Bartonella henselae bacilli in cardiac valve of a patient with blood culture-negative endocarditis. The bacilli appear as black granulations.
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Endocarditis

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

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Endocarditis can be classified by etiology as either infective or non-infective, depending on whether a foreign micro-organism is causing the problem.

Infective endocarditis

As the valves of the heart do not actually receive any blood supply of their own, which may be surprising given their location, defense mechanisms (such as white blood cells) cannot enter. So if an organism (such as bacteria) establish hold on the valves, the body cannot get rid of them.

Normally, blood flows pretty smoothly through these valves. If they have been damaged (for instance in rheumatic fever) bacteria have a chance to take hold.

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When should patients with mitral valve prolapse get endocarditis prophylaxis?
From Journal of Family Practice, 3/1/04 by Daniel Triezenberg

* EVIDENCE-BASED ANSWER

Patients with suspected mitral valve prolapse (MVP) (Figure 1) should undergo echocardiography before any procedure that may place them at risk for bacteremia. Patients with MVP and documented absence of mitral regurgitation or valvular thickening likely do not need antibiotic prophylaxis against subacute bacterial endocarditis (SBE). Patients with MVP with documented mitral regurgitation, valvular thickening, or an unknown degree of valvular dysfunction may benefit from antibiotics during procedures that often lead to bacteremia (strength of recommendation: C).(1)

[FIGURE 1 OMITTED]

* EVIDENCE SUMMARY

Only disease-oriented evidence and expert opinion address prevention for endocarditis. A randomized trial would require an estimated 6000 patients to demonstrate benefit. (2)

Endocarditis occurs in MVP at a rate of 0.1 cases/100 patient-years. (3) However, MVP is the most common predisposing/precipitating cause of native valve endocarditis. (4,5) In animal models, antibiotics prevent endocarditis following experimental bacteremia. The antibiotic can be administered either just before or up to 2 hours after the bacteremic event. (2) It is worth noting that most bacteremia is not associated with medical procedures. Since endocarditis is often fatal, recommendations have been developed based on these animal models. Estimates of effectiveness of prophylaxis from case-control studies in humans (not limited to patients with MVP) estimate effectiveness from 49% to 91%. (2)

For patients with MVP who do not have evidence of mitral regurgitation on physical examination or echocardiography, the risk of morbidity may be greater from antibiotic therapy than the risk of endocarditis. Prophylaxis for these patients is not recommended. Patients with MVP associated with regurgitation are at moderate risk and may benefit from antibiotic prophylaxis.

* RECOMMENDATIONS FROM OTHERS

The American Heart Association has published recommendations in 1985, (6) 1990, (7) and 1997. (1) The 1997 recommendations are summarized in Figure 2. The Swiss Working Group for Endocarditis Prophylaxis published similar recommendations in 2000. (8) Recommended prophylactic regimens appear in Table 1. Table 2 shows a modified list of procedures for which prophylaxis is recommended.

TABLE 2

Procedures for which endocarditis prophylaxis is, or is not, recommended

Endocarditis prophylaxis recommended

Respiratory tract

Tonsillectomy or adenoidectomy Surgical operations that involve respiratory mucosa Bronchoscopy with a rigid bronchoscope

Gastrointestinal tract

Sclerotherapy for esophageal varices Esophageal stricture dilation Endoscopic retrograde cholangiography with biliary obstruction Biliary tract surgery Surgical operations that involve intestinal mucosa

Genitourinary tract

Prostatic surgery Cystoscopy Urethral dilation

Endocarditis prophylaxis not recommended

Respiratory tract

Endotracheal intubation Flexible bronchoscopy, with or without biopsy Tympanostomy tube insertion

Gastrointestinal tract Endoscopy with or without gastrointestinal biopsy

Genitourinary tract Circumcision Vaginal hysterectomy Vaginal delivery Cesarean section

In uninfected tissue Incision or biopsy of surgically scrubbed skin Urethral catheterization Uterine dilatation and curettage Therapeutic abortion Sterilization procedures Insertion or removal of intrauterine devices

Cardiac Transesophageal echocardiography Cardiac catheterization, including balloon angioplasty and coronary stents Implanted cardiac pacemakers, implanted defibrillators

Modified from Dajani et al, 1997. (1)

* CLINICAL COMMENTARY

Guidelines assist decision-making regarding who needs SBE prophylaxis It is unfortunate, but not surprising, that the evidence for SBE prophylaxis for patients with MVP is disease-oriented evidence and expert opinion. Too often, the easy thing to do in a busy practice is not necessarily in the best interest of either the patient or the public. However-despite the low incidence of SBE--the high mortality of the disease and community standard of care often drive clinicians to write that prescription for antibiotics.

With the improved resolution and sensitivity of newer generations of echocardiograms, clinicians often face the dilemma of the patient with MVP and "trivial" or "minimal" mitral regurgitation. Unfortunately, no guidelines assist us in our decision-malting regarding these patients.

Another consideration for the clinician is the American Heart Association's recommendation for SBE prophylaxis for patients with MVP and thickened leaflets, regardless of whether there is associated mitral valve regurgitation.

One significant change that should lessen the frequency of unnecessary antibiotic prescribing was published recently. The echocardiographic criteria for diagnosing MVP were changed in the 2003 updated guidelines from the American College of Cardiology, American Heart Association, and American Society of Echocardiography. Valve prolapse of 2 mm or more above the mitral annulus is required for diagnosis. (10) This change has effectively lowered the prevalence of MVP from 4% to 8% of the general population down to 2% to 3%.

David M. Bercaw, MD, Christiana Care Health Systems, Wilmington, Del

REFERENCES

(1.) Dajani AS, Taubert KA, Wilson W, et al. Prevention of bacterial endocarditis. Recommendations by the American Heart Association. JAMA 1997; 277:1794-1801.

(2.) Durack DT. Prevention of infective endocarditis. N Engl J Med 1995; 332:38-44.

(3.) Zuppiroli A, Rinaldi M, Kramer-Fox R, Favilli S, Roman MJ, Devereux RB. Natural history of mitral valve prolapse. Am J Cardiol 1995; 75:1028-1032.

(4.) Awadallah SM, Kavey RE, Byrum CJ, Smith FC, Kveselis DA, Blackman MS. The changing pattern of infective endocarditis in childhood. Am J Cardiol 1991; 68:90-94.

(5.) McKinsey DS, Ratts TE, Bisno AL. Underlying cardiac lesions in adults with infective endocarditis. The changing spectrum. Am J Med 1987; 82:681-688.

(6.) Shulman ST, Amren DP, Bisno AL, et al. Prevention of bacterial endocarditis: A statement for health professionals by the Committee on Rheumatic Fever and Bacterial Endocarditis of the Council on Cardiovascular Diseases in the Young of the American Heart Association. Am J Dis Child 1985: 139:232-235.

(7.) Dajani AS, Bisno AL, Chung KJ, et al. Prevention of bacterial endocarditis. Recommendations by the American Heart Association. JAMA 1990: 264:2919-2922.

(8.) Moreillon P. Endocarditis prophylaxis revisited: experimental evidence of efficacy and new Swiss recommendations. Swiss Working Group for Endocarditis Prophylaxis. Schweiz Med Wochenschr 2000; 130:1013-1026.

(9.) Cheitlin MD, Armstrong WF, Aurigemma GP, et al. ACC/AHA/ASE 2003 guideline update for the clinical application of echocardiography: a report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines. Am Coll Cardiol 2003; 42:954-970.

Daniel Triezenberg, MD, Jennifer Helmen, BA, Michelle Pearson, MD, Saint Joseph Regional Medical Center, South Bend, Ind

COPYRIGHT 2004 Dowden Health Media, Inc.
COPYRIGHT 2004 Gale Group

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