Archive for the 'medical words' Category

Medical Word of the Day: Omphalocele

Omphalocele: (audio pronunciation)

A birth defect in which part of the intestine, covered only by a thin transparent membrane, protrudes outside the abdomen at the umbilicus. The underlying error is a failure during embryonic development for a section of the intestines (the midgut) to return from outside the abdomen and reenter the abdomen, as it should. The opening in the abdominal wall cannot close because, to do so, would pinch off part of the intestines. An omphalolocele must be repaired by surgery.

Omphalocele Illustrationclick to enlarge

With an omphalocele, the part of the intestine that sticks out is covered by two thin transparent membranes called the amnion (the amniotic membrane) and peritoneum (the abdominal membrane). The liver and spleen may also be within the omphalocele.

An omphalocele is caused by an error in the normal embryonic development of the intestinal tract. During embryogenesis (the time during which the embryo forms), there are initially three distinct portions of the intestinal tract (the foregut, midgut and hindgut) that extend the length of the embryo. Much of the midgut is then herniated (protruded) outside the abdomen at the umbilicus (belly button). The midgut later reenters the abdomen (belly) and the opening in the abdominal wall closes. The error responsible for an omphalocele is a failure for the midgut to return and reenter the abdomen. The opening in the abdominal wall cannot close because to do so would pinch off part of the intestines.

About 1 in 5,000 babies is born with an omphalocele. The omphalocele can be an isolated birth defect (all by itself). Or it may occur in children who have additional malformations as for example a congenital heart defect. Omphalocele is a characteristic malformation in certain chromosome abnormalities as the trisomy 13 (Patau) syndrome and the trisomy 18 (Edwards) syndrome. It also is seen in some genetic disorders such the Beckwith-Wiedemann syndrome.

“Omphalo-” indicates a relationship to the umbilicus (the navel) and the suffix “-cele” refers to a hernia or rupture, so omphalocele literally = a hernia or rupture at the umbilicus.

Immediate care:

Because some or all of the abdominal organs are outside the body, infection is a concern, especially if the protective membrane around the organs breaks. Also, an organ may lose its blood supply if it becomes pinched or twisted.  A loss of blood flow can damage the affected organ.  Omphalocele can often be detected on fetal ultrasound in the second and third trimesters of pregnancy.  A fetal echocardiogram (ultrasound of the heart) may also be done to check for heart abnormalities before the baby is born.  After birth, the omphalocele can be noted by the physician during the physical examination. X-rays (diagnostic tests that use invisible electromagnetic energy beams to produce images of internal tissues, bones, and organs onto film) may also be done after birth to evaluate abnormalities of other organs or body parts.

Surgical Repair:

Specific treatment for an omphalocele will be determined by: the baby’s gestational age, overall health, and medical history extent of the condition the baby’s tolerance for specific medications, procedures, or therapies.
For a small omphalocele (only a portion of the intestine protruding outside the abdominal cavity), shortly after birth, an operation is done to return the organs to the abdomen and close the opening in the abdominal wall.
For a large omphalocele (most of the abdominal organs, including intestine, liver, and spleen, are present outside the abdominal cavity), the repair is done in stages and may include the following:
Initially, sterile, protective sheeting is placed over the abdominal organs.
Because the abdomen may be small and underdeveloped, it may not be able to hold all of the organs at once. Therefore, the exposed organs are gradually moved back into the abdomen over several days or weeks. The abdominal wall is closed surgically once the organs have been returned to the abdominal cavity.
Because the abdominal cavity may be small and underdeveloped and the organs may be swollen, a baby with an omphalocele may have breathing difficulties as the organs are returned to the abdomen. The baby may need help from mechanical ventilation while the swelling is decreasing and the size of the abdominal cavity is increasing.
Post-Operative Care:

The infant is cared for post-operatively in a neonatal intensive care unit. The baby is placed in an isolette (incubator) to keep warm and prevent infection. Oxygen is given and mechanical ventilation is often required. Intravenous fluids, antibiotics, and pain medications will be given. A nasogastric tube will be in place to keep the stomach emptied of gastric secretions. Feedings are started by nasogastric tube as soon as bowel function resumes. Feedings are started very slowly and often infants are reluctant to feed. These babies may need feeding therapy and lots of encouragement.

Prognosis:

Babies who have damage to the intestines or other abdominal organs may have long-term problems with digestion, elimination, and infection.

Greg Olson :: Ubiquity :: 303-962-8700 :: greg@ubiquitygroup.com

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Surgical Procedure of the Week: Cardiac

The medical word of the day typically has longer definitions, along with images. The surgical procedure of the week is a quick overview of a variety of procedures and the definitions.

Heart Illustrationclick to enlarge

Lets review cardiac procedures and the definitions.

Cardiac Surgical Procedures:

Aneurysmectomy [ann-ure-is-meck-ta-me] removal of an aneurysm

Arterial anastomosis [ann-ass-to-moe-sis] end-to-end union of two different arteries or two separate segments of the same artery

Atriotomy [a-tree-ott-toe-me] - incision of the atrium

Biopsy - arterial, etc. - carried out to examine a specimen of an arterial vessel wall.

Arterial biopsy often confirms inflammation of the vessel wall, or arteritis, [aart-urh-ite-iss]a type of vasculitis [vass-kule-ite-iss].

Cardiolysis - freeing of pericardial adhesions from surrounding tissues, involving resection of ribs and sternum (open chest surgery)

Cardioplasty - surgical repair of the heart to relieve spasm

Cardiorrhaphy - suture of the heart (note the two rr’s)

Cardiotomy - incision of the heart

Pericardiectomy - excision of a portion of the pericardium

Pericardiocentesis - [pair-ee-kard-ee-oh-sent-ee-suss] the pericardium is surgically punctured in order to remove a small sample of the pericardial fluid for laboratory examination. This test is performed while the patient is in a semisitting position and under EKG monitoring. The fluid removed is tested for protein, sugar, and LDH. Most often it is used to determine the cause of pericarditis (bacterial, fungal, tubercular or viral), or to confirm suspected carcinomatous infiltration of the pericardium.

Phleborrhaphy, [flee-bore-uh-fee] or venorrhaphy - suturing of a vein

Phlebotomy, venisection, [veen-ee-section] venipuncture - opening or piercing of a vein for removal of blood, or for the introduction of fluids or medications via an IV

Thrombectomy - removal of a thrombus

Valvotomy, mitral commissurotomy - [come-iss-sure-ott-tomy] surgical incision of a mitral valve to increase the size of the orifice; used in treating mitral stenosis

Venotomy [veen] - surgical incision of a vein

Greg Olson :: Ubiquity :: 303-962-8700 :: greg@ubiquitygroup.com

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Ubiquity specializes in generating demand for life science companies.  We help bioscience and med tech companies create a better human health experience by driving investor interest, awareness and product desire.

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Medical Word of the Day: Elliptocytosis

Topic: Blood

Red blood cells - elliptocytosis Elliptocytosis is a hereditary disorder of the red blood cells (RBCs). In this condition, the RBCs assume an elliptical shape, rather than the typical round shape.

Elliptocytosis:(audio pronunciation)

Hematologic disorder characterized by elliptically shaped red blood cells (elliptocytosis) with variable breakup of red cells (hemolysis) and varying degrees of anemia. Inherited as a dominant trait. Due to mutation (change) in one of the genes encoding proteins of the red cell membrane skeleton.  Elliptocytosis is frequently harmless. In mild cases, fewer than 15% of red blood cells are oval-shaped. However, some people may have crises in which the red blood cells rupture, releasing their hemoglobin. Persons with this disease can develop anemia, jaundice, and gallstones.

In 1956 Newton Morton brilliantly showed that there were at least 2 forms of elliptocytosis, one form linked to the Rh blood group and another form not linked to Rh (now known to be on chromosome 1). The Rh-linked form, called EL1, in is due to a mutation in erythrocyte membrane protein 4.1. Forms of elliptocytosis not linked to Rh are due to mutations in the alpha-spectrin gene, the beta-spectrin gene, or the band 3 gene. The linkage between elliptocytosis and Rh was one of the first autosomal linkages discovered.

Greg Olson :: Ubiquity :: 303-962-8700 :: greg@ubiquitygroup.com

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Medical Word of the Day: Hemolysis

Topic: Blood Cells
Hemolysis:

(audio pronunciation)                                                                                                                                                                                   The destruction of red blood cells which leads to the release of hemoglobin from within the red blood cells into the blood plasma. Etymology: The word “hemolysis” is made up of “hemo-”, blood + “lysis”, the disintegration of cells.

Hemoglobin:                                                                                                                                                                                                                         The oxygen-carrying pigment and predominant protein in the red blood cells. Hemoglobin forms an unstable, reversible bond with oxygen. In its oxygenated state it is called oxyhemoglobin and is bright red. In the reduced state it is called deoxyhemoglobin and is purple-blue.

Each hemoglobin molecule is made up of four heme groups surrounding a globin group. Heme contains iron and gives a red color to the molecule. Globin consists of two linked pairs of polypeptide chains. The development of each chain is controlled at a separate genetic locus. Changes in the amino acid sequence of these chains results in abnormal hemoglobins. For example, hemoglobin S is found in sickle-cell disease, a severe type of anemia in which the red cells become sickle-shaped when oxygen is in short supply.

When red blood cells die, the hemoglobin within them is released and broken up: the iron in hemoglobin is salvaged, transported to the bone marrow by a protein called transferrin and used again in the production of new red blood cells; the remainder of the hemoglobin becomes a chemical called bilirubin that is excreted into the bile which is secreted into the intestine, where it gives the feces their characteristic yellow-brown color.

 Additional Definitions:

Polypeptide: A peptide consisting of 2 or more amino acids. Amino acids make up polypeptides which, in turn, make up proteins.

Bilirubin: A yellow-orange compound produced by the breakdown of hemoglobin from red blood cells.

Locus: The place, in Latin.. In genetics, a locus is the place a gene occupies on a chromosome. One locus, two loci.

Transferrin: A plasma protein that transports iron through the blood to the liver, spleen and bone marrow.

Hemoglobin S: The most common type of abnormal hemoglobin and the basis of sickle cell trait and sickle cell anemia.

Greg Olson :: Ubiquity :: 303-962-8700 :: greg@ubiquitygroup.com :: Follow on Twitter:: @ubiquity

Ubiquity specializes in generating demand for life science companies.  We help bioscience and med tech companies create a better human health experience by driving investor interest, awareness and product desire.

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Medical Word of the Day: Polymyositis

Polymyositis:  (Webster definition with audio pronunciation) A chronic inflammatory disease of muscle that begins when white blood cells, the immune cells of inflammation, spontaneously invade muscles, especially the muscles closest to the trunk or torso, resulting in sometimes severe muscle pain, tenderness and weakness.

There are commonly periods of increased symptoms, called flares or relapses, and periods of decreased symptoms, known as remissions. The disease is slightly more common in females than males. It affects all age groups, although its onset is most common in middle childhood and in the twenties. It occurs throughout the world. It can be associated with skin rash and is then referred to as “dermatomyositis.” It also can affect other areas of the body and is, therefore, a systemic illness.

Occasionally, polymyositis is associated with other diseases of connective tissue such as systemic lupus erythematosus, scleroderma, and rheumatoid arthritis. Polymyositis is also associated with modestly increased risk of cancer, including non-Hodgkin lymphoma, lung and bladder cancer.

Polymyositis treatment:

Initially, polymyositis is treated with high doses of corticosteroids. These are medications related to cortisone and can be given by mouth or intravenously. They are given because they can have a powerful effect to decrease the inflammation in the muscles. They usually are required for years and their continued use will be based on what the doctor finds related to symptoms, examination, and muscle enzyme blood test.

Greg Olson :: Ubiquity :: 303-962-8700 :: greg@ubiquitygroup.com :: Follow on Twitter:: @ubiquity
Ubiquity specializes in generating demand for life science companies.  We help bioscience and med tech companies create a better human health experience by driving investor interest, awareness and product desire.

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Medical Word of the Day: Hydrocephalus

Topic: Neuro: Medical Word of the Day: Hydrocephalus

This is a word that is near and dear to our hearts at Ubiquity. My business partner’s newphew has hydrocephalus. We actively support an orginization based near Seattle, Washington: The Hydrocephalus Research Guild. This is a special interest guild of Seattle Children’s Guild Association, Seattle, WA. HRG seeks to fund research at Seattle Children’s to find better hydrocephalus.  We need to find better treatment for hydrocephalus.

Hydrocephalus has been described as a ticking time bomb by those who suffer from it. There is no cure and very little research being conducted for a cure. Hydrocephalus is the number one reason for brain surgery in children in the U.S. The most significant treatment, a shunt, was developed in 1952 with little innovation since then.

What is Hydrocephalus:
Hydrocephalus is an abnormal buildup of cerebrospinal fluid (CSF) in the ventricles of the brain. The fluid is often under increased pressure and can compress and damage the brain.

Hydrocephalus can arise before birth or any time afterward. It may be due to many causes including a birth defect, hemorrhage into the brain, infection, meningitis, tumor, or head injury. Most forms of hydrocephalus are the result of obstructed CSF flow in the ventricular system. With physical obstruction of CSF flow in the ventricular system is usually the cause of the hydrocephalus. Hydrocephalus is a common companion of spina bifida (meningomyelocele).

What is termed “hydrocephalus ex-vacuo” occurs when there is damage to the brain caused by stroke or injury, and there may be an actual shrinkage of brain substance. “Hydrocephalus ex-vacuo” is essentially only hydrocephalus by default; the CSF pressure itself is normal.

Normal pressure hydrocephalus (NPH) can also occur due to a gradual blockage of the CSF drainage pathways in the brain. Although the ventricles enlarge, the pressure of the CSF remains within normal range. NPH is characterized by memory loss dementia, gait disorder, urinary incontinence and a general slowing of activity.

Left Image: Hydrocephalus brain scan image.   Right Image:  Normal Scan.  The dark space is the extra fluid in the brain which is actually cerebrospinal fluid.

Hydrocephalus brain scan click to enlarge

Learn more about hydrocephalus at HRG.

What can you do to help? You can support HRG in many ways. Support HRG

  1. Become a corporate sponsor.
  2. Donate an auction item.
  3. Make a tax-deductible contribution.
  4. Buy tickets to the event.
  5. Volunteer for the event.
  6. Become a member of the HRG.

Greg Olson :: Ubiquity :: 303-962-8700 :: greg@ubiquitygroup.com :: Follow on Twitter:: @ubiquity
Ubiquity specializes in generating demand for life science companies.We help bioscience and med tech companies create a better human health experience by driving investor interest, awareness and product desire.

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Medical Work of the Day: Transillumination

2-23-2009: Medical Word o the Day: Transillumination

Transillumination: The passing of a strong beam of light through a part of the body for medical inspection. A method of examination by the passage of light through tissues or a body cavity.

A common use of transillumination is in infancy. The infant’s skull should normally not transilluminate (let a beam of light pass through it). But in hydranencephaly, a condition in which the cerebral hemispheres are almost totally absent, the head appears normal, but when transilluminated, light shines completely through.

This is just one example of the use of transillumination, a simple, inexpensive, painless procedure. 

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