Endocarditis

Endocarditis
Mitral valve vegetations in a patient with bacterial endocarditis.
ICD-10	I33
ICD-9	421
DiseasesDB	4224
MedlinePlus	001098
eMedicine	emerg/164  med/671 ped/2511
MeSH	D004696

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Related Key Words and Synonyms: Infective endocarditis, IE, subacute bacterial endocarditis, acute bacterial endocarditis, fungal endocarditis, nosocomial infective endocarditis, NIE, intravenous drug abuse endocarditis, intravenous drug abuse infective endocarditis, IVDA endocarditis, IVDA IE, prosthetic valve endocarditis, PVE, pacemaker endocarditis, PM infective endocarditis, PM IE, endocardial infection, native valve endocarditis, NVE, HACEK infection, bloodstream infection, marantic endocarditis

Overview

Endocarditis is an inflammation of the inner layer of the heart, the endocardium. The most common structures involved are the heart valves.

Endocarditis can be classified by etiology as either non-infective or infective, depending on whether a microorganism is the source of the problem.

Traditionally, infective endocarditis has been clinically divided into acute and subacute (because the patients tend to live longer in subacute as opposed to acute) endocarditis. This classifies both the rate of progression and severity of disease. Thus subacute bacterial endocarditis (SBE) is often due to streptococci of low virulence and mild to moderate illness which progresses slowly over weeks and months, while acute bacterial endocarditis (ABE) is a fulminant illness over days to weeks, and is more likely due to Staphylococcus aureus which has much greater virulence, or disease-producing capacity.

This terminology is now discouraged. The terms short incubation (meaning less than about six weeks), and long incubation (greater than about six weeks) are preferred.

Infective endocarditis may also be classified as culture-positive or culture-negative. Culture-negative endocarditis is due to micro-organisms that require a longer period of time to be identified in the laboratory. Such organisms are said to be 'fastidious' because they have demanding growth requirements. Some pathogens responsible for culture-negative endocarditis include Aspergillus species, Brucella species, Coxiella burnetii, Chlamydia species, and HACEK bacteria.

Finally, the distinction between native-valve endocarditis and prosthetic-valve endocarditis is clinically important. Prosthetic-valve endocarditis constitutes 10-20% of cases of endocarditis. The greatest risk is during the first 6 months after valve surgery. Staphylococcus epidermidis is the most common cause. The infection often extends into the anulus and cardiac tissues.

Patients who inject narcotics intravenously may introduce infection which will travel to the right side of the heart. In other patients without a history of intravenous exposure, endocarditis is more frequently left-sided.

Non-infective endocarditis

Non-infective or marantic endocarditis is rare. A form of sterile endocarditis is termed Libman-Sacks endocarditis; this form occurs more often in patients with lupus erythematosus and the antiphospholipid syndrome. Non-infective endocarditis may also occur in patients with cancer, particularly mucinous adenocarcinoma.

Infective endocarditis

Given the poor vascular supply of the heart valves, entrance of infection fighting components of the bloodstream (such as white blood cells) are reduced. So if an organism (such as bacteria) establishes a foothold in the valves, the bodies ability to fight the infection inside the valve structures is reduced.

Normally, blood flows smoothly through these valves. If they have been damaged (for instance in rheumatic fever) the trauma of non-laminar flow can increase the risk of infection.

Historical Background of Endocarditis

• 1554: Earliest report of endocarditis in medical books
• 1669: Accurately described tricuspid valve endocarditis
• 1646: Described unusual "outgrowths" from autopsy of patient with endocarditis; detected murmurs by placing hand on patient's chest
• 1708: Described unusual structures in entrance of aorta
• 1715: Described abnormality in aortic valve and mitral valve
• 1749: Described valvular lesions
• 1769: Linked infectious disease and endocarditis; observed association with the spleen
• 1784: Accurately drew intracardiac abnormalities
• 1797: Showed relationship between rheumatism and heart disease
• 1799: Described inflammatory process associated with endocarditis
• 1806: Described unusual structures in heart as "vegetations," syphilitic virus as causative agent of endocarditis, and theory of antiviral treatment of endocarditis
• 1809: Indicated vegetations were not "outgrowths" or "buds" but particles adhering to heart wall
• 1815: Elucidated inflammatory processes associated with endocarditis
• 1816: Invented cylindrical stethoscope to listen to heart murmurs; dismissed link between venereal disease and endocarditis
• 1832: Confirmed Laennec's observations
• 1835-40: Named endocardium and endocarditis; described symptoms; prescribed herbal tea and bloodletting as treatment regimen; described link between acute rheumatoid arthritis and endocarditis
• 1852: Described consequences of embolization of vegetations throughout body. Described cutaneous nodules (named "Osler's nodes" by Libman)
• 1858-71: Examined fibrin vegetation associated with endocarditis by microscope; coined term "embolism;" discussed role of bacteria, vibrios, and micrococci in endocarditis
• 1861: Confirmed Virchow's theory on emboli
• 1862: Described granulations or foreign elements in blood and valves, which were motile and resistant to alkalis
• 1868-70: Described infected arterial blood as originating from heart; proposed scarlet fever as cause of endocarditis
• 1869: Established "parasites" on skin transported to heart and attached to endocardium; named "mycosis endocardii"
• 1872: Detected microorganisms in vegetations of endocarditis
• 1878: All cases of endocarditis were infectious in origin
• 1878: Combined experimental physiology and infection to produce animal model of endocarditis in rabbit; noted valve had to be damaged before bacteria grafted onto valve
• 1878: Micrococci enter vessels that valves were fitted into; valves exposed to abnormal mechanical attacks over long period created favorable niche for bacterial colonization
• 1879: Virchow's student; employed early animal model of endocarditis
• 1879: Proposed etiology of endocarditis was based on infectious model and treatment should focus on eliminating "parasitic infection"
• 1880: Working with Pasteur, proposed use of routine blood cultures
• 1881-86: Believed endocarditis could appear during various infections; noted translocation of respiratory pathogen from pulmonary lesion to valve through blood
• 1883: Believed microorganisms were result, not cause, of endocarditis
• 1884: Named disease "infective endocarditis"
• 1886: Demonstrated various bacteria introduced to bloodstream could cause endocarditis on valve that had previous lesion
• 1885: Synthesized work of others relating to endocarditis
• 1899: Described streptococcal, staphylococcal, pneumococcal, and gonococcal endocarditis
• 1903: First described "endocarditis lenta"
• 1909: Credited by Osler as first to observe cutaneous nodes (named "Osler's nodes" by Libman) in patients with endocarditis
• 1909: Analyzed 150 cases of endocarditis and published diagnostic criteria relating to signs and symptoms
• 1910: Described initial classification scheme to include "subacute endocarditis," with clinical signs/symptoms; absolute diagnosis required blood cultures
• 1981: Described Beth Israel criteria based on strict case definitions
• 1994: New criteria utilizing specific echocardiographic findings
• 1995: Antibiotic treatment of adults with infective endocarditis caused by streptococci, enterococci, staphylococci, and HACEK (a) microorganisms
• 1996: Modified Duke Criteria to allow serologic diagnosis of Coxiella burnetii
• 1997: Guidelines for preventing bacterial endocarditis
• 1997: Suggested modifications to Duke criteria for clinical diagnosis of native valve and prosthetic valve endocarditis: analysis of 118 pathologically proven cases
• 1998: Guidelines for antibiotic treatment of streptococcal, enterococcal, and staphylococcal endocarditis
• 1998: Antibiotic treatment of infective endocarditis due to viridans streptococci, enterococci, and other streptococci; recommendations for surgical treatment of endocarditis
• 2000: Updated and modified Duke Criteria
• 2002: Duke Criteria to include a molecular diagnosis of causal agents
• 2001-3: Described etiology of Bartonella spp., Tropheryma whipplei, and Coxiella burnetii in endocarditis

Epidemiology and Demographics

The incidence of IE is approximately 2-4 cases per 100,000 persons per year worldwide. This rate has not changed in the past 5-6 decades.

IE may occur in a person of any age. The frequency is increasing in elderly individuals, with 25-50% of cases occurring in those older than 60 years of age. The occurrence of IE is 3 times more common in males than in females.

Risk Factors

Adults and children with underlying cardiac conditions placing them at highest risk for adverse outcomes of infective endocarditis (IE) including those with:

• Prosthetic cardiac valve or prosthetic cardiac valve repair
• Previous infective endocarditis
• Congenital heart disease (CHD) associated with
  • Unrepaired cyanotic CHD, including palliative shunts and conduits
  • Completely repaired congenital heart defect with prosthetic material or device, whether placed by surgery or by catheter intervention, during the first 6 months after the procedure
  • Repaired CHD with residual defects at the site or adjacent to the site of a prosthetic patch or prosthetic device (which inhibit endothelialization)
• Cardiac transplantation patients who develop cardiac valvulopathy

Screening

Among those patients at high risk, careful monitoring should be undertaken to detect the early development of complications such as:

1. Valvular dysfunction, usually insufficiency of the mitral or aortic valves;
2. Myocardial or septal abscesses
3. Congestive heart failure
4. Metastatic infection
5. Embolic phenomenon

Pathophysiology & Etiology

As previously mentioned, altered blood flow around the valves is a risk factor for the development of endocarditis. The valves may be damaged congenitally, from surgery, by auto-immune mechanisms, or simply as a consequence of old age. The damaged part of a heart valve becomes covered with a blood clot, a condition known as non-bacterial thrombotic endocarditis (NBTE).

In a healthy individual, a bacteremia (where bacteria get into the blood stream through a minor cut or wound) would normally be cleared quickly with no adverse consequences. If a heart valve is damaged and covered with thrombus, these structures can provide a nidus for bacteria to attach themselves and an infection can be established.

The bacteremia is often caused by dental procedures, such as a cleaning or extraction of a tooth. It is important that a dentist or a dental hygienist therefore be told of any heart problems before beginning the procedure. Prophylactic antibiotics are administered to patients with certain heart conditions as a precaution.

Another cause of infective endocarditis is a scenario in which an excess number of bacteria enter the bloodstream. Colorectal cancer, serious urinary tract infections, and IV drug use can all introduce large numbers of such bacteria. When a large burden of bacteria are introduced, a normal heart valve may be infected. A more virulent organism (such as Staphylococcus aureus, but see below for others) is often responsible for infecting a normal valve.

Infections of the tricuspid valve and less frequently the pulmonic valve tend to occur in intravenous drug users given the high pathogen burden from their introduction in the vein. The diseased valve is most commonly affected when there is a pre-existing disease. In rheumatic heart disease this is the aortic valve and the mitral valves, on the left side of the heart.

Complications of endocarditis can occur as a result of the locally destructive effects of the infection. These complications include perforation of valve leaflets, perforation of fistula between blood vessels or cardiac chambers, abscesses and disruption of conduction system.

Natural History and Complications

Complications of infective endocarditis include the following:

• Cardiac

1. Murmur
2. New aortic diastolic murmur suggests dilatation of the aortic annulus or eversion, rupture, or fenestration of an aortic leaflet
3. Sudden onset of loud mitral pansystolic murmur suggests rupture of chorda tendineae or fenestration of a mitral valve leaflet
4. Congestive heart failure
5. Cardiac rhythm disturbances
6. Occasionally, pericarditis

• Cutaneous

1. Petechiae of the conjunctiva, oropharynx, skin, and legs
2. Linear subungual splinter haemorrhages of the lower or middle nail bed
3. Osler’s nodes
4. Janeway lesions

• Musculoskeletal

1. Myalgias
2. Arthralgias
3. Arthritis
4. Low back pain
5. Rheumatoid factor in up to 50% of patients with endocarditis for > 6 wk
6. Clubbing of fingers in < 15% of patients

• Ocular

1. Petechial hemorrhages,
2. Flame-shaped hemorrhages,
3. Roth's spots,
4. Cotton-wool exudates in the retina

• Embolic

1. Significant arterial emboli occur in 30%–50% of patients, causing the following:

   Stroke

   Monocular blindness

   Acute abdominal pain, ileus, and melena

   Pain and gangrene in the extremities

2. CNS emboli are common
3. Coronary emboli, often asymptomatic, can cause myocardial infarction
4. Pulmonary emboli common in right-sided endocarditis, causing pulmonary infarcts or focal pneumonitis

• Splenic

1. Splenomegaly in 15%–30% of patients
2. Splenic infarcts in up to 40% of patients
3. Splenic abscesses in ~ 5% of patients

• Renal

1. Microscopic hematuria in ~ 50% of patients
2. Embolic renal infarction
3. Diffuse membranoproliferative glomerulonephritis

• Mycotic aneurysms

Occur in any artery in 2%–8% of patients, causing the following:

1. Pain or headache
2. Pulsatile mass
3. Fever
4. Sudden expanding hematoma
5. Signs of major blood loss

• Neurologic

1. Neurologic complications occur in 25%–40% of cases
2. Strokes caused by cerebral embolisms in ~ 15% of cases, causing the following:

   Altered level of consciousness

   Seizures

   Fluctuating focal neurologic signs

3. Cerebral aneurysms occur in 1%–5% of cases, causing the following:

   Headache

   Focal signs

   Acute intracerebral or subarachnoid hemorrhage caused by rupture

   Mild meningeal irritation resulting from slow leakage

4. Brain abscesses may occur in acute endocarditis caused by Staphylococcus aureus
5. Seizures

Diagnosis

In general, a patient should fulfill the Duke Criteria in order to establish the diagnosis of endocarditis.

As the Duke Criteria relies heavily on the results of echocardiography, research has addressed when to order an echocardiogram by using signs and symptoms to predict occult endocarditis among patients with intravenous drug abuse and among non drug abusing patients . Unfortunately, this research is over 20 years old and it is possible that changes in the epidemiology of endocarditis and bacteria such as staphylococcus make the following estimates incorrectly low.

Among patients who do not use illicit drugs and have a fever in the emergency room, there is a less than 5% chance of occult endocarditis. Mellors in 1987 found no cases of endocarditis nor of staphylococcal bacteremia among 135 febrile patients in the emergency room. The upper confidence interval for 0% of 135 is 5%, so for statistical reasons alone, there is up to a 5% chance of endocarditis among these patients. In contrast, Leibovici found that among 113 non-selected adults admitted to the hospital because of fever there were two cases (1.8% with 95%CI: 0% to 7%) of endocarditis.

Among patients who do use illicit drugs and have a fever in the emergency room, there is about a 10% to 15% prevalence of endocarditis. This estimate is not substantially changed by whether the doctor believes the patient has a trivial explanation for their fever. Weisse found that 13% of 121 patients had endocarditis. Marantz also found a prevalence of endocarditis of 13% among such patients in the emergency room with fever. Samet found a 6% incidence among 283 such patients, but after excluding patients with initially apparent major illness to explain the fever (including 11 cases of manifest endocarditis), there was a 7% prevalence of endocarditis.

Among patients with staphylococcal bacteremia (SAB), one study found a 29% prevalence of endocarditis in community-acquired SAB versus 5% in nosocomial SAB. However, only 2% of strains were resistant to methicillin and so these numbers may be low in areas of higher resistance.

Common Causes

Many types of organism can cause infective endocarditis. These are generally isolated by blood culture, where the patient's blood is removed, and any growth is noted and identified.

Alpha-haemolytic streptococci, that are present in the mouth will often be the organism isolated if a dental procedure caused the bacteraemia.

If the bacteraemia was introduced through the skin, such as contamination in surgery, during catheterisation, or in an IV drug user, Staphylococcus aureus is common.

A third important cause of endocarditis is Enterococci. These bacteria enter the bloodstream as a consequence of abnormalities in the gastrointestinal or urinary tracts. Enterococci are increasingly recognized as causes of nosocomial or hospital-acquired endocarditis. This contrasts with alpha-haemolytic streptococci and Staphylococcus aureus which are causes of community-acquired endocarditis.

Some organisms, when isolated, give valuable clues to the cause, as they tend to be specific.

• Candida albicans, a yeast, is associated with IV drug users and the immunocompromised. Fungal endocarditis accounts for 5% of cases of native endocarditis and 10% of cases of prosthetic valve endocarditis. A diagnosis of fungal endocarditis is difficult, because many patients are afebrile with a normal white blood cell count (WBC). The fungus is often difficult to culture, and blood cultures typically negative. Fungal infections often result in large vegetations, systemic embolization, myocardial invasion, and are extremely resistant to medical therapy. Early surgical intervention is warranted because medical mortality approaches 100% Anti-fungal therapy for life is required.
• Pseudomonas species, which are very resilient organisms that thrive in water, may contaminate street drugs that have been contaminated with drinking water. P. aeruginosa can infect a child through foot punctures, and can cause both endocarditis and septic arthritis.
• Streptococcus bovis and Clostridium septicum, which are part of the natural flora of the bowel, are associated with colonic malignancies. When they present as the causative agent in endocarditis, it usually call for a concomitant colonoscopy due to worries regarding hematogenous spread of bacteria from the colon due to the neoplasm breaking down the barrier between the gut lumen and the blood vessels which drain the bowel.
• HACEK organisms are a group of bacteria that live on the dental gums, and can be seen with IV drug abusers who contaminate their needles with saliva. Patients may also have a history of poor dental hygiene, or pre-existing valvular disease.

Differential Diagnosis of Risk Factors for or Causes of Endocarditis

History and Symptoms

A. Subacute Bacterial Endocarditis (SBE)

• Insidious onset
• Fever
• Sweats
• Weakness
• Myalgias
• Arthralgias
• Malaise
• Anorexia
• Fatigue
• Splenomegaly, clubbing, and Osler’s nodes in long-standing SBE

B. Acute Bacterial Endocarditis

• Abrupt onset
• Rigors
• Fevers as high as 102.9° to 105.1° F (39.4° to 40.6° C), often remittent

C. Endocarditis Associated with Parenteral Drug Use

1. High fevers, chills, rigors, malaise, cough, and pleuritic chest pain
2. Septic pulmonary emboli causing sputum production, hemoptysis, and signs suggesting pneumonia
3. Cardiac murmurs
4. Tricuspid insufficiency
5. Metastatic infections
6. Neurologic manifestations
7. Peripheral emboli

D. Prosthetic Valve Endocarditis

1. Occurs in 1%–2% of cases at 1 yr and in 4%–5% of cases at 4 yr after implantation
2. Infection of perivalvular tissues
3. Valvular dysfunction
4. Myocardial abscesses
5. Fever
6. Petechiae, Roth's spots, Osler's nodes, Janeway lesions
7. Emboli

Physical Examination

Vital Signs

A fever will likely be present. Rigors may be present.

Skin

• Petechiae 10 - 40%
• Splinter haemorrhage 5 - 15%
• Osler’s nodes 7 - 10% (tender subcutaneous nodules in pulp of digits)
• Janeway lesion 6 - 10% (erythematous, nontender lesions on palm or sole)

Eyes

• Conjunctival hemorrhage
• Roth's spots in the retina

Roth's spots (white centered hemorrhage)

Ear Nose and Throat

In patients in whom there is new acute onset of aortic regurgitation, bobbing of the uvula may be present.

Heart

• Heart Murmurs: 80 - 85%

Lungs

Signs of heart failure may present

Abdomen

• Abdominal pain may be present due to mesenteric embolization or ileus
• Splenomegaly may be found in 15-30% patients. Left upper quadrant (LUQ) pain may be present as a result of a splenic infarct from embolization
• Flank pain may be present as a result of an embolus to the kidney

Extremities

Osler's nodes

• Janeway lesions (painless hemorrhagic cutaneous lesions on the palms and soles)
• Gangrene of fingers may occur
• The fingers may show splinter haemorrhages
• Osler's nodes (painful subcutaneous lesions in the distal fingers)

Neurologic

Septic emboli may result in stroke and focal neurologic findings

Intracranial hemorrhage may occur

Symptoms Frequency

• Fever 80 - 85%, often spiking
• Chills 42 - 75%
• Anorexia 25 - 55%
• Malaise 25 - 40%
• Weight loss 25 - 35%
• Back pain
• Stroke may be present in 10 - 15% of patients as a result of cerebral embolization
• Chest pain may be present as a result of embolzation in the coronary artery. The infarcts are usually not transmural. Pulmonary emboli, often septic, occur in 75% of patients with tricuspid endocarditis
• Abdominal pain may be present due to mesenteric embolization or ileus
• Blindness may be present due to retinal embolization in 3% of patients

Laboratory Findings

An elevated erythrocyte sedimentation rate is present

A marked leukocytosis is present

A positive serum rheumatoid factor may be present (in approximately 50% of patients with subacute disease). It becomes negative after successful treatment.

The serum BUN and Cr may be elevated if glomerulonephritis is present

Urinalysis

Glomerulonephritis may be present

Electrocardiogram

There is no spesific EKG changes for diagnosis of Infective Endocarditis. EKG may help to detect the 10% of patients who develop a conduction delay during Infective Endocarditis by documenting an increased PR interval.

Chest X Ray

There are no specific chest x-ray findings specific for the diagnosis of endocarditis. Non specific findings would include findings of congestive heart failure.

MRI and CT

• A CT scan of the head should be obtained in patients who exhibit CNS symptoms or findings consistent with a mass effect (eg, macroabscess of the brain).

Echocardiography

Echocardiography is useful for risk stratification. Although the data are inconsistent, evidence suggests that vegetation size can predict embolic complications. In general, transthoracic echocardiography (TTE) is adequate for diagnosis of infective endocarditis in cases where cardiac structures-of-interest are well visualized.

Specific situations where transesophageal echocardiography (TEE) is preferred over TTE include the presence of a prosthetic valvular device, suspected periannular complications, children with complex congenital cardiac lesions, patients with S. Aureus caused bacteremia and pre-existing valvular abnormalities that make TTE interpretation more difficult (e.g. calcific aortic stenosis).

The transthoracic echocardiogram has a sensitivity and specificity of approximately 65% and 95% if the echocardiographer believes there is 'probabable' or 'almost certain' evidence of endocarditis.

Aims of echocardiography

1. Determine the presence, location and size of vegetations
2. Assess the damage to the valve apparatus and determine the haemodynamic effects.
3. The dimensions and function of the ventricles.
4. Identify any abscess formation
5. Need for surgical intervention.

Echocardiographic features

• Irregular echogenic mass attached to valve leaflet
• attachment of the vegetation is on the upstream side of the valve leaflet
• independent movement of the mass (chaotic)
• minimum size of the vegetation identifiable on trans thoracic echocardiography is 3mm and by transoesophageal route is 2mm.
• With treatment and time, the vegetation shrinks and can get fibrosed or calcified - may not disappear completely.
• Large vegetations occur with fungal endocarditis or staph. aureus endocarditis.
• the haemodynamical effect is mostly due to regurgitation as a result of valve destruction.

Local complications

• Abscess
• Fistula
• Perforation
• Prosthetic dehiscence

When to do trans esophageal echocardiogram?

• Prosthetic valve endocarditis
• Poor trans thoracic views
• continuing sepsis in spite of adequate antibiotic therapy
• new PR prolongation
• No signs of endocarditis on trans thoracic echocardiography, but high clinical suspicion.

• Video 1: 2 D Echo shows Mitral Valve Vegetation,

<youtube v=5LogTcWG_u4/>

• Video 2: 2 D Echo shows Aortic and Mitral Valve Vegetations

<youtube v=fyrI9RR5DZY/>

• Video 3: 2D Echo Tricuspid Valve Vegetation

<googlevideo>-5198562295572873918&hl=en</googlevideo>

• Fungal Endocarditis 1

<googlevideo>7982129228294522803&hl=en</googlevideo>

• Fungal Endocarditis 2

<googlevideo>365208208714072490&hl=en</googlevideo>

• Fungal Endocarditis 3

<googlevideo>-4564538766847216719&hl=en</googlevideo>

• Fungal Endocarditis 4

<googlevideo>-6464177311760516420&hl=en</googlevideo>

• Fungal Endocarditis 5

<googlevideo>-6146773792630914635&hl=en</googlevideo>

Other Imaging Findings

• Various radionuclide scans using, for example, gallium Ga 67–tagged white cells and indium In 111–tagged white cells, have proven to be of little use in diagnosing IE.

Radionuclide scans of the spleen are useful to help rule out a splenic abscess, which is a cause of bacteremia that is refractory to antibiotic therapy.

Pathology

In acute phase

• Aneurysms
• Infected thrombi or vegetations
• Valve ulcers or erosions
• Rupture of chordaes
• Endocardial jet lesions
• Flail leaflets or cusps
• Abcess formation (annular and ring)

In chronic phase

• Perforations
• Nodular calcifications
• Tissue defects of valves
• Fibrosis of valves

Gross Pathology

Images shown in this section are courtesy of Professor Peter G. Anderson D.V.M. PhD, and published with permission.

© PEIR, University of Alabama at Birmingham, Department of Pathology

• 

  Thrombotic Nonbacterial Endocarditis: (Gross) An excellent example of thrombi on aortic valve.

• 

  Thrombotic Nonbacterial Endocarditis: (Gross) Mitral valve lesion appears that have been present for at least several days.

• 

  Bacterial Endocarditis: (Gross) Perforated aortic valve cusp is shown.

• 

  Thrombotic Nonbacterial Endocarditis: (Gross) Aortic valve with two small vegetations.

• 

  Thrombotic Nonbacterial Endocarditis: (Gross) Mitral valve thrombi in chorda.

• 

  (Gross) A very good example of focal necrotizing lesions in distal portion of digit associated with bacterial endocarditis

• 

  Bacterial Endocarditis: (Gross) A lesion on non-coronary cusp of aortic valve.

• 

  Bacterial Endocarditis: (Gross) An excellent view of mitral scarring due to rheumatic fever healing infectious lesion.

• 

  Bacterial Endocarditis: (Gross) Aortic valve prosthesis ring infection extending into left atrium.

• 

  Bacterial Endocarditis: (Gross) An excellent close-up view of mitral valve vegetations

• 

  Bacterial Endocarditis: (Gross) vegetations on mitral valve and left atrial endocardium due to actinomycosis

• 

  Bacterial Endocarditis: (Gross) An excellent image of vegetation on aortic valve

• 

  Bacterial Endocarditis: (Gross) An excellent image of vegetations on mitral valve evidence of rheumatic scarring

• 

  Thrombotic Nonbacterial Endocarditis: (Gross) Mitral valve, an excellent example

• 

  Thrombotic Nonbacterial Endocarditis: (Gross) Mitral valve: an excellent image, identical to acute rheumatic lesion

• 

  Verrucous Nonbacterial Endocarditis: (Gross) An excellent example of an infant heart

• 

  Purpura of cerebrum, cerebellum and brain stem in 36 years old female with Cushing syndrome and bacterial endocarditis caused by Staphylococcus aureus

• 

  Spleen infarct: (Gross) A typical small infarct with necrotic central portion (originated from infected marantic endocarditis on aortic and mitral valves)

• 

  Kidney infarct: (Gross) A natural color close-up and excellent image of yellow infarct marantic endocarditis on aortic and mitral valves

• 

  Thrombotic Nonbacterial Endocarditis Infected: (Gross) Natural color of pulmonary valve. An excellent example of patient with multiple myeloma

• 

  Thrombotic Non Bacterial Endocarditis: (Gross) Natural color of pulmonary valve.

• 

  Thrombotic Non Bacterial Endocarditis: (Gross) Natural color and good example of tricuspid valve lesions

• 

  Disseminated intravascular coagulation in endocarditis; tricuspid valve showing NBTE in DIC

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  Eye: Bacterial Endocarditis complicated as petechiae. Septic emboli to conjunctiva

Bacterial Endocarditis

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Treatment

High dose antibiotics are administered by the intravenous route to maximize diffusion of antibiotic molecules into vegetation(s) from the blood filling the chambers of the heart. This is necessary because neither the heart valves nor the vegetations adherent to them are supplied by blood vessels. Antibiotics are continued for a long time, typically two to six weeks. Specific drug regimens differ depending on the classification of the endocarditis as acute or subacute (acute necessitating treating for Staphylococcus aureus with oxacillin or vancomycin in addition to gram-negative coverage). Fungal endocarditis requires specific anti-fungal treatment, such as amphotericin B.

Surgical removal of the valve is necessary in patients who fail to clear micro-organisms from their blood in response to antibiotic therapy, or in patients who develop cardiac failure resulting from destruction of a valve by infection. A removed valve is usually replaced with an artificial valve which may either be mechanical (metallic) or obtained from an animal such as a pig; the latter are termed bioprosthetic valves.

Infective endocarditis is associated with a 10-25% mortality.

Pharmacotherapy

Effective treatment requires identification of the etiologic agent and determination of its antimicrobial susceptibility.

Antibiotic therapy for subacute or indolent disease can be delayed until results of blood cultures are known; in fulminant infection or valvular dysfunction requiring urgent surgical intervention, begin empirical antibiotic therapy promptly after blood cultures have been obtained.

For prosthetic valve endocarditis, treatment should be continued for 6–8 weeks.

Acute Pharmacotherapies

Penicillin-Susceptible Viridans and Other Nonenterococcal Streptococci

The minimum inhibitory concentration [MIC] <0.2 µg/ml

• Penicillin G: preferred regimen

Dose: 12–18 million units I.V. daily in divided doses q. 4 hour for 4 weeks

• Penicillin G + gentamicin or ceftriaxone: preferred regimen

Dose: penicillin G, 12–18 million units I.V. daily in divided doses q. 4 hour for 4 weeks; gentamicin, 3 mg/kg I.M. or I.V. daily in divided doses q. 8 hour for 2 weeks (peak serum concentration should be ~ 3 µg/ml and trough concentrations < 1 µg/ml); ceftriaxone, 2 g I.V. daily as a single dose for 2 weeks

• Vancomycin: for patients with history of penicillin hypersensitivity

Dose: 30 mg/kg I.V. daily in divided doses q. 12 hour for 4 weeks

Relatively Penicillin-Resistant Streptococci

A- MIC 0.2–0.5 µg/ml

• Penicillin G + gentamicin: preferred regimen

Dose: penicillin G, 20–30 million units I.V. daily in divided doses q. 4 hour for 4 weeks; gentamicin, 3 mg/kg I.M. or I.V. daily in divided doses q. 8 hr for 2 wk (peak serum concentration should be ~ 3 µg/ml and trough concentrations < 1 µg/ml)

B- MIC > 0.5 µg/ml

• Penicillin G + gentamicin: preferred regimen

Dose: penicillin G, 20–30 million units I.V. daily in divided doses q. 4 hour for 4 week; gentamicin, 3 mg/kg I.M. or I.V. daily in divided doses q. 8 hour for 4 week (peak serum concentration should be ~ 3 µg/ml and trough concentrations < 1 µg/ml)

• Vancomycin: regimen for patients with history of penicillin hypersensitivity

Dose: 30 mg/kg I.V. daily in divided doses q. 12 hour for 4 weeks

Enterococci

• Penicillin G + gentamicin: preferred regimen

Dose: penicillin G, 20–30 million units I.V. daily in divided doses q. 4 hr for 4–6 weeks; gentamicin, 3 mg/kg I.M. or I.V. daily in divided doses q. 8 hour for 4–6 weeks (peak serum concentration should be ~ 3 µg/ml and trough concentrations < 1 µg/ml)

• Ampicillin + gentamicin

Dose: ampicillin, 12 g I.V. daily in divided doses q. 4 hour for 4–6 weeks; gentamicin, dose as above

• Vancomycin + gentamicin: regimen for patients with history of penicillin hypersensitivity

Dose: vancomycin, 30 mg/kg I.V. daily in divided doses q. 12 hour for 4–6 weeks; gentamicin, dose as above

Staphylococci (Methicillin Susceptible) in the Absence of Prosthetic Material

• Nafcillin or oxacillin + gentamicin (optional): preferred regimen

Dose: nafcillin or oxacillin, 12 g I.V. daily in divided doses q. 4 hour for 4–6 weeks; gentamicin, 3 mg/kg I.M. or I.V. daily in divided doses q. 8 hr for 3–5 days (peak serum concentration should be ~ 3 µg/ml and trough concentrations <1 µg/ml)

• Cefazolin + gentamicin (optional): alternative regimen for patients with history of penicillin hypersensitivity

Dose: cefazolin, 12 g I.V. daily in divided doses q. 4 hour for 4–6 weeks; gentamicin, dose as above

• Vancomycin: alternative regimen for patients with history of penicillin hypersensitivity

Dose: 30 mg/kg I.V. daily in divided doses q. 12 hr for 4–6 weeks

Staphylococci (Methicillin Resistant) in the Absence of Prosthetic Material

• Vancomycin

Dose: 30 mg/kg I.V. daily in divided doses q. 12 hour for 4–6 weeks

Staphylococci (Methicillin Susceptible) in the Presence of Prosthetic Material

• Nafcillin or oxacillin + rifampin + gentamicin

Dose: nafcillin or oxacillin, 12 g I.V. daily in divided doses q. 4 hour for 6–8 weeks; rifampin, 300 mg p.o., q. 8 hour for 6–8 weeks; gentamicin (administer during the initial 2 weeks), 3 mg/kg I.M. or I.V. daily in divided doses q. 8 hour for 2 weeks

Staphylococci (Methicillin Resistant) in the Presence of Prosthetic Material

• Vancomycin + rifampin + gentamicin

Dose: vancomycin, 30 mg/kg I.V. daily in divided doses q. 12 hour for 6–8 weeks; rifampin, 300 mg p.o., q. 8 hour for 6–8 weeks; gentamicin (administer during the initial 2 weeks), 3 mg/kg I.M. or I.V. daily in divided doses q. 8 hour for 2 weeks

HACEK Organisms

• Ceftriaxone or another third-generation cephalosporin

Dose: 2 g I.V. daily as a single dose for 4 weeks

Antithrombotic Therapy

• Anticoagulants can cause or worsen hemorrhage in patients with endocarditis but may be carefully administered when needed
• Prothrombin time should be carefully maintained at INR of 2.0–3.0
• Anticoagulation should be reversed immediately in the event of CNS complications and interrupted for 1–2 wk after acute embolic stroke
• Avoid heparin administration during active endocarditis if possible

Surgery and Device Based Therapy

Indications for Surgery

Indications for surgical debridement of vegetations and infected perivalvular tissue, with valve replacement or repair as needed are listed below:

1. Moderate to severe congestive heart failure due to valve dysfunction
2. Unstable valve prosthesis
3. Uncontrolled infection for > 1–3 week despite maximal antimicrobial therapy
4. Persistent bacteremia
5. Fungal endocarditis
6. Relapse after optimal therapy (prosthesis)
7. Vegetation in Situ
8. Prosthetic valve endocarditis with perivalvular invasion
9. Endocarditis caused by Pseudomonas aeruginosa or other gram-negative bacilli that has not responded after 7–10 days of maximal antimicrobial therapy
10. Perivalvular extension of infection and abscess formation
11. Staphylococcal infection of prosthesis
12. Persistent fever (culture negative)
13. Large vegetation (>10 mm = increased embolism)
14. Relapse after optimal therapy (native valve)
15. Vegetations that obstruct the valve orifice

Principles of Surgical Management

1. Excise all infected valve tissue
2. Drain and debride abscess cavities
3. Repair or replace damaged valves
4. Repair associated pathology such as septal defect, fistulas

Aortic Valve - Surgical Options

If the infection limited is limited to the leaflets, then replace the aortic valve.

If the infection extends to anulus or beyond, then debride the infected tissues, drain any abscesses to the pericardial sac and replace the aortic root.

Atrioventricular Valve - Surgical Options

If the infection is limited to the leaflets, then perform a vegectomy, repair perforations, and perform a reduction annuloplasty

If the infection extends to the anulus or beyond, then perform valve replacement, debride and abliterate abscesses. In some cases the tricuspid valve may be excised, but 20-30% of patients will develop congestive heart failure.

Surgical Outcomes

Operative mortality is 15 - 20%. The development of an infection of a prosthetic valve during operation for native valve endocarditis is 4%, it is higher (12 - 16%) if active endocarditis is present at the time of the surgery. Late survival at 5 years for native valve endocarditis is 70 - 80% and for prosthetic valve endocarditis is 50 - 80%.

Prevention of Infective Endocarditis

Primary Prevention

Amoxicillin is the preferred choice for oral therapy because it is well absorbed in the gastrointestinal (GI) tract and provides high and sustained serum concentrations. For individuals who are allergic to penicillins or amoxicillin, the use of cephalexin or another first-generation oral cephalosporin, clindamycin, azithromycin, or clarithromycin is recommended.

Because of possible cross-reactions, a cephalosporin should not be administered to patients with a history of anaphylaxis, angioedema, or urticaria after treatment with any form of penicillin, including ampicillin or amoxicillin.

Patients who are unable to tolerate an oral antibiotic may be treated with ampicillin, ceftriaxone, or cefazolin administered intramuscularly or intravenously. For ampicillin-allergic patients who are unable to tolerate an oral agent, therapy is recommended with parenteral cefazolin, ceftriaxone, or clindamycin.

• List of antibiotics can be used for prophylaxis of Infective Endocarditis;

1. Amoxicillin
2. Ampicillin
3. Cefazolin
4. Ceftriaxone
5. Cephalexin
6. Clindamycin
7. Azithromycin
8. Clarithromycin

• POTENTIAL HARM: The administration of prophylactic antibiotics is not risk free. Additionally, the widespread use of antibiotic therapy promotes the emergence of resistant microorganisms most likely to cause endocarditis, such as viridans group streptococci and enterococci. The frequency of multidrug-resistant viridans group streptococci and enterococci has increased dramatically during the past 2 decades. This increased resistance has reduced the efficacy and number of antibiotics available for the treatment of infective endocarditis.

• CONTRAINDICATIONS: Cephalosporins should not be used in an individual with a history of anaphylaxis, angioedema, or urticaria with penicillins or ampicillin.

Antibiotic Prophylaxis with Dental Procedures

Background

• Endodontic procedures have been associated with a high incidence of bacteremia since the 1920s. Therefore, dental procedures were implicated as an independent risk factor for the development of bacterial endocarditis.
  • However, only 4%-7.5% of all bacterial endocarditis cases are related to endodontic associated bacteremia.

AHA Guidelines

In 1955, the American Heart Association (AHA) published the first of ten subsequent IE prevention guidelines. Most recent, 2007 guidelines underwent changes intended to clarify patient eligibility criteria for receiving IE prophylaxis.

• Major changes include, the consideration that frequent exposures to bacteremias associated with daily activities are considered more likely to induce IE then are endodontic-procedural induced bacteremias.

1. Optimal oral hygiene is emphasized as an important practice for IE prevention.
2. A patient’s lifetime acquisition risk of IE is no longer a consideration for initiating prophylactic antibiotic therapy.
3. The AHA now recommends the administration of single-dose prophylactic antibiotics prior to endodontic procedure only to patients with cardiac conditions associated with the highest risk of adverse outcomes following the acquisition of bacterial endocarditis.

2007 AHA Guideline Recommendation for Which patients require Antiobiotic Prophylaxis Prior to Dental Procedure are those with documented

1. Prosthetic cardiac valve.
2. Previous IE
3. Cardiac transplantation recipients who develop cardiac valvulopathy.
4. Congential heart disease:
   • Unrepaired cyanotic CHD: shunts and conduits
   • Completely repaired congential heart defect during 1st 6months following procedure.
   • Repaired CHD with residual defects at site of prostetic patch or device.

Endodontic Procedures and Endocarditis risk

• Following dental intervention, the absolute risk for developing IE is estimated at 1 case per 14 million dental procedures.
• IE acquisition risk estimates following an endodontic induced bacteremia in patients with congenital heart disease are 1 per 475,000; rheumatic heart disease, 1 per 142,000; prosthetic heart valve, 1 per 114,000; and previous IE, 1 per 95,000 dental procedures.
• Inocula of 1 x 108 (100 million) colony forming units [cfu]/mL or greater are required to consistently induce experimental endocarditis.
  • Recent human quantitative blood culture data support the implication that endodontic associated bacteremia inocula are of insufficient magnitude to induce endocarditis. Bacteremia intensities immediately following invasive human dental procedures are 1.5 cfu/ml-5.9 cfu/ml 10 fold less then necessary to induce IE in the animal model.

• The most recent case-control study of 104 patients with known, high-risk structural heart disease discovered that patients who developed IE were actually less likely to have experienced an endodontic procedure within the 180 days prior to diagnosis than did control patients who did not develop IE (OR 0.2 [95% CI 0.04-0.7]).

• Among high-risk patients with underlying structural heart disease, kidney disease (OR 16.9 [95% CI 1.5-193.0]), diabetes (OR 2.7 [95% CI 1.4-5.2]) and skin flora infection (OR 3.5 [95% CI 0.7-17.0]) were associated with a greater risk for the development of bacterial endocarditis.
• Daily activities such as chewing and oral hygiene practices result in bacteremias more frequently, of longer duration and of greater magnitude in comparison to high-risk endodontic procedures.

These findings have led the AHA to conclude that the cumulative background bacteremia associated with chewing, daily dental hygiene practices, kidney disease, diabetes, and skin colonization present a greater risk of significant bacteremia than any single invasive dental procedure.

Prophylactic Antibiotic Efficacy

• The efficacy of antibiotic regimens for IE prophylaxis has never been assessed under the scrutiny of a randomized controlled trial.
• Evidence supporting pre-endodontic chemoprophylaxis efficacy is extrapolated from data demonstrating reductions in bacteremia magnitudes immediately following the administration of antibiotics.

Antibiotic prophylaxis is reasonable for patients with the conditions who undergo any dental procedure that involves the gingival tissues or periapical region of a tooth and for those procedures that perforate the oral mucosa. Although Infective Endocarditis prophylaxis is reasonable for these patients, its effectiveness is unknown.

Efficacy Assesment

The Cochran Collaboration assessed whether prophylactic administration of penicillin to moderate- to high-risk patients prior to endodontic intervention conferred a mortality, serious illness or endocarditis incidence benefit.

• The pooled, adjusted Odds Ratio across all studies for the development of IE among patients receiving prophylaxis was non-significant (0.56 [95% CI (0.15-2.15)]).

The Cochrane Collaboration concluded; it is unclear whether antibiotic prophylaxis is effective and there is a lack of evidence to support published guidelines using penicillin as chemoprophylaxis for IE.

' To date, only 4 case-control studies has assessed antibiotic efficacy for IE prevention.'

1. Strom et al discovered the administration pre-endodontic procedural antibiotics did not provide a protective benefit against the development of IE (OR 0.5 [CI .01-9.6]).
2. Van Der Meer et al,8/48 case pts (16%) received antibiotics.26/200 control pts (13%) received antibiotics.Stratified Odds Ratio: 0.51 (0.11-2.29).Protective Efficacy 49%.
3. Lacassin et al6/37 case pts (23%) received antibiotics.6/33 control pts (27%) received antibiotics.Matched and Adjusted Odds Ratio: 0.2 (0-0.8) Protective Efficacy 20%.
4. Imperiale et al

1/8 case pts (13%) received antibiotics.15/24 control pts (63%) received antibiotics. Matched Odds Ratio: .09 (CI upper limit of 0.93) (p=.025)Protective Efficacy 91%.

Safety Concerns with Antibiotic Prophylaxis

Adverse reactions associated with the administration of beta-lactam antibiotics are common.

• Ranging in severity from purititus to fatal anaphylactic shock, the frequency of all adverse reactions from the administration of penicillin to the general population is 0.7% to 10%.
• Fatal anaphylaxis among patients receiving single-dose penicillin, ampillicin or amoxicillin therapy is approximately 20 cases per 1 million patients treated.
• Single-dose, cephalosporin-associated fatal anaphylaxis risk is estimated at 0.5-5.7 cases per 10 million patients treated.
• Macrolide and clindamycin single-dose fatal anaphylaxis risk is estimated at 0-5 cases per 1 million patients treated.

With the highest associated mortality rate of all the recommended antibiotic regimens, the risk of anaphylaxis with the initiation of beta-lactam IE prophylactic therapy must be considered.

1. The risk of mortality associated with the single-dose administration of beta-lactam antibiotics for IE prophylaxis is estimated at 1-3 anaphylactic deaths per 1 million patients treated.
2. According to the AHA, single dose administration of a beta-lactam antibiotic for IE prophylactic therapy is a safe practice as it has never resulted in a reportable case of fatal anaphylaxis.

Cost Effectiveness of Oral Antibiotic Prophylaxis

To date, one report has addressed the cost-effectiveness of providing chemoprophylaxis to patients of moderate- and high-risk of IE acquisition prior to endodontic procedure.

1. The risk of drug-induced anaphylaxis and associated loss of QALYs with prophylactic oral amoxicillin or ampicillin to moderate-risk patients rendered this practice ineffective and therefore the authors did not complete a cost-effectiveness analysis.
2. The estimated cost-effectiveness ratio for the prophylaxis of 10 million moderate-risk patients with clarithromycin, clindamycin or cephalexin, was $88,007, $101,142 and $99,373 per QALY saved, respectively.
3. Cost-effectiveness ratio for the use of clarithromycin in patients with the prior diagnosis of endocarditis was $40,334, and in patients with prosthetic valves, $16,818 per QALY saved.
4. Cost-effectiveness ratio of treating 10 million high-risk patients administered single dose clindamycin was $46,678 (prior endocarditis) and $19,936 (prosthetic valve) per QALY saved. #Cephalexin was associated with a cost-effectiveness of $37,916 per QALY saved in patients with a history of IE and $14,060 per QALY saved, in patients with a prosthetic valves.

The cost-effective analyses suggest that the 2007 AHA IE prevention guidelines advocating chemoprophylaxis to patients with a high-risk of adverse outcomes upon acquisition of IE is a reasonable, cost-effective practice.

The term of prophylaxis required procedure include biopsies, suture removal, and placement of orthodontic bands, but it does not include routine anesthetic injections through non-infected tissue, the taking of dental radiographs, placement of removable prosthodontic or orthodontic appliances, placement of orthodontic brackets, or adjustment of orthodontic appliances.

SUMMARY for antibiotic prophlaxis prior to endodontic procedure

• The presumed correlation of endodontic induced bacteremia, and new onset IE made pre-procedural antibiotic prophylaxis a reasonable practice for the preceding 60 years. However, there is a paucity of evidence in support of providing chemoprophylaxis for effective IE prevention.
• Chewing, dental hygiene practices, kidney disease, diabetes, and skin colonization present a greater risk of significant bacteremia and greater cumulative IE acquisition risk than any single invasive dental procedure.
• The AHA recommends reducing the incidence of bacteremia with the optimization of oral hygiene in at-risk patients and does not recommend indiscriminant pre-procedural chemoprophylaxis as a safe, IE prevention practice.

• Case-control studies have reported conflicting results on the protective efficacy conferred from providing pre-procedural antibiotic prophylaxis to at-risk patients.

The AHA acknowledges that even if chemoprophylaxis conferred 100% efficacy, few cases of IE would be prevented as the incidence of endodontic induced IE is so low.

The AHA now recommends the administration of pre-endodontic procedural prophylactic antibiotics to patients with the highest risk of adverse outcomes subsequent to the development of IE.

• Acknowledging an estimated 10-20 fold greater risk of single-dose fatal anaphylaxis with amoxicillin compared to single dose cephalosporin, macrolide and clindamycin regimens, the AHA believes prophylaxis with amoxicillin is a safe practice as there have been no reports of fatal anaphylaxis from a single-dose of pre-dental IE prophylaxis oral amoxicillin.
• The 2007, AHA guidelines appropriately advocate against providing chemoprophylaxis to moderate-risk patients and appropriately advocate for chemoprophylaxis to high-risk patients prior to endodontic procedure as this is a cost-effective practice for IE prevention.

Finally, there are other events that are not dental procedures and for which prophylaxis is not recommended, such as shedding of deciduous teeth and trauma to the lips and oral mucosa.

In this limited patient population, prophylactic antimicrobial therapy should be directed against Streptococcus viridans.

As a summary; individuals at the highest risk group who need procedures listed below require proper antibiotic prophylaxis;

• Any type of dental extractions
• Any type of periodontal procedures and gingival surgery
  • Placement of dental implants and avulsed teeth replantation
  • Dental canal or root surgery
  • Antibiotic fibres or strips placement at subgingival area
  • Initial placement of orthodontic brackets
  • Intraligamentous injection of local anesthetic drugs
  • Bleeding during prophylactic cleaning of teeth or implants

Antibiotic prophylaxis with Respiratory Tract Procedures

Currently there is no published data conclusively demonstrate a link between these procedures and Infective Endocarditis.

Antibiotic prophylaxis is reasonable for high risk patients who undergo an invasive procedure of the respiratory tract that involves incision or biopsy of the respiratory mucosa, such as tonsillectomy and adenoidectomy.

Antibiotic prophylaxis for bronchoscopy is not usually recommended unless the procedure involves incision of the respiratory tract mucosa. For high risk patients who undergo an invasive respiratory tract procedure to treat an established infection, such as drainage of an abscess or empyema, antibiotic regimen should contain an agent active against Streptococcus viridans.

If the infection is known or suspected to be caused by Staphylococcus aureus, the regimen should contain an agent active against S aureus, such as an antistaphylococcal penicillin or cephalosporin, or vancomycin in patients unable to tolerate a beta-lactam. Vancomycin should be administered if the infection is known or suspected to be caused by a methicillin-resistant Staphylococcus aureus.

As a summary; individuals at the highest risk group who need procedures listed below require proper antibiotic prophylaxis;

• Tonsillectomy
• Adenoidectomy
• Rigid bronchoscopic manipulations
• Respiratory mucosa related surgery

Antibiotic prophylaxis with GI or Genitourinary (GU) Tract Procedures

The administration of prophylactic antibiotics solely to prevent endocarditis is not recommended for patients who undergo GU or GI tract procedures, including diagnostic esophagogastroduodenoscopy or colonoscopy.

The significance of the increased frequency of multiresistant strains of enterococci on prevention of IE in patients who undergo GI or GU tract procedures is unknown. The high prevalence of resistant strains of enterococci adds further doubt about the efficacy of prophylactic therapy for GI or GU tract procedures. Patients with infections of the GI or GU tract may have intermittent or sustained enterococcal bacteremia.

For patients with high risk conditions who have an established GI or GU tract infection or for those who receive antibiotic therapy to prevent wound infection or sepsis associated with a GI or GU tract procedure, it may be reasonable that the antibiotic regimen include an agent active against enterococci, such as penicillin, ampicillin, piperacillin, or vancomycin; however, currently no published studies demonstrate that such therapy would prevent enterococcal IE.

For patients with high risk conditions and scheduled for an elective cystoscopy or other urinary tract manipulation who have an enterococcal urinary tract infection or colonization, antibiotic therapy to eradicate enterococci from the urine before the procedure may be reasonable. If the urinary tract procedure is not elective, it may be reasonable that the empiric or specific antimicrobial regimen administered to the patient contain an agent active against enterococci.

Amoxicillin or ampicillin is the preferred agent for enterococcal coverage for these patients. Vancomycin may be administered to patients unable to tolerate ampicillin. If infection is caused by a known or suspected strain of resistant enterococcus, consultation with an infectious diseases expert is recommended.

As a summary; individuals at the highest risk group who need procedures listed below require proper antibiotic prophylaxis;

• Sclerotherapy of esophageal varices
• Dilatation of esophageal stricture
• Endoscopic retrograde cholangiopancreatography – ERCP (especially when biliary obstruction is present)
• Biliary tract surgery
• Surgery of intestinal mucosa

Antibiotic prophylaxis with Procedures on Infected Skin, Skin Structure, or Musculoskeletal Tissue

These infections are often polymicrobial, but only staphylococci and beta hemolytic beta-hemolytic streptococci are likely to cause Infective Endocarditis.

For patients with high risk conditions who undergo a surgical procedure that involves infected skin, skin structure, or musculoskeletal tissue, it may be reasonable that the therapeutic regimen administered for treatment of the infection contain an agent active against staphylococci and beta-hemolytic streptococci, such as an antistaphylococcal penicillin or a cephalosporin.

Vancomycin or clindamycin may be administered to patients unable to tolerate a beta-lactam or who are known or suspected to have an infection caused by a methicillin-resistant staphylococcus aureus.

Primary Prevention in Specific Situations and Circumstances

Patients Already Receiving Antibiotics

If a patient is already receiving long-term antibiotic therapy with an antibiotic that is also recommended for Infective Endocarditis prophylaxis for a dental procedure, it is prudent to select an antibiotic from a different class rather than to increase the dosage of the current antibiotic. For example, antibiotic regimens used to prevent the recurrence of acute rheumatic fever are administered in dosages lower than those recommended for the prevention of Infective Endocarditis.

Individuals who take an oral penicillin for secondary prevention of rheumatic fever or for other purposes are likely to have viridans group streptococci in their oral cavity that are relatively resistant to penicillin or amoxicillin. In such cases, the provider should select either clindamycin, azithromycin, or clarithromycin for IE prophylaxis for a dental procedure, but only for patients shown in the table above. Because of possible cross-resistance of viridans group streptococci with cephalosporins, this class of antibiotics should be avoided.

If possible, it would be preferable to delay a dental procedure until at least 10 days after completion of the antibiotic therapy. This may allow time for the usual oral flora to be reestablished.

Patients Who Receive Anticoagulants

Intramuscular injections for Infective Endocarditis prophylaxis should be avoided in patients who are receiving anticoagulant therapy. In these circumstances, orally administered regimens should be given whenever possible. Intravenously administered antibiotics should be used for patients who are unable to tolerate or absorb oral medications.

Patients Who Undergo Cardiac Surgery

Patients who undergo surgery for placement of prosthetic heart valves or prosthetic intravascular or intracardiac materials are at risk for the development of infection. Because the morbidity and mortality of infection in these patients are high, perioperative prophylactic antibiotics are recommended.

Early-onset prosthetic valve endocarditis is most often caused by S. aureus, coagulase-negative staphylococci, or diphtheroids. No single antibiotic regimen is effective against all these microorganisms. Prophylaxis at the time of cardiac surgery should be directed primarily against staphylococci and should be of short duration. A first-generation cephalosporin is most often used, but the choice of an antibiotic should be influenced by the antibiotic susceptibility patterns at each hospital. For example, a high prevalence of infection by methicillin-resistant Staphylococcus aureus (MRSA) should prompt the consideration of the use of vancomycin for perioperative prophylaxis.

The majority of nosocomial coagulase-negative staphylococci are methicillin-resistant. Nonetheless, surgical prophylaxis with a first-generation cephalosporin may be recommended for these patients. In hospitals with a high prevalence of methicillin-resistant strains of S. epidermidis, surgical prophylaxis with vancomycin may be reasonable but has not been shown to be superior to prophylaxis with a cephalosporin.

Prophylaxis should be initiated immediately before the operative procedure, repeated during prolonged procedures to maintain serum concentrations intraoperatively, and continued for no more than 48 hours postoperatively to minimize emergence of resistant microorganisms. The effects of cardiopulmonary bypass and compromised renal function on antibiotic concentrations in serum should be considered and dosages adjusted as necessary before and during the procedure.

Secondary Prevention and Follow-Up

Short-Term Follow-Up

The majority of patients with IE are cured with appropriate medical and, if necessary, surgical treatment. Before completing antimicrobial therapy, the patient should receive TTE (Class IIb, Level of Evidence: C) to establish a new baseline for subsequent comparison.

A referral to a program to assist in cessation of drug use should be made for IDU patients. Patients should be educated about the signs of endocarditis and urged to seek immediate medical attention should they occur. A thorough dental evaluation should be obtained and all active sources of oral infection should be eradicated.

All catheters used to infuse antimicrobial treatment should be promptly removed at the end of therapy. In the short-term follow-up, patients should be monitored for development of several complications. A relapse of endocardial infection is a primary concern. Patients should be aware that relapses can occur and that new onset of fever, chills, or other evidence of systemic toxicity mandates immediate evaluation, including obtaining ≥3 sets of blood cultures from different phlebotomy sites after a thorough history and physical examination.

Long-Term Follow-Up

Months to years after completion of medical therapy for IE, patients need ongoing observation and education regarding recurrent infection and delayed onset of worsening valvular dysfunction. Ongoing daily dental hygiene should be stressed, with serial evaluations by a dentist who is familiar with this patient population.

Patients should be questioned about the symptoms of decreased cardiac output and CHF. A thorough cardiac examination will be needed. Additional evaluations with TTE will be necessary in selected patients with positive findings from history and physical examination. Patients must be reminded to seek immediate medical evaluation for fever. This is necessary because IE can mimic a panoply of febrile illnesses.

Antibiotic therapy should not be initiated for treatment of undefined febrile illnesses without obtaining previous blood cultures. Antibiotics prescribed for nonspecific or unproved febrile syndromes are the major cause of (blood) culture negative endocarditis and should be strongly discouraged.

Cost-Effectiveness of Therapy

Although cost-effectiveness calculations suggest that TEE should be the first examination in adults with suspected IE, particularly in the setting of staphylococcal bacteriemia, many patients are not candidates for immediate TEE because of oral intake during the preceding 6 hours or because the patients are in institutions that cannot provide 24-hour TEE services. When TEE is not clinically possible or must be delayed, early TTE should be performed without delay.

Future or Investigational Therapies

Considering infective endocarditis to be an "emerging" problem in the 21st century may seem unusual, given that the illness has been well documented over the last 450 years. However, such emergence can be attributed to several factors:

1. The emergence of antimicrobial resistance in classic infective endocarditis microflora, namely, the gram-positive cocci;
2. The existence of antimicrobial resistance in complex ecologic biofilms;
3. The changing pattern of causal agents now regarded as important pathogens of infective endocarditis, e.g., Bartonella spp., T. whipplei, and fungi;
4. Changing epidemiologic trends of persons who acquire infective endocarditis, including injection drug users, persons with HIV/AIDS, children with congenital heart defects, and persons undergoing body piercing.

Furthermore, the way we provide inpatient medical care has also been associated with the emergence of nosocomial infective endocarditis, which can result from invasive procedures such as catheterization, although no cardiac surgery has been performed.

The forthcoming years will likely witness the emergence of even more changing trends of infective endocarditis, which as yet have not been well recognized.

External Links and Patient Resources

• Brief Communication: Treatment of Enterococcus faecalis Endocarditis with Ampicillin plus Ceftriaxone
• Infective Endocarditis in Adults
• Temporal Trends in Infective Endocarditis

For Patients:

• A.H.A. Patient Information for Infective Endocarditis

Acknowledgements

The content on this page was first contributed by: C. Michael Gibson, M.S., M.D.