appeared on the Science-Based Medicine blog.

One of the most interesting aspects of working as a community-based pharmacist is the insight you gain into the actual effectiveness of the different health interventions. You can see the most elaborate medication regimens developed, and then see what happens when the “rubber really hits the road”: when patients are expected to manage their own treatment plan. Not only do we get feedback from patients, there’s a semi-objective measure we can use — the prescription refill history.

The clinical trial, from where we derive much of our evidence on treatments, is very much an idealized environment. The relationship to the “real world” may be tenuous. Patients in trials are usually highly selected, typically those that are able to comply with the intervention planned. They may need to be free of any other diseases which could complicate evaluation. Patients that qualify for enrollment enter an environment where active monitoring is the norm, and may be far more intense than normal clinical practice. All of these factors mean that trial results may be meaningful, but not completely generalizable to the patient that may eventually be given the intervention. It’s for this reason we use the term “efficacy” to describe clinical trial results, while “effectiveness” is what we’re more interested in: those real-word effects that are far more relevant, yet more elusive to our decision-making.  Efficacy measures a drug’s effect on an endpoint, and estimates risk and benefit in a particular setting. Effectiveness adds in real-world tolerance, the ability to tolerate the regimen, and all the other factors that are present when real patients take a drugs under less-than-ideal conditions. Consequently, effectiveness is a much more useful predictor of outcome than efficacy. Unfortunately, measurements of real-world effectiveness, possibly as a “phase 4″ or real-world trial, are rarely conducted. For the rest of Scott’s post click here.

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Guest Blog: What’s All That Other Stuff In My Medicine?

Scott Gavura
Friday, October 14th, 2011

Scott Gavura, BScPhm, MBA, RPh, works in the Ontario cancer system and has a professional interest in improving the cost-effective use of drugs at the population level, primarily focusing on evaluating new drugs.  He is a registered pharmacist in Ontario. He blogs on the Science-Based Pharmacy blog which he describes as “Turning an eye on the profession, separating fact from fiction on both sides of the counter”. This post originally appeared on the Science-Based Medicine blog.

If you read enough supplement advertisements, like I do, you’ll often see the purity of a product often cited as one of its merits. It’s usually some phrase like:

Contains no binders! No fillers! No colours! No excipients! No starch! No gluten! No coatings! No flow agents!

It’s a point of pride for supplement manufacturers to advertise that their product contains nothing but the labelled ingredient. And that’s also seen as an important benefit to many that purchase supplements. The perception from many consumers (based on my personal experience) seems to be that products are inferior if they contain non-drug ingredients. By this measure, drug products are problematic. Pharmaceuticals all contain an array of binders, coatings, supplements and fillers.  Even (gasp) artificial ingredients and sweeteners! And they’re often, though not always, disclosed on the package label.

But rather than being a negative feature, these supplementary, non-medicinal ingredients play a critical role in ensuring that drug products are of consistent and reproducible quality. Without them, we’d have products that are potentially unstable, we’d be unclear if they were actually being absorbed, and we wouldn’t know if they actually delivered any active ingredients into the body. In short, we’d be in the same situation we’re currently in with many herbal remedies and other types of supplements…Read More.

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Guest Blog: Who’s to Blame for Drug Shortages?

Scott Gavura
Tuesday, September 6th, 2011

Scott Gavura, BScPhm, MBA, RPh, works in the Ontario cancer system and has a professional interest in improving the cost-effective use of drugs at the population level, primarily focusing on evaluating new drugs.  He is a registered pharmacist in Ontario. He blogs on the Science-Based Pharmacy blog which he describes as “Turning an eye on the profession, separating fact from fiction on both sides of the counter”.

horizontalline

All the best efforts to practice science-based medicine are for naught when the optimal treatment is unavailable. And that’s increasingly the case – even for life-threatening illnesses. Shortages of prescription drugs, including cancer drugs, seem more frequent and more significant than at any time in the past. Just recently manufacturing deficiencies at a large U.S.-based contract drug manufacturer meant that over a dozen drugs stopped being produced. This lead to extensive media coverage, speculating on the causes and implications of what seems like a growing problem. So who’s to blame?

First, some perspective. Drug shortages are not a new problem, something that’s well known to every pharmacist reader of this blog. I’ve worked in almost every healthcare setting – and dealing with shortages is a time-consuming and frustrating part of the profession. However, the perception, even among health professionals, is that this situation is worsening. Statistics back this up. U.S. sources accurately track the prevalence of drug shortages and it hit a record high in the first half of 2011, with over 180 drugs reported to be in short supply. Before you blame the dysfunctional American health care system – it’s not just there. The same issues are occurring in Canada, and the United Kingdom, an some are worldwide. Managing shortages is a problem that affects all aspects of a patient’s treatment.

For the rest of this post click here.

Guest Blog: Good Idea, Bad Execution: Dosing Errors, A Preventable Harm

Scott Gavura
Wednesday, December 15th, 2010

Scott Gavura, BScPhm, MBA, RPh, works in the Ontario cancer system and has a professional interest in improving the cost-effective use of drugs at the population level, primarily focusing on evaluating new drugs.  He is a registered pharmacist in Ontario. He is a contributing blogger on the Science-Based Medicine blog whose only goal is to promote high standards of science in medicine.  A collection of his posts can be found here.


In my last post, I noted how cough and cold products for children have largely been withdrawn from the market due to their lack of efficacy, and the risks related to toxicity. Today’s post is going to dive a little more deeply into factors that can contribute to toxicity in the pediatric population. Let’s start with a vignette that may be familiar to parents:

The new father is wakened from a blissful, deep sleep by a crying child. Once Dad realizes when and where he is, and the source of the crying, he silently curses the short duration of action of the acetaminophen liquid he gave his child at bedtime. It has probably worn off already, and the fever is back. Stumbling into his child’s room in the dark, he can feel the heat radiating off his body. He fumbles around for the Tylenol, and something to measure it with. He can’t find the dropper bottle, but finds a bottle of syrup. It’s hard to measure the dose in the dark, and the medicine cup he finds is hard to read. “I think the dose is a teaspoon…that’s 5mL”. He pours the medicine into his child’s throat, tucks him back into bed, and both are back asleep within minutes.

Did this parent measure the acetaminophen dose correctly? What factors could contribute to a dosing error in this situation?

Dosing errors are among the most common and most preventable causes of adverse drug events in children. Why children? Drugs for children are often in liquid form for ease of measurement and administration. Typically dosed based on milligrams per kilogram, liquid formulations allow us to (in theory) deliver the exact dose that’s appropriate. But measurement isn’t always easy or intuitive. What’s the best way to measure 2.5mL (half a teaspoon)? How easy is it to confuse teaspoons (5mL) and tablespoons (15mL)? And what instructions should health professionals give parents and caregivers to ensure they can measure and administer a dose accurately? Despite the prevalence of dosing errors, there has been little evidence telling us what health professionals, or parents, can do better. Until now…

Click here to read the rest of Scott’s post.