Pharmaceutical companies report misleading RELATIVE, not ABSOLUTE (real) risk reduction percentages

Relative risk reduction figures do not consider the number of people in the study

When claiming a study’s risk-reduction results in favor of their drug, pharmaceutical companies usually claim RELATIVE risk percentages, which do not consider the number of subjects in the test groups.   Reporting RELATIVE risk reduction percentages, not ABSOLUTE (REAL) risk reduction percentages fits the old British adage . . . “There are LIES, BLOODY LIES and STATISTICS!”. To know the REAL risk reduction and effectiveness of a drug, you need to know the “Number needed to treat” (NNT). Drug manufacturers rely on the premise that statistics is a daunting subject for many people, including busy medical professionals who only have time to read a study’s summary.

Number Needed to Treat (NNT) answers the question:

“In a clinical trial, how many people  have to take a particular drug compared to those taking placebo to avoid one incidence of a specific medical issue?”

( NNT is treatment time specific. Studies of different duration are not comparable)

The pharmaceutical companies would rather you remained ignorant of the NNT, since it enables you to see that their results are nowhere near as impressive as they would have you believe.

An example of RELATIVE vs. ABSOLUTE risk-reduction

Based on the following study, Pfizer claims says that taking their drug Lipitorâ„¢ can decrease the chance of having a heart attack by 36%:

The Anglo-Scandinavian Cardiac Outcomes Trial lipid lowering arm: extended observations 2 years after trial closure

The study claimed an impressive 36% RELATIVE-risk reduction in heart attacks in a double-blind drug trial for people with multiple risk factors for heart disease who took atorvastatin ( Lipitor™) for 3.3 years.   The number of people enrolled in that trial was 10,305:

158 out of 5137 people (3.1%   i.e 3.1 out of 100) taking placebo had a heart attack;

104 out of 5168 people (2.0%   i.e. 2 out of 100) taking atorvastatin had a heart attack;

In other words, according to this study, if you have a bunch of risk factors for heart disease and your doctor prescribes you Lipitorâ„¢ your chances of having a heart attack in the next 3.3 years are 2 out of 100. If you don’t take Lipitorâ„¢, your chances of having a heart attack in the next 3.3 years are 3.1 out of 100). So in real risk terms, this is a REAL reduction of ~1% (i.e. 3.1% compared to 2%) – not really that impressive is it?  The NNT is 100, meaning 100 people need to take Lipitorâ„¢ for 3.3 years to prevent 1 heart attack.

So where does the impressive 36% risk reduction figure come from?   —-  3.1% of patients taking a placebo had a heart attack compared to 2% of patients taking Lipitor.” The study reports this as a RELATIVE risk reduction (comparing these two percentages) of about 36%, calculated as:

(3.1 – 2.0) / 3.1     x    100 = 35.4%

The same study claims a RELATIVE risk reduction of 22% in fatal and non-fatal strokes.  Whereas the REAL / ABSOLUTE risk reduction is a mere 0.6%! 

General NNT values for statin drugs w/treatment time 5 years

GROUP

NON-fatal Heart Attack

Death from any Cause

People who had a previous heart attack *NNT=~20NNT=~48
People who have risk factors for heart disease **NNT=70-250, depending on # of risk factorsNNT=500+ In actual clinical trials, there was no significant reduction in deaths or serious events, so a precise NNT is unavailable. Regardless, NNT>100 is pretty much irrelevant

* For people who had a previous heart attack – one person out of ~20 people treated for 5 years could prevent a NON-fatal heart attack, and the death of one person due to any cause could be prevented out of ~48 people treated

** People who have risk factors for heart disease – one person out of between 70 and 250 people (depending on how many risk factors they have) could prevent one NON-fatal heart attack, and the death of one person due to any cause could be prevented out of ~500 or more people treated (i.e. has an insignificant effect).

 

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When claiming a study's risk-reduction results in favor of their drug, pharmaceutical companies usually claim misleading RELATIVE risk percentages, which do not consider the number of subjects in the test groups. . .