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PA H10 | Hemostasis & Bleeding Disorders — Practice Quiz

Practice 14 questions · Untimed · Unlimited attempts

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Q1 PA20.1 1 pt

A 35-year-old woman presents with prolonged bleeding after a dental extraction. Her platelet count is 220 × 10⁹/L. Prothrombin time (PT) is normal. Activated partial thromboplastin time (aPTT) is prolonged. A 1:1 mixing study with normal plasma corrects the aPTT to normal. Which factor deficiency is most consistent with these findings?

A Factor VII
B Factor VIII
C Factor V
D Factor II (prothrombin)

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Q2 PA20.1 1 pt

A 9-year-old boy is brought to the emergency department after a fall from a bicycle. He has a large haemarthrosis of the right knee and deep muscle haematomas. His older brother had a similar episode last year. Platelet count and PT are normal; aPTT is prolonged. Which inheritance pattern and coagulation arm is most likely affected?

A Autosomal dominant; extrinsic pathway
B Autosomal recessive; common pathway
C X-linked recessive; intrinsic pathway
D X-linked dominant; extrinsic pathway

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Q3 PA20.2 1 pt

A 28-year-old woman presents with menorrhagia since menarche and easy bruising. She reports that her gums bleed for 20 minutes after brushing. Platelet count is 180 × 10⁹/L, PT is normal, and aPTT is mildly prolonged. Ristocetin cofactor activity is markedly reduced. What is the most likely diagnosis?

A Glanzmann thrombasthenia
B von Willebrand disease
C Bernard-Soulier syndrome
D Haemophilia A

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Q4 PA20.2 1 pt

A 6-year-old girl has had nosebleeds since age 2, multiple episodes of prolonged bleeding from minor cuts, and no joint bleeds. Her platelet count is 12 × 10⁹/L. Blood film shows no platelet clumps and normal platelet morphology. PT and aPTT are normal. Bone marrow biopsy shows increased megakaryocytes. Which diagnosis is most likely?

A Aplastic anaemia
B Immune thrombocytopenic purpura (ITP)
C Thrombotic thrombocytopenic purpura (TTP)
D Disseminated intravascular coagulation (DIC)

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Q5 PA20.2 1 pt

A 45-year-old woman presents with confusion, fever, purpuric rash, and oliguria. Blood film shows numerous schistocytes. Platelet count is 18 × 10⁹/L. PT and aPTT are normal. Lactate dehydrogenase is markedly elevated. Which mechanism best explains her thrombocytopenia?

A Anti-platelet IgG antibody formation
B Deficiency of ADAMTS13 leading to ultra-large vWF multimer accumulation
C Consumption of coagulation factors and platelets by fibrin thrombi
D Decreased thrombopoietin production by the liver

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Q6 PA20.2 1 pt

A 7-year-old boy is referred because of repeated episodes of petechiae on his lower limbs and prolonged bleeding from cuts. Peripheral blood film shows giant platelets. Platelet count is 40 × 10⁹/L. Ristocetin-induced platelet agglutination is absent. PT and aPTT are normal. Which protein is most likely deficient?

A GPIIb/IIIa (αIIbβ3)
B GPIb/IX/V complex
C ADAMTS13
D Factor VIII

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Q7 PA20.1 1 pt

A surgeon preparing a patient for elective cholecystectomy notices that the PT is prolonged (INR 2.1) while the aPTT is normal and platelet count is 260 × 10⁹/L. The patient is otherwise well and takes no anticoagulants. Which vitamin-K-dependent factor has the shortest half-life and would be depleted first in vitamin K deficiency?

A Factor II (prothrombin)
B Factor VII
C Factor IX
D Factor X

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Q8 PA20.2 1 pt

CLINICAL VIGNETTE: A 32-year-old primigravida at 36 weeks gestation develops abruptio placentae and is transferred to the ICU. She begins oozing from IV sites and her gums. Investigations: platelets 35 × 10⁹/L; PT 28 s (control 12 s); aPTT 68 s (control 32 s); fibrinogen 0.8 g/L (normal >2 g/L); D-dimer markedly elevated; blood film shows schistocytes. Which best describes the underlying pathophysiology?

A Platelet antibody-mediated destruction in the spleen
B Systemic thrombin generation consuming platelets, fibrinogen, and coagulation factors
C Deficiency of ADAMTS13 causing platelet-rich microvascular thrombi
D Failure of vitamin K-dependent carboxylation of clotting factors

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Q9 PA20.2 1 pt

CLINICAL VIGNETTE: A 55-year-old man with decompensated cirrhosis presents with haematemesis. Investigations show: PT 22 s (INR 1.9), aPTT 55 s, platelets 60 × 10⁹/L, fibrinogen 1.6 g/L, D-dimer mildly elevated. Which feature best distinguishes this coagulopathy from DIC?

A Prolonged PT and aPTT are present
B Thrombocytopenia is present
C Fibrinogen is relatively preserved and D-dimer is only mildly elevated compared to DIC
D Schistocytes are absent

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Q10 PA20.1 1 pt

A 24-year-old man with known Haemophilia A undergoes a mixing study: his aPTT is 78 s (normal <38 s), and after 1:1 mixing with normal plasma his aPTT corrects to 36 s. A second patient with systemic lupus erythematosus has an aPTT of 72 s; after mixing with normal plasma the aPTT remains prolonged at 65 s. Which best explains the different mixing study results?

A The haemophilia patient has a factor inhibitor; the SLE patient has a factor deficiency
B The haemophilia patient has a factor deficiency; the SLE patient has an inhibitor (lupus anticoagulant)
C Both patients have factor deficiencies at different intrinsic pathway steps
D Both patients have inhibitors acting at different points in the common pathway

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Q11 PA20.2 1 pt

CLINICAL VIGNETTE: A 4-year-old boy presents with gingival bleeding and easy bruising for 3 weeks following a febrile illness. Platelet count is 22 × 10⁹/L. PT and aPTT are normal. Peripheral blood film shows no schistocytes and normal platelet morphology (small platelets). Direct antiglobulin test is negative. Which first-line management is most appropriate?

A Immediate platelet transfusion
B Intravenous immunoglobulin (IVIG) or corticosteroids
C Rituximab (anti-CD20)
D Splenectomy

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Q12 PA20.2 1 pt

A 14-year-old girl presents with heavy menstrual bleeding since menarche. Platelet aggregation studies show absent aggregation with ADP, collagen, and arachidonic acid, but normal agglutination with ristocetin. Platelet count is 240 × 10⁹/L and platelet morphology is normal. Which protein is deficient?

A GPIb/IX/V complex (vWF receptor)
B GPIIb/IIIa (fibrinogen receptor, αIIbβ3)
C von Willebrand factor
D ADAMTS13 protease

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Q13 PA20.2 1 pt

A 65-year-old man develops septicaemia following bowel perforation. Over 48 hours, progressive bleeding from wounds and catheter sites is noted. Investigations: PT 34 s, aPTT 72 s, platelets 28 × 10⁹/L, fibrinogen 0.5 g/L, D-dimer >10 µg/mL (markedly elevated), blood film shows schistocytes. Which single test result best distinguishes this coagulopathy from vitamin K deficiency?

A Prolonged PT
B Prolonged aPTT
C Markedly reduced fibrinogen with elevated D-dimer
D Thrombocytopenia

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Q14 PA20.1 1 pt

A 19-year-old man presents with spontaneous haemarthrosis of the left ankle and a deep thigh haematoma. His sister is a known carrier of haemophilia. Platelet count, PT, and bleeding time are normal. aPTT is prolonged; mixing study corrects. Specific factor assays show Factor IX activity at 2% of normal. Which statement correctly describes this condition?

A Haemophilia A; autosomal recessive; Factor VIII deficiency
B Haemophilia B; X-linked recessive; Factor IX deficiency
C Haemophilia B; autosomal recessive; Factor IX deficiency
D von Willebrand disease type 3; autosomal recessive; vWF deficiency

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