Thyroid Malfunction Can Result in Serious Consequences

Exophthalmos. (Dr. Noorali Bharwani)
Exophthalmos. (Dr. Noorali Bharwani)

It is estimated 200 million people in the world have some form of thyroid condition. One in every three Canadians has a thyroid disorder. Of those, as many as 50 per cent are undiagnosed. Most thyroid disorders are five to seven times more common in women.

Thyroid hormones are produced in the thyroid gland from iodine and an amino acid, tyrosine. The normal function of the thyroid gland is to produce and secrete hormones. There are two hormones which are closely related: T3 (triiodothyronine) and T4 (thyroxine).

These hormones have enormous impact on our health, affecting all aspects of our metabolism. They maintain the rate at which our body uses fats and carbohydrates, help control our body temperature, influence our heart rate, and help regulate the production of protein. These hormones are important for normal growth and development of children.

Problems with the thyroid can be caused by iodine deficiency and autoimmune diseases, in which the immune system attacks the thyroid, leading either to hyperthyroidism (Graves’ disease) or hypothyroidism (Hashimoto’s disease).

Graves’ disease – overactive thyroid

This condition was first described by Caleb Parry in 1786, but the pathogenesis of thyroid disease was not discovered until later. Parry was an Anglo-Welsh physician credited with one of the earliest descriptions of the exophthalmic (bulging eyeballs) goiter, published in 1825.

Now the condition is known as Graves’ disease. It is named after Robert J. Graves, an Irish physician who described it in 1835. Graves’ disease is an autoimmune disease characterized by hyperthyroidism (over active thyroid gland). We don’t know why this happens.

Graves’ disease is the most common cause of hyperthyroidism. The condition accounts for at least 90 per cent of all patients with hyperthyroidism. It is an autoimmune condition. The immune system normally produces antibodies to protect us and are designed to target a specific virus, bacteria or other foreign substance. Here, it is attacking our own system. An enemy within us!

Clinically, hyperthyroidism presents with palpitations, nervousness, tremor, heat intolerance, weight loss, muscular weakness and quite often there is goiter.

In Graves’ eye disease, the eyes are painful, red and watery – particularly in sunshine or wind. The eye lids and tissues around the eyes are swollen with fluid. The eyeballs bulge out of their sockets (exophthalmos). Because of eye muscle swelling, the eyes are unable to move normally and there may be blurred or double vision. Some patients have decreased colour vision as well.

With treatment, in most patients, the eyes tend to get somewhat better when the thyroid abnormality has been treated.

Hashimoto’s disease – underactive thyroid

There is another autoimmune thyroid condition called Hashimoto’s thyroiditis. It is named after Japanese physician Hakaru Hashimoto (1881−1934), who first described the symptoms in 1912. It affects more women than men.

This condition is characterized by the destruction of thyroid cells by various cell- and antibody-mediated immune processes. This condition is the most common cause of hypothyroidism. The treatment of choice for Hashimoto thyroiditis is thyroid hormone replacement.

Hypothyroidism causes many symptoms: weight gain, lethargy, cold intolerance, menstrual irregularities, depression, constipation, and dry skin. Deficiency of thyroid hormones in children leads to dwarfism and mental retardation.

Treatment of hypothyroidism with synthetic thyroid hormone is usually simple, safe and effective. Finding an adequate replacement dosage of thyroid may take a little time.

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Are we making any progress in the management of pancreatic cancer?

"We can learn a lot from trees: they're always grounded but never stop reaching heavenward." -Everett Mamor
"We can learn a lot from trees: they're always grounded but never stop reaching heavenward." -Everett Mamor

Some years ago, my sister died of pancreatic cancer. She was only 60-years old. Not long ago, a friend of mine died of the same illness. Over the years, as a general surgeon, I have looked after many patients with pancreatic cancer. None of them lived more than six to 12 months after diagnosis.

Most common pancreatic cancer is pancreatic adenocarcinoma and this represents more than 90 per cent of diagnoses.

Long-term prognosis for pancreatic cancer depends on the size and type of the tumor, lymph node involvement and degree of metastasis at the time of diagnosis. The earlier pancreatic cancer is diagnosed and treated, the better the prognosis. Is this possible?

Unfortunately, pancreatic cancer usually shows little or no symptoms until it has advanced and spread. Therefore, most cases (up to 80 percent) are diagnosed at later, more difficult-to-treat stages.

Compared with many other cancers, the combined five-year survival rate for pancreatic cancer – the percentage of all patients who are living five years after diagnosis – is very low at just five to 10 per cent. This is because far more people are diagnosed as stage IV when the disease has metastasized.

With this information in my mind, I was curious to read an article on this subject in the Canadian Medical Association Journal (Advances in the management of pancreatic ductal adenocarcinoma, CMAJ June 7, 2021).

The article says the incidence of pancreatic carcer is rising and is projected to become the third leading cause of cancer death in Canada. The reason for this is not known. Observational studies have shown that smoking, obesity and a prolonged history of diabetes, are associated with a higher risk of developing pancreatic cancer. A family history of pancreatic cancer in a first degree relative is reported in about 10 per cent of patients.

Surgical resection remains the only opportunity to cure pancreatic cancer, and only about 20 per cent of patients present with resectable disease.

The CMAJ article has five recommendations for the management of pancreatic cancer:

  1. Germline testing is now recommended for all patients with pancreatic cancer. Pancreatic cancer is associated with numerous hereditary syndromes and the results of germline testing can help guide treatment selection.
  2. In suitable patients, modified FOLFIRINOX is the adjuvant chemotherapy regimen of choice, after surgical resection.
  3. Neoadjuvant approaches for resectable disease are increasingly common and should be considered in patients with high-risk features such as an elevated carbohydrate antigen 19.9 level at diagnosis.
  4. Patients with borderline resectable or locally advanced pancreatic cancer should have induction combination chemotherapy, when possible, before consideration of surgical resection or a local therapy.
  5. If resources allow, patients with advanced pancreatic cancer should have molecular profiling of their tumours to detect uncommon but therapeutically targetable somatic alterations.

These five treatment options are not easy to understand for people who are not involved in the management of pancreatic cancer. And cure for pancreatic cancer is nowhere in sight. Cure is only possible if the cancer is diagnosed early. Only up to 10 per cent of patients who receive an early diagnosis become disease-free after treatment. For rest of the pancreatic cancer patients the prognosis is poor.

If the tumour is resectable and there are no metastases then the person can live for 2.5 years after their diagnosis and have a five-year survival rate of 20 to 30 percent.

For early detection of cancer, we put many individuals through screening tests like pap smears, mammograms, colonoscopies etc. Should we put individuals age 60-years and older to go through ultrasound, computerized tomography (CT) scans, magnetic resonance imaging (MRI) and endoscopic ultrasound (EUS) to pick up early pancreatic cancer? Can the health care system afford the cost of it? How many people will benefit? How many lives will be saved? Something for us to think about.

Be safe. Take care.

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Antihistamines Should Be Used Properly

Pacific Ocean. (Dr. Noorali Bharwani)
Pacific Ocean. (Dr. Noorali Bharwani)

Antihistamines are used to treat hay fever and other allergies. They work by preventing the effects of histamine, which is produced by the body. Histamine can cause itching, sneezing, runny nose, and watery eyes.

Allergic reaction occurs when our body’s immune system mistakes a harmless substance for a harmful one, and the body releases chemicals to fight it. This reaction is what causes the symptoms.

Hay fever is an allergic reaction to substances in the air like pollen. This can be indoors or outdoors. Besides pollen, one can have allergy to dust mites, or tiny flecks of skin and saliva shed by cats, dogs, and other animals with fur or feathers.

Allergic rhinitis refers to inflammation of the nasal passages due to the release of histamine and other mediators in the nose. Allergy testing helps with the diagnosis. Allergic rhinitis may be seasonal (usually due to grass, tree or weed pollens) or perennial (due to triggers such as pet hair, house dust mite or mould). Allergic rhinitis can lead to increased asthma symptoms.

Allergic conjunctivitis is another condition similar to allergic rhinitis. It can be seasonal due to pollens or perennial due to allergens present all year.

An article titled “How to use antihistamines,” was published in the Canadian Medical Association Journal (CMAJ April 6, 2021) which says, “Antihistamines are among the most commonly and incorrectly used medicines worldwide.”

The article says antihistamine use is most strongly supported for treating allergic rhino-conjunctivitis (hay fever) and urticaria (hives). It says we should not use antihistamines for conditions where antihistamines have questionable utility, such as in managing asthma, eczema, or cough.

Older (first generation) antihistamines are associated with substantial and sometimes fatal adverse effects. They cause sedation, injury and impairment in sleep. They interfere with mental and cognitive function, including impaired performance at school.

Older antihistamines should be avoided in the elderly. Overdose can result in death. Examples of older antihistamines are: Benadryl, Chlor-Tripolon, and Atarax.

The CMAJ article says, “Newer antihistamines are safer, as affordable and as efficacious as first-generation antihistamines.”

Compared with first-generation antihistamines, systematic reviews of randomized controlled trials have found newer antihistamines to be safer, longer lasting (12–24 hours) and faster acting. Their effect is felt in 50 minutes compared to 80 minutes for the first-generation antihistamines.

Warning – no antihistamine should be consumed with alcohol. And antihistamines should not be used for anaphylaxis. For this purpose, epinephrine is the drug of choice.

What you should know about second generation antihistamines.

Second generation antihistamines are newer medicines. Many treat allergy symptoms without causing sleepiness. The CMAJ article gives a summary of preferred antihistamines for allergy and urticaria: Bilastine, Cetirizine (Reactine), Desloratadine (Aerius), Fexofenadine (Allegra), Loratadine (Claritin), Rupatadine (Rupall).

It is important to remember some antihistamines are mixed with other medicines. These could include pain relievers or decongestants. These are meant to treat many symptoms at the same time. It is a good idea to treat just the symptoms that you have. If you have only a runny nose, don’t choose a medicine that also treats headache and fever.

There are other uses of antihistamines. For example: to prevent motion sickness, nausea, vomiting, and dizziness. In addition, since antihistamines may cause drowsiness as a side effect, some of them may be used to help people go to sleep, relieve anxiety, and produce sleep before surgery.

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Benefits and risks of COVID-19 vaccines.

Cactus in Arizona. (Dr. Noorali Bharwani)
Cactus in Arizona. (Dr. Noorali Bharwani)

“There is solid medical and scientific evidence that the benefits of vaccines far outweigh the risks. Despite this, there have been concerns about the safety of vaccines for as long as they have been available in the U.S,” says Centre for Disease Control and Prevention (CDC) on its website under the title of Vaccine Safety.

“Vaccine risks are rare,” according to Dr. Supirya Sharma. She said this last year. She is a senior medical advisor for Canada’s health department. “The benefits outweigh the potential risks, but it is still a drug and still a vaccine and there are potential risks even if they’re rare,” Sharma said. “That’s why we continue to monitor it.”

Sharma has said that the three vaccines authorized in Canada so far offer excellent protection and, along with public health measures, can help slow the spread of the virus and potentially help stop it from mutating even further.

“We knew this was going to happen, that we would have variants,” she said, in an interview with The Canadian Press.

There is still a lot we are learning about COVID-19 vaccines.

We know that COVID-19 has caused very serious illness and death for a lot of people.

The biggest benefit is vaccines vastly reduce your chances of getting COVID-19. They also to an even greater degree protect against hospitalisation and death. We don’t know how long protection lasts for those who are vaccinated. It’s concerning seeing breakthrough infections, and the worry is that they might increase if vaccine protection does, as suspected, fall over time.

The US Centers for Disease Control and Prevention led a nationwide study of vaccination involving more than 3,600 adults hospitalized for Covid-19 between March and August.

The study found Pfizer vaccine provided 88 per cent protection against hospitalization, and Moderna was 93 per cent effective. Johnson & Johnson’s Janssen vaccine comes in third, but still provides 71 per cent protection.

Vaccine failure

According to an article in The Conversation Canada (September 9, 2021) titled “Four factors that increase the risk of vaccinated people getting COVID” are:

  1. Vaccine type
  2. Time since vaccination
  3. Variants
  4. Your immune system

Two weeks after your second COVID-19 vaccine dose, the protective effects of vaccination will be at their highest. At this point, you’re fully vaccinated. If you still get COVID-19 after this point, you’ve suffered a “breakthrough” infection.

In the UK, research has found that 0.2 per cent of the population – or one person in every 500 – experiences a breakthrough infection once fully vaccinated. But not everyone is at the same risk. Four things appear to contribute to how well you are protected by vaccination.

1. Vaccine type

The first is the specific vaccine type you received and the relative risk reduction that each type offers. Relative risk reductions for the Moderna vaccine reduced a person’s risk of developing symptomatic COVID-19 by 94 per cent, while the Pfizer vaccine reduced this risk by 95 per cent. The Johnson & Johnson and AstraZeneca vaccines performed less well, reducing this risk by about 66 pr cent and 70 per cent respectively.

2. Time since vaccination

It’s becoming increasingly evident that length of time since vaccination is also important and is one of the reasons why the debate over booster immunisations is growing in intensity.

Some reports suggests that the Pfizer vaccine’s protection wanes over the six months following vaccination. Report from Israel also suggests that this is the case. It’s too soon to know what happens to vaccine efficacy beyond six months in the double vaccinated, but it’s likely to reduce further.

3. Variants

Current information suggests the vaccines are slightly less protective against variants.

4. Your immune system

If your immunity is compromise due to your age or other medical conditions, you will have lower levels of vaccine-induced protection against COVID-19. This raises the question – who should get a booster shot?

There is solid medical and scientific evidence that the benefits of vaccines far outweigh the risks. Get your shot and don’t forget the importance of wearing your mask, washing your hands and maintaining social distance.

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