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Cardiovascular
Neutropenia and Normocytic Anaemia
Neutropenia
Differentials
Common: Acute infections (EBV, CMV, hepatitis, influenza)
Others: Autoimmune (SLE), bone marrow suppression (malignancies, chemo), drug reactions
When to Refer
WCC <1 × 10⁹/L
Persistent/recurrent infections
Systemic illness
Key Points
Febrile Neutropenia: Emergency → IV antibiotics
Severe/Prolonged: Consider G-CSF
Normocytic Anaemia
Differentials
Anaemia of chronic disease (RA, T2DM, HF, IHD, IBD)
Acute blood loss
Early iron deficiency
Haemolytic anaemia (e.g., sickle cell)
Key Points
Reticulocyte Count: Distinguish underproduction vs haemolysis
Haemolysis Workup: LDH, bilirubin, haptoglobin
Chronic Disease: Check CRP, ESR
Note:
Neutropenia: Acute infections are most common and often self-limiting
Normocytic Anaemia: Chronic inflammation suppresses erythropoiesis despite adequate iron
Neutropenia and Normocytic Anaemia
NEUTROPENIA
Differential Diagnoses
Acute Infections (viral: EBV, CMV, influenza, hepatitis)
Often self-limiting, mild neutropenia resolving once infection clears
Autoimmune Conditions (SLE, RA)
Immune-mediated peripheral destruction or bone marrow suppression
Bone Marrow Suppression
Malignancies (leukaemia, myelodysplastic syndromes), infiltration, aplastic anaemia
Chemotherapy or radiation-induced (common iatrogenic cause)
Drug-Induced
Certain antibiotics (trimethoprim-sulfamethoxazole), antipsychotics, anticonvulsants can cause neutropenia
Monitor FBC if on long-term or high-risk medications
When to Refer
WCC <1 × 10^9/L or severe neutropenia (ANC <0.5 × 10^9/L)
High risk of severe infections (bacterial/fungal)
Persistent / Recurrent Infections suggesting inadequate immune defence
Systemic Illness with unexplained cytopenias or suspicion of bone marrow failure
Key Points
Febrile Neutropenia: Medical emergency → urgent hospital referral for broad-spectrum IV antibiotics
Sepsis risk is high, especially with ANC <0.5 × 10^9/L
Severe / Prolonged Neutropenia
Consider G-CSF (granulocyte colony-stimulating factor) to stimulate neutrophil production if recurrent infections or post-chemotherapy
Evaluate marrow function (bone marrow biopsy if indicated)
Common, Mild Neutropenia
Often benign, especially with mild viral infections in children or transient autoimmune neutropenia
Monitor FBC trend over weeks to ensure recovery
NORMOCYTIC ANAEMIA
Differential Diagnoses
Anaemia of Chronic Disease (ACD) / Anaemia of Chronic Inflammation
Associated with RA, CKD, T2DM, HF, IBD, malignancies
Inflammatory cytokines reduce erythropoietin responsiveness and iron mobilisation
Ferritin often normal or elevated, low TIBC, normal/low serum iron
Acute Blood Loss
Initially normocytic before iron deficiency develops if bleeding continues
Early Iron Deficiency
MCV may remain normal initially, eventually becomes microcytic
Haemolytic Anaemia
RBC destruction (hereditary spherocytosis, sickle cell disease, autoimmune haemolysis)
Reticulocytosis with elevated unconjugated bilirubin, LDH, low haptoglobin
Key Investigations
Reticulocyte Count
Differentiates underproduction (low retic) vs increased RBC destruction or blood loss (high retic)
Haemolysis Workup
LDH, bilirubin, haptoglobin, peripheral smear (schistocytes, spherocytes, sickle cells)
Markers of Inflammation
CRP, ESR often elevated in chronic disease
Renal and Endocrine Status
CKD or hypothyroidism may present with normocytic anaemia
Bone Marrow Assessment
If unexplained cytopenias or suspicion of marrow pathology
Management
Anaemia of Chronic Disease
Address underlying inflammatory condition (RA control, infection treatment, better CKD management)
IV iron supplementation may help if functional iron deficiency present (low transferrin saturation, normal/high ferritin)
Erythropoiesis-stimulating agents in selected CKD patients with severe anaemia
Acute Blood Loss
Identify and treat source of bleeding (GI bleed, trauma)
RBC transfusion if haemodynamically unstable or Hb <70 g/L in most stable adults (target higher threshold in cardiac disease)
Early Iron Deficiency
Oral iron therapy (100–200 mg elemental iron daily) or IV iron if malabsorption or intolerance
Reassess MCV and iron studies over 2–3 months
Haemolytic Anaemia
Tailor therapy based on aetiology (e.g. steroids for autoimmune, hydroxycarbamide for sickle cell, splenectomy in certain conditions)
Supportive Care
Regular follow-up, monitor CBC trends to ensure response to therapy
Treat comorbidities (CKD, hypothyroidism) contributing to anaemia
Check for B12/folate deficiency if RBC indices shift or if clinical suspicion
Notes:
Neutropenia and normocytic anaemia may co-exist in marrow disorders (myelodysplasia) or systemic diseases (SLE, chronic infections)
Febrile Neutropenia requires urgent IV antibiotics and possible G-CSF if severe/prolonged
For normocytic anaemia, always check reticulocyte count to distinguish underproduction vs blood loss/haemolysis
Anaemia of Chronic Disease is common in older adults with multiple comorbidities (HF, T2DM, CKD) – treat underlying cause, consider IV iron if functional deficiency
Consider referral to haematology if complex aetiologies, persistent cytopenias, or uncertain diagnosis
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