| 🩸 Disseminated Intravascular Coagulation |
- Bleeding from venepuncture sites, gums, GI tract or wounds.
- Petechiae, ecchymoses, purpura or skin necrosis.
- Microvascular thrombosis causing renal, respiratory or neurological dysfunction.
- Usually secondary to sepsis, trauma, malignancy, obstetric catastrophe or major haemorrhage.
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- FBC: thrombocytopenia.
- Prolonged PT and APTT.
- Raised D-dimer.
- Low fibrinogen, especially in severe/obstetric DIC.
- Blood film may show schistocytes.
- Check lactate, renal function and underlying cause.
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- Treat underlying cause urgently.
- Sepsis pathway and IV antibiotics if infection suspected.
- Blood products guided by bleeding and labs: platelets, FFP, cryoprecipitate/fibrinogen concentrate.
- Haematology and ICU input if severe bleeding, shock or organ failure.
- Heparin only in selected predominantly thrombotic DIC under specialist advice.
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| 🧠 Thrombotic Thrombocytopenic Purpura |
- Thrombocytopenia plus microangiopathic haemolytic anaemia.
- Neurological symptoms: confusion, headache, seizures, stroke-like episodes.
- Fever, renal impairment, abdominal pain or cardiac involvement may occur.
- The classic pentad is uncommon - do not wait for all five features.
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- FBC: severe thrombocytopenia.
- Blood film: schistocytes.
- LDH and bilirubin raised; haptoglobin low.
- Coagulation usually normal or near-normal, unlike DIC.
- ADAMTS13 activity and inhibitor testing, but do not delay treatment.
- Use PLASMIC score if locally used.
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- Urgent haematology emergency.
- Plasma exchange urgently.
- High-dose corticosteroids.
- Caplacizumab and rituximab may be used under specialist guidance.
- Avoid platelet transfusion unless life-threatening bleeding or essential procedure.
- Transfer to specialist TTP centre if needed.
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| 💉 Heparin-Induced Thrombocytopenia |
- Platelet fall usually 5–10 days after heparin exposure.
- Platelet count falls by >50% from baseline, even if still “normal”.
- Venous or arterial thrombosis: DVT, PE, limb ischaemia, stroke, MI.
- Skin necrosis or acute systemic reaction after heparin bolus may occur.
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- Calculate 4Ts score to estimate probability.
- FBC trend and blood film to exclude pseudothrombocytopenia.
- HIT immunoassay and functional assay according to local lab pathway.
- Imaging for thrombosis if symptoms/signs.
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- Stop all heparin immediately, including flushes and heparin-coated lines.
- Start non-heparin anticoagulation if intermediate/high probability and bleeding risk acceptable.
- Options include argatroban, fondaparinux or DOAC depending on clinical setting/local policy.
- Avoid platelet transfusion unless serious bleeding.
- Avoid starting warfarin until platelets recover and specialist plan in place.
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| 🧪 Acute Haemolytic Transfusion Reaction |
- Fever, chills, rigors during or soon after transfusion.
- Flank/back pain, chest pain, dyspnoea, hypotension.
- Haemoglobinuria, dark urine or renal failure.
- DIC, shock and death can occur.
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- Stop transfusion and check patient/sample identity.
- Send blood bag and giving set to transfusion lab.
- Repeat FBC, U&E, clotting, LDH, bilirubin, haptoglobin.
- Direct antiglobulin test.
- Blood cultures if bacterial contamination possible.
- Urine for haemoglobin.
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- Stop transfusion immediately.
- Maintain IV access with sodium chloride 0.9% using a new giving set.
- Call senior clinician and transfusion lab.
- ABCDE, fluids, treat shock, monitor urine output.
- Manage DIC/AKI with haematology, renal and ICU support.
- Do not restart the unit.
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| 🧬 Acute Leukaemia with Tumour Lysis Syndrome |
- Fatigue, pallor, fever, bruising, bleeding or infections.
- Bone pain, lymphadenopathy, hepatosplenomegaly.
- TLS: nausea, weakness, arrhythmia, seizures, AKI.
- Electrolyte pattern: hyperkalaemia, hyperphosphataemia, hypocalcaemia, hyperuricaemia.
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- FBC and blood film: blasts, anaemia, thrombocytopenia or high WCC.
- U&E, calcium, phosphate, urate, LDH, creatinine.
- Clotting/fibrinogen, especially if acute promyelocytic leukaemia suspected.
- ECG if hyperkalaemia/hypocalcaemia.
- Bone marrow and flow cytometry under haematology.
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- Urgent haematology referral.
- IV hydration and close fluid balance.
- Rasburicase or allopurinol according to TLS risk/local policy.
- Correct life-threatening electrolytes immediately.
- Avoid potassium/phosphate-containing fluids.
- Renal/ICU support if severe TLS or AKI.
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| 🧫 Neutropenic Sepsis |
- Fever, rigors or sepsis in a patient receiving chemotherapy or with neutropenia.
- May be afebrile or subtly unwell, especially older or immunosuppressed patients.
- Symptoms may be minimal despite severe infection.
- Common sources: line infection, chest, urinary, skin, gut translocation.
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- FBC: neutrophils often <0.5 × 10⁹/L, or expected to fall.
- Blood cultures including central line cultures if present.
- U&E, LFT, CRP, lactate, glucose.
- Urine, sputum, CXR or other tests guided by symptoms.
- Do not delay antibiotics for investigations.
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- Medical emergency: give IV antibiotics urgently according to local neutropenic sepsis policy.
- Use sepsis pathway and assess NEWS2.
- IV fluids and oxygen if needed.
- Early haematology/oncology and microbiology advice.
- Consider ICU if shock, hypoxia or organ dysfunction.
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| 🧯 Severe Thrombocytopenia / Major Bleeding |
- Petechiae, bruising, epistaxis, gum bleeding, menorrhagia or GI bleeding.
- Severe headache, neurology or trauma raises concern for intracranial bleeding.
- Causes include ITP, marrow failure, sepsis, DIC, drugs, TTP, leukaemia.
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- Repeat FBC and blood film to exclude platelet clumping.
- Coagulation, fibrinogen, D-dimer if DIC possible.
- Haemolysis screen if TTP suspected.
- Medication review.
- Bone marrow tests if marrow failure/malignancy suspected.
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- Assess bleeding site and severity.
- Platelet transfusion for major/life-threatening bleeding or procedures, guided by haematology.
- In ITP, use steroids/IVIG for significant bleeding under specialist advice.
- Avoid platelet transfusion in suspected TTP unless life-threatening bleeding.
- Stop antiplatelets/anticoagulants if safe and clinically appropriate.
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| 🫁 Massive PE with Haemodynamic Instability |
- Sudden breathlessness, pleuritic chest pain, syncope or collapse.
- Hypotension, shock, hypoxia and tachycardia.
- Signs of right heart strain: raised JVP, loud P2, RV dysfunction.
- May complicate malignancy, thrombophilia, surgery or immobility.
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- CTPA if stable enough.
- Bedside echo may show RV strain in unstable patient.
- ECG: sinus tachycardia, RBBB or right heart strain; S1Q3T3 is uncommon.
- Troponin/BNP may support risk stratification.
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- ABCDE, oxygen, IV access and senior/ICU input.
- Anticoagulation if no contraindication.
- Systemic thrombolysis for high-risk PE with shock, unless contraindicated.
- Consider catheter-directed therapy or surgical embolectomy if thrombolysis contraindicated/fails.
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| 🧬 Sickle Cell Acute Painful Episode |
- Severe bone, chest, abdominal or limb pain.
- May have fever, dehydration or anaemia.
- Triggers: infection, cold, dehydration, hypoxia, stress.
- Always look for complications, not just pain.
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- Pain score and observations including oxygen saturations on air.
- FBC, reticulocytes, U&E, LFT, CRP if clinically indicated.
- Group and save if severe anaemia/possible transfusion.
- CXR if chest symptoms, hypoxia or fever.
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- Offer analgesia within 30 minutes of presentation.
- Use patient’s individual care plan if available.
- Oxygen if hypoxic.
- Hydration: avoid both dehydration and fluid overload.
- Antibiotics if infection suspected.
- Haematology advice for severe pain, anaemia, pregnancy or complications.
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| 🫁 Sickle Acute Chest Syndrome |
- Chest pain, cough, fever, wheeze or breathlessness.
- Hypoxia or falling oxygen saturations.
- New pulmonary infiltrate on CXR.
- Can progress rapidly to respiratory failure.
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- CXR.
- Oxygen saturations and ABG/VBG if severe.
- FBC, reticulocytes, U&E, LFT, CRP, blood cultures if febrile.
- Group and save/crossmatch.
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- Admit and involve haematology early.
- Oxygen, analgesia and careful fluids.
- Broad-spectrum antibiotics according to local policy.
- Incentive spirometry if able.
- Simple or exchange transfusion if severe, worsening hypoxia or specialist indication.
- ICU if respiratory failure or rapid deterioration.
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| 🌊 Hyperviscosity Syndrome |
- Headache, dizziness, confusion or visual disturbance.
- Mucosal bleeding, retinal haemorrhages or papilloedema.
- Dyspnoea, heart failure or neurological deficits.
- Associated with Waldenström macroglobulinaemia, myeloma, very high WCC or polycythaemia.
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- FBC, blood film and plasma viscosity/serum viscosity if available.
- U&E, calcium, immunoglobulins, serum protein electrophoresis/free light chains.
- Fundoscopy for retinal changes.
- Assess for end-organ compromise.
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- Urgent haematology referral.
- Plasma exchange for paraprotein-related hyperviscosity.
- Leukapheresis may be considered in selected leukostasis cases.
- Hydration and treat underlying disorder.
- Avoid red cell transfusion before viscosity addressed unless life-threatening anaemia and specialist advice.
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| ⚪ Hyperleucocytosis / Leukostasis |
- Very high WCC, usually acute leukaemia.
- Respiratory symptoms: dyspnoea, hypoxia, pulmonary infiltrates.
- Neurological symptoms: headache, confusion, visual changes, stroke-like features.
- May coexist with DIC or tumour lysis.
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- FBC and urgent blood film.
- U&E, calcium, phosphate, urate, LDH.
- Clotting/fibrinogen.
- CXR/CT if respiratory symptoms.
- Flow cytometry/bone marrow under haematology.
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- Urgent haematology emergency.
- IV hydration and TLS prophylaxis/treatment.
- Cytoreduction with hydroxycarbamide or urgent chemotherapy under specialist direction.
- Leukapheresis may be considered in selected cases.
- Avoid unnecessary red cell transfusion until specialist advice because it can worsen viscosity.
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