Lesson 4 Testing Medicines Scientifically

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Presentation transcript:

Lesson 4 Testing Medicines Scientifically Beth Elmore Wizards Science Mill Creek Middle 2011-2012

Testing Medicines Scientifically How can we be certain that the foods we eat are safe, that the cosmetics we use won’t harm us, and that medical products are effective? In the United States, the Federal Food, Drug, and Cosmetic Act and several other laws protect the public’s safety. Before the Federal Food, Drug, and Cosmetic Act was passed in 1938, most products were not regulated. How are medicines, such as over-the-counter and prescription drugs, tested?

Materials For each student Book pages printed from online textbook Student Sheet 1.1, “Anticipation Guide: Ideas about Experimental Design,” from Activity 1

Reading The Role of the FDA Today, the U.S. Food and Drug Administration (FDA) enforces the laws on medical product safety and effectiveness. The FDA approves medicines that have been proven to be safe and effective for people to use. To be approved, a product must undergo and pass scientific tests. Usually, new medicines are first tested on animals to see whether they cause any harmful side effects. Only then are the medicines tested by volunteers in clinical trials. The results of clinical trials must show that the medicine Is both safe and effective before it can be approved for Use by the public.

Listen as your teacher reads aloud Listen as your teacher reads aloud. Stop when you see this yellow pencil and close your book. Write down the main ideas you just heard. Informed Consent In clinical trials, volunteers are chosen carefully. They must not be allergic to drugs similar to the one that will be tested. Also, they cannot be taking certain other medications. These things might make it more likely for them to experience harmful side effects. The volunteers must be told about any risks, such as possible side effects. They sign an informed consent form. This form states that they have been told (informed) about the risks and that they agree (consent) to participate in the trial.

Treatment and Control Groups The volunteers are then divided into two groups. One group receives a pill or liquid that contains the medicine being tested. The other group receives a pill or liquid that looks the same but contains only an inactive ingredient, such as sugar. This inactive pill is called a placebo (pla-SEE-bo). Neither the patients nor their doctors know who is receiving the medicine and who is receiving the placebo. The placebo is used as a control. It helps to prove that any improvement in the patient is due to the medicine and not to other aspects of the medical treatment. For example, just going to see a doctor may result in an improvement in a patient’s condition.

The Placebo Effect Why is it necessary to use placebos in clinical trials? For many years, scientists observed that people in clinical trials who receive placebos were more likely to show an improvement than other patients with the same disease. This improvement in the health of people receiving placebos is known as the placebo effect. Scientists give several explanations for the placebo effect. One factor is the regular, and often better, medical care that patients receive in a clinical trial. Another factor is the Psychological effect of participating in a clinical trial. A patient who is getting regular medical attention and a pill may have a more positive attitude toward his or her health. He or she may also be more careful about diet, exercise, or other factors related to the illness. As a result, this person may be more likely to recover because of this positive attitude, and not as a result of anything in the pill. Today, scientists and doctors are studying this connection Between a person’s mental attitude and his or her physical health to understand how they influence each other.

The Placebo Effect The placebo effect sometimes makes it difficult to determine if a treatment is effective. For example, the use of vitamin C to treat colds is controversial. Some studies suggest that vitamin C improves cold symptoms. Other studies suggest that vitamin C doesn’t work any better than a placebo, and that people who feel better from vitamin C are experiencing a placebo effect. Studies of high blood pressure, asthma, pain, depression, and cough have shown that about 30–40% of patients taking a placebo experience some relief of their symptoms. This relief can sometimes be measured objectively: for example, blood pressure actually drops in some patients taking placebos.

Analysis 1. In clinical trials of medicines, why is one group of volunteers given a placebo? Explain. 2. Activity 3, “Testing Medicines: A Clinical Trial,” simulated a clinical trial that investigated whether a headache medicine was effective. A person reporting a better or worse taste with the pink lemon drink (compared with the yellow lemon drink) represented a person feeling better after taking a pill for headache relief. In this simulation: a. What represented the medicine? b. What represented the placebo? c. Look at your data on Student Sheet 3.1, “Analysis of Clinical Trial.” How many people experienced the placebo effect? d. Look at your data on Student Sheet 3.1. How many people in the placebo group were unaffected by the placebo? 3. What is the purpose of a placebo? 4. In your own words, what is the placebo effect?

Analysis 5. Complete the “After” column for statements 5–9 on Student Sheet 1.1 “Anticipation Guide: Ideas about Experimental Design.” 6. Imagine a clinical trial to test a treatment for serious illnesses, such as heart disease or cancer. What is the trade-off of giving placebos to some people participating in this clinical trial?

Analysis Feel the same Feel better Feel worse Total number of in the group Control group (received placebo) 60 35 5 100 Treatment group (received medicine) 10 80 7. With your group, review the data shown above from a clinical trial of a cold medicine. You will record your answers to be turned in for a group grade. Have 1 person copy and complete a table like the one shown above to compare the number of people who feel better as a result of the medicine vs. the placebo. b. Is the medicine effective in a high percentage of the population? Explain your answer. c. Compare the percentage of people who feel worse in the placebo group vs. the percentage who feel worse in the treatment group. What difference do you observe? What could explain this difference? d. Would you conclude that this medicine is safe and effective for treating colds? Explain the evidence for your conclusion.

Analysis Feel the same Feel better Feel worse Total number of in the group Control group (received placebo) 50 46 4 100 Treatment group (received medicine) 41 55 8. Review the data shown above from a clinical trial of a stomachache pill. Think about whether the medicine works and how often side effects occur. Explain why this medicine should or should not be sold. Support your answer with evidence about the safety and effectiveness of this medicine. Homework: 9. Reflection: a. What evidence do you use to decide if cold, stomachache, or other over-the-counter medicines work for you? b. What effect do you think a positive attitude has on your everyday health? What about when you are sick?

End of lesson