Drugs

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    Drugs - Presentation Transcript

    1. Commonly Used Drugs Julie Beauregard, MLIS
    2. Outline
      • Antibiotics
      • Diuretics
      • Non-steroidal anti-inflammatory drugs (NSAIDs)
      • Beta-blockers
      • Steroids
      • Anticoagulants
    3. Antibiotics Adapted from a presentation by Jennifer Lyon, delivered at EBL’s Knowledge Building session in 2007.
    4. What Antibiotics Do
      • Antibiotics may either kill bacteria (“bacteriocidal”) or stop bacteria from dividing and producing more bacteria (“bacteriostatic”).
    5. Classifying Antibiotics
      • Antibiotics can be classified by:
      • Their biological source
        • Plant, mold, soil microorganisms
      • Their spectrum of action or coverage
        • Broad/wide spectrum - effective against a wide range of bacteria
        • Narrow spectrum - effective mainly against specific categories of bacteria
          • e.g. Gram-positive or Gram-negative bacteria but not both
        • Limited spectrum - effective against a single organism or disease
      • Their mode of action
        • How they fight bacteria
    6. Types of Bacteria
      • Bacteria can be classified in a number of ways. The ways that are most commonly considered for antibiotic coverage are:
          • Gram Stain
          • Shape
          • Use of Oxygen
    7. Gram-negative vs. Gram-positive Bacteria
      • Gram-negative or gram-positive classification represents a difference in the composition of the bacterial cell wall.
      • Antibiotic “coverage” is based on whether it is effective against gram-positive, gram-negative or both types of bacteria.
      http://helios.bto.ed.ac.uk/bto/microbes/shape.htm
    8. Bacterial Shape
      • The most common shapes are cocci (spherical), bacilli (rods), and spirochetes (spiral/helical).
      http://www.merck.com/mmhe/sec17/ch190/ch190a.html
    9. Use of Oxygen
      • Aerobic bacteria
        • Staphylococcus, Streptococcal
      • Anaerobic bacteria
        • Clostridia
      • Facultative bacteria
        • Salmonella, E. coli
    10. Antibiotic Modes of Action
      • Inhibit synthesis of bacterial cell wall
      • Act directly on the cell membrane of the bacteria, causing it to break open
      • Inhibit bacterial protein synthesis
      • Affect bacterial metabolism and growth
    11. Antibiotic Modes of Action
      • Inhibit synthesis of bacterial cell wall
        • Beta-lactams
        • Polypeptides
          • bacitracin (Baciguent®; BaciiM®)
        • Glycopeptides
          • vancomycin (Vancocin®), ramoplanin
          • oritavancin, dalbavancin, telavancin
        • Cycloserine (Seromycin®)
    12. Beta-Lactam Antibiotics
      • Biggest class of antibiotics
        • Penicillins
          • benzylpenicillin (Penicillin G), amoxicillin (Amoxil®)
        • Cephalosporins/Cephamycins
          • cephalexin (Keflex®), cefadroxil (Duricef®), cefdinir (Omnicef®)
        • Carbapenems
          • imipenem (Primaxin®), ertapemem (Invanz®), meropenem (Merrem®)
        • Monobactam
          • aztreonam (Azactam®)
    13. The Penicillin Family of Antibiotics
      • Natural Penicillins
        • Benzylpenicillin (Penicillin G)
        • phenoxymethyl penicillin (Penicillin V)
      • Synthetic Penicillins
        • Penicillinase-resistant or anti-staph penicillins
          • Methicillin, Oxacillin, Nafcillin, Cloxacillin, Dicloxacillin
        • Aminopenicillins (Second Generation)
          • Ampicillin, Amoxicillin
        • Carboxypenicillins (Third Generation)
          • Carbenicillin, Ticarcillin
        • Ureidopenicillins (Fourth Generation)
          • Piperacillin
        • Penicillin plus ß-lactamase inhibitors
          • Amoxicillin-clavulanic acid, ampicillin-sulbactam, ticarcillin-clavulanic acid, piperacillin-tazobactam
    14. Antibiotic Modes of Action
      • Act directly on the cell membrane of the bacteria, causing it to break open
        • Polymyxins
          • Colistin (polymyxin E)
          • Polymyxin B
          • Surfactin
        • Daptomycin (Cubicin®)
    15. Antibiotic Modes of Action
      • Inhibit bacterial protein synthesis
        • Aminoglycosides
          • gentamicin (Genoptic®; Gentak®), streptomycin
        • Chloramphenicol
        • Tetracyclines
          • tetracycline (Sumycin®), doxycycline (Adoxa®; Doryx®; Monodox®)
        • Macrolides
          • erythromycin (Erythrocin®; Eryderm®)
          • azithromycin (Zithromax®)
        • Clindamycin ( Cleocin®; ClindaMax®)
    16. Antibiotic Modes of Action
      • Affect bacterial metabolism and growth
        • Rifamycin
          • rifampin (Rifadin®)
        • Quinolines/Fluoroquinolones
          • ciprofloxacin (Cipro®; Ciloxan®; Proquin®)
          • levofloxacin (Levaquin®; Quixin®; Iquix®)
        • Antimetabolites
          • Sulfonamides
          • trimethoprim (Primsol®; Proloprim®)
    17. Nicknames
      • Physicians tend to use shortened nicknames for some antibiotics.
        • vancomycin (Vancocin®)=Vanc
        • clindamycin (ClindaMax®)=Clinda
        • azithromycin (Zithromax®)=Zithro
    18. References
      • Access Medicine [database on the Internet]. Drug Index. McGraw-Hill. c2008.
      • Calderwood SB. Overview of beta-lactam antibiotics. UpToDate [database on the Internet]. c2008 [updated 2008 Oct 16; cited 200 May 13].
      • Centers for Disease Control and Prevention. Atlanta: CDC; [updated 2008 Apr 30; cited 2008 May 13]. Vancomycin-resistant enterococci (VRE). Available at: http://www.cdc.gov/ncidod/dhqp/ar_VRE_publicFAQ.html .
      • Hentges DJ. Anaerobes: Genral Characteristics, Chapt. 17. In: Samuel Baron, editor. Medical Microbiology. Galvenston, TX, University of Texas.. Available at: http://www.gsbs.utmb.edu/microbook/ch017.htm .
      • Porter RS, editor. Anaerobic Bacteria In: Merck Manual Online. Whitehouse Station, NJ, c2008 [cited 2008 May 13]. Available from: http://www.merck.com/mmpe/sec14/ch178/ch178a.html
      • Porter RS, editor. Bacterial Infections In: Merck Manual Home Edition Online. Whitehouse Station, NJ, c2008 [cited 2008 May 13]. Available from: http://www.merck.com/mmhe/print/sec17/ch190/ch190a.html .
      • Wikipedia [database on the Internet]. Antibiotic. [updated 2008 May 12; cited 2008 May 13]. Available from: http://en.wikipedia.org/wiki/Antibiotic .
      • Wright AJ. The penicillins. Mayo Clin Proc. 1999 Mar;74(3):290-307. Erratum in: Mayo Clin Proc 1999. Nov;74(11):1184.
    19. Diuretics
      • Diuretics (also called ‘water pills’) are a class of drugs that reduces fluid volume in the body.
      What are Diuretics?
      • Diuretics cause the kidneys to increase the volume of urine excreted (diuresis), as well as increase the rate of sodium excretion (natriuresis).
        • Sodium levels that are too high for too long, can cause volume overload and edema.
      How do Diuretics Work?
    20. Common Conditions for Diuretic Use
      • Hypertension
      • Edema
      • Heart failure
      • Liver cirrhosis
      • Kidney disorders
      • Overdose/poisoning
      • Glaucoma
      • Osteoporosis
      • Kidney stones
      • These types work in different parts of the nephron.
        • Loop
        • Thiazide
        • Potassium-sparing
      Major Types of Diuretics
    21. http://kidney.niddk.nih.gov/kudiseases/pubs/glomerular/
    22. Loop Diuretics
      • Most powerful class of diuretic
        • Act rapidly, within 1 hour
        • Large output of urine
        • Short duration of action, complete within 6 hours
        • Effective for emergency use
        • Inhibits Na + and Ca + re-absorption in loop of Henle
      • Used primarily to treat edema related to congestive heart failure, hepatic cirrhosis and nephrotic syndrome
      • Also used to treat drug overdose and hypertension
    23. Loop Diuretics: Side Effects
      • Common Side Effects:
        • Hypokalemia=low potassium
        • Hypotension
        • Weakness, lethargy, cramps, and dizziness
      • Osteoporosis in postmenopausal women
      • Kidney stones
      • Hyperglycemia
      • Gout
    24. Loop Diuretics Commonly Prescribed the U.S.
      • furosemide (Lasix®)
      • bumetanide (Bumex®)
      • torsemide (Demadex®)
      • ethacrynic acid (Edecrin®)
    25. Thiazide Diuretics
      • This is a moderate diuretic
        • Acts within 1-2 hours
        • Diuretic effects last for 12-24 hours
        • Effective for long-term use
        • Inhibits Na + and Cl - re-absorption from distal convoluted tubules
        • Decreases Ca + excretion
      • Used as first line therapy for uncomplicated hypertension
      • Also used to treat edema associated with heart, liver and renal disease, as well as kidney stones and osteoporosis
    26. Thiazide Diuretics: Side Effects
      • Common Side Effects:
        • Cramps, dizziness, weakness, lethargy
        • Hypokalemia=low potassium
        • Hyponatremia=low sodium
        • Hypercalcemia=high calcium
        • Hyperglycemia
      • Rare Side Effects:
        • Rashes, vertigo, headache, GI upsets, photosensitivity, reversible impotence, pancreatitis, blood diseases.
    27. Thiazide Diuretics Commonly Prescribed the U.S.
      • Hydrochlorothiazide (or HCTZ) (Microzide®, Hydrocot®)
      • Trichlormethiazide (Aquacot®, Naqua®)
      • Chlorothiazide (Diuril®)
      • Bendroflumethiazide (Naturetin-5®)
      • Methyclothiazide (Aquatensen®, Enduron®)
      • Polythiazide (Renese®)
    28. Potassium-sparing Diuretics
      • Mild diuretics
        • Diuretic effect lasts for several hours
        • Do not cause K + to be depleted
        • Na + channel blocker acting in the cortical collecting ducts
      • Potassium-sparing diuretics do not worsen diabetes or gout
      • Because of their mild diuretic effects, they are often combined with other diuretics for treatment congestive heart failure
    29. Potassium-sparing Diuretics: Side Effects
      • Potassium retention (hyperkalemia) causing muscle weakness and abnormal heartbeat.
      • Nausea and gastrointestinal problems are common side effects
    30. Potassium-sparing Diuretics Commonly Prescribed the U.S.
      • triamterene (Dyrenium®)
      • eplerenone (Inspra®)
      • amiloride (Midamor®)
      • spironolactone (Aldactone®)
        • Shown to cause tumors in lab rats, carries black box warning
    31. References
      • Beers MH, Jones TV, editors. Problems with Electrolyte Balance. In: Merck Manual of Health and Aging Online. Merck Research Laboratories, Whitehouse Station, NJ: c2005. [cited 2008 May 13]. Available at: http://www.merck.com/pubs/mmanual_ha/sec3/ch18/ch18d.html.
      • Jackson EK. Diuretics. In: Goodman and Gilman’s Pharmacological Basis of Therapeutics, 11th Edition. [book on the Internet]. Brunton LL, editor. McGraw Hill: 2007. [cite 2008 May 13].
      • Oxford Reference Online. Thiazide Diuretics. In: An A-Z of Medicinal Drugs. [book on the Internet]. Oxford University Press, c2003. [cited 2008 May 13].
      • Oxford Reference Online. Loop Diuretics. In: An A-Z of Medicinal Drugs. [book on the Internet]. Oxford University Press, c2003. [cited 2008 May 13].
      • Oxford Reference Online. Potassium-sparing Diuretics. In: An A-Z of Medicinal Drugs. [book on the Internet]. Oxford University Press, 2003. [cited 2008 May 13].
      • Mayo Foundation for Medical Education and Research. Diuretics. [updated 2008 Dec 22; cited 2008 May 13]. Available at: http://www.mayoclinic.com/health/diuretics/HI00030 .
    32. NSAIDs: Non-steroidal Anti-inflammatory Drugs
    33. What are NSAIDs?
      • NSAIDs are a group of drugs that control pain and reduce inflammation and fever. These drugs also have cardioprotective effects and may prevent certain cancers.
    34. How do NSAIDs work?
      • NSAIDs inhibit the enzyme cyclooxygenase (COX), which regulates prostaglandin synthesis.
      • Main types of prostaglandins.
        • ’ Maintenance ’--produced by COX-1 enzyme, regulates gastric mucosal lining, vascular homeostasis, platelet aggregation and renal blood flow. Expressed in most tissues.
        • ‘ Inflammatory ’--produced by COX-2 enzyme, increases inflammation and pain. Expressed in the brain, bones, kidneys and female reproductive system.
      • Nonselective NSAIDs
      • Selective COX-2 Inhibitors
    35. Conditions for NSAID Use
      • Pain, Fever, Inflammation/redness
        • Headaches, arthritis, sports injuries, cold and allergies, acute gout, lupus, menstrual pain
      • Cardiovascular Disease/Antiplatelet Therapy
        • Myocardial infarction, stroke, unstable angina, peripheral vascular disease
      • Cancer Treatment and Prevention
        • Colorectal cancer
    36. Commonly Used NSAIDs
      • Non-selective NSAIDs
      • aspirin (Bayer®, Excedrin®)
      • ibuprofen (Motrin®, Advil®, Nuprin®)
      • naproxen (Aleve®)
      • etodolac (Lodine®)
      • indomethacin (Indocin®)
      • meclofenamate (Meclomen®)
      • piroxicam (Feldene®)
      • nabumetone (Relafen®)
      • COX-2 Inhibitors
      • celecoxib (Celebrex®)
      • rofecoxib (Vioxx®)
      • valdecoxib (Bextra ®)
    37. Pharmacological Action
      • Absorbed mostly from the stomach and intestinal mucosa
      • Absorption approaches 100%
      • Metabolized by the liver
    38. Adverse Effects
      • Most side effects are due to the inhibition COX-1
      • Gastrointestinal
        • Upper gastrointestinal bleeding
        • Ulcer perforation
        • Dyspepsia
        • Diarrhea
        • Nausea and vomiting
      • Renal
        • Salt and fluid retention
        • Acute renal insufficiency due to vasoconstriction
    39. Adverse Effects (cont’d)
      • Cardiovascular
        • Worsening of hypertension
        • Worsening of heart failure
        • Increased risk of stroke
      • Hepatic
        • Acute liver injury
      • Central Nervous System
        • Aseptic Meningitis
        • Psychosis
        • Cognitive dysfunction
    40. NSAIDs and Cancer Treatment and Prevention
      • If COX-2 enzyme is over-expressed, it produces large quantities of prostaglandin A1 and A2, which then bind to a tumor suppressor, p53, inhibiting its activity.
        • p53 promotes apoptosis (programmed cell death) when cellular DNA is damaged and cannot be repaired (e.g. tumor cells).
      • Regular aspirin use has been associated with a 20-40% reduction in the risk of colorectal cancer.
    41. References
      • Dube C; Rostom A; Lewin G; Tsertsvadze A; Barrowman N; Code C; Sampson M; Moher D. The use of aspirin for primary prevention of colorectal cancer: a systematic review prepared for the U.S. Preventive Services Task Force. Ann Intern Med. 2007 Mar 6;146(5):365-75.
      • Johnsen JI, Lindskog M, Ponthan F, Pettersen I, Elfman L, Orrego A, Sveinbjornsson B, Kogner P. Cyclooxygenase-2 is expressed in neuroblastoma, and nonsteroidal anti-inflammatory drugs induce apoptosis and inhibit tumor growth in vivo. Cancer Res. 2004 Oct 15;64(20):7210-5.
      • Ogbru O. Nonsteroidal Antiinflammatory Drugs (NSAIDs). MedicineNet, Inc; [updated 2005 Sept 18; cited 2008 May 13]. Available at: http://www.medicinenet.com/nonsteroidal_antiinflammatory_drugs/article.htm
      • Solomon, DH. NSAIDs: Mechanism of Action. UpToDate. [Database on the Internet]. c2008 [updated 2008 Jan; cited 2008 May 13].
    42. References cont’d
      • Solomon, DH. NSAIDs: Overview of adverse effects. UpToDate. [Database on the Internet]. c2008 [updated 2008 Jan; cited 2008 May 13].
      • Solomon, DH. NSAIDs: Cardiovascular effects. UpToDate. [Database on the Internet]. c2008 [updated 2008 Feb 8; cited 2008 May 13].
      • Solomon, DH. Overview of selective COX-2 inhibitors. UpToDate. [database on the Internet]. c2008 [updated 2006 Apr 10; cited 2008 May 13].
      • Su M, Nagdev A. NSAID Intoxication. UpToDate. [Database on the Internet]. c2008 [updated 2008 Jan; cited 2008 May 13].
    43. Beta-blockers
    44. What are Beta-blockers?
      • Beta-blockers (or ß-blockers) are a class of drugs that reduce blood pressure and improve blood flow.
      • Other names:
        • beta-adrenergic blocking agent
        • beta-adrenergic antagonist
        • beta-adrenergic receptor blocking agent
        • beta antagonist
    45. How do Beta-blockers Work?
      • Beta-blocking drugs occupy β receptors and competitively reduce receptor occupancy by catecholamines.
        • β1-receptors are primarily found in the heart and in the kidneys.
        • β2-receptors are primarily found in bronchial and peripheral vascular smooth muscles.
      • Catecholamines are hormones/neurotransmitters produced by the adrenal glands. They are released into the blood during times of physical or emotional stress.
        • The major catecholamines are dopamine, norepinephrine, and epinephrine (which used to be called adrenaline).
    46. Conditions for Beta-blocker Use
      • Hypertension
      • Angina
      • Arrhythmia
      • Heart Failure
      • Myocardial Infarction prevention
      • Glaucoma
      • Generalized Anxiety Disorder
      • Tremors
      • Hyperthyroidism
      • Migraines
    47. Common Beta-blockers
      • Nonselective
      • propranolol (Inderal®)
      • sotalol (Betapace®)
      • nadolol (Corgard®)
      • timolol (Blocadren®)
      • Beta-1 Selective
      • atenolol (Tenormin®)
      • metoprolol (Lopressor®, Toprol-XL®)
      • bisoprolol (Zebeta®)
      • acebutolol (Sectral®)
      • nebivolol (Bystolic®)
    48. Side Effects of Beta-blockers
      • Fatigue, weakness
      • Dizziness
      • Cold hands
      • Increase triglycerides; decrease HDL cholesterol
      • Airway resistance
    49. References
      • Colucci WS. Molecular and cellular mechanisms of myocardial failure. Am J Cardiol 1997 Dec 4;80(11A):15L-25L.
      • Hoffman BB. Adrenoceptor Antagonist Drugs, Chapter 10. In: Bertram G. Katzung editor. Basic & Clinical Pharmacology, 10 th Edition [Book on the Internet]. McGraw-Hill, c2007. [cited 2008 May 13].
      • Kannam JP, Aroesty JM, Gersh BJ. Beta blockers in the management of stable angina pectoris. UpToDate. [Database on the Internet]. c2008 [updated 2008 Feb 3; cited 2008 May 13].
      • Lexi-Comp [Database on the Internet]. Beta-Blockers. Lexi-Comp, Inc. c2008.
      • Mayo Foundation for Medical Education and Research. Beta blockers. [updated 2006 Dec 22; cited 2008 May 13]. Available at: http://www.mayoclinic.com/health/beta-blockers/HI00059
    50. References cont’d
      • MedlinePlus Encyclopedia. Catecholamines—blood. National Library of Medicine. [updated 2007 Jan 22; cited 2008 May 13]. Available at: http://www.nlm.nih.gov/medlineplus/ency/article/003561.htm
      • Noth I, Schmidt GA. Management of the patient with severe COPD and coronary artery disease. UpToDate. [Database on the Internet]. c2008 [updated 2008 Feb 13; cited 2008 May 13].
      • Podrid PJ. Major side effects of beta blockers. UpToDate. [Database on the Internet]. c2008 [updated 2008 Feb 13; cited 2008 May 13].
      • Rosenson RS, Reeder GS, Kennedy HL. Beta blockers in the management of acute
      • coronary syndrome. UpToDate. [Database on the Internet]. c2008 [updated 2008 Feb 7; cited 2008 May 13].
      • lRoss DS. Beta blockers in the treatment of hyperthyroidism. UpToDate. [Database on the Internet]. c2008 [updated 2006 Apr 18; cited 2008 May 13].
    51. Steroids
    52. Categories of Steroids
      • Corticosteroids
        • Glucocorticoids (e.g. cortisol)
        • Mineralocorticoids (e.g. aldosterone)
      • Sex Steroids/Hormones
        • androgens, estrogens, and progestagens
        • Anabolic steroids (related to testosterone)
    53. What are Glucocorticoids?
      • Glucocorticoids are produced in the adrenal gland (e.g. cortisol)
        • Cortisol is a hormone (also called the “stress hormone”) produced by the adrenal gland that increases blood pressure, controls inflammation and has immunosuppressive activity.
      • Glucocorticoids suppress the immune system’s response (white blood cells) to injury or trauma, thus reducing inflammation.
        • Administered locally or systemically
    54. What are Mineralocorticoids?
      • Mineralocorticoids are produced in the adrenal gland (i.e. aldosterone)
        • Aldosterone helps regulates electrolyte and water balance in the cells by retaining sodium and excreting potassium in the urine.
          • Maintains blood pressure
          • Administered systemically
    55. Conditions for Corticosteroid Use
      • Glucocorticoids
      • Adrenal insufficiencies
      • Arthritis
      • Asthma
      • Autoimmune diseases (e.g. lupus, multiple sclerosis)
      • Skin conditions (e.g. eczema, rashes)
      • Organ transplantation
      • Cancer
      • Mineralocorticoids
      • Adrenal insufficiencies (e.g Addison’s disease)
      • Idiopathic orthostatic hypotension
      • Acid in the blood
    56. Common Corticosteroids
      • hydrocortisone
        • Cortef®, Hydrocortone®, Cortaid®, Cortizone®, etc
      • cortisone
        • Generic only
      • prednisolone
        • Econopred ® , Omnipred ® , Orapred ® , Pediapred ® , Pred Forte ® , Pred Mild ® , Prelone ®
      • prednisone
        • Sterapred®
      • methylprednisolone
        • Medrol®, Methylpred-DP®, Depo-Medrol®, Solu-Medrol®
    57. Common Corticosteroids (cont’d)
      • triamcinolone
        • Aristocort®, Azmacort®, Kenalog®, Nasacort®, Tri-Nasal®, Triderm®
      • betamethasone
        • Celestone®, Beta-Val®, Dibprolene®, Luxiq®
      • dexamethasone
        • Dexamethasone Intensol®, DexPak®, Maxidex®, TaperPak®
      • fludrocortisone
        • Florinef®
    58. Adverse Effects of Corticosteroids
      • Short-term side effects:
        • Glaucoma
        • Edema
        • Hypertension
        • Weight gain
        • Mood swings
        • Increased blood sugar
      • Long-term side effects:
        • Cataracts
        • Infections
        • Osteoporosis and bone fractures
        • Irregular menstruation
        • Skin degradation
    59. Discontinuing Corticosteroids
      • Withdrawing steroids are indicated when:
        • Therapeutic effect has been reached
        • No therapeutic effect has been achieved
        • Risk of side effects outweigh benefit of the treatment
      • Gradually tapering steroids is necessary to:
        • Allow the adrenal glands to begin producing normal levels of natural cortisol
        • Prevent fatigue, lightheadedness and body aches
      • Immediate discontinuation may be necessary if:
        • The patient develops steroid-induced acute psychosis
        • The patient has a serious eye condition
    60. References
      • Brown ES, Chandler PA. Mood and Cognitive Changes During Systemic Corticosteroid Therapy. Prim Care Companion J Clin Psychiatry. 2001 Feb;3(1):17-21.
      • Chrousos GP. Adrenocorticosteroids & Adrenocortical Antagonists. Chapter 39. In: Bertram G. Katzung editor. Basic & Clinical Pharmacology, 10 th Edition [Book on the Internet]. McGraw-Hill, c2007. [cited 2008 May 13].
      • Cleveland Clinic Foundation. Corticosteroids. c2008. [cited 2008 May 13]. Available at: http://www.clevelandclinic.org/health/health-info/docs/0200/0215.asp?index=4812
      • e.hormone. The Hormones: Corticoids. Center for Bioenvironmental Research at Tulane and Xavier Universities. [cited 2008 May 13]. Available at: http://e.hormone.tulane.edu/learning/corticoids.html
      • Furst DE, Saag KG. Glucocorticoid withdrawal. UpToDate. [Database on the Internet]. c2008 [updated 2006 Dec 20; cited 2008 May 13].
      • Goldstein BG, Goldstein AO. General principles of dermatologic therapy and topical glucocorticoid use. UpToDate. [Database on the Internet]. c2008 [updated 2007 Nov 5; cited 2008 May 13].
      • Lexi-Comp [Database on the Internet]. Lexi-Comp, Inc. c2008.
    61. References cont’d
      • Mayo Foundation for Medical Education and Research. Prednisone and corticosteroids: Balance the risks and benefits. [updated 2006 June 7; cited 2008 May 13].Available at: http://www.mayoclinic.com/health/steroids/HQ01431
      • MedlinePlus Encyclopedia. Steroids. National Library of Medicine. [updated 2008 May 7; cited 2008 May 13]. Available at: http://www.nlm.nih.gov/medlineplus/steroids.html
      • National Cancer Institute. NCI Drug Dictionary—prednisolone. [cited 2008 May 13]. Available at: http://www.cancer.gov/Templates/drugdictionary.aspx?CdrID=43296
      • National Institute on Drug Abuse. NIDA InfoFacts: Steroids (Anabolic-Androgenic). [updated 2007 Mar; cited 2008 May 13]. Available at: http://www.nida.nih.gov/infofacts/steroids.html
      • National Jewish Medical and Research Center. About Steroids (Inhaled and Oral Corticosteroids). [updated 2006 Feb; cited 2008 May 13]. Available at: http://www.njc.org/disease-info/treatments/long-term/steroids/corticosteroids.aspx
      • Porter RS, editor. Rhematoid Arthritis (RA). In: Merck Manual Home Edition Online. Whitehouse Station, NJ, c2008 [cited 2008 May 13]. Available from: http://merck.com/mmhe/sec05/ch067/ch067b.html#sb067_1
    62. Anticoagulants
    63. What are Anticoagulants?
      • Anticoagulants (also called blood thinners) are a group of drugs that decrease the formation of blood clots .
    64. Indications of Anticoagulants
      • Anticoagulants are used prophylactically and therapeutically for:
        • Thromboembolic events
          • Pulmonary embolism
          • Deep vein thrombosis
        • Unstable angina
        • Myocardial infarction
        • Stroke
    65. Categories of Anticoagulants
      • Vitamin K antagonists
        • warfarin (Coumadin®)
      • Inhibitors of thrombin
        • Unfractionated heparin (UFH)
          • Hep-Lock®, HepFlush-10®
        • Low molecular weight heparin (LMWH)
          • enoxaparin (Lovenox®), dalteparin (Fragmin®)
        • Newer Anticoagulants
          • fondaparinux (Arixtra®)--related to heparin
          • bivalirudin (Angiomax®)
          • Lepirudin (Refludan®)
          • argatroban (no generic)
    66. How do Anticoagulants Work?
      • Warfarin depletes vitamin K, which is required for producing many blood clotting factors
        • Administered by mouth
        • Dietary vitamin K is restricted
      • Heparin increases the activity of antithrombin III, which inactivates the clotting factor thrombin
        • Administered by injection
      • Newer anticoagulants inhibit the activity of thrombin by directly binding to it
        • Administered by injection
    67. Adverse Events
      • Warfarin:
      • Hemorrhage, bleeding, hematomas, anemia, nausea, vomiting, diarrhea, headache
      • Heparin:
      • UFH: Hemorrhage, bleeding, thrombocytopenia, skin necrosis, bruising, fever headache, GI issues, osteoporosis, elevated liver enzymes
      • LMWH: Hemorrhage, bleeding, bruising, GI issues, fever
    68. Antiplatelets
      • What are antiplatelets?
        • Antiplatelets inhibit platelets from aggregating to form blood clots
      • Commonly used antiplatelets
        • aspirin (Bayer®, Excedrin®),
        • clopidogrel (Plavix®)
        • abciximab (ReoPro®)
      • Conditions
        • Stroke, myocardial infarction, arteriosclerosis
      • Adverse effects
        • Bleeding, hemorrhage, GI issues, headache, fever, hypotension, thrombocytopenia
    69. References
      • Cucchiara B, Messe SR. Antiplatelet therapy for secondary prevention of stroke. UpToDate. [Database on the Internet]. c2008 [updated 2007 Apr 24; cited 2008 May 13].
      • First Consult [Database on the Internet]. Principles of anticoagulation. Elsevier Inc. c2008. [cited 2008 May 13].
      • Hennekens CH. Patient Information: Aspirin and heart disease. UpToDate, Inc. c2008. [updated 2007 Sept 18; cited 2008 May 13]. Available at: http://www.uptodate.com/patients/content/topic.do?topicKey=~6cTQKoLyIHUj1&selectedTitle=1~133&source=search_result
      • Lexi-Comp [Database on the Internet]. Lexi-Comp, Inc. c2008.
      • Lip, GYH, Pineo GF. Bauer KA. Patient Information: Deep vein thrombosis (DVT). UpToDate, Inc. c2008. [updated 2007 June 19; cited 2008 May 13]. Available at: http://patients.uptodate.com/topic.asp?file=blod_dis/7159&title=Heparin#18
    70. References cont’d
      • National Heart Lung and Blood Institute. How is pulmonary embolism treated? [cited 2008 May 13]. Available at: http://www.nhlbi.nih.gov/health/dci/Diseases/pe/pe_treatments.html
      • Porter RS, editor. Bleeding and Clotting Disorders. In: Merck Manual Home Edition Online. Whitehouse Station, NJ, c2008 [cited 2008 May 13]. Available at: http://www.merck.com/mmhe/sec14/ch173/ch173a.html
      • Porter RS, editor. Acute Coronary Syndromes (ACS). In: Merck Manual Online. Whitehouse Station, NJ, c2007 [updated 2007 Dec; cited 2008 May 13]. Available at: http://www.merck.com/mmpe/sec07/ch073/ch073c.html
      • Valentine KA, Hull RD. Patient Information: Warfarin (Coumadin®). UpToDate, Inc. c2008. [updated 2007 July 25; cited 2008 May 13]. Available at: http://patients.uptodate.com/topic.asp?file=blod_dis/6066&title=Anticoagulants
    71. Free Resources
      • FDA – fda.gov, especially http://www.fda.gov/cder/index.html
      • MedlinePlus Drugs and Supplements - http://www.nlm.nih.gov/medlineplus/druginformation.html
    72. Exercise
    73. Matching
      • Diuretic
      • Steroid
      • Anticoagulant
      • NSAID
      • Beta-Blocker
      • Antibiotic
      clindamycin propranolol Coumadin® hydrochlorothiazide
    74. Matching
      • Antiplatelet
      • Beta-blocker
      • Steroid
      • Antibiotic
      • Anticoagulant
      • NSAID
      prednisone celecoxib rifampin Plavix®
    75. Clinical Question: Antibiotics
      • Is there clinical evidence indicating that a dual treatment strategy of Cell Wall Active and Protein Synthesis Inhibitor antibiotics is more effective than either therapy alone for pneumonia in pediatric patients?
    76. Clinical Question: Diuretics
      • What kinds of cutaneous drug reactions are caused by the diuretic hydrochlorothiazide?
    77. Clinical Question: NSAIDs
      • Is there any evidence for increased risk of complications such as gastrointestinal (GI) bleeding with increased duration of NSAID use for arthritis?
    78. Clinical Question: Beta-Blockers
      • In adults with a history of chronic obstructive pulmonary disease (COPD), what is the probability of adverse events when giving them beta-blockers for treatment of hypertension?
    79. Clinical Question: Steroids
      • Does the evidence support the use of systemic steroids in the prevention of post-extubation airway obstruction in critically ill adults?
    80. Clinical Question: Anticoagulants
      • What are the major complications associated with using anticoagulants, such as heparin, in the context of intracranial hemorrhage (ICH) secondary to cerebral venous thrombosis (CVT)?

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