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62 Cards in this Set

  • Front
  • Back

Risk factors for acute rejection after transplant

1. increased HLA mismatch


2. factors affecting previous sensitization


3. ethnicity


4. age


5. donor source


6. prolonged preservation time


7. noncompliance

Induction phase

**early phase intended to provide highly potent, multifocal suppression of hte immune system for several days to a few weeks




1. steroids


2. monoclonal antibodies


3. polyclonal antibody

Maintenance Phase

**immunosuppression regimen designed to provide chronic, balanced immunodeficiency

Types of medications used in Solid Organ Transplant

1. Calcineurin inhibitors


2. Steroids


3. Antimetabolites


4. mTOR inhibitor

Calcineurin Inhibitors

1. Cyclosporine (Sandimmune, Neoral)


2. Tacrolimus (Prograf)

Cyclosporine

MOA: inhibits calcineurin-dependent translocation of the cytosolic subunit of NFAT - inhibits IL-2 mediated monoclonal T-cell proliferation




ADRs: seizures, hallicinations, insomnia, gingival hyperplasia, HTN, hepatotoxicity, Nephrotoxcity

Tacrolimus

MOA: inhibits translocation of the cytocolic subunit of NFAT - inhibits IL-2 mediated monoclonal T-cell proliferation




ADRs: seizures, hallucinations, insomnia, alopecia, HTN, QT prolongation, hetapo & nephro toxicity, anemia

mTOR inhibitors

1. Sirolimus (Rapamune)


2. Everolimus (Zortress)

MOA of mTOR inhibitors

bind to FKBP-12 to form a complex that binds and inhibits activation of its target protein that is critical in IL-2 mediated cell-cycle progression

Everolimus

ADRs: fatigue, headache, oral ulcers, nephrotoxicity (with calcineurin inhibitors), HTN, anorexia, N/D, rash, acne, anemia

Sirolimus

ADRs: anorexia, oral ulcers, diarrhea, esophagitis, gastritis, nephrotoxicity (with calcineurin inhibitors), HTN, rash, acne, arthralgias

Selective T-cell co-stimulation Blocker

Belatacept

Belatacept

MOA: binds to co-stimulation proteins CD80 & CD86 on the APC, to prevent binding to hte T-cell proteins




ADRs: headache, insomnia, anxiety, HTN, N/V/D, anemia, hematuria, proteinuria,acne, UTI

Antiproliferative Agents fOR SOT

1. Azathioprine


2. Mycophenolate mofetil


3. Mycophenolate sodium

Azathioprine

MOA: purine analogue pro-drug; can be incorporated directly into DNA as thiopurine as well as interfere with RNA and DNA synthesis




ADRs: retinopathy, N/V/D, pancreatitis, rash, skin cancer, leukopenia

Mycophenolate

MOA: noncompetitive, reversible inhibition of inosine monophosphate dehydrogenase - inhibits purine synthesis




ADRs: N/V/D, ab pain, leukopenia, anemia

Corticosteroids

MOA: bind to glucocorticoid receptors where the complexes bind to regulatory DNA sequences




ADRs: delirium, mood swings, insomnia, glaucoma, HTN, increased appetite, PUD, edema, HLD, hirsutism, impaired wound healing, arthralgia, myopathy

Basiliximab

*monoclonal antibody*




MOA: monoclonal IgG specifically binds to CD25 - competitively inhibits IL-2 and facilitates preferential ilimination of activated lymphocytes




ADRs: severe acute hypersensitivity reactions

Antithymocyte globulin (Equine & Rabbit)

*polyclonal antibody*




MOA: includes IgG directed against multiple surface markers - targets multiple phases of immunity




ADR: infusion related (fever, chills, dyspnea), rash, leukopenia

Peptic Ulcer Disease

group of disorders of hte upper GI tract characterized by ulcerative lesions that depend on acid and pepsin for their formation

Clinical presentation of PUD

epigastric pain 1-3 hours after meals relieved by ingestion of food or antacids

PPIs

MOA: suppress gastric acid secretion specifically by inhibiting the H+-K+-ATPase enzyme system on the surface of gastric parietal cells




ADRs: increased risk of CDAD, increased risk of osteoporosis-related fractures, lower Mg levels chronically, headache, diarrhea, nausea




**take 30-60 minutes before first meal of day**

MOA of H2RAs

suppress gastric acid secretion by reversibly blocking histamine-2 receptors on the surface of the gastric parietal cell




ADRs: headache, diarrhea, nausea




**take antacids 1-2 hours before or after**

Sucralfate

MOA: when exposed to gastric acid, forms a viscous adhesive that binds positively charged protein molecules in the ulcer crater forming a protective barrier




ADRs: constipation




**take 1 hour before meals and at bedtime**

Misoprostol

MOA: synthetic prostaglandin E1 analog that moderately inhibits acid secretion and enhances gastric mucosal defense




ADRs: diarrhea, ab cramping, nausea, flatulence, headache




**Take with or after meals and at bedtime**

Treatment of PUD

1. PPI/H2RA


2. Sucralfate


3. Misoprostol


4. Antibiotic (H. pylori)

Typical Reflux Syndrome

presence of troublesome heartburn, regurgitation, or both




may have epigastric pain, sleep problems

Reflux Chest Pain Syndrome

GERD causes chest pain that is similar to ischemic cardiac pain

Reflux esophagitis

visible breaks in the distal esophageal mucosa

Reflux Stricture

persistent luminal narrowing of hte esophagus caused by GERD

Barrett's Esophagus

esophageal squamous epithelium from the gastroesophageal junction is replaced with metaplastic columnar epithelium

Proton Pump Inhibitors

1. Omeprazole (Prilosec) 20-40mg qd


2. Esomeprazole (Nexium) 20-40mg qd


3. Lansoprazole (Prevacid) 15-30mg BID


4. Dexlansoprazole (Dexilant) 30-60mg qd


5. Rabeprazole (Aciphex) 10-20mg qd


6. Pantoprazole (Protonix) 40-80mg qd

Histamine-2 Receptor Antagonists (H2RAs)

1. Cimetidine (Tagamet)


2. Randitidine (Zantac)


3. Nizatadine (Axid)


4. Famotidine (Pepcid)

Antibacterials for H. pylori

1. Clarithromycin (Biaxin)


2. Amoxicillin (Amoxil)


3. Metronidazole (Flagyl)


4. Tetracycline

Antacids and Absorbents

1. Magnesium hydroxide (Milk of magnesia)


2. Aluminum hydroxide (ALternaGEL)


3. Aluminum carbonate (Basaljel)


4. Mag hydroxide + Aluminum hydrox (Maalox)


5. Magaldrate (Riopan)


6. Calcium Carbonate (Tums)


7. Sodium bicarbonate


8. Alginic acid + aluminum hyrox + Mag hydrox (Gaviscon)

Antacids

MOA: neutralize gastric acid and inhibit the conversion of pepsinogen to pepsin, thus raising the pH of gastric contents




ADRs: Mag - diarrhea; Alu - constipation

Ulcerative Colitis

chronic mucosal inflammatory condition confined to the rectum and colon




S/Sx: bloody diarrhea, rectal urgency, tenesmus

Crohn's Disease

a transmural inflammation of hte GI tract that can affect any part of hte GI tract from mouth to anus




S/Sx: chronic or nocturnal diarrhea, abdominal pain, weight loss, fever, rectal bleeding, pallor

Treatment of mild to moderate distal colitis

1. oral aminosalicylates


2. topical mesalamine


3. topical steroids

Treatment of mild to moderate extensive ulcerative colitis

1. aminosalicylates


2. oral steroids


3. thiopurines


4. infliximab

Treatment of Severe colitis

1. infliximab & hospitalization


2. IV steroids


3. IV cyclosporine


4. thiopurines

Treatment of mild to moderate Crohn's localized to ileum or right colon

1. controlled-release oral budesonide


2. oral mesalmine


3. oral sulfasalazine


4. rectal aminosalicylates

Treament of moderate to severe Crohn's disease

1. Oral steroids


2. Azathioprine and 6-mercaptopurine


3. parenteral methotrexate


4. infliximab, adalimumab, certolizumab

Treatment of severe to fulminant Crohn's disease

1. IV steroids & hydration


2. high dose flagyl or cipro


3. azathioprine, 6-mercaptopurine, infliximab

mesalamine

MOA: inhibits COX and may also inhibit production of COX, thromboxane synthetase, platelet-activating factor synthetase, and IL-1 in macrophages




ADRs: better tolerated than sulfasalazine (nausea, headaches)

infliximab, adalimumab

MOA: chimeric monoclonal antibody that inhibits human TNF which inhibits subsequent cytokine-triggered inflammatory processes




ADRs: infusion-related/injection site reactions, URIs, headache, rash, cough, nausea

certolizumab

MOA: pegylated humanized antibody Fab fragment of TNF monoclonal antibody - inhibits TNF which inhibits cytokine inflammatory processes




ADRs: injection-site reaction, URI, rash, UTI

Sulfasalazine

MOA: cleaved by bacteria in the gut to form mesalamine




ADRs: nausea, vomiting, anorexia, headache




IRXN: digoxin

Immunosuppressant agents for ulcerative colitis and Crohn's

1. corticosteroids


2. azathioprine


3. 6-mercaptopurine


4. cyclosporine


5. tacrolimus

Irritable Bowel Syndrome

abdominal pain or discomfort that occurs in association with altered bowel habits over a period of 3 months




S/Sx: crampy/achy ab pain, diarrhea, constipation, heartburn, dyspepsia, nausea

Aminosalicylates for Ulcerative Colitis & Crohn's

1. Sulfasalazine (Azulfidine)


2. Mesalamine (Asacol, Pentasa, Lialda, Canasa)


3. Balsalazide (Colazal)

Immunomodulators used in UC & Crohns

1. infliximab (Remicade)


2. adalimumab (Humira)


3. Cerolizumab pegol (Cimzia)


4. Natalizumab (Tysabri)

Antispasmodic/anticholinergics used in IBS1

1. dicyclomine (bentyl)

2. hyoscyamine





Dicyclomine (Bentyl

MOA: decreases GI motility by relaxing smooth muscle in the gut




ADRs: CNS depression, dry mouth, urinary retention, constipation, decreased sweating

Hyoscyamine

MOA: anticholinergic agent that decreases GI motility by decreasing smooth muscle tone through antimuscarinic activity in the gut




ADRs: CNS depression, dry mouth, urinary retention, constipation, decreased sweating

Amitriptyline (Elavil)

MOA: TCA, delays intestinal transit and may blunt perception of visceral distension




ADRs: CNS depression, dry mouth, urinary retention, constipation, decreased sweating

Tegaserod (Zelnorm)

MOA: partial 5-HT4 agonist that stimulates the peristaltic reflex and intestinal secretion, inhibits visceral sensitivity by binding to receptors in the gut




ADRs: diarrhea, nausea, headache, abdominal pain, increased risk of CV events

Loperamide (Imodium)

MOA: inhibits peristalsis by directly affecting the circular and longitudinal muscles of the intestinal wall

Diphenoxylate (Lomotil)

MOA: a meperidine congener that directly affects the circular smooth muscle in the gut slowing GI transit time

Alosetron (Lotrenox)

MOA: selective 5-HT3 antagonist that inhibits activation of nonselective cation channels in hte gut




ADRs: constipation, ab pain, nausea (obstruction, perforation, toxic megacolon, ischemic colitis, death have occured)

Lubiprostone (Amitiza)

MOA: C-2 chloride channel activator that increases secretion of saltwater into the intestinal lumen




ADRs: nausea, diarrhea, headache




**approved ONLY FOR women with constipation-dependent IBS**

Linaclotide (Linzess)

MOA: guanylate cyclase-C agonist which increases intra- and extracellular levels of cGMP. this stimulates the secretion of chloride and bicarb in the lumen increasing the transit time




ADRs: diarrhea, ab pain, flatulence, URI, ab distention, sinusitis