eMedicine Specialties > Emergency Medicine > Cardiovascular

Mitral Valve Prolapse: Treatment & Medication

Author: Michael C Plewa, MD, Research Coordinator, Consulting Staff, Department of Emergency Medicine, Lucas County Emergency Physicians, Inc, and Saint Vincent Mercy Medical Center
Coauthor(s): Richard Worthington, MD, Assistant Clinical Professor, Program Instructor, Department of Emergency Medicine, St Vincent Mercy Medical Center
Contributor Information and Disclosures

Updated: Dec 22, 2008

Treatment

Prehospital Care

The prehospital treatment of patients with chest pain, dyspnea, palpitations, a neurologic deficit, or syncope should include cardiac monitoring, supplemental oxygen, and intravenous catheter placement.

Emergency Department Care

  • Patients with symptoms of chest pain, dyspnea, palpitations, a neurologic deficit, or syncope should be placed on oxygen, put in a supine or Fowler position, and monitored.
    • Pulse oximetry
    • Cardiac monitoring
    • Frequent vital signs, including one set of orthostatic vital signs when possible
  • Anxious patients should be reassured regarding their status, and many may benefit from psychosocial intervention.

Consultations

  • Consult a cardiologist in cases of diagnostic uncertainty, ventricular dysrhythmia, or risk of sudden death as well as when symptoms of severe MR are present.
  • Consider consulting a cardiothoracic surgeon in patients with significant exertional dyspnea and congestive heart failure that is related to MR.

Medication

Medications generally are not necessary. Beta-blockers may be helpful if palpitations are severe.

Antiplatelet agents such as aspirin, aspirin with extended-release dipyridamole (Aggrenox), or clopidogrel (Plavix) are indicated for patients with transient ischemic attack or stroke.17 Some authors recommend prophylaxis with antiplatelet agents in all patients with mitral valve prolapse (MVP) and murmur because of a small but significant increase in risk of stroke (10%).18

Orthostatic hypotension and presyncope symptoms may be treated with sodium chloride tablets; however, if this treatment is not successful, fludrocortisone 0.05-0.10 mg/d PO may be used.

Magnesium supplementation may improve symptoms of the classic MVP syndrome.5

Significant mitral regurgitation (MR) in the setting of hypertension (systolic blood pressure >140 mm Hg) may be improved with the use of angiotensin-converting enzyme inhibitors. No evidence exists as yet to support the use of these medications to halt the progression of MVP to MR.

Antibiotics

Antibiotic prophylaxis to prevent infective endocarditis is no longer recommended prior to dental or surgical procedures for any patient with MVP (even those with a murmur or nontrivial MR on echo and men older than 45 years with valve thickening) unless there is a history of endocarditis.19  Antibiotic prophylaxis to prevent infective endocarditis is no longer recommended prior to genitourinary or gastrointestinal procedures, even with a history of endocarditis.19,20

Patients with MVP with prior endocarditis who are undergoing a dental, respiratory tract, infected skin, or musculoskeletal tissue procedure (eg, contaminated wound repair or abscess incision and drainage) should receive prophylaxis for infective endocarditis with amoxicillin 2 g (50 mg/kg) PO 1 hour prior to the procedure. Patients with MVP with prior endocarditis who are unable to take oral medications may be treated with ampicillin 2 g (50 mg/kg) IM or IV, or cefazolin or ceftriaxone 1 g (50 mg/kg) IM or IV 1 hour prior to the procedure.

Patients with MVP with prior endocarditis who are allergic to penicillin may be treated 1 hour before the procedure with cephalexin 2 g (50 mg/kg) PO, clindamycin 600 mg (20 mg/kg) PO, or azithromycin or clarithromycin 500 mg (15 mg/kg) PO. Clindamycin 600 mg (20 mg/kg), or cefazolin or ceftriaxone 1 g (50 mg/kg), may be administered IM or IV 30 minutes before the procedure, as an alternative to the PO route.


Amoxicillin (Amoxil, Biomox, Polymox)

DOC; interferes with the synthesis of cell wall mucopeptide during active multiplication, resulting in a bactericidal activity against susceptible bacteria.

Adult

2 g PO 1 h before the procedure; alternatively, 3 g PO 1 h before the procedure, followed by 1.5 g PO 6 h after the initial dose

Pediatric

50 mg/kg PO 1 h before procedure

May reduce efficacy of oral contraceptives

Pregnancy

B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals

Precautions

Adjust dose in renal impairment; may enhance chance of candidiasis


Ampicillin (Marcillin, Omnipen)

Alternative parenteral agent. Interferes with bacterial cell wall synthesis during active multiplication, causing bactericidal activity against susceptible organisms. Given in place of amoxicillin in patients who are unable to take medication orally.

Adult

2 g IV/IM 30 min before the procedure

Pediatric

50 mg/kg IV/IM 30 min before the procedure

Probenecid and disulfiram elevate ampicillin levels; allopurinol decreases ampicillin effects and has additive effects on ampicillin rash; may decrease effects of oral contraceptives

Pregnancy

B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals

Precautions

Adjust dose in renal failure; evaluate rash and differentiate from hypersensitivity reaction

Beta-blockers

Blood pressure control may prevent chordal rupture and the progression of MVP to severe MR. Clonidine has been shown to diminish symptoms of the classic (disputed) MVP syndrome. Beta-blocking agents (eg, propranolol, atenolol, pindolol) may also be effective in those with neurocardiogenic syncope.


Atenolol (Tenormin)

Selectively blocks beta1-receptors with little or no effect on beta2 types.

Adult

50 mg PO qd, increase to 100 mg/d

Pediatric

Not established; 1-2 mg/kg/dose PO qd suggested

Coadministration with aluminum salts, barbiturates, calcium salts, cholestyramine, NSAIDs, penicillins, and rifampin may decrease effects; haloperidol, hydralazine, loop diuretics, and MAOIs may increase toxicity of atenolol

Documented hypersensitivity; congestive heart failure; pulmonary edema; cardiogenic shock; AV conduction abnormalities and heart block (without a pacemaker)

Pregnancy

C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus

Precautions

Beta-adrenergic blockade may reduce symptoms of acute hypoglycemia and mask signs of hyperthyroidism; abrupt withdrawal may exacerbate symptoms of hyperthyroidism and cause thyroid storm; monitor patients closely and withdraw drug

Antiarrhythmics

Digoxin has been effective in treating supraventricular tachycardia and in the prevention of symptoms of classic MVP syndrome (eg, chest pain, fatigue).


Digoxin (Lanoxin)

Cardiac glycoside with direct inotropic effects in addition to indirect effects on the cardiovascular system. Effects on the myocardium involve both a direct action on cardiac muscle that increases myocardial systolic contractions and indirect actions that result in increased carotid sinus nerve activity and enhanced sympathetic withdrawal for any given increase in mean arterial pressure.

Adult

0.125-0.375 mg PO qd; digitalization must be individualized

Pediatric

5-10 years: 20-35 mcg/kg PO divided bid
>10 years: 10-15 mcg/kg PO qd
Maintenance dose: 25-35% of PO loading dose
Digitalization must be individualized

Medications that may increase digoxin levels include alprazolam, benzodiazepines, bepridil, captopril, cyclosporine, propafenone, propantheline, quinidine, diltiazem, aminoglycosides, oral amiodarone, anticholinergics, diphenoxylate, erythromycin, felodipine, flecainide, hydroxychloroquine, itraconazole, nifedipine, omeprazole, quinine, ibuprofen, indomethacin, esmolol, tetracycline, tolbutamide, and verapamil
Medications that may decrease serum digoxin levels include aminoglutethimide, antihistamines, cholestyramine, neomycin, penicillamine, aminoglycosides, oral colestipol, hydantoins, hypoglycemic agents, antineoplastic treatment combinations (including carmustine, bleomycin, methotrexate, cytarabine, doxorubicin, cyclophosphamide, vincristine, procarbazine), aluminum or magnesium antacids, rifampin, sucralfate, sulfasalazine, barbiturates, kaolin/pectin, and aminosalicylic acid

Documented hypersensitivity; beriberi heart disease; idiopathic hypertrophic subaortic stenosis; constrictive pericarditis; carotid sinus syndrome

Pregnancy

C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus

Precautions

Hypokalemia may reduce positive inotropic effect of digitalis; IV calcium may produce arrhythmias in digitalized patients; hypercalcemia predisposes patient to digitalis toxicity, and hypocalcemia can make digoxin ineffective until serum calcium levels are normal; magnesium replacement therapy must be instituted in patients with hypomagnesemia to prevent digitalis toxicity; patients diagnosed with incomplete AV block may progress to complete block when treated with digoxin; exercise caution in hypothyroidism, hypoxia, and acute myocarditis

More on Mitral Valve Prolapse

Overview: Mitral Valve Prolapse
Differential Diagnoses & Workup: Mitral Valve Prolapse
Treatment & Medication: Mitral Valve Prolapse
Follow-up: Mitral Valve Prolapse
Multimedia: Mitral Valve Prolapse
References

References

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Further Reading

Contributor Information and Disclosures

Author

Michael C Plewa, MD, Research Coordinator, Consulting Staff, Department of Emergency Medicine, Lucas County Emergency Physicians, Inc, and Saint Vincent Mercy Medical Center
Michael C Plewa, MD is a member of the following medical societies: American Academy of Emergency Medicine, American College of Emergency Physicians, American Medical Association, Physicians for Social Responsibility, and Society for Academic Emergency Medicine
Disclosure: Nothing to disclose.

Coauthor(s)

Richard Worthington, MD, Assistant Clinical Professor, Program Instructor, Department of Emergency Medicine, St Vincent Mercy Medical Center
Richard Worthington, MD is a member of the following medical societies: American College of Emergency Physicians, Ohio State Medical Association, and Society for Academic Emergency Medicine
Disclosure: Nothing to disclose.

Medical Editor

Robert M McNamara, MD, FAAEM, Chair and Professor, Department of Emergency Medicine, Temple University School of Medicine
Robert M McNamara, MD, FAAEM is a member of the following medical societies: American Academy of Emergency Medicine, American Medical Association, Pennsylvania Medical Society, and Society for Academic Emergency Medicine
Disclosure: Nothing to disclose.

Pharmacy Editor

Francisco Talavera, PharmD, PhD, Senior Pharmacy Editor, eMedicine
Disclosure: Nothing to disclose.

Managing Editor

Paul Blackburn, DO, FACOEP, FACEP, Program Director, Department of Emergency Medicine, Maricopa Medical Center; Assistant Professor, Department of Surgery, University of Arizona
Paul Blackburn, DO, FACOEP, FACEP is a member of the following medical societies: American College of Emergency Physicians, American College of Osteopathic Emergency Physicians, American Medical Association, and Arizona Medical Association
Disclosure: Nothing to disclose.

CME Editor

John D Halamka, MD, MS, Associate Professor of Medicine, Harvard Medical School, Beth Israel Deaconess Medical Center; Chief Information Officer, CareGroup Healthcare System and Harvard Medical School; Attending Physician, Division of Emergency Medicine, Beth Israel Deaconess Medical Center
John D Halamka, MD, MS is a member of the following medical societies: American College of Emergency Physicians, American Medical Informatics Association, Phi Beta Kappa, and Society for Academic Emergency Medicine
Disclosure: Nothing to disclose.

Chief Editor

David FM Brown, MD, Assistant Professor, Department of Medicine, Division of Emergency Medicine, Harvard Medical School; Associate-Chief, Attending Physician, Department of Emergency Medicine, Massachusetts General Hospital
David FM Brown, MD is a member of the following medical societies: American College of Emergency Physicians and Society for Academic Emergency Medicine
Disclosure: Schering  Honoraria Speaking and teaching

 
 
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