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Books on the topic 'Antifungal antibiotic'

Author: Grafiati
Published: 4 June 2021
Last updated: 1 February 2022

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1

Ólafsson, Jón Hjaltalín, and Roderick James Hay, eds. Antibiotic and Antifungal Therapies in Dermatology. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-39424-4.

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2

Chipeleme, Alex. Synthetic studies on the antifungal antibiotic-ambruticin. Salford: University of Salford, 1994.

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3

Grayson, M. Lindsay. Kucers' the use of antibiotics: A clinical review of antibacterial, antifungal, antiparasitic and antiviral drugs : Antibiotics. London: Hodder Arnold, 2010.

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4

International, Telesymposium on Recent Trends in the Discovery Development and Evaluation of Antifungal Agents (1987). Recent trends in the discovery, development and evaluation of antifungal agents: Proceedings of an international telesymposium, May 1987. Barcelona: J.R. Prous Science, 1987.

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5

A, Hunter P., Darby G. K, and Russell Nicholas J, eds. Fifty years of antimicrobials: Past perspectives and future trends : Fifty-third Symposium of the Society for General Microbiology held at the University of Bath April 1995. Cambridge: Cambridge University Press, 1995.

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6

Ólafsson, Jón Hjaltalín, and Roderick James Hay. Antibiotic and Antifungal Therapies in Dermatology. Springer, 2016.

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7

Whitney, Laura, and Tihana Bicanic. Antifungal stewardship. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780198758792.003.0016.

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Although the principles of antifungal stewardship are similar to those of antibiotic stewardship, there are a number of key differences, as outlined in this chapter. Antifungal prescribing occupies a specialist niche: it occurs much less frequently than antibacterial prescribing due to the smaller, but increasing, population at risk of fungal infection. Antifungal stewardship is thus less established compared with programmes directed at antibacterials, with a narrower and more complex evidence base. This chapter provides examples of successful stewardship programmes in different settings, allowing readers to understand the challenges of antifungal stewardship and how to address these and enabling them to build a successful stewardship programme at their own institution.
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8

A, Kucers, ed. The use of antibiotics: A clinical review of antibacterial, antifungal, and antiviral drugs. 5th ed. Oxford: Butterworth-Heinemann, 1997.

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9

Kucers, A., S. M. Crowe, M. L. Grayson, and J. F. Hoy. The Use of Antibiotics: A Clinical Review of Antibacterial, Antifungal and Antiviral Drugs. 5th ed. A Hodder Arnold Publication, 1997.

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10

A, Sutcliffe Joyce, and Georgopapadakou Nafsika H. 1950-, eds. Emerging targets in antibacterial and antifungal chemotherapy. New York: Chapman and Hall, 1992.

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11

Recent Trends in the discovery, development and evaluation of antifungal agents. J.R. Prous Science Publishers, 1987.

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12

John, Mills, M. Lindsay Grayson, Johan W. Mouton, Suzanne Crowe, and James S. McCarthy. Kucers' the Use of Antibiotics: A Clinical Review of Antibacterial, Antifungal, Antiparasitic and Antiviral Drugs, Seventh Edition - Three Volume Set. Taylor & Francis Group, 2017.

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13

André, Bryskier, ed. Antimicrobial agents: Antibacterials and antifungals. Washington, D.C: ASM Press, 2005.

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14

Andre, M. D. Bryskier. Antimicrobial Agents: Antibacterials and Antifungals. ASM Press, 2005.

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15

Wilson, A. P. R., and Preet Panesar. Antimicrobial drugs in critical illness. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199600830.003.0053.

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The pharmacokinetics of antimicrobials are altered in critically-ill patients, particularly in the presence of renal or hepatic failure. Maintaining a choice or diversity of antibiotics is important due to the emergence of resistance. Antibiotic use should also be kept to the minimum and local protocols need to be established. For community-acquired infection, co-amoxiclav or a parenteral cephalosporin can be used, while for hospital-acquired infection, piperacillin/tazobactam, ciprofloxacin, or ceftazidime are recommended. For suspected vascular catheter infection or methicillin-resistant Staphylococcus aureus (MRSA) infection, teicoplanin or vancomycin should be used, with meropenem or imipenem reserved for second line treatment. Prophylactic antibiotics should not be continued once a surgical patient has returned from the theatre. Patients with febrile neutropenia receive piptazobactam, meropenem, ceftazidime or ciprofloxacin and a glycopeptide. Antifungals, usually caspofungin or liposomal amphotericin, are used if fungal infection is suspected, especially after failed antibacterial treatment. Cephalosporin use has declined as they have been linked with emergence of MRSA and Clostridium difficile. However, this reflects overuse and they still have a place as part of a diverse choice of antibiotics. Vancomycin and teicoplanin use has increased greatly in order to treat MRSA and line infections, but resistance remains unusual. Carbapenem use has increased rapidly with the emergence of extended spectrum beta-lactamase producing Gram-negative bacteria.
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16

(Editor), P. A. Hunter, G. K. Darby (Editor), and N. J. Russell (Editor), eds. Fifty Years of Antimicrobials: Past Perspectives & Future Trends. Cambridge University Press, 1995.

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