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A Review of vancomycin use
in the Medical/Surgical floor
Chibuzo Anyama
Lamar University
MSNE 5356
Advanced Pharmacology
Drug Chosen: vancomycin
• Common prescriptions in the medical/surgical
floor: lisinopril (Zestril), promethazine
(Phenergan), vancomycin (Vancocin), aspirin
(Ecotrin), propranolol (Inderal), hydromorphone
(Dilaudid), furosemide (Lasix), etc.
• Drug Chosen: vancomycin (Vancocin)
Pathophysiological Condition
Treated
• Condition: community acquired methicillin
resistant staphylococcus aureus (CA-MRSA) skin
infection (cellulitis).
• Transmission- Skin contact
• Facilitating conditions- Immunocompromised
(antineoplastic, steroid medications, cuts,
laceration, puncture wounds, etc.)
• Crowded living conditions
Intended Drug Response
• Vancomycin- A tricyclic glycopeptide antibiotic
• Binds with high affinity to D-alanine (D-ala) and D-
lactate (D-ala) C-terminals of MRSA bacteria,
compromising the cell wall integrity (Bruniera, 2015).
• Higher osmotic pressure within bacterial cell cytoplasm
pulls water from external cell environment into cell.
• Osmotic burst (bacteriolysis) of the bacterial cell results
in cell death –i.e. vancomycin is bactericidal (Medinaz,
2017).
Potential Interactions
• Vancomycin when co-administered with cisplatin
(antineoplastic agent), aminoglycosides (gentamicin,
kanamycin, and neomycin), cyclosporine, aspirin, and
loop diuretics like furosemide, would cause additive
nephrotoxicity and ototoxicity.
• Vancomycin potentiates effect of non-depolarizing
neuromuscular blocking agents (NMBAs)-pancuronium ,
atracurium , and vecuronium.
• Piperacillin-tazobactam (Zozyn) coadministration with
vancomycin- increases risk of acute kidney injury (AKI)
(Bamgbola, 2016).
Adverse Drug Reactions
• Hypersensitivity reaction -urticaria,
exfoliative dermatitis, macular rashes, etc.
• Events related to infusion –phlebitis,
erythema, flushing, hypotension,
tachycardia, red man syndrome.
• Ototoxicity
• Nephrotoxicity
Side Effects of Vancomycin
•Nausea and vomiting
•Back and neck pain
•Chills and fever
•Vertigo, dizziness, and tinnitus (may
be symptom before the onset of
ototoxicity).
Pharmacokinetics of
Vancomycin
• Absorption -Poorly administered in gastrointestinal (GI)
tract when administered by mouth (PO).
• Distribution -lipophilic drug, large volume distribution,
widely distributed, crosses placenta, and 20-30% enters
CSF (Davis, 2017).
• Metabolism -Poorly metabolized (5%) (Bruniera et al.,
2015).
• Excretion -IV 90% renal excretion. PO excreted in feces
(Bruniera et al., 2015).
• Half-life: 4-11 hours in adults but longer in adults with
renal failure i. e. 7 days (Bruniera et al., 2015)
Drug Binding Issues
• No drug is known to affect the binding of
vancomycin (VCM) at the D-ala and D-ala
C-terminals of the peptidoglycan cell walls
of staphylococcus bacteria cell.
• Hypoalbuminemia only elongates
vancomycin half-life (Mizuno et al., 2013).
• Ototoxic and nephrotoxic drugs has
additive effects on vancomycin but does
not affect the binding of vancomycin.
Improving Interprofessional team
member communication.
• Teach back or repeat back method to be applied
not only to patients but also among members of
the interprofessional team.
• Physicians to take more time to listen to patients
without early interrruption.
• Adequate staffing to encourage structured
interdisciplinary rounding.
• The need for physicians and other prescribers to
communicate more with each other.
Application to the practice
setting
• Closely monitor kidney function while administering
vancomycin especially on renal patients.
• Piperacillin-tazobactam, cisplatin, aminoglycosides,
cyclosporine, aspirin, and loop diuretics like furosemide,
etc., need to be avoided during vancomycin therapy.
• Effective interdisciplinary team communication
necessary for improved outcomes including VCM therapy
outcomes.
• Effective listening, teach back method, structured
interdisciplinary rounding need to be applied.
References
• Bamgbola, O. (2016). Review of vancomycin-induced renal toxicity: an update.
Therapeutic Advances in Endocrinology and Metabolism, 7(3), 136–147.
http://doi.org/10.1177/2042018816638223
• Bruniera, F. R., Ferreira, F. M., Saviolli, L. R. M., Bacci, M. R., Feder, D., Pedreira,
M. G., . . . Fonseca, F. L. (2015). The use of vancomycin with its therapeutic
and adverse effects: a review. European Review for Medical and
Pharmacological Sciences, 19(4), 694-700.
• Davis, F. A. (2017). Davis’s drug guide for nurses (15th ed.). Philadelphia, PA: F. A.
Davis
• Medinaz, [Medinaz]. (2017, September 3). Vancomycin Mechanism of action.
Retrieved from https://www.youtube.com/watch?v=gf-Za1kYfdo
• Mizuno, T., Mizokami, F., Fukami, K., Ito, K., Shibasaki, M., Nagamatsu, T., &
Furuta, K. (2013). The influence of severe hypoalbuminemia on the half-life
of vancomycin in elderly patients with methicillin-resistant Staphylococcus
aureus hospital-acquired pneumonia. Clinical Interventions in Aging, 8,
1323–1328. http://doi.org/10.2147/CIA.S52259

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Chibuzo anyama a review of vancomycin use in the medical

  • 1. A Review of vancomycin use in the Medical/Surgical floor Chibuzo Anyama Lamar University MSNE 5356 Advanced Pharmacology
  • 2. Drug Chosen: vancomycin • Common prescriptions in the medical/surgical floor: lisinopril (Zestril), promethazine (Phenergan), vancomycin (Vancocin), aspirin (Ecotrin), propranolol (Inderal), hydromorphone (Dilaudid), furosemide (Lasix), etc. • Drug Chosen: vancomycin (Vancocin)
  • 3. Pathophysiological Condition Treated • Condition: community acquired methicillin resistant staphylococcus aureus (CA-MRSA) skin infection (cellulitis). • Transmission- Skin contact • Facilitating conditions- Immunocompromised (antineoplastic, steroid medications, cuts, laceration, puncture wounds, etc.) • Crowded living conditions
  • 4. Intended Drug Response • Vancomycin- A tricyclic glycopeptide antibiotic • Binds with high affinity to D-alanine (D-ala) and D- lactate (D-ala) C-terminals of MRSA bacteria, compromising the cell wall integrity (Bruniera, 2015). • Higher osmotic pressure within bacterial cell cytoplasm pulls water from external cell environment into cell. • Osmotic burst (bacteriolysis) of the bacterial cell results in cell death –i.e. vancomycin is bactericidal (Medinaz, 2017).
  • 5. Potential Interactions • Vancomycin when co-administered with cisplatin (antineoplastic agent), aminoglycosides (gentamicin, kanamycin, and neomycin), cyclosporine, aspirin, and loop diuretics like furosemide, would cause additive nephrotoxicity and ototoxicity. • Vancomycin potentiates effect of non-depolarizing neuromuscular blocking agents (NMBAs)-pancuronium , atracurium , and vecuronium. • Piperacillin-tazobactam (Zozyn) coadministration with vancomycin- increases risk of acute kidney injury (AKI) (Bamgbola, 2016).
  • 6. Adverse Drug Reactions • Hypersensitivity reaction -urticaria, exfoliative dermatitis, macular rashes, etc. • Events related to infusion –phlebitis, erythema, flushing, hypotension, tachycardia, red man syndrome. • Ototoxicity • Nephrotoxicity
  • 7. Side Effects of Vancomycin •Nausea and vomiting •Back and neck pain •Chills and fever •Vertigo, dizziness, and tinnitus (may be symptom before the onset of ototoxicity).
  • 8. Pharmacokinetics of Vancomycin • Absorption -Poorly administered in gastrointestinal (GI) tract when administered by mouth (PO). • Distribution -lipophilic drug, large volume distribution, widely distributed, crosses placenta, and 20-30% enters CSF (Davis, 2017). • Metabolism -Poorly metabolized (5%) (Bruniera et al., 2015). • Excretion -IV 90% renal excretion. PO excreted in feces (Bruniera et al., 2015). • Half-life: 4-11 hours in adults but longer in adults with renal failure i. e. 7 days (Bruniera et al., 2015)
  • 9. Drug Binding Issues • No drug is known to affect the binding of vancomycin (VCM) at the D-ala and D-ala C-terminals of the peptidoglycan cell walls of staphylococcus bacteria cell. • Hypoalbuminemia only elongates vancomycin half-life (Mizuno et al., 2013). • Ototoxic and nephrotoxic drugs has additive effects on vancomycin but does not affect the binding of vancomycin.
  • 10. Improving Interprofessional team member communication. • Teach back or repeat back method to be applied not only to patients but also among members of the interprofessional team. • Physicians to take more time to listen to patients without early interrruption. • Adequate staffing to encourage structured interdisciplinary rounding. • The need for physicians and other prescribers to communicate more with each other.
  • 11. Application to the practice setting • Closely monitor kidney function while administering vancomycin especially on renal patients. • Piperacillin-tazobactam, cisplatin, aminoglycosides, cyclosporine, aspirin, and loop diuretics like furosemide, etc., need to be avoided during vancomycin therapy. • Effective interdisciplinary team communication necessary for improved outcomes including VCM therapy outcomes. • Effective listening, teach back method, structured interdisciplinary rounding need to be applied.
  • 12. References • Bamgbola, O. (2016). Review of vancomycin-induced renal toxicity: an update. Therapeutic Advances in Endocrinology and Metabolism, 7(3), 136–147. http://doi.org/10.1177/2042018816638223 • Bruniera, F. R., Ferreira, F. M., Saviolli, L. R. M., Bacci, M. R., Feder, D., Pedreira, M. G., . . . Fonseca, F. L. (2015). The use of vancomycin with its therapeutic and adverse effects: a review. European Review for Medical and Pharmacological Sciences, 19(4), 694-700. • Davis, F. A. (2017). Davis’s drug guide for nurses (15th ed.). Philadelphia, PA: F. A. Davis • Medinaz, [Medinaz]. (2017, September 3). Vancomycin Mechanism of action. Retrieved from https://www.youtube.com/watch?v=gf-Za1kYfdo • Mizuno, T., Mizokami, F., Fukami, K., Ito, K., Shibasaki, M., Nagamatsu, T., & Furuta, K. (2013). The influence of severe hypoalbuminemia on the half-life of vancomycin in elderly patients with methicillin-resistant Staphylococcus aureus hospital-acquired pneumonia. Clinical Interventions in Aging, 8, 1323–1328. http://doi.org/10.2147/CIA.S52259