eMedicine Specialties > Pediatrics: Cardiac Disease and Critical Care Medicine > Cardiology

Pericarditis, Bacterial: Treatment & Medication

Author: John Berger, MD, Departments of Critical Care Medicine and Pediatric Cardiology, Assistant Professor, George Washington University and Children's National Medical Center
Contributor Information and Disclosures

Updated: Jul 15, 2008

Treatment

Medical Care

Proper treatment of life-threatening illness requires proper antimicrobial therapy, pericardial decompression and drainage, and intensive supportive care.

  • Antibiotics
    • Until a definitive agent is identified, empiric therapy includes antibiotics to treat both S aureus and gram-negative bacilli.
    • Initial antibiotics should include a combination of penicillinase-resistant penicillin and third-generation cephalosporin.
    • In areas of high antibiotic resistance, consider the use of vancomycin and a third-generation cephalosporin.
    • Include an aminoglycoside if the patient is postoperative from cardiac surgery, is immunocompromised, or has a genitourinary coinfection.
    • Duration of therapy is empiric but generally continues for 3-4 weeks with an antibiotic specific to the organism isolated.
  • Pericardial drainage
    • Although needle pericardiocentesis may be life saving in tamponade and confirming the diagnosis, it rarely provides complete and long-lasting resolution of the effusion.
    • Avoid repeated attempts at needle pericardiocentesis because they are associated with increased morbidity rates.
    • Open surgical drainage has been used in most cases of purulent pericarditis.
    • Continuous drainage using specialized pericardial catheters and echographic monitoring has had reported success in treating bacterial pericarditis. However, the pericardial fluid may be too thick or loculated to be drained adequately by a catheter.
    • Delay in adequate pericardial drainage is associated with increased mortality rates.
  • Supportive care
    • Almost all patients require intensive supportive care.
    • In patients with tamponade, supportive therapies are of little or no benefit until emergent pericardial drainage is performed.
    • Drugs that depress the heart rate, produce vasodilatation, or decrease intravascular volume are contraindicated because they further compromise cardiac output. Do not administer digoxin to an infant with purulent pericarditis who shows signs of congestive heart failure.
    • Application of positive pressure mechanical ventilation and positive end-expiratory pressure (PEEP) must be performed carefully because the increased intrathoracic pressure can lead to lethal falls in ventricular preload and worsened shock.
    • Although systolic function of the heart may not be depressed, inotropic agents may be required to treat hypotension that persists after pericardial drainage.
    • Plasma volume expansion is helpful in maintaining cardiac output.

Surgical Care

  • Pericardial drainage
    • If pericardiocentesis is unsuccessful in resolving tamponade, emergent surgical drainage is indicated.
    • Surgical drainage is indicated in most patients after the acute emergency resolves.
    • Delay in adequate pericardial drainage is associated with increased mortality rates.
    • Various surgical procedures have been used to provide adequate pericardial drainage, and optimal approach is controversial. Techniques for drainage include placement of a large bore subxiphoid drainage tube (with or without irrigation), creation of a pericardial window and placement of a drain, or pericardiectomy.
    • Proponents of pericardiectomy argue that thick clots and fibrin are not removed through a tube and that it prevents the possibility of late pericardial constriction and recurrent tamponade.
  • Pericardiectomy: Late pericardiectomy may be required in the rare patient who develops constrictive pericarditis as a complication of the infection.

Consultations

  • Critical care specialist: Most patients with bacterial pericarditis present with severe hemodynamic compromise. Patients should be referred to specialists proficient in the use of vasoactive agents and mechanical ventilation.
  • Cardiologist: Patients with cardiomegaly and cardiovascular compromise require cardiology consultation and echocardiography to rule out myocardial or pericardial disease.
  • Cardiovascular surgeon: Emergent consultation with a cardiovascular surgeon is warranted in patients who have incomplete resolution of pericardial tamponade despite pericardiocentesis. Consultation should be considered in patients with recurrent effusions or constrictive pericarditis.

Activity

No activity restrictions are required in patients who have recovered from bacterial pericarditis.

Medication

Antibiotic agents

Empiric antimicrobial therapy must be comprehensive and should cover all likely pathogens in the context of the clinical setting. Initial empiric coverage requires a combination of a penicillinase-resistant penicillin and third-generation cephalosporin. In areas of high antibiotic resistance, substitute vancomycin for the penicillin antibiotic.


Oxacillin

Bactericidal antibiotic that inhibits cell wall synthesis. Used in the treatment of infections caused by penicillinase-producing staphylococci. May be used to initiate therapy when a staphylococcal infection is suspected.

Adult

2 g IV q6h

Pediatric

200 mg/kg/d IV divided q6h; not to exceed adult dose

Oxacillin decreases effects of contraceptives and tetracycline; administered concomitantly with disulfiram and probenecid, may increase oxacillin levels; effect of anticoagulants increase when large IV doses of oxacillin given

Pregnancy

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

Precautions

Use with caution in patients with hypersensitivity to cephalosporins or severe renal impairment; adjust dosage in patients with renal failure


Nafcillin

Bactericidal antibiotic that inhibits cell wall synthesis. Used in the treatment of infections caused by penicillinase-producing staphylococci. May be used to initiate therapy when a staphylococcal infection is suspected.

Adult

2 g IV q6h

Pediatric

200 mg/kg/d IV divided q6h; not to exceed adult dose

Associated with warfarin resistance when administered concurrently; effects may decrease with bacteriostatic action of tetracycline derivatives; may increase hepatic metabolism of cyclosporine; probenecid inhibits nafcillin elimination

Pregnancy

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

Precautions

Use extravasation precautions; adjust dosage in severe renal and/or hepatic impairments; caution with hypersensitivity to cephalosporins


Vancomycin (Vancocin, Vancoled)

Indicated for patients with suspected or known infection with resistant organisms. To avoid toxicity, assay vancomycin trough levels 30 min before fourth dose. Use CrCl to adjust dose in patients diagnosed with renal impairment.

Adult

500 mg IV q6h

Pediatric

60 mg/kg/d IV divided q6h; not to exceed 4 g/d

Erythema, histaminelike flushing and anaphylactic reactions may occur when administered with anesthetic agents; coadministration with other nephrotoxic or ototoxic drug (eg, aminoglycosides, cisplatin, loop diuretics) increases risk of toxicity; enhanced effect of neuromuscular blockade when coadministered with nondepolarizing muscle relaxants

Documented hypersensitivity; previous hearing loss

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

Caution in renal dysfunction (adjust dose) or myelosuppression; red man syndrome is caused by too rapid IV infusion (dose given over a few min) but rarely happens when dose given as 2-h infusion


Cefotaxime (Claforan)

Arrests bacterial cell wall synthesis, which, in turn, inhibits bacterial growth. Third-generation cephalosporin with gram-negative spectrum. Lower efficacy against gram-positive organisms.

Adult

2.5 g IV q6h

Pediatric

200 mg/kg/d IV divided q6h; not to exceed adult dose

Probenecid may increase cefotaxime levels; coadministration with furosemide and aminoglycosides may increase nephrotoxicity

Pregnancy

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

Precautions

Caution with history of hypersensitivity to penicillin, impaired renal function (adjust dose), or colitis


Ceftriaxone (Rocephin)

Third-generation cephalosporin with broad-spectrum gram-negative activity; lower efficacy against gram-positive organisms; higher efficacy against resistant organisms. Arrests bacterial growth by binding to one or more penicillin binding proteins.

Adult

4 g/d IV divided q12-24h

Pediatric

75 mg/kg/d IV divided q12-24h; not to exceed adult dose

Probenecid may increase ceftriaxone levels; coadministration with ethacrynic acid, furosemide, and aminoglycosides may increase nephrotoxicity

Documented hypersensitivity; hyperbilirubinemic neonates, especially premature neonates

Pregnancy

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

Precautions

Use with caution in patients with gallbladder, biliary, liver, or pancreatic disease; use with caution in patients with a history of colitis or penicillin hypersensitivity; adjust dose in severe renal insufficiency (high doses may cause CNS toxicity)


Gentamicin (Garamycin)

Aminoglycoside antibiotic for gram-negative coverage. Dosing regimens are numerous; adjust dose based on CrCl and changes in volume of distribution. To avoid toxicity, assay trough levels 30 min before fourth dose and peak levels 30-60 min following.

Adult

3-6 mg/kg/d IV qd or divided q8-12h

Pediatric

2-2.5 mg/kg IV q8h

Coadministration with other aminoglycosides, cephalosporins, penicillins, and amphotericin B may increase nephrotoxicity; because aminoglycosides enhance effects of neuromuscular blocking agents prolonged respiratory depression may occur; coadministration with loop diuretics may increase auditory toxicity of aminoglycosides; possible irreversible hearing loss of varying degrees may occur (monitor regularly)

Documented hypersensitivity; non–dialysis dependent renal insufficiency

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

Narrow therapeutic index (not intended for long-term therapy); caution in renal failure (not on dialysis), myasthenia gravis, hypocalcemia, and conditions that depress neuromuscular transmission; adjust dose in renal impairment

More on Pericarditis, Bacterial

Overview: Pericarditis, Bacterial
Differential Diagnoses & Workup: Pericarditis, Bacterial
Treatment & Medication: Pericarditis, Bacterial
Follow-up: Pericarditis, Bacterial
Multimedia: Pericarditis, Bacterial
References

References

  1. Dupuis C, Gronnier P, Kachaner J, et al. Bacterial pericarditis in infancy and childhood. Am J Cardiol. Oct 15 1994;74(8):807-9. [Medline].

  2. Feldman WE. Bacterial etiology and mortality of purulent pericarditis in pediatric patients. Review of 162 cases. Am J Dis Child. Jun 1979;133(6):641-4. [Medline].

  3. Jayashree M, Singhi SC, Singh RS, Singh M. Purulent pericarditis: clinical profile and outcome following surgical drainage and intensive care in children in Chandigarh. Ann Trop Paediatr. Dec 1999;19(4):377-81. [Medline].

  4. Kocheril AG, Luttmann C, Sadaniantz A. Pneumococcal pericarditis successfully treated with catheter drainage and intravenous antibiotics. Cathet Cardiovasc Diagn. Dec 1991;24(4):286-7. [Medline].

  5. Morgan RJ, Stephenson LW, Woolf PK, Singh M. Surgical treatment of purulent pericarditis in children. J Thorac Cardiovasc Surg. Apr 1983;85(4):527-31. [Medline].

  6. Sinzobahamvya N, Ikeogu MO. Purulent pericarditis. Arch Dis Child. Jul 1987;62(7):696-9. [Medline].

  7. Strauss AW, Santa-Maria M, Goldring D. Constrictive pericarditis in children. Am J Dis Child. Jul 1975;129(7):822-6. [Medline].

  8. Zahn EM, Houde C, Benson L, Freedom RM. Percutaneous pericardial catheter drainage in childhood. Am J Cardiol. Sep 1 1992;70(6):678-80. [Medline].

Further Reading

Keywords

bacterial pericarditis, purulent pericarditis, inflammation of the pericardium, bacterial infection, pericardium, pericardial effusion, pneumonia, empyema, tamponade, constrictive pericarditis, Haemophilus influenzae, malnutrition, Staphylococcus aureus, respiratory distress, meningitis, acute myocarditis, acute osteomyelitis, arthritis, soft tissue infection, hypovolemia, small airway obstruction, epiglottitis, asthma, Neisseria meningitidis, Streptococcus pneumoniae, Pseudomonas aeruginosa, Salmonella species, Francisella tularensis, anaerobic bacteria and fungi, Histoplasma species, coccidioidomycosis, blastomycosis, Aspergillus species, Candida species, Mycoplasma pneumoniae

Contributor Information and Disclosures

Author

John Berger, MD, Departments of Critical Care Medicine and Pediatric Cardiology, Assistant Professor, George Washington University and Children's National Medical Center
John Berger, MD is a member of the following medical societies: American Academy of Pediatrics and Society of Critical Care Medicine
Disclosure: Nothing to disclose.

Medical Editor

Ira H Gessner, MD, Professor Emeritus, Pediatric Cardiology
Ira H Gessner, MD is a member of the following medical societies: American Academy of Pediatrics, American College of Cardiology, American Heart Association, American Pediatric Society, and Society for Pediatric Research
Disclosure: Nothing to disclose.

Pharmacy Editor

Mary L Windle, PharmD, Adjunct Assistant Professor, University of Nebraska Medical Center College of Pharmacy, Pharmacy Editor, eMedicine.com, Inc
Disclosure: Pfizer Inc Stock Investment from broker recommendation; Avanir Pharma Stock Investment from broker recommendation

Managing Editor

Hugh D Allen, MD, Professor, Department of Pediatrics, Division of Pediatric Cardiology and Department of Internal Medicine, Ohio State University College of Medicine
Hugh D Allen, MD is a member of the following medical societies: American Academy of Pediatrics, American College of Cardiology, American Heart Association, American Pediatric Society, American Society of Echocardiography, Society for Pediatric Research, Society of Pediatric Echocardiography, and Western Society for Pediatric Research
Disclosure: Nothing to disclose.

CME Editor

Gilbert Herzberg, MD, Assistant Professor, Department of Pediatrics, Section of Pediatric Cardiology, New York Medical College
Gilbert Herzberg, MD is a member of the following medical societies: American Academy of Pediatrics
Disclosure: Nothing to disclose.

Chief Editor

Stuart Berger, MD, Professor of Pediatrics, Division of Cardiology, Medical College of Wisconsin; Chief of Pediatric Cardiology, Medical Director of Pediatric Heart Transplant Program, Medical Director of The Heart Center, Children's Hospital of Wisconsin
Stuart Berger, MD is a member of the following medical societies: American Academy of Pediatrics, American College of Cardiology, American College of Chest Physicians, American Heart Association, and Society for Cardiac Angiography and Interventions
Disclosure: Nothing to disclose.

 
 
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