Sandbox ID Cardiovascular: Difference between revisions

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::::::* >7 days of age and > 2000g 75 mg/kg/day in divided doses every 8 h
::::::* >7 days of age and > 2000g 75 mg/kg/day in divided doses every 8 h
::::::* >7 days of age and 1200 g - 100 mg/kg/day in divided doses every 6 h
::::::* >7 days of age and 1200 g - 100 mg/kg/day in divided doses every 6 h
:::::* [[Oxacillin]]  
::::* [[Oxacillin]]  
:::::* Neonates  
:::::* Neonates  
::::::*0–4 weeks of age and 1200 g- 50 mg/kg/day in divided doses every 12 h
::::::*0–4 weeks of age and 1200 g- 50 mg/kg/day in divided doses every 12 h

Revision as of 03:14, 15 June 2015

Aortitis, infectious

  • Preferred regimen (3): Oxacillin 1.0 to 2.0g IV or IM q4h / q6h OR Nafcillin 1.0 to 2.0 g IV or IM q4h / q6h OR Dicloxacillin 500 mg to 1.0 g IV or IM q4h /q6h
  • Preferred regimen (4): Vancomycin 1.0 g (15 mg/kg, up to 3.0 to 4.0 g/d) IV q12h.
Note: Antimicrobial treatments are most effective when bactericidal, broadspectrum antibiotics are begun after obtaining blood cultures and prior to surgery. Dose of Cefotaxime sodium should be decreased by 50% in those with a creatinine clearance (CCr) of ≤ 20 mL/min. Ciprofloxacin should be used cautiously in those with a CCr ≤ 50 mL/min or when given concomitantly with drugs whose metabolism may be altered.

Cardiovascular implantable electronic device infections

  • Early post-implantation inflammation[2][3][4]
  • Penicillin allergy or MRSA Colonisation
Note: Benefit of and need for antimicrobial therapy in early post-implantation inflammation is unclear.
  • Early post-implantation inflammation in penicillin-allergic or MRSA-colonized patient
  • Uncomplicated generator pocket infection
  • ICED-LI or ICED-IE or complicated generator pocket infection pending blood cultures, e.g. in severe sepsis
Note: Gentamicin or other anti-Gram-negative agents may be appropriate depending on local epidemiology.
  • ICED-LI or ICED-IE or generator pocket infection with negative blood cultures
Note: Duration of antimicrobial therapy should be at least 4 to 6 weeks for complicated infection (ie, endocarditis, septic thrombophlebitis, or osteomyelitis or if bloodstream infection persists despite device removal and appropriate initial antimicrobial therapy.

Endocarditis, prophylaxis

  • Antibiotic Prophylactic Regimens for Dental Procedures[5][6][7]
  • Oral regimen
  • Preferred regimen: Amoxicillin 2 g single dose 30-60 minutes before procedure.
  • Pediatric dose: Amoxicillin 50 mg/kg single dose 30-60 minutes before procedure.
  • Unable to take oral medication
  • Preferred regimen: Ampicillin 2 g IM or IV single dose 30-60 minutes before procedure OR Cefazolin 1 g IM or IV single dose 30-60 minutes before procedure OR Ceftriaxone 1 g IM or IV single dose 30-60 minutes before procedure.
  • Allergic to penicillins or ampicillin— Oral regimen
  • Preferred regimen: Cephalexin 2 g single dose 30-60 minutes before procedure OR Clindamycin 600 mg single dose 30-60 minutes before procedure OR Azithromycin 500 mg single dose 30-60 minutes before procedure OR Clarithromycin 500 mg single dose 30-60 minutes before procedure.
  • Allergic to penicillins or ampicillin and unable to take oral medication
  • Preferred regimen: Cefazolin 1 g IM or IV single dose 30-60 minutes before procedure OR Ceftriaxone 1 g IM or IV single dose 30-60 minutes before procedure OR Clindamycin 600 mg IM or IV.
  • Gastrointestinal/Genitourinary Procedures
  • Antibiotic prophylaxis solely to prevent IE is no longer recommended for patients who undergo a GI or GU tract procedure.
Note: Routine administration of prophylactic antibiotics prior to GI and GU procedures including diagnostic esophagogastroduodenoscopy or colonoscopy is not recommended. However, for the high risk patients who already have an established GI or GU tract infection, it is reasonable to administer antibiotics against enterococci which includes the following: Ampicillin 2 g IM or IV single dose, piperacillin, or vancomycin.
  • Regimens for Respiratory Tract Procedures
  • Oral regimen
  • Preferred regimen: Amoxicillin 2 g single dose 30-60 minutes before procedure.
  • Pediatric dose: Amoxicillin 50 mg/kg single dose 30-60 minutes before procedure.
  • Unable to take oral medication
  • Allergic to penicillins or ampicillin— Oral regimen
  • Allergic to penicillins or ampicillin and unable to take oral medication
  • Regimens for Procedures on Infected Skin, Skin Structure, or Musculoskeletal Tissue

Intravascular catheter-related infections

  • Pathogen based treatment[8]
  • Staphylococcus aureus
  • Neonates
  • 0–4 weeks of age and 1200 g- 50 mg/kg/day in divided doses every 12 h
  • <7 days and 1200–2000 g- 50 mg/kg/day in divided doses every 12 h
  • >7 days of age and > 2000g 75 mg/kg/day in divided doses every 8 h
  • >7 days of age and 1200 g - 100 mg/kg/day in divided doses every 6 h
  • Neonates
  • 0–4 weeks of age and 1200 g- 50 mg/kg/day in divided doses every 12 h
  • Postnatal age 7 days and 1200–2000 g- 50–100 mg/kg/day in divided doses every 12 h
  • Postnatal age 7 days and >2000 g, 75–150 mg/kg/day in divided doses every 8 h
  • Postnatal age 7 days and 1200–2000 g- 75–150 mg/kg/day in divided doses every 8 h
  • Postnatal age 7 days and >2000 g, 100–200 mg/kg/day in divided doses every 6 h;
  • Infants and children Nafcillin 100–200 mg/kg/day in divided doses every 4–6 h
  • Methicillin resistant Staphylococcus aureus
  • Coagulase-negative staphylococci
  • Methicillin resistant
  • Enterococcus faecalis/Enterococcus faecium
  • Gram-negative bacilli
  • ESBL negative
  • ESBL positive
  • Enterobacter species and Serratia marcescens
  • Acinetobacter
  • Stenotrophomonas maltophilia
  • Pseudomonas aeruginosa
  • Burkholderia cepacia
  • Fungi
  • Candida albicans or other Candida species
  • Preferred regimen: Capsiofungin 70-mg loading dose, then 50 mg per day OR micafungin, 100 mg per day OR anidulafungin, 200 mg loading dose followed by 100 mg per day OR fluconazole, 400–600 mg per day.
  • Altered regimen: Lipid amphotericin B preparations.
  • Uncommon pathogens
  • Corynebacterium jeikeium (group JK)
  • Chryseobacterium (Flavobacterium)
  • Ochrobacterium anthropi
  • Malassezia furfur

Note

  • Scheduled replacement of intravascular catheters has been proposed as a method to prevent phlebitis and catheter related infections. No specific recommendation can be made regarding routine replacement of catheters that need to be in place for >7 days
  • Peripheral Venous Catheters: Short peripheral catheter sites commonly are rotated at 72–96-hour intervals. There is no need to replace peripheral catheters more frequently than every 72-96 hours to reduce risk of infection and phlebitis in adults. Replace peripheral catheters in children only when clinically indicated. Replace midline catheters only when there is a specific indication.
  • Midline Catheters: Midline catheters were in place a median of 7 days, but for as long as 49 days.
  • Hemodialysis Catheters: Hemodialysis catheters should be avoided in favor of arteriovenous fistulas and grafts. If temporary access is needed for dialysis, a cuffed catheter is preferable to a noncuffed catheter, even in the ICU setting, if the catheter is expected to stay in place for >3 weeks.
  • Pulmonary Artery Catheters: Pulmonary Artery Catheters typically remain in place an average of 3 days.
  • An umbilical catheter may be replaced if it is malfunctioning, and there is no other indication for catheter removal, and the total duration of catheterization has not exceeded 5 days for an umbilical artery catheter or 14 days for an umbilical vein catheter.

Mediastinitis, acute

  • Treatment secondary to cardiac infection and surgery[9].
  • Prophylaxis
  • Methicillin susceptible staphylococcus aureus infection
  • Methicillin susceptible staphylococcus aureus infection
Note
  • Preoperative antibiotics should be administered to all patients to reduce the risk of mediastinitis in cardiac surgery.
  • A deep sternal wound infection should be treated with aggressive surgical debridement in the absence of complicating circumstances.
  • Primary or secondary closure with muscle or omental flap is recommended. Vacuum therapy in conjunction with early and aggressive debridement is an effective adjunctive therapy.
  • Use of a continuous intravenous insulin protocol to achieve and maintain an early postoperative blood glucose concentration less than or equal to 180 mg/dL while avoiding hypoglycemia is indicated to reduce the risk of deep sternal wound infection.
  • The use of intranasal mupirocin is reasonable in nasal carriers of S. aureus.

Myocarditis, viral

Note
  • Mainstay of therapy for myocarditis is supportive care and standard management of CHF. Ribavarin and interferon alpha improved survival in mice with acute myocarditis.[10]
  • Temporary pacemaker insertion is indicated in patients with symptomatic bradycardia and/or heart block during the acute phase of myocarditis.
  • ICD implantation is not indicated during the acute phase of myocarditis.
  • ICD implantation can be beneficial in patients with life-threatening ventricular arrhythmias who are not in the acute phase of myocarditis, as indicated in the ACC/AHA/NASPE 2002 Guideline Update for Implantation of Cardiac Pacemakers and Antiarrhythmia Devices.
  • Antiarrhythmic therapy can be useful in patients with symptomatic NSVT or sustained VT during the acute phase of myocarditis.

Pericarditis, fungal

  • Fungal Pericarditis[11]
Note: Corticosteroids and NSAIDs can support the treatment with antifungal drugs. Pericardiocentesis or surgical treatment is indicated for haemodynamic impairment. Pericardiectomy is indicated in fungal constrictive pericarditis.
Note: Corticosteroids and NSAIDs can support the treatment with antifungal drugs. Pericardiocentesis or surgical treatment is indicated for haemodynamic impairment. Pericardiectomy is indicated in fungal constrictive pericarditis.
  • Preferred regimen: Combination of three antibiotics including Penicillin.
Note: Corticosteroids and NSAIDs can support the treatment with antifungal drugs. Pericardiocentesis or surgical treatment is indicated for haemodynamic impairment. Pericardiectomy is indicated in fungal constrictive pericarditis.

Pericarditis, tuberculous

Note: Intrapericardial drainage is done if needed. If constriction develops inspite of medical therapy, pericardiectomy is indicated[11].

Pericarditis, viral

  • Viral pericarditis[11]
  • CMV pericarditis
  • Preferred regimen: immunoglobulin 1 time per day 4 ml/kg on day 0, 4, and 8; 2 ml/kg on day 12 and 16.
Note: Symptomatic treatment is given to the patients with viral pericarditis while in large effusions and cardiac tamponade pericardiocentesis is necessary. The use of corticosteroid therapy is contraindicated except in patients with secondary tuberculous pericarditis, as an adjunct to tuberculosis treatment. Drainage, if needed is done.
  • Coxsackie B pericarditis
  • Preferred regimen: Interferon alpha or beta 2,5 Mio. IU/m2 surface area s.c. 3×per week.
Note: Symptomatic treatment is given to the patients with viral pericarditis while in large effusions and cardiac tamponade pericardiocentesis is necessary. The use of corticosteroid therapy is contraindicated except in patients with secondary tuberculous pericarditis, as an adjunct to tuberculosis treatment. Drainage, if needed is done.
  • Adenovirus and parvovirus B19 perimyocarditis
  • Preferred regimen: Immunoglobulin 10 g intravenously at day 1 and 3 for 6–8 hours
Note: Symptomatic treatment is given to the patients with viral pericarditis while in large effusions and cardiac tamponade pericardiocentesis is necessary. The use of corticosteroid therapy is contraindicated except in patients with secondary tuberculous pericarditis, as an adjunct to tuberculosis treatment. Drainage, if needed is done.

Rheumatic fever, primary prophylaxis


Rheumatic fever, secondary prophylaxis


Septic pelvic vein thrombophlebitis

  • Right ovarian vein thrombosis
Note: Repeat CT scan after 3 months. If negative, stop anticoagulation. If still positive for thrombi, anticoagulate for 3 additional months.
  • Pelvic branch vein thrombosis
  • Negative for pelvic thrombi

References

  1. Foote EA, Postier RG, Greenfield RA, Bronze MS (2005). "Infectious Aortitis". Curr Treat Options Cardiovasc Med. 7 (2): 89–97. PMID 15935117.
  2. Sandoe JA, Barlow G, Chambers JB, Gammage M, Guleri A, Howard P; et al. (2015). "Guidelines for the diagnosis, prevention and management of implantable cardiac electronic device infection. Report of a joint Working Party project on behalf of the British Society for Antimicrobial Chemotherapy (BSAC, host organization), British Heart Rhythm Society (BHRS), British Cardiovascular Society (BCS), British Heart Valve Society (BHVS) and British Society for Echocardiography (BSE)". J Antimicrob Chemother. 70 (2): 325–59. doi:10.1093/jac/dku383. PMID 25355810.
  3. Harrison JL, Prendergast BD, Sandoe JA (2015). "Guidelines for the diagnosis, management and prevention of implantable cardiac electronic device infection". Heart. 101 (4): 250–2. doi:10.1136/heartjnl-2014-306873. PMID 25550318.
  4. Baddour LM, Epstein AE, Erickson CC, Knight BP, Levison ME, Lockhart PB; et al. (2010). "Update on cardiovascular implantable electronic device infections and their management: a scientific statement from the American Heart Association". Circulation. 121 (3): 458–77. doi:10.1161/CIRCULATIONAHA.109.192665. PMID 20048212.
  5. Nishimura RA, Otto CM, Bonow RO, Carabello BA, Erwin JP, Guyton RA; et al. (2014). "2014 AHA/ACC Guideline for the Management of Patients With Valvular Heart Disease: executive summary: a report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines". Circulation. 129 (23): 2440–92. doi:10.1161/CIR.0000000000000029. PMID 24589852.
  6. Vahanian A, Alfieri O, Andreotti F, Antunes MJ, Baron-Esquivias G, Baumgartner H; et al. (2013). "[Guidelines on the management of valvular heart disease (version 2012). The Joint Task Force on the Management of Valvular Heart Disease of the European Society of Cardiology (ESC) and the European Association for Cardio-Thoracic Surgery (EACTS)]". G Ital Cardiol (Rome). 14 (3): 167–214. doi:10.1714/1234.13659. PMID 23474606.
  7. Wilson W, Taubert KA, Gewitz M, Lockhart PB, Baddour LM, Levison M; et al. (2007). "Prevention of infective endocarditis: guidelines from the American Heart Association: a guideline from the American Heart Association Rheumatic Fever, Endocarditis, and Kawasaki Disease Committee, Council on Cardiovascular Disease in the Young, and the Council on Clinical Cardiology, Council on Cardiovascular Surgery and Anesthesia, and the Quality of Care and Outcomes Research Interdisciplinary Working Group". Circulation. 116 (15): 1736–54. doi:10.1161/CIRCULATIONAHA.106.183095. PMID 17446442.
  8. Mermel LA, Allon M, Bouza E, Craven DE, Flynn P, O'Grady NP; et al. (2009). "Clinical practice guidelines for the diagnosis and management of intravascular catheter-related infection: 2009 Update by the Infectious Diseases Society of America". Clin Infect Dis. 49 (1): 1–45. doi:10.1086/599376. PMC 4039170. PMID 19489710.
  9. Hillis LD, Smith PK, Anderson JL, Bittl JA, Bridges CR, Byrne JG; et al. (2011). "2011 ACCF/AHA Guideline for Coronary Artery Bypass Graft Surgery. A report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines. Developed in collaboration with the American Association for Thoracic Surgery, Society of Cardiovascular Anesthesiologists, and Society of Thoracic Surgeons". J Am Coll Cardiol. 58 (24): e123–210. doi:10.1016/j.jacc.2011.08.009. PMID 22070836.
  10. Mandell, Gerald (2010). Mandell, Douglas, and Bennett's principles and practice of infectious diseases. Philadelphia, PA: Churchill Livingstone/Elsevier. ISBN 978-0443068393.
  11. 11.0 11.1 11.2 Maisch B, Seferović PM, Ristić AD, Erbel R, Rienmüller R, Adler Y; et al. (2004). "Guidelines on the diagnosis and management of pericardial diseases executive summary; The Task force on the diagnosis and management of pericardial diseases of the European society of cardiology". Eur Heart J. 25 (7): 587–610. doi:10.1016/j.ehj.2004.02.002. PMID 15120056.
  12. Blumberg HM, Burman WJ, Chaisson RE, Daley CL, Etkind SC, Friedman LN; et al. (2003). "American Thoracic Society/Centers for Disease Control and Prevention/Infectious Diseases Society of America: treatment of tuberculosis". Am J Respir Crit Care Med. 167 (4): 603–62. doi:10.1164/rccm.167.4.603. PMID 12588714.
  13. Gerber MA, Baltimore RS, Eaton CB, Gewitz M, Rowley AH, Shulman ST; et al. (2009). "Prevention of rheumatic fever and diagnosis and treatment of acute Streptococcal pharyngitis: a scientific statement from the American Heart Association Rheumatic Fever, Endocarditis, and Kawasaki Disease Committee of the Council on Cardiovascular Disease in the Young, the Interdisciplinary Council on Functional Genomics and Translational Biology, and the Interdisciplinary Council on Quality of Care and Outcomes Research: endorsed by the American Academy of Pediatrics". Circulation. 119 (11): 1541–51. doi:10.1161/CIRCULATIONAHA.109.191959. PMID 19246689.
  14. Nishimura RA, Otto CM, Bonow RO, Carabello BA, Erwin JP, Guyton RA; et al. (2014). "2014 AHA/ACC guideline for the management of patients with valvular heart disease: a report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines". J Am Coll Cardiol. 63 (22): e57–185. doi:10.1016/j.jacc.2014.02.536. PMID 24603191.
  15. Javier Garcia, Ramzi Aboujaoude, Joseph Apuzzio & Jesus R. Alvarez (2006). "Septic pelvic thrombophlebitis: diagnosis and management". Infectious diseases in obstetrics and gynecology. 2006: 15614. doi:10.1155/IDOG/2006/15614. PMID 17485796.