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1

Sutcliffe, Joyce A., and Nafsika H. Georgopapadakou, eds. Emerging Targets in Antibacterial and Antifungal Chemotherapy. Boston, MA: Springer US, 1992. http://dx.doi.org/10.1007/978-1-4615-3274-3.

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2

Ray, A. B. Medicinal properties of plants: Antifungal, antibacterial, and antiviral activities. Lucknow: International Book Distributing Co., 2004.

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3

Bōkin Bōbaizai Jiten Shuppan Iinkai, ed. Bōkin bōbaizai jiten. Ōsaka-shi: Nihon Bōkin Bōbai Gakkai, 1986.

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4

Stig, Lindholm. Design, synthesis, and antibacterial activity of some pyridylguanidines. Helsinki: Suomalainen Tiedeakatemia, 1990.

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5

Gifford, Jennifer Ann. Antifungal activity of trihalogenmethylthio compounds in controlled release paints. Birmingham: University of Birmingham, 1994.

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6

Stevens, Paul James Edward. The antibacterial activity of some analogues of nalidixic acid. Uxbridge: Brunel University, 1985.

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7

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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8

Fund, Pacific West Cancer, and National Cancer Coalition, eds. Cecropins: A class of lytic peptides : promising antibacterial and antitumor activity. Seattle, Wash: Distributed by National Cancer Coalition, 1997.

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9

McDonald, Claire. Cecropins: A class of lytic peptides : promising antibacterial and antitumor activity. Seattle, Wash: Distributed by National Cancer Coalition, 1997.

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10

L, Dien Ariani. A bioautographic TLC assay [sic] for the detection of antibacterial activity of some Zingiberaceae in jamu gendong. Surabaya: Pusat Penelitian Obat Tradisional, Universitas Katolik Widya Mandala, 1997.

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11

Emami, Saeed. New quinolones with potential anti-MRSA activity. Hauppauge, N.Y: Nova Science, 2009.

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12

Dougherty, Thomas J., and Michael J. Pucci. Antibiotic discovery and development. New York: Springer, 2012.

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13

Walton, Katherine E., and Sally Ager. Antimicrobial agents. Edited by Rob Pickard. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199659579.003.0002.

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Antimicrobial resistance is a growing problem, which can be exacerbated by inappropriate use of antimicrobial agents. An understanding of the judicious use of antimicrobial agents, also known as antimicrobial stewardship, is therefore of fundamental importance to safe clinical practice. Patient factors should also be considered, including age, clinical status, special factors such as pregnancy or immunosuppression, co-morbidities, allergies, medication which may result in potential drug interactions, previous microbiology results, and antimicrobial treatment history. Important antimicrobial characteristics include the drug’s spectrum of activity, routes of administration, potential side effects, and cost. This chapter provides an overview of the ways in which antibacterial agents work and how bacteria develop resistance. It also outlines the principles of safe antimicrobial prescribing for prophylaxis and therapy, and highlights the key features, clinical indications, and potential adverse effects of antibacterial and antifungal agents commonly used in urology.
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14

Emerging Targets in Antibacterial and Antifungal Chemotherapy. Springer, 2012.

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15

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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16

CYANOBACTERIA: ANTIBACTERIAL ACTIVITY. New India Publishing Agency, 101 Vikas Surya Plaza, CU Block, Pitampura, New Delhi-110088, 2009.

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17

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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18

Molan, P. C. Antibacterial Activity of Honey. International Bee Research Association, 1992.

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19

Antibacterial Activity of Nanomaterials. MDPI, 2018. http://dx.doi.org/10.3390/books978-3-03897-050-7.

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20

Estes, Lynn L., and John W. Wilson. Antimicrobials. Oxford University Press, 2012. http://dx.doi.org/10.1093/med/9780199755691.003.0412.

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This chapter approaches the field of infectious diseases from 3 perspectives. This third section reviews antimicrobial agents. The mechanisms of action, spectrums of activity, clinical uses, routes of excretion, and toxic effects of various antimicrobial agents are emphasized. Antibacterials such as penicillins, cephalosporins, carbapenems, aminoglycosides, tetracyclines, and fluoroquinolones are reviewed. Antifungals such as the azoles, polyenes, and echinocandins are also covered. Antivirals such as acyclovir, famciclovir, oseltamivir, and foscarnet are included as well.
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21

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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22

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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23

H, Bentley P., Ponsford R, Royal Society of Chemistry (Great Britain). Fine Chemicals and Medicinals Group., and International Symposium on Recent Advances in the Chemistry of Anti-Infective Agents (1st : 1992 : Cambridge, England), eds. Recent advances in the chemistry of anti-infective agents. Cambridge [UK]: Royal Society of Chemistry, 1993.

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24

Shellenberger, Jill Suzanne. Antibacterial activity of two species of bryozoans from northern Puget Sound. 1996.

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25

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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26

Carton, James. Infectious diseases. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780198759584.003.0002.

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This chapter describes infectious diseases, including common types of microbes (bacteria, viruses, fungi, protozoa, helminths) and antimicrobial agents (antibacterial, antiviral, and antifungal agents), as well as some common systemic infectious diseases such as human immunodeficiency virus (HIV), tuberculosis (TB), infectious mononucleosis, malaria, syphilis, Lyme disease, and leishmaniasis.
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27

Paola, Bonsi, ed. Up to date review of toxicological data of some plant volatiles with antifungal activity. Roma: Istituto superiore di sanità, 1999.

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28

Yu, Yupei. A quantitative structure activity relationships study of antiinfectives based on the nalidixic acid structure. 1987.

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29

Bassett, Pamela. Antibacterials and antifungals: Technologies, trends and market opportunities (D & MD reports). 2nd ed. D & MD, 2001.

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30

Harrison, Mark. Infections. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780198765875.003.0042.

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This chapter describes the pharmacology of infections as they apply to Emergency Medicine, and in particular the Primary FRCEM examination. The chapter lists notifiable diseases and outlines the key details of antibacterial drugs, penicillins, cephalosporins tetracyclines, aminoglycosides, macrolides, the management of tuberculosis, quinolones, urinary tract infections, antifungal preparations, herpes virus infections, and antimalarials. This chapter is laid out exactly following the RCEM syllabus, to allow easy reference and consolidation of learning.
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31

Press, Renea. Virus Transmission Protect: Travelling, Virus Transmission, Cow, Antibacterial, Gas Mask, Patient, Travelling, Test Tube for Girls 8-12 Picture Quiz Words Activity and Coloring Books 55 Funny. Independently Published, 2020.

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32

Dougherty, Thomas J., and Michael J. Pucci. Antibiotic Discovery and Development. Springer, 2016.

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33

Retter, Andrew. Management of the bone marrow transplant recipient in ICU. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199600830.003.0375.

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Bone marrow transplants are an exciting and rapidly evolving area of haematology providing life-saving therapy to many patients and the number performed annually is increasing. Transplants are generally not considered as first line therapy due to their inherent toxicity and high rate of complications. The patients tend to have more heavily pre-treated disease with it attendant toxicities and a decreased physiological reserve. Admission rates vary between series from 15 to 30%. It is increasingly important that intensivists are aware of the basic principles of bone marrow transplantation and its’ possible morbidities. There are two types of transplant autologous transplants, where the patient’s own stem cells are returned to them and transplants from a donor. Only allogeneic transplants are associated with graft-versus-host disease. Allograft recipients also require immunosuppression to prevent transplant rejection. It is essential that this immunosuppression is continued when patients are admitted to intensive care. Transplant patients are always severely immunocompromised and prone to prolonged periods of neutropenia. They routinely receive antiviral, antifungal, and antibacterial prophylaxis, which must be continued on their admission. They remain vulnerable to unusual infections presenting in an atypical fashion. It is essential to have both a very low clinical threshold of suspicion for infection and detailed local protocols established to guide empirical antimicrobial therapy. Although traditionally poor, the prognosis is slowly improving.
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34

Daham, Sultan A. The antibacterial activity of chlorhexidine in combination with dodecyl trimethyl ammonium bromide and some other antimicrobial agents: The uptake of chlorhexidine and dodecyl timethyl ammonium bromide by escherichia coli and their effects on growth and viability.... Bradford, 1987.

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