medicine 2 Flashcards
emergency treatment for anaphylaxis?
IV hydrocortisone and adrenaline
RCHOP drugs
Rituximab, cyclophosphamide, vincristine, doxorubicin and prednisolone
Poor prognostic factors for ALL:
Presentation <2 or >10
B or T cell surface markers
WCC>20 at diagnosis
Poor prognostic factors for HL:
B symptoms
Age >45
Wcc> 15
hb <10.5
albumin <40
lymphocytes <600
male
Blood film findings:
Howell-Jolly –> hyposplenic conditions e.g. megaloblastic anaemia, post splenectomy
Heinz –> G6PD deficiency
Shistocytes –> metallic heart valves or haemolytic anaemia
Rouleaux –> MM + other inflammatory conditions, alongside raised ESR
Drugs that induce thrombocytopenia:
aspirin, heparin, diuretics, quinine, sulfonamides, thiazide diuretics
Things that can induce a sickle cell crisis:
Infection
Hypoxia
Dehydration
Management of SCD:
- hydroxycarbamide –> increases fetal Hb which can’t sickle
- exchange transfusion if severe anaemia
- vaccinations and abx, to avoid infections as this can precipitate vaso-occlusive crises
Investigation findings in DIC:
Thrombocytopenia
PT increased
D-dimer increased
Fibrinogen decreased
Presentation of tumour lysis syndrome:
~2 days post high dose chemo for leukaemia or lymphoma.
Oliguria, abdo pain and weakness.
High potassium, phospahte and urea.
Low calcium.
AKI
Presentation of sideroblastic anaemia:
Microcytic anaemia refractory to iron therapy, with abnormally high serum ferritin and iron.
Hereditary causes of haemolytic anaemia:
Sickle cell
Thalassaemia
G6PD deficiency
Hereditary spherocytosis
Causes of a prolonged PT:
DIC
Vit K deficiency (2,5,7,10)
Chronic Liver Disease
Causes of a prolonged APTT:
DIC
Haemophilia A+B
VWB Disease
Drugs that may enhance the effect of warfarin, and therefore need lower dosing / monitoring of it:
Alcohol
Amiodarone
Antibiotics
SSRIs + SNRIs
Aspirin
Clopidogrel