bleeding SA
Approach to bleeding
Haemostasis | · Stages: 1. Primary haemostasis = platelet plug 2. Secondary haemostasis = fibrin plug (requires coagulation cascade) 3. Clot lysis |
Primary haemostatic disorders | Clinical signs: petechia, mucosal bleeds, multiple sites of bleeding Investigations: haematology (platelet count), BMBT, vWF Causes: · Thrombocytopenia o Defective platelet production – bone marrow neoplasia, drug/chemical/toxin-induced bone marrow suppression, bone marrow infection o Accelerated platelet removal – IMTP (most common cause), DIC o Platelet loss – splenomegaly, acute ongoing haemorrhage · Thrombocytopathia – treat symptomatically o Inherited thrombopathias o Drug-induced defects of platelet function, e.g. NSAIDs o Platelet dysplasia, e.g. neoplasia · vWF dysfunction o Dobermans predisposed o Diagnosis: normal platelet count, prolonged BMBT, low vWF antigens o Treatment: plasma transfusion, cryoprecipitate, desmopressin (for type 1) |
Secondary haemostatic disorders | Clinical signs: deep bleeds, single site, haematomas, mucosal bleeds Investigations: WBCT, OSPT, APTT, specific factor assays Causes: · Congenital o Haemophilia – either factor 8 or factor 9 deficient – will have increased APTT · Acquired o Vitamin K antagonism (rat bait) – stops production of factors 2, 7, 9, 10 (takes few days so don’t see CS for few days) § If can make vomit on same day then risk of side effects is very low o Hepatic disease – all clotting factors made in liver – incr. OSPT and APTT |
Approach to bleeding patient | Signalment – Clinical signs: · Primary coagulopathy o Petechiae/ecchymoses – little bleeds common (differentiate from vasodilation – push microscope slide into lesion – if doesn’t fade = petechiae) o Bleeding from MMs o Usually >1 site of bleeding · Secondary coagulopathy o Deep or cavity bleeds (little bleeds not seen) o Haematomas common o Sometimes only 1 site of bleeding Investigations: · Haematology – platelet count – normal = rule out IMTP o Take blood sample from peripheral vein (cephalic) – easier to apply pressure bandage · Buccal mucosal bleeding time (conscious dog, small nick, hold gum up and see how long takes to stop bleeding) – increased = primary coagulopathy · vWF antigen measurement – normal = rule out vWF · Whole blood clotting time – increased = thrombocytopenia, vit K antagonism o Measures intrinsic + extrinsic pathways (also incr. if low platelets) · One stage prothrombin time – increased = hepatic disease, vit K antagonism o Measures extrinsic + common pathways · Activated partial thromboplastin time – increased = hepatic disease, vit K antagonism, haemophilia o Measures intrinsic + common pathways Management: · Avoid SC injections, DON’T use IM injections · Minimise movement, cage rest · Handle very gently (bruises easily) |
Thrombosis | · Causes hypoxia and tissue damage (but hard to detect) · To test fibrinolysis – test fibrinogen, FDP (degradation products), D-dimer (breakdown products) o D-dimer increased when more thrombin activated (animal in pro-thrombotic state) = DIC, feline thromboembolism disease, PLN, cushings |
DIC | · Disseminated intravascular coagulation – balance of haemostasis tips (animal turns prothrombotic or wont form any clots) · Always an underlying causes – potential triggers: o Endothelial damage o Platelet activation, e.g. FIP, endotoxemia o Release of tissue procoagulants – trauma, pancreatitis, bacterial infections, neoplasia o Specific groups of diseases known to cause DIC: § Infectious agents – bacterial sepsis, FIP, babesia, rickets § Neoplasia – metastatic tumours, haemangiosarcoma § Inflammation/necrosis – trauma, IMHA, pancreatitis, hepatitis, GDV, vasculitis § IV haemolysis – IMHA, acute transfusion reactions, snake/insect bites · Two types: o Overt DIC – body able to compensate for a bit, may see few clinical signs as small clots thrown (but no clinically detectable abnormalities) o Overt DIC – body can no longer compensate, lots of clots thrown (cats), bleeding (dogs) ® haemorrhage and end-organ damage · Diagnosis: o Thrombocytopenia o Hypofibrinogenemia (as coagulation factors used up) o Schistocytes · Treatment: treat underlying cause |