Notes

Slide Show

Outline

1	CLSC412 HEMOSTASIS
2	Unit Objectives - 1
3	Unit Objectives - 2
4	Definition of Hemorrhage
5	Types of Hemorrhage
6	Localized vs Generalized
7	Localized Hemorrhage
8	Generalized Hemorrhage-1
9	Generalized Hemorrhage-2
10	Acquired vs Congenital
11	Acquired Hemorrhage
12	Congenital Hemorrhage
13	Anatomic vs Systemic
14	Anatomic Hemorrhage
15	Systemic Hemorrhage
16	Acquired Hemorrhagic Disorders
17	Liver Disease - 1
18	Liver Disease - 2
19	D.I.C. in Liver Disease
20	Systemic Fibrinolysis & Liver
21	Thrombotic Episodes & Liver
22	Lab Tests & Liver Disease
23	Therapy in Liver Disease
24	Renal Failure - 1
25	Renal Failure - 2
26	Nephrotic Syndrome
27	Vitamin K Deficiency/Antagonism
28	Vitamin K factor abnormalities
29	Autoanti-VIII inhibitor
30	Alloanti-VIII inhibitor
31	Acquired von Willebrand Disease
32	Congenital Hemorrhagic Disorders
33	Congenital von Willebrand Disease-1
34	Congenital von Willebrand Disease-2
35	Congenital von Willebrand Disease-3
36	Congenital von Willebrand Disease-4
37	Other Causes of Decreased vWF
38	Lab Detection of vW
39	Therapy in vW
40	Congenital Hemorrhagic Disorders
41	Hemophilia
42	Hemophilia A - 1
43	Hemophilia A - 2
44	Hemophilia A - 3
45	Clinical Features of Hemophilia A
46	Complications of Hemophilia A
47	Lab Findings in Hemophilia A
48	Therapy in Hemophilia A
49	VIII Inhibitors in Hemophilia A - 1
50	VIII Inhibitors in Hemophilia A - 2
51	Therapy in Hemophilia A with Inhibitors
52	Hemophilia B
53	Lab Features in Hemophilia B
54	Inhibitors in Hemophilia B
55	Hemophilia C
56	Other Single-Factor-Deficiencies - 1
57	Other Single-Factor-Deficiencies - 2
58	Hemorrhagic Coagulation Disorders
59	g-carboxylation cycle
60	Cascade Theory of Coagulation-I