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52 Cards in this Set

  • Front
  • Back
most common cause of inherited thrombophilias?
- factor V leiden 40-50%
- other causes: prothrombin gene mutation, hyperhomocysterinemia, protein C, protein S, antithrombin III deficiency, antiphospholipid
epidural spinal cord compression
- common complication of cancer
- cancers that tend to met to spinal cord: prostate, breast, lung, non-Hodgkins, RCC
- sx: thoracic radicular pain that wraps around the abdomen, lower exremity weakness and sensory changes
- TREAT IMMEDIATELY b/c cord compression: high dose corticosteroids followed by MRI to confirm dx, followed by radiation therapy vs surgery
best prognostic sign for CNS lymphoma?
- increase in CD4 count
first step in treatment of sickle cell crisis?
- IV fluids
- presence of sickling in bood smear is not useful
splenic sequestration crisis
- high risk in young children with SCC
- check CBC - large fall in hemoglobin secondary to vaso-occlusion in spleen and splenic pooling
- spleen can enlarge rapidly --> hypovolemic shock --> immediate blood transfusion
greatest correlation w/ dvlp colon cancer? what protects?
- alcohol possibly due to decreased alcohol intake
- protects: NSAIDS, HRT, high fiber, exercise
risk of multiple blood transfusions?
- development of alloantibodies --> difficulty in finding compatibility
autoantibodies vs alloantibodies in finding match for blood transfusion?
- alloantibodies develop in patient with long hx of transfusions
- autoantibodies usually become an issue in pts with AI anemia and taking certain drugs (methyldopa and procainamide)
HLA allosensitization
- increases risk of graft rejection in pts awaiting organ or bone marrow transplantation
patient with isolated thrombocytopenia- everything else is normal including PT, PTT, plasma fibrinogen, etc?
- idiopathic thrombocytopenic purpura
- platelet destruction secondary to specific autoantibodies
- don't give plt transfusion because they will just be destroyed anyway by antibodies
- no need to treat if plt btw 30-50
- if severe, tx with corticosteroids esp in adults or IVIG if CS fails
tx of HUS and TTP?
- plasmapheresis
side effects of metoclopromide
- D2 receptor blocker
- causes EPS when used in high doses
- being replaced by odansetron 5HT3 receptor blocker
tx of platelet dsfx in pt who is acutely bleeding?
- desmopressin, dialysis, estrogen tx, cryoprecipitate infusion
clotting tests
- PT: aka factor II, produced by liver, requires vit K, prolonged in liver disease
- PTT: detects deficiencies in all clotting factors except VII, XIII, used to monitor heparin therapy
- bleeding time: prolonged in thrombocytopenic purpura, plt abnormalities, vascular abnormalitiy, leukemia, severe liver disease, DIC, factor deficiency, hemophilia
Heparin induced thrombocytopenia
- Type I: w/in 2 days of heparin therapy, not as large drop (to 100), plt count return to normal once d/c heparin
- type II: 4-10 days after heparin, Ab driven, associated with venous and arterial thrombosis, so major manifestations: DVT, PE, venous limb gangrene, cerebral sinus thrombosis, stroke, MI
- prevent by using LMWH over unfractionated and using heparin < 5 days to decrease risk of Ab formation
tx of HIT?
- d/c heparin and warfarin if pt is on it (don't restart warfarin until plt count > 100) --> start lepirudin (don't use in renal insufficiency) or argatroban (dose adjust in hepatic dysfunction)
what blood smear is consistent with iron deficiency anemia?
- microcytic/hypochromic anemia with anisocytosis
- most common source is GI bleed in males --> fecal occult test
microcytic vs macrocytic anemia?
- microcytic: iron deficiency
- macrocytic: check b12, folate
febrile transfusion reaction
- 10 minutes after transfusion, pt gets chills and spikes a fever
- pathophys: pt's ab reacts to donor's leukocytes
- prevent by cell washing, using frozen deglycerolized red cells, other leukocyte depletion techniques
dx acute hemolytic transfusion reactions
- classic triad that you rarely see: fever, back pain, red or pink colored urine
- to r/o stop transfusion and get tests: direct antiglobulin/Coombs test and measurement of plasma-free hemoglobin level, UA to see hemoglobin
what calcium abnormality occurs with transfusions?
- hypocalcemia --> calcium gluconate infusion
tx of DVT secondary to reversible cause vs idiopathic?
- treat w/ warfarin for 3-6 months
- idiopathic: at least 6 months, reassess on whether to continue
1 unit of platelet should raise the plts by how much? when to recheck plts after transfusion?
- 5,000
- 10-60min after copmletion
platelet refractoriness
- absolute platelet increment of less than 2,000 per unit
- most common cause is alloimmuniation
plt count rises appropriately after transfusion but then falls w/in 24 hours
- DIC, sepsis, active bleeding, drugs that reduce plt survival
superior vena cava syndrome
- dyspnea, cough, facial fullness, neck pain --> hoarseness, dysphagia, chest pain, syncope
- Pex: dilated veins in arms and neck
- best dx test is CT w/ contrast
- 80% bronchogenic carcinoma
use and risk of tamoxifen? testing?
- use in estrogen receptor positive breast cancer for 5 years
- risk of uterine cancer
- only do further testing if pt is post menopausal w/ abnormal sx e.g. bleeding or vaginal sx --> U/S or biopsy
tx for non-operable head and neck cancer?
- both chemo and radiation
ABO incompatibility
- fever and hypotension
- stop transfusion and HYDRATE with normal saline (not LR)
- also consider dopamine infusion and osmotic diuresis
tx of metastatic prostate cancer?
- e.g. met to spine
- palliative rather than curative
- androgen depletion: LHRH (leutinizing hormone releasing hormone) eg. leuprolide but causes initial T surge followed by decrease so also give antiandrogen e.g. flutamide for that first week T surge
pt with lobular carcinoma in situ on core needle biopsy, next step?
- nonmalignant lesion but increased risk of lobular or ductal carcinoma
- do excisional biopsy because may actually be DCIS or invasive cancer
- follow up yearly surveillance or consider SERMS: tamoxifen, raloxifene or prophylactic bilateral mastectomy
pt with elevated PSA and shoulder pain
- get radioiostope bone scan
elderly pts with bone pain?
- always suspect multiple myeloma
- will see hyperCa2+ and renal dysfx
-to dx get: SPEP, UPEP, skeletal survey, bone marrow biopsy
pt with multiple myeloma- what test to assess for bone lesions?
- whole body xray b/c looking or lytic lesions (not radionucleotide bone scan that look for blastic lesions)
hyperviscosity syndrome
- increased serum vicosity due to high protein content
- seen in multiple myeloma, Waldestrom's macroglobulinemia
- sx: HA, dizziness, vertigo, nystagmus, hearing loss, visual impairment, mucosal hemorrhage from impaired plt function
- ddx ARF: not as acute
- hypercalcemia: no mucosal bleeding or blurry vision
** HY
patient presents with elevated Hg/Hct... next step?
- get EPO
- if pt has hx of lung disease then secondary to hypoxia and pt with high EPO
- if low EPO then think myeloproliferative d/o
side effect of methotrexate?
- macrocytic anemia
- methotrexate inhibits folate conversion --> folate deficiency
what drugs cause macrocytic anemia?
- trimethoprim, methotrexate, phenytoin --> interferes with folate
- give folinic acid (leucovorin)
common primary sites of origin of brain metastasis
- order of frequency: lung, breast, unknown, melanoma, colon cancer
pernicious anemia
- autoimmune destruction of parietal cells
- dx by measurement of autoantibodies against intrinsic factor (which is produced by parietal cells and is needed to bind to B12 for body to absorb)
- schilling test is second line
- see atrophy in fundus and body, not antrum **high yield
bcr/abl translocation?
- CML
- tx with tyrosine kinase inhibitor to control disease; then if stable and w/ donor tx with bone marrow transplant
pt treated with EPO for anemia secondary to renal disease --> inadequate response in 4-6 wks... next step?
- look if pt has other causes of anemia as well ---> measure ferritin and transferrin saturation
- avoid blood transfusion in ESRD because can sensitize pt for allograft rejection
treatment of multiple brain metastasis
- whole brain radiation to improve survival by a couple of months
- chemotherapy has poor penetration
pt with pancoast's tumor: what finding requires immediate therapy?
- asymmetric chest movement and lower DTR --> phrenic nerve involvement or invasion of intervertebral foramina --> risk of spinal cord compression
- Horner's is bad prognostically but not an emergency
anemia of chronic disease
- seen in pts with cancer or chronic inflammation (e.g. RA) --> suppress RBC in bone marrow
- see low iron, high ferritin, normal transferritin
- bone marrow biopsy: decreased sideroblast, increased iron storage in macrophages
- tx underlying disease, give EPO or blood transfusions
- EPO ineffective if pt's EPO is already >500
neutropenic fever
- isolate fever >101 and lasts more than an hour
- don't get many other symptoms
- emergency
pt with anemia, normal MCV
- get retic count to ddx disease of RBC production vs destruction
- ESR may be useful because anemia of chronic disease will look similar; ESR would be elevated
palliative pain tx for pt with spine metastasis?
- radiation therapy
patient with squamous cell carcinoma refuses excision... next step?
- do radiation therapy
work up of lung cancer
get CT
HER2/neu overexpression
- worse prognosis
- bad response to treatment
- tx with monoclonal ab to Her2/neu e.g. herceptin (trastuzumab)
note: IM/IV EPO is not more effective then oral EPO, so don't choose if oral EPO is ineffective
ok