Tuesday, October 12, 2021

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                                      R78.81-Bacteremia






Bacteremia is when there are bacteria present in your bloodstream. Another term that you may have heard for bacteremia is “blood poisoning,” however this isn’t a medical term.In some cases, bacteremia can be asymptomatic, meaning there are no symptoms. In other cases, symptoms may be present and there’s a potential risk for serious complications.Read on to learn more about bacteremia, its symptoms, and how it can be treated.

You may have heard of bacteremia being associated with conditions like septicemia and sepsis. These terms are all closely related, but have slightly different meanings.

Strictly speaking, bacteremia refers to the presence of bacteria in the bloodstream. Bacteria can sometimes enter your bloodstream due to things like cleaning your teeth or undergoing a minor medical procedure.

In many healthy people, bacteremia will clear up on its own without causing illness. However, when an infection is established within the bloodstream, this type of bacteremia is differentiated as septicemia.

If left untreated, a bloodstream infection can lead to more serious complications. One of these is sepsis, which is caused by a strong immune response to the infection.

Sepsis and septic shock can lead to organ failure and even death.

A variety of different bacteria can cause bacteremia. Some of these bacteria can go on to establish an infection in the bloodstream.

Examples of such bacteria include:

Some common ways in which bacteremia occurs include:

  • through a dental procedure such as a routine teeth cleaning or through a tooth extraction
  • from a surgery or procedure
  • an infection spreading from another part of the body into the bloodstream
  • via medical devices, particularly in-dwelling catheters and breathing tubes
  • through severe injuries or burns

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                                       Q24.0 Dextrocardia






Dextrocardia is a rare congenital condition where the heart points toward the right side of the chest instead of the left.The condition is usually not life-threatening, although it often occurs alongside more serious complications, such as heart defects and organ disorders in the abdomen. Dextrocardia in isolation, without any other heart defects, is unusual.

Dextrocardia is a congenital condition, which is present at birth. There are two major types of dextrocardia.

Dextrocardia situs inversus

In this type of dextrocardia, the tip of the heart and its four chambers are pointing towards the right side of the body

Dextrocardia with situs inversus totalis

With this type of dextrocardia, abdominal and chest organs and other vessels, such as the liver, stomach, and spleen are also out of position. In fact, the other organs are in the opposite position, or in mirror-image reversal, to where they should be.

Non-dominant (also called autosomal recessive) genes cause dextrocardia.

These abnormal genes cause the primitive, or cardiac, tube to reverse direction while a fetus is developing in the womb.

Depending on the extent and timing of the reversal, the heart and abdominal organs may also develop in a reversed form.

As it is recessive genes that cause dextrocardia, an individual must inherit a copy of the abnormal gene from both parents to develop the condition.

Dextrocardia affects an estimated 1 out of every 12,000 peopleTrusted Source. Dextrocardia situs inversus totalis affects approximately 1 out of every 10,000 children. Gender, race, and ethnicity do not seem to have any impact on whether or not a person develops the condition.

Sympotoms

Many people with congenital dextrocardia do not always know they have it, as the condition may not produce many symptoms. Often doctors only discover the irregularity while carrying out chest or heart imaging examinations for unrelated complications.

However, one telltale symptom of dextrocardia is that people with this condition have maximum heart sounds on the right of the chest instead of the left.

In severe cases, typically in infants with additional heart defects or another disease, certain symptoms need medical treatment.

Symptoms that require medical attention include:

  • unexplained and continual exhaustion
  • inability to gain weight
  • chronic infections, especially of the sinus and lungs
  • difficulty breathing
  • jaundiced or yellowed skin
  • blue-tinted skin, especially around the fingers and toes

Although the reversed organs themselves may function normally, their irregular positioning often makes the diagnosis of other conditions tricky. For example, in someone with dextrocardia situs inversus, appendicitis will cause sharp pain in the lower left part of the abdomen instead of the right.

When these anatomical differences occur, they can also make surgery difficult.

Other complications associated with dextrocardia may include:

  • bowel disorders, usually from obstruction due to malrotation (reversal)
  • bronchial diseases, such as like chronic pneumonia, associated primarily with a loss of cilia (hair-like projections) from mucosal tissues
  • esophageal disorders
  • cardiovascular disorders
  • heart failure or disease
  • infection and sepsis


Most cases of dextrocardia are diagnosed using an electrocardiogram (EKG) and chest X-ray.

An EKG that shows inverted or reversed electrical waves usually points to dextrocardia.

Once a doctor suspects dextrocardia, they may use a computed tomography (CT) scan or a magnetic resonance imaging (MRI) scan to confirm the condition.

Related conditions

Dextrocardia may be caused by, associated with, or related to other conditions. Complicating conditions include:

Kartagener syndrome

Kartagener syndrome is when dextrocardia situs inversus is accompanied by primary ciliary dyskinesia, an inherited condition where the cilia that help move mucus become immobile.

Roughly 20 percent of those with dextrocardia also have Kartagener syndrome.

Dextroversion

Dextroversion occurs when the heart is abnormally positioned further to the right and rotated to the right. The right ventricle has usually moved behind the left, but the left ventricle has stayed left. This complication is diagnosed using an electrocardiograph (ECG).

Dextroposition

Dextroposition occurs when the heart is displaced or moved to the right. Unlike dextrocardia, the other organs are not mirrored.

This condition is usually associated with acquired diseases of the lungs, diaphragm, or pleura (the membrane surrounding the lungs).

Surgeries and muscle damage or deformities may also contribute to the development of dextroposition.

Doctors will often use an ECG test to distinguish between dextroposition and dextrocardia.[KG3]

Transposition of the great vessels (TGA)

TGA occurs when the major vessels of the heart are connected in reverse due to the reversal of the heart chambers. This condition is pretty rare.

Congenitally corrected transposition of the great arteries (CCTGA)

This condition occurs when the lower half of the heart is reversed, specifically the lower ventricles and the connected valves.

The condition is even rarer than TGA, and the cause is still unknown. According to the Adult Congenital Heart Association, around 0.5 to 1 percentTrusted Source of all babies born with heart problems have CCTGA.

Tricuspid atresia

This condition is a congenital defect where the tricuspid valve fails to develop. The tricuspid valve prevents blood from flowing back into the right atrium from the right ventricle.

Single, double-outlet, or double-inlet ventricles

These cases occur when the aorta, which typically transports oxygenated blood from the left ventricle to the rest of the body, and the pulmonary artery, which carries deoxygenated blood from the right ventricle to the lungs, both connect in the same (left or right) ventricle.

Pulmonary stenosis or atresia

This occurs when the pulmonary (pulmonic) valve of the heart that allows blood to leave the heart narrows (stenosis) or fails to develop (atresia).

Heterotaxy

Heterotaxy happens when mirrored internal organs do not develop or function properly. Depending on the organs involved and the severity of the case, heterotaxy can be life-threatening.

Endocardial cushion defect

This is a congenital heart defect where the tissues that separate the chambers of the heart fail to develop, interfering with blood flow. This condition is also known as atrioventricular canal defect.

Treatment and outlook

Many people with dextrocardia do not display symptoms so the condition can go untreated.

Infants with dextrocardia, which is accompanied by heart defects, may require surgery. Many children will be given medication that increases the force of the heartbeat and lowers their blood pressure before surgery.

For those with Kartagener syndrome, treatment of sinus and lung symptoms may help lessen the chances or impact of dextrocardia.

Treatment options include:

  • expectorant or mucous clearing medications
  • antibiotics for bacterial infections
  • treating cases of bronchitis and sinusitis

Genetic counseling may be helpful for those with dextrocardia who are looking to start a family.

For most people with dextrocardia situs inversus, life expectancy is normal. In cases of isolated dextrocardia, congenital heart defects are more frequent and associated with greater health risks.



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                    A40.9 - Streptococcal Sepsis Unspecified




 Sepsis is a potentially life-threatening condition that occurs when the body's response to an infection damages its own tissues. When the infection-fighting processes turn on the body, they cause organs to function poorly and abnormally.Sepsis may progress to septic shock. This is a dramatic drop in blood pressure that can lead to severe organ problems and death.

Sepsis is a medical emergency caused by the body's response to an infection and can be life-threatening. Sepsis is the consequence of widespread inflammation (swelling) in the body. Inflammation and blood clotting during sepsis causes reduced blood flow to limbs and vital organs, and can lead to organ failure and even death. Over 1.5 million people in the United States are diagnosed with sepsis yearly, and approximately 30% of patients do not survive.

Early treatment with antibiotics and intravenous fluids improves chances for survival.

Sepsis can affect anyone, but those at particular risk include:

  • The very old (older than 65 years old) or very young or pregnant women
  • People with pre-existing infections or medical conditions such as diabetes, lung disease, cancer and kidney disease
  • People with weakened immune systems
  • Patients who are in the hospital
  • People with severe injuries, such as large burns or wounds
  • Patients with catheters (IVs, urinary catheters) or a breathing tube

Symptoms





Signs and symptoms of sepsis

To be diagnosed with sepsis, you must have a probable or confirmed infection and all of the following signs:

  • Change in mental status
  • Systolic blood pressure — the first number in a blood pressure reading — less than or equal to 100 millimeters of mercury (mm Hg)
  • Respiratory rate higher than or equal to 22 breaths a minute

Signs and symptoms of septic shock

Septic shock is a severe drop in blood pressure that results in highly abnormal problems with how cells work and produce energy. Progression to septic shock increases the risk of death. Signs of progression to septic shock include:

  • The need for medication to maintain systolic blood pressure greater than or equal to 65 mm Hg.
  • High levels of lactic acid in your blood (serum lactate). Having too much lactic acid in your blood means that your cells aren't using oxygen properly.

When to see a doctor

Most often, sepsis occurs in people who are hospitalized or who have recently been hospitalized. People in an intensive care unit are more likely to develop infections that can then lead to sepsis.

Any infection, however, could lead to sepsis. See your doctor about an infection or wound that hasn't responded to treatment. Signs or symptoms, such as confusion or rapid breathing, require emergency care.

Causes





While any type of infection — bacterial, viral or fungal — can lead to sepsis, infections that more commonly result in sepsis include infections of:

  • Lungs, such as pneumonia
  • Kidney, bladder and other parts of the urinary system
  • Digestive system
  • Bloodstream (bacteremia)
  • Catheter sites
  • Wounds or burns

Risk factors

Several factors increase the risk of sepsis, including:

  • Older age
  • Infancy
  • Compromised immune system
  • Diabetes
  • Chronic kidney or liver disease
  • Admission to intensive care unit or longer hospital stays
  • Invasive devices, such as intravenous catheters or breathing tubes
  • Previous use of antibiotics or corticosteroids

Complications

As sepsis worsens, blood flow to vital organs, such as your brain, heart and kidneys, becomes impaired. Sepsis may cause abnormal blood clotting that results in small clots or burst blood vessels that damage or destroy tissues.

Most people recover from mild sepsis, but the mortality rate for septic shock is about 40%. Also, an episode of severe sepsis places you at higher risk of future infections.




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                     K90.81  Whipple's Disease




Whipple disease is a systemic disease most likely caused by a gram-positive bacterium, Tropheryma whipplei (formerly T whippelii).  Although the first descriptions of the disorder described a malabsorption syndrome with small intestine involvement, the disease also affects the joints, central nervous system, and cardiovascular system. T whipplei infection is recognized to be a major cause of culture-negative endocarditis.  Because fewer than 1000 reported cases have been described, clinical experience with this disorder is sparse. 

  • heart
  • lungs
  • brain
  • joints
  • skin
  • eyes

It’s a relatively rare disease, but it can be life-threatening.

It’s widely believed that there’s a genetic predisposition to developing the illness. White men between 40 and 60 are more likelyTrusted Source to contract the condition than any other group. The rate for Whipple’s disease also tends to be higher in places that lack freshwater and proper sanitation. Currently, there’s no known way to prevent Whipple’s disease.

Whipple’s disease prevents your body from properly absorbing nutrients. Because of this, it affects many different parts of the body and is associated with a variety of symptoms. In advanced stages of the disease, the infection may spread from the intestines to other organs such as the:

  • heart
  • lungs
  • brain
  • joints
  • eyes

The most common signs and symptoms of Whipple’s disease include:

  • chronic joint pain
  • chronic diarrhea that can be bloody
  • significant weight loss
  • stomach pain and bloating
  • decreased vision and eye pain
  • fever
  • fatigue
  • anemia, or low red blood cell count

The following signs and symptoms don’t occur as frequently but can indicate that the condition is getting worse:

  • skin discoloration
  • inflamed lymph nodes
  • a chronic cough
  • pain in the chest
  • pericarditis, or swelling of the sac surrounding the heart
  • heart failure
  • a heart murmur
  • poor vision
  • dementia
  • numbness
  • insomnia
  • muscle weakness
  • tics
  • trouble walking
  • poor memory


Infection with the T. whipplei bacteria is the one and only known cause of Whipple’s. The bacteria will lead to the development of internal sores and cause bodily tissues to thicken.

The villi are finger-like tissues that absorb nutrients in the small intestine. When the villi begin to thicken, their natural shape begins to change. This damages the villi and prevents them from effectively absorbing nutrients. This leads to many of the symptoms of Whipple’s disease.

A diagnosis of Whipple’s disease is complicated, especially because symptoms are similar to other more common conditions that range from celiac disease to neurological disorders. Your doctor will try to rule out these other conditions before diagnosing you with Whipple’s disease.

Endoscopy

The first sign your doctor will look for to determine if you have Whipple’s disease is lesions. An endoscopy is the insertion of a small flexible tube down your throat to the small intestine. The tube has a mini camera attached. Your doctor will observe the condition of your intestinal walls. Thick walls with creamy, ragged covers are a potential sign of Whipple’s.

Biopsy

During an endoscopy, your doctor may remove tissue from your intestinal walls to test for the presence of the T. whipplei bacteria. This procedure is called a biopsy and can confirm an infection.

Polymerase Chain Reaction

Polymerase chain reaction is a highly sensitive test that amplifies the DNA of the T. whipplei from your tissue samples. If the bacteria have been in your tissue, there will be DNA evidence of it. This test can confirm the existence of the T. whipplei bacteria in your tissue.

Blood Tests

Your doctor might order a complete blood count. This will help determine if you have a low count of red blood cells and low amounts of albumin, which are both signs of anemia. Anemia is an indication that you might have Whipple’s disease

An aggressive course of antibiotics is usually the first step in treatment, including two weeks of antibiotics through an intravenous (IV). In addition, you’ll likely be on daily antibiotics for one to two years.

Other treatment options include:

  • ingesting proper amounts of fluids
  • taking antimalarial medication for 12 to 18 months
  • using iron supplements to assist with anemia
  • taking vitamin D, vitamin K, calcium, and magnesium supplements
  • maintaining a high-calorie diet to help with nutrient absorption
  • taking corticosteroids to help ease inflammation
  • taking nonsteroidal pain medication, such as ibuprofen

Whipple’s disease is a bacterial infection that can lead to death if it’s not treated properly.

After treatment begins, many of the symptoms will go away within a month. The best thing you can do is continue to take your antibiotics. Relapses are common. When they occur, additional symptoms, such as neurological problems, can show up as well.



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                                        R78.81-Bacteremia Bacteremia  is when there are bacteria present in your bloodstream. Another term t...