Use of vancomycin in pediatric patients with congenital heart disease at Queen Sirikit Heart Center of The Northeast Khon Kaen University

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Wanapa Hinwiset
Patiwat Plangklang
Somboon Sukanusat
Weerawooth Sooma
Yupaporn Preechagoon

Abstract

Background: Congenital heart disease (CHD) is a defect in the structure of the heart and great vessels which is present at birth. The CHD is high risk of infection such as infective endocarditis (IE) and postoperative septic complications from cardiac surgery. One of microorganism is methicillin-resistant S. Aureus (MRSA). Vancomycin is use in MRSA infection resistant to penicillin. Vancomycin also has narrow therapeutic index, many adverse drug reactions and is is expensive medication so in this study was studies utility of vancomycin in the pediatric patients with congenital heart disease i.e. indication, dosage and interval, therapeutic drug monitoring, adverse drug reactions and outcome also has been used in the pediatric patients with congenital heart disease at Queen Sirikit Heart Center of The Northeast Khon Kean University. Method: The data was retrospectively collected from inpatients medical record who received vancomycin at Queen Sirikit Heart Center of The Northeast Khon Kean University. Inclusion criterias are congenital pediatric patients age from 0 to 18 years old who received vancomycin and can be searched for inpatient medical record. Exclusion criteria are patient who can not searched for inpatient medical record and do not utility of vancomycin in inpatient medical record for 2 years. Results were shown in frequency and percentage. The study was approved from the Helsinki of the clinical ethics committee of Khon Kaen University. Result: Vancomycin was used in 137 patients but only 86 patients were recruited into the study. Indications were documented therapy and prophylaxis of 7.0% and 3.5%, respectively. On the other hand, unevaluated indications were 61.6% and 27.9% respectively. Dosage and interval, rate of administration and fluids were appropriate in 82.6%, 96.5% and 57.0%, respectively. Appropriate duration was reported to be 95.3%. Therapeutic drug monitoring (TDM) have been prescribed in the patients i.e.complete blood count, serum creatinine, vancomycin level, blood pressure, body temperature and urinalysis of 76.7%, 75.6%, 57.0%, 93.0%, 95.4% and 43.3%, respectively. Adverse drug reactions were occurred thrombocytopenia, nephrotoxicity and neutropenia of 17.7%, 7.0% and 1.2%, respectively. Patients were treated by monotherapy and combination therapy of 51.2% and 48.8%, respectively. The treatment is equally improve of 36.0%. Conclusion: This study found most of indications which are sepsis, acute febrile illness and pneumonia of 61.6%. Appropriate dose, administration of vancomycin in rate, duration and diluent. Therapeutic drug monitoring prescribed in most of patients. Although adverse drug reactions has low but should be close monitoring vancomycin for most effectiveness less adverse drug reaction and suitable for each patient. Keyword: Vancomycin, Congenital heart disease, pediatrics

Article Details

Section
Pharmaceutical Practice

References

Ascher SB, Smith PB, Clark RH, et al. Sepsis in young infants with congenital heart disease. Early Human Development 2012; 88S2: S92-S97.

Burgess LD and Drew RH. Comparison of the Incidence of the Vancomycin-Induced Nephrotoxicity in Hospitalized Patients with and without concomitant Piperacillin-Tazobactam. Pharmacotherapy 2014; 34(7): 670–676.

Calderwood SB, Swinski LA, Waternaux CM, et al. Risk factors for the development of prosthetic valve endocarditis. Circulation 1985; 72: 31-37.

Chaikitpinyo A, Panamonta M, Wongswadiwat Y, et al. Rheumatic and congenital heart diseases among school children of Khon Kaen, Thailand: declining prevalence of rheumatic heart disease. Asian Biomed 2014; 8: 645-650.

Clinical Practice Guidelines by the Infectious Diseases Society of America for the Treatment of Methicillin-Resistant Staphylococcus Aureus Infections in Adults and Children. Clin Infect Dis 2011; 1–38.

Cohen LS, Wechsler AS, Mitchel JH, et al. Depression of cardiac function by streptomycin and other antimicrobial agents. Am J Cardiol 1970; 26: 505-511.

Christie DJ, van Buren N, Lennon SS, et al. Vancomycin-dependent antibodies associated with thrombocytopenia and refractoriness to platelet transfusion in patients with leukemia. Blood 1990; 75: 518-523.

Dehghan F, Khorami N, Taleghani Taleghani T, et al. Drug Utilization Evaluation of Vancomycin in Pediatric Department. Novel Biomed 2018; 6(1): 9-14.

Drisyamol KA and Mahesh NM. Vancomycin induced Red man syndrome. Int J Clin Pharmacol Res 2016; 6: 127-132.

Drouet M, Chai F, Barthélémy C, et al. Influence of Vancomycin Infusion Methods on Endothelial Cell Toxicity. Antimicrob. Agents Chemother 2015; 59(2): 930-934.

Drygalski A, Curtis BR, Bougie DW, et al. Vancomycin-Induced Immune Thrombocytopenia. N Engl J Med 2007; 356:904-910.

Edwards F, Engelman R, Houck P, et al. Workforce on Evidence Based Surgery, Society of Thoracic Surgeons. The Society of Thoracic Surgeons practice guideline series: Antibiotic prophylaxis in cardiac surgery, Part 1: duration of prophylaxis. Ann Thorac Surg 2006; 81: 397-404.

Engelman R, Shahian D, Shemin R, et al. Workforce on Evidence-Based Medicine, Society of Thoracic Surgeons. The Society of Thoracic Surgeons practice guideline series: Antibiotic prophylaxis in cardiac surgery, part II: Antibiotic choice. Ann Thorac Surg 2007; 83(4): 1569-1576.

European Society of Cardiology. Guideline on the prevention diagnosis and treatment of infection endocarditis. Eur Heart J 2009; 30: 2369-2413.

Farbert BF and Moellering RC. Retrospective study of the toxicity of preparations of vancomycin from 1974 to 1981. Antimicrob Agents Chemother 1983; 23(1): 138-141.

Forouzesh A, Moise PA, Sakoulas G. Vancomycin Ototoxicity: a Reevaluation in an Era of Increasing Doses. Antimicrob Agents Chemother 2009; 53(2): 483-486.

Furtun J, Cetella T, Davila PM, et al. Infective endocarditis in congenital heart disease: a frequent community-acquired complication. Infection 2013; 41: 167-174.

Hadaway L. Infiltration and extravasation. Am J nurs 2007; 107(8): 64-72.

Hadaway L, Chamallas SN. Vancomycin: new perspectives on an old drug. J Infus Nurs 2003; 26(5): 278-284.

Hal SJ, Paterson DL, Lodise TP. Systematic Review and Meta-Analysis of Vancomycin-Induced Nephrotoxicity Associated with Dosing Schedules That Maintain Troughs between 15 and 20 Milligrams per Liter. Antimicrob Agents Chemother 2013; 57(2): 734-744.

Hanrahan TP, Kotapati C, Roberts MJ, et al. Factors associated with vancomycin nephrotoxicity in the critically ill. Anaesth Intensive Care 2015; 43(5): 594-600.

Hawes ML. A proactive approach to combating venous depletion in the hospital setting. J Infus Nurs 2007; 30(1): 33-44.

Hing WC, Bek SJ, Lin RTP, et al. A retrospective drug utilization evaluation of vancomycin usage in pediatric patients. J Pharm Ther 2004; 29: 1529-1538.

Katayanagi T. Nasal Methicillin-Resistant S. Aureus is a Major Risk for Mediastinitis in Pediatric Cardiac Surgery. Ann Thorac Cardiovasc Surg 2015; 21: 37–44.

Keyserling HL, Sinkowitz-Cochran RL, Harris JM, et al. Vancomycin Use In Hospitalized Pediatric Patients. Pediatrics 2003; 112: e104-e111.

Kokotis K. Preventing chemical phlebitis. Nursing 1998; 28(11): 41-46.

LA. Trissel. Handbook on Injectable Drugs.16th Edition. Bethesda, Maryland: American society of health-system pharmacists, inc; 2011.

Laura L, Marianne B. Incidence of Vancomycin-Induced Red Man Syndrome in Pediatric Patients: Case Series. Infect Dis Clin Pract 2016; 24(2): 106-108.

Logsdon BA, Lee KR, Luedtke G, et al. Evaluation of vancomycin use in a pediatric teaching hospital based on CDC criteria. Infect Control Hosp Epidemiol 1997; 18: 780–782.

Mahmoodian A, Abbasi S, Farseal S. A new approach to Vancomycin utilization evaluation: A cross-sectional study in intensive care unit J Res Pharm Pract. 2016; 5: 279-84.

Marinho DS, Huf G, Ferreira BL, et al. The study of vancomycin use and its adverse reactions associated to patients of a Brazilian university hospital. BMC Res Notes 2011; 4: 236.

Mizon P, Kiefel V, Mannessier L, et al. Thrombocytopenia induced by vancomycin-dependent platelet antibody. Vox Sanguinis 1997; 73: 49-51.

Mackett RL, Guay DR. Vancomycin-induced neutropenia. Can Med Assoc J 1985; 132(1): 39–40.

Moureau N. Is the pH of vancomycin an indication for central venous access?. J Vasc Access 2014: 1-2.

National Drug Committee. National List of Essential Medicine 2008. 2008: 31.

Newfield P, Roizen MF. Hazards of rapid administration of vancomycin. Ann Intern Med 1979; 91: 581.

Pai MP, Mercier RC, Koster SA. Epidemiology of Vancomycin-Induced Neutropenia In Patients Receiving Home Intravenous Infusion Therapy. Ann Pharmacother 2006; 40(2): 224-228.

Piper C, Korfer R, Horstkotte D. Valve Disease Prosthetic valve endocarditis. Heart 2001; 85: 590-593.

Rocha JL. Kondo W, Baptista MI, et al. Uncommon vancomycin-induced side effects. Braz J Infect Dis 2002; 6:196-200.

Rodvold KA, Erdman SM, Pryka RD. Vancomycin. In: Schumacher GE, editor. Therapeutic drug monitoring. Norwalk: Appleton & Lange 1996: 587-664.

Rodvold KA, Everett JA, Pryka RD, et al. Pharmacokinetics and administration of vancomycin in neonates, infants and children. Clinical Pharmacokinetics 1997; 33(1): 32-51.

Rushani D, Kaufman R, Ionescu-Ittu R, et al. Circulation 2013; 128: 1412-1419.

Schwartz MD. Vancomycin-induced neutropenia in a patient positive for an antineutrophil antibody. Pharmacotherapy 2002; 22: 783-788.

So-YA, Eui-Kyung H, Joo-Hee K,Jeong-Eun K, et al. Vancomycin associated Spontaneous Cutaneous Adverse Drug Reactions. Allergy Asthma Immunol Res 2011; Jul; 3(3): 194-198.

Taketomo CK. Pediatric Dosage Handbook 17th Edition. Lexi-Comp, inc; 2010.

The Hospital Infection Control Practices Advisory Committee. Recommendations for preventing the spread of vancomycin resistance. Hospital Infection Control Practices Advisory Committee (HICPAC). Infect Control Hosp Epidemiol 1995; 16: 105–113.

Van Hal SJ, Paterson DL, Lodise TP. Systeminc review and meta-analysis of vancomycin-induced nephrotoxicity associated with dosing schedules that maintain troughs between 15 and 20 milligrams per liter. Antimicrob Agents Chemother 2013; 57(2): 734-744.

Wilson W, Taubert KA, Gewitz M, et al. 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 2007; 116(15): 1736-1754.