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Docs Tag: blood

Congenital Heart Defects

What is congenital heart disease?

Congenital heart disease is a heart condition you are born with. The word congenital means “present at birth.” Congenital heart disease can range from very minor conditions which never cause problems, to more serious conditions that require treatment.

A congenital heart defect happens when the chambers, walls or valves of your heart – or the blood vessels near the heart – don’t develop normally before birth. There are many different types of defects listed below.

1. Holes in the heart (septal defects)

When a baby is born with an abnormal opening in the wall that separates the right and left chambers of the heart (the septum), blood can leak between the chambers instead of flowing normally to the rest of the body. This may cause the heart to become enlarged.

The most common holes in the heart are:

  • Atrial septal defect (ASD) Normally, oxygen-rich blood that’s already been to the lungs flows from the left atrium to the left ventricle, out the aorta and to the body. An abnormal opening between the right and left atria (the upper chambers of the heart) allows some blood from the left atrium to leak back into the right atrium. Your heart has to work extra hard to move the extra blood out to the lungs. The seriousness of the problem depends on the size of the opening.

    Patent foramen ovale (PFO) is one type of atrial septal defect. The hole between the left and right atria usually closes within the first few years of life. Even if it doesn’t close, the hole may not cause any complications unless you have a second heart defect. PFOs are very common and many people will never know they have one.

  • Ventricular septal defect (VSD) If there is a hole between your right and left ventricles, oxygen-rich blood returning from your lungs leaks from the left ventricle into the right ventricle instead of being pumped into the aorta and out to the rest of your body. Depending on the size of the opening, you may need surgery to close the hole.

2. Obstruction of blood flow

Stenosis is a narrowing or obstruction in heart valves, arteries or veins that affects the flow of blood. Atresia is when a passageway in the body is abnormally shut or has not formed properly. Different types of stenosis and atresia can partly or completely block blood flow in the heart.

  • Pulmonary valve stenosis If your pulmonary valve narrows, the flow of oxygen-poor blood from the right ventricle through the pulmonary arteries to your lungs is restricted. This interferes with the blood’s ability to pick up oxygen and deliver it to the rest of your body. The right ventricle has to work harder to pump blood through the narrowed pulmonary valve and the pressure in the heart is often increased.
  • Pulmonary atresia The pulmonary valve lets blood flow from the right ventricle to the lungs via the pulmonary artery. In pulmonary atresia, the pulmonary valve does not form properly and it remains closed at birth. Blood is not able to flow properly to the lungs to get oxygenated. If left untreated, this condition is fatal. Visit About Kid’s Health to learn more.
  • Tricuspid atresia The tricuspid valve controls blood flow between the right atrium and the right ventricle. In tricuspid atresia, the valve does not form properly and there is no opening between these two chambers. Blood is not able to flow from the right atrium into the right ventricle and then onto the lungs, to get oxygenated. If left untreated, this condition is fatal. Visit About Kid’s Health to learn more.
  • Aortic stenosis When the aortic valve narrows, blood flow is restricted from the heart through the main artery to your body (aorta) and onwards to the rest of the body. As a result, the left ventricle has to contract harder to push blood across the aortic valve. This eventually weakens the heart muscle and makes your heart less efficient. Surgery may be necessary. Aortic stenosis can be treated, but life-long follow-up will be needed.
  • Coarctation of the aorta This is the narrowing of the largest artery in the body. When the aorta is pinched or constricted, the flow of blood to the lower part of the body is reduced and blood pressure above the constriction is increased. The heart is forced to pump harder in order to deliver enough blood to the rest of your body. Coarctation of the aorta can range from mild to severe. It usually occurs with other heart defects. The condition can be treated, but life-long follow-up will be needed.
  • Patent ductus arteriosus The ductus arteriosus is a passageway for blood between the aorta and pulmonary artery that normally closes a few days after birth. If it fails to close properly, too much blood flows to the lungs. The condition is common in premature babies, but rare in full-term babies. How serious it is depends on how large the opening is and how premature the baby is. In some circumstances an open ductus is necessary for survival – where blood flow is blocked, or if the blood vessels supplying the lungs and body are switched (transposition of the great arteries).

    Medication in the first few weeks of life can either close (or keep open) the ductus arteriosus. As your baby gets older and if the medication isn’t working, the ductus can be closed off using a cardiac catheterization procedure. This will restore normal circulation.

  • Blue babies (cyanotic defects) When blood that is pumped from the lungs and heart to the body contains less-than-normal amounts of oxygen, it causes a blue discoloration of the skin, lips, gums, nail beds, and the areas around the eyes and mouth (cyanosis). There are several different conditions that can lead to a blue baby.
    • Tetralogy of fallot is a combination of four defects that make the level of oxygen in the blood too low:
      • A large hole in the wall between the two ventricles allows some oxygen-rich blood to be pumped to the right side of the heart instead of to the rest of the body through the aorta. (See ventricular septal defect above.)
      • A narrowing of the pulmonary valve can block the flow of blood from the right side of the heart to the lungs. (See pulmonary valve stenosis above.)
      • A more-muscular-than-normal right ventricle can cause the heart muscle to become stiff over time, eventually making the heart weak (right ventricular hypertrophy).
      • An aorta that lies directly over the right ventricle allows a mixture of oxygen-rich and oxygen-poor blood to flow into the aorta (overriding aorta).
    • Transposition of the great arteries In this condition, your baby’s pulmonary artery and the aorta are reversed. Their aorta is connected to the right ventricle, so most of the blood returning to the heart from the body is pumped back out to their body without first getting oxygen from the lungs. The pulmonary artery is connected to the left ventricle, so that most of the oxygen-rich blood returning from their lungs goes back to the lungs again. The condition is often detected during the first week of life and can be corrected with surgery during your baby’s first month.

      Other defects between the right and left sides of the heart often co-exist with transposition of the great arteries. An atrial septal defect, ventricular septal defect or ductus arteriosus can actually help oxygenated blood circulate to the body.

    • Ebstein’s anomaly The tricuspid valve controls blood flow between the right atrium and the right ventricle. Ebstein’s anomaly is a rare condition in which the tricuspid valve is located lower than normal and has abnormal flaps (leaflets). This can cause blood to leak backwards through the valve and prevent the heart from working efficiently. This causes the ventricle to be too small and the atrium to be too large. Many children with Ebstein’s anomaly have mild cases that don’t cause symptoms. If your child’s tricuspid valve is leaking badly, heart valve surgery may be necessary.
  • Hypoplastic left heart syndrome Children born with this syndrome have an underdeveloped left side of their heart.
    • The left ventricle is underdeveloped and too small.
    • The mitral valve is not formed or too small.
    • The aortic valve is not formed or too small.
    • A part of the aorta (the ascending aorta) is underdeveloped or too small.

    Children with this condition often have an atrial septal defect as well (see above).

  • Information taken from https://www.heartandstroke.ca/heart/conditions/congenital-heart-disease

Crohn’s and Colitis

WHAT ARE CROHN’S AND COLITIS?

Inflammatory bowel disease (IBD) describes a group of conditions, the two main forms of which are Crohn’s disease and ulcerative colitis. IBD also includes indeterminate colitis.

Crohn’s disease and ulcerative colitis are diseases that inflame the lining of the GI (gastrointestinal) tract and disrupt your body’s ability to digest food, absorb nutrition, and eliminate waste in a healthy manner.

Below you fill find more information about the anatomy and function of the gastrointestinal (GI) tract, Crohn’s disease and ulcerative colitis.

Dr. Mike Evans is founder of the Health Design Lab at the Li Ka Shing Knowledge Institute, an Associate Professor of Family Medicine and Public Health at the University of Toronto, and a staff physician at St. Michael’s Hospital. This video was made possible through the Gastrointestinal Society, with the support of Crohn’s and Colitis Canada.

ANATOMY AND FUNCTION OF THE GI TRACT

In order to understand Crohn’s disease and ulcerative colitis, it is first helpful to understand the anatomy and function of the healthy gastrointestinal (GI) tract. Below is a medical illustration of the GI tract. When you eat, food travels through the GI tract in the following order:

Digestive-SystemNumbered-1.gif

Mouth [ 1 ]

Esophagus [ 2 ] (tube that connects the mouth to the stomach)

Stomach [ 3 ] (food is mixed with stomach acid and enzymes to break down the material into smaller pieces called chyme)

Small Bowel [ 4 ] (or the ‘Small Intestine’) is made up of three sections: Duodenum [ 7 ] (about 8 cm in length); Jejunum [ 8 ] (around 3 metres long); and Ileum [ 9 ] (about 3 metres in length).

The functions of the small bowel are to digest your food and absorb the nutrients. In particular, the jejunum and ileum are the organs responsible for absorbing nutrients from your food. Without the small bowel, we would not be able to convert food into useable nutrition.

Ileocecal Valve [ 5 ] (regulates the amount of material passed from the small bowel to the large bowel and prevents “dumping” all at once)

Large Bowel [ 6 ] (also called the Large Intestine or the Colon). The colon is much wider in diameter than the small bowel and is approximately 1.5 metres long. The different sections of the colon are identified as the:

  • Cecum [ 10 ] and appendix [ 11 ] 
  • Ascending colon
  • Hepatic flexure (a bend in the gut at close to the location of the liver)
  • Transverse colon
  • Splenic flexure (another bend located near the spleen)
  • Descending colon
  • Sigmoid colon
  • Rectum [ 12 ]
  • Anus [ 13 ]

The main functions of the colon are to extract water and salt from stool, and store it until it can be expelled via the anus.

Stool is the by-product of digestion through the GI tract. When stool first enters the colon from the small bowel, it is very watery. As it traverses the large bowel, water is reabsorbed and the stool gradually becomes firmer.
In a healthy individual, it is usually composed of water, dead and living bacteria, fiber (undigested food), intestinal mucous, and sloughed-off lining of the gut. It is not normal to have blood in feces, nor large amounts of mucous. Stool from an individual without any gut disease is soft enough to pass comfortably from the rectum and anus, and (depending on the person) is typically expelled one or two times a day.

Bowel movements are an entirely different matter for someone with Crohn’s or colitis. Individuals with these diseases face some very real challenges related to feelings of urgency, diarrhea, and bloody stool.

WHAT IS CROHN’S DISEASE

Digestive-SystemNumbered-1.gif

Crohn’s disease is named after the doctor who first described it in 1932 (also known as ‘Crohn disease’).

Inflammation from Crohn’s can strike anywhere in the gastrointestinal (GI) tract, from mouth to anus, but is usually located in the lower part of the small bowel and the upper colon.

Patches of inflammation are interspersed between healthy portions of the gut, and can penetrate the intestinal layers from inner to outer lining.

Crohn’s can also affect the mesentery, which is the network of tissue that holds the small bowel to the abdomen and contains the main intestinal blood vessels and lymph glands.

 

WHAT IS ULCERATIVE COLITIS

Digestive-SystemNumbered-1.gif

Ulcerative colitis is more localized in nature than Crohn’s disease. Typically, the disease affects the colon (large intestine) including the rectum and anus, and only invades (inflames) the inner lining of bowel tissue.

It almost always starts at the rectum, extending upwards in a continuous manner through the colon. Colitis can be controlled with medication and in severe cases can even be treated through the surgical removal of the entire large intestine.

WHAT IS INDETERMINATE COLITIS:

Indeterminate colitis is a term used when it is unclear if the inflammation is due to Crohn’s disease or ulcerative colitis.

SYMPTOMS OF CROHN’S DISEASE AND ULCERATIVE COLITIS

Crohn’s disease and ulcerative colitis are (lifelong) diseases. People with these diseases experience acute periods of active symptoms (active disease or flare), and other times when their symptoms are absent (remission).

Symptoms can include abdominal pain and cramping; severe diarreha; rectal bleeding; blood in stool; weight loss and diminished appetite.

Visit our Signs and Symptoms page for more information. 

COMPARING CROHN’S DISEASE AND ULCERATIVE COLITIS

There are similarities and differences between Crohn’s disease and ulcerative colitis. We’ve already described above how Crohn’s disease and ulcerative colitis involve different areas of the gastrointestinal tract.

Other characteristics of Crohn’s disease and ulcerative colitis that may differ include: symptoms; the effect of surgery; treatment options; complications or extra-intestinal manifestations; and impact of smoking.

These characteristics are summarized in the table below:

Crohn’s Disease Ulcerative Colitis
Occurrence More females than males
All ages, peak onset 15-35 years
Similar for females and males
All ages, usual onset 15-45 years
Symptoms Diarrhea, fever, sores in the mouth and around the anus, abdominal pain and cramps, anemia, fatigue, loss of appetite, weight loss Bloody diarrhea, mild fever, abdominal pain and cramps, anemia, fatigue, loss of appetite, weight loss
Terminal ileum involvement Common Never
Colon involvement Common Always
Rectum involvement Common Always
Peri-anal disease Common Never
Distribution of disease Patchy areas of inflammation Continuous areas of inflammation but can be patchy once treated
Endoscopic findings Deep and snake-like ulcers Diffuse ulceration
Depth of inflammation May be transmural, extending through the entire thickness of the wall of an organ or cavity deep into tissues Shallow, mucosal
Fistulas between organs Common Never
Stenosis Common Never
Granulomas on biopsy Common Never
Effect of surgery Often return following removal of affected parts. Decreased likelihood of pregnancy. Usually cured by removal of colon (colectomy). Decreased likelihood of pregnancy after ileoanal pouch.
Treatment options Drug treatment (corticosteroids, immune modifiers, biologic therapies). Exclusive formula diet in children. Surgery (repair fistulas, remove obstruction, resection, and anastomosis). Drug treatment (5-aminosalicylates, sulfasalazine, corticosteroids, immune modifiers, biologic therapies). Surgery (rectum/colon removal) with creation of an internal pouch (ileoanal pouch).
Cure No existing cures. Maintenance therapy is used to reduce the chance of relapse. Through colectomy only. Maintenance therapy is used to reduce the chance of relapse.
Bowel complications Blockage of intestine due to swelling or formation of scar tissue. Abscesses, sores, or fistulas. Malnutrition. Colon cancer. Bleeding from ulcerations. Perforation (rupture) of the bowel. Malnutrition. Colon cancer.
Extra-intestinal disease Osteoporosis. Liver inflammation (primary sclerosing cholangitis). Blood clots. Pain and swelling in the joints (arthritis). Growth failure (in children). Mental Illness. Liver inflammation (primary sclerosing cholangitis). Blood clots. Eye inflammation (iritis). Pain and swelling in the joints (arthritis). Mental illness.
Smoking Higher risk of acquiring for smokers Higher risk of acquiring for ex-smokers
Mortality risk Increased risk of colorectal cancer and overall mortality. Increased risk of lymphoma and skin cancer (due to treatments). Increased risk of colorectal cancer. Uncertain change in mortality risk. Increased risk of lymphoma and skin cancer (due to treatments).

Image reference. Impact of Inflammatory Bowel Disease in Canada. 2018.

Information taken from https://crohnsandcolitis.ca/About-Crohn-s-Colitis/What-are-Crohns-and-Colitis

 

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Bone Marrow/Stem Cell Transplant

What is the Difference Between a Bone Marrow Transplant and a Stem-cell Transplant?

There are two different types of transplants: bone marrow transplants and peripheral blood stem-cell transplants (PBSCTs). The difference between the two depends on where the stem cells are taken from. In bone marrow transplants, the stem cells are taken from the bone marrow. In PBSCTs, the stem cells are taken from the circulating blood. PBSCTs are now more commonly performed than bone marrow transplants, as the procedure is easier and the body is able to regenerate new stem cells faster.

Transplants fall into three basic donor categories:

syngeneic transplant is when the cells are donated by an identical twin. Allogeneic is when the donor’s basic cell is almost identical to the patient’s as with a close relative (brother or sister). Rarely is the basic cell type matched by an unrelated relative.

Autologous is when the patient’s own stem cells are removed from his or her bone marrow or bloodstream. With types of NHL that have spread to the bloodstream or bone marrow, it may be difficult to obtain uncontaminated cells or cells that can be used, even after treating them in a laboratory to remove or kill the NHL cells.

Marrow or cell transplantation is done to replace healthy cells that have been destroyed by cancer treatment. Bone marrow or stem cells that have been removed from a donor are carefully frozen and stored while the patient receives high-dose chemotherapy and sometimes whole-body radiation treatment. This process kills all or most normal stem and bone marrow, while destroying cancer cells. This leaves them defenseless against infection and unable to form blood. After therapy, the frozen marrow or cells are thawed and put back in the body. During the recovery period, all of the body’s systems must be carefully monitored for rejection, infection and the need for any supportive treatments.

Information taken from https://www.lymphoma.ca/lymphoma/patient-journey/treatment/bone-marrow-transplant

 

Valvular Heart Disease

What is valvular heart disease?
The heart has four chambers. The two upper chambers are called the left and right atrium, and the two lower chambers are called the left and right ventricle. The four valves at the exit of each chamber maintain one-way continuous flow of blood through the heart to the lungs and the rest of the body.
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The four valves are the tricuspid valve, pulmonary valve, mitral valve and aortic valve.

  • Oxygen-poor blood coming into your heart from your body flows into the right atrium. The tricuspid valve is the valve between the right atrium and the right ventricle. It opens so blood can be pumped to the right ventricle.
  • The pulmonary valve controls blood flow between the right ventricle and the lungs. It opens to let the heart pumps blood out of the ventricles into the pulmonary artery toward the lungs so it can pick up oxygen. The oxygen-rich blood flows back from the lungs into the left atrium.
  • The mitral valve lies between the left atrium and the left ventricle. It opens so the oxygen-rich blood from the left atrium can be pumped into the left ventricle.
  • The aortic valve controls blood flow from the left ventricle into the aorta (the main artery in your body). When this valve opens, the oxygen-rich blood is pumped to the aorta and then out to fuel the rest of your body.

In between each step, the valve closes to prevent blood from flowing backwards and mixing oxygen-poor blood with oxygen-rich blood. The one-way continuous flow of blood delivers oxygen throughout your body.

Heart valve disease occurs when one or more of the heart valves do not open or close properly. When it affects more than one heart valve, it is called multiple valvular heart disease.

  • Stenosis is when the valve opening becomes narrow and restricts blood flow.
  • Prolapse is when a valve slips out of place or the valve flaps (leaflets) do not close properly.
  • Regurgitation is when blood leaks backward through a valve, sometimes due to prolapse.

Heart valve disease can be classified as mild, moderate or severe. It can lead to an enlarged heart or heart failure. Heart failure is a serious medical condition where the heart cannot pump enough blood to meet the body’s need for oxygen.

Many valvular heart diseases can be treated with medication, or surgery and other procedures to repair or replace the valve.

The four valves are the tricuspid valve, pulmonary valve, mitral valve and aortic valve.

  • Oxygen-poor blood coming into your heart from your body flows into the right atrium. The tricuspid valve is the valve between the right atrium and the right ventricle. It opens so blood can be pumped to the right ventricle.
  • The pulmonary valve controls blood flow between the right ventricle and the lungs. It opens to let the heart pumps blood out of the ventricles into the pulmonary artery toward the lungs so it can pick up oxygen. The oxygen-rich blood flows back from the lungs into the left atrium.
  • The mitral valve lies between the left atrium and the left ventricle. It opens so the oxygen-rich blood from the left atrium can be pumped into the left ventricle.
  • The aortic valve controls blood flow from the left ventricle into the aorta (the main artery in your body). When this valve opens, the oxygen-rich blood is pumped to the aorta and then out to fuel the rest of your body.

In between each step, the valve closes to prevent blood from flowing backwards and mixing oxygen-poor blood with oxygen-rich blood. The one-way continuous flow of blood delivers oxygen throughout your body.

Heart valve disease occurs when one or more of the heart valves do not open or close properly. When it affects more than one heart valve, it is called multiple valvular heart disease.

  • Stenosis is when the valve opening becomes narrow and restricts blood flow.
  • Prolapse is when a valve slips out of place or the valve flaps (leaflets) do not close properly.
  • Regurgitation is when blood leaks backward through a valve, sometimes due to prolapse.

Heart valve disease can be classified as mild, moderate or severe. It can lead to an enlarged heart or heart failure. Heart failure is a serious medical condition where the heart cannot pump enough blood to meet the body’s need for oxygen.

Many valvular heart diseases can be treated with medication, or surgery and other procedures to repair or replace the valve.

Information taken from https://www.heartandstroke.ca/heart/conditions/valvular-heart-disease

Haemophilia

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Blood Pressure Test

What is a Blood Pressure test?

Throughout your body, your heart pumps blood through blood vessels.  The heart can pump the blood fast and slow.  For example, think about a garden hose.  If the water is just trickling out, the water is moving slow and at a low force, but if you turn on the hose all the way, the water shoots out really fast and at a high force.  This is how your blood vessels work; your heart can pump blood through the vessels slow or fast.  To measure how your blood is moving around your body, the blood pressure test is used.

A blood pressure test (sphygmomanometer) measures the force (how fast or slow) of the blood moving through your blood vessels.  You may remember hearing numbers when nurses and doctors are talking about your blood pressure.  For example you may hear 120 over 80.  The first number 120 means how fast your blood is being pushed out of your heart and into the blood vessels, this is called systolic.  The other number 80 means this is how fast your blood is going back to your heart, this is called diastolic.  A blood pressure test measures both how fast your blood is being pushed out of your heart and how fast your blood is going back to your heart.

Why do I need to have a Blood Pressure test?

Usually when you are in the hospital, your blood pressure is checked everyday, sometimes it can even be checked a few times a day.  This just lets the doctor and nurse know how your blood is moving around your body.

What does a Blood Pressure machine look like?

Blood Pressure Cuff/Machine

The blood pressure machine has a small computer and a blood pressure cuff.  The cuff is made of material with some Velcro on it.  The cuff is attached to the computer by a rubber cord.  It is on a cart or a small pole so that the nurses can move it around from room to room, or sometimes it is attached to the wall in your room.   No picture is taken, just the numbers show up on the small computer screen for the nurses to write down and tell the doctor.

Sometimes the nurse will use a blood pressure cuff that is not attached to a computer.  When the nurse uses this type of blood pressure cuff, they use a pump to pump air into the cuff to fill it with air and read the numbers from the side of the cuff where the pump is.

What happens when I have a Blood Pressure test?

A nurse will come to you with the blood pressure machine.   She may ask you to roll up your sleeve.  She will then place the cuff around your arm, just above your elbow.  Sometimes the nurses may put the cuff on part of your leg.  The nurse will then attach the Velcro to make sure it says in place.  A button will then be pushed on the machine, and the cuff will start to fill with air.  If the blood pressure cuff is not one that connects to a computer, then the nurse will use a pump on the side of the cuff to help the cuff fill with air.  Once it has filled, you will notice that the cuff is very puffy and gives your arm a tight hug/squeeze.  The machine will beep that it is done and the nurse will remove the cuff from your arm.

What will the Blood Pressure test feel like?

The nurse will wrap a small cuff around a part of your arm or your leg.  When the machine is on, the cuff fills with air.  The cuff will get snug (tight) around your arm or leg.  Do not worry, the cuff will stop filling with air when it is done, and the air will be let out of the cuff.  It is important to relax and stay still so that the test will be short.  If you move your arm or leg around, the test will take longer which means the snug cuff will be on your arm or leg longer.  The test should take less then a few minutes and will be done a few times a day, sometimes even at night.  Sometimes it can help to think of something else, like your favourite place or song, while having the blood pressure done.  Other ideas to try to help you lie still are quiet activities like blowing bubbles or watching your favourite movie.

Preparing for the test

There is nothing that you need to do to prepare for a blood pressure test.  You do not have to go anywhere to have the test done; your nurse will come into your room with the machine and check it for you.

Remember

If you have any questions about the test, always ask!

This content has been reviewed and approved by health care team members at McMaster Children’s Hospital in Hamilton, Ontario.