Geriatrics and Haematology Flashcards

1
Q

What is vascular dementia?

A

Dementia arising after minor strokes

symptoms:
-Several months/years of sudden or stepwise deterioration of cognitive function
-Focal neurological abnormalities e.g. visual disturbance, sensory or motor symptoms
-difficulty with attention and concentration
-Seizures
-Memory disturbance
-Gait disturbance
-Speech disturbance
-Emotional disturbance

reduce chance of further strokes

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2
Q

How do you treat pressure ulcers?

A

-moist wound = Hydrocolloid dressings and hydrogels
-The use of soap should be discouraged to avoid drying the wound
-wound swabs should not be done routinely as the vast majority of pressure ulcers are colonised with bacteria. The decision to use systemic antibiotics should be taken on a clinical basis (e.g. Evidence of surrounding cellulitis)
-consider referral to the tissue viability nurse
-surgical debridement may be beneficial for selected wounds

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3
Q

What would be the treatment for hypochromatic microcytic anaemia and macrocytic Hyperchromatic anaemia?

A

Hypochromatic microcytic anaemia = iron

Hyperchromatic macrocytic anaemia = B12/folate

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4
Q

As Hodgkin’s lymphoma and non-Hodgkin’s lymphoma present similarly, how would you differentiate them?

A

Hodgkin’s lymphoma = Reed-Sternberg cells, pain with alcohol and B symptoms are earlier

Non-Hodgkin’s = B symptoms later

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5
Q

What scoring system is used for patients at risk of pressure ulcers?

A

Waterlow score

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6
Q

What are the symptomatic differences between B12 and folate deficiency?

A

B12 = pale, glossitis, mouth ulcers, pins and needles (paraesthesia), dementia

Folate = reduced sense of taste, diarrhoea, numbness and tingling in the feet and hands, muscle weakness

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7
Q

What would left lower quadrant pain and low-grade fever in an elderly patient suggest?

A

diverticulitis

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8
Q

How do you treat a DVT?

A

Wells score can be calculated

2 or more = high risk of DVT

high risk = ultrasound and then DOACs (apixaban for at least 3 months) unless ultrasound is negative then do a D-dimer—> use low weight heparin instead of DOACs if renal impairment or antiphospholipid syndrome

low risk = D-dimer and if this is positive do a ultrasound

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9
Q

What can taking ‘poppers’ cause and how do you treat it?

A

can cause Methaemoglobinaemia

Features:
-‘chocolate’ cyanosis
-a typical brownish blue coloration of the skin and mucous membranes and the brown coloured blood
-dyspnoea, anxiety, headache
-severe: acidosis, arrhythmias, seizures, coma
-normal pO2 but decreased oxygen saturation

Management:
-ascorbic acid
-IV methylene blue if acquired

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10
Q

What is myelofibrosis?

A

Features:
e.g. elderly person with symptoms of anaemia e.g. fatigue (the most common presenting symptom)
massive splenomegaly
hypermetabolic symptoms: weight loss, night sweats etc

Laboratory findings: anaemia
high WBC and PLATELET count early in the disease
‘tear-drop’ poikilocytes on blood film
unobtainable bone marrow biopsy - ‘dry tap’ therefore trephine biopsy needed
high urate and LDH (reflect increased cell turnover)

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11
Q

What level do you offer a platelet transfusion?

A

platelet count of <30 x 10 9 AND ARE SIGNIFICANTLY BLEEDING

platelet transfusions have the highest risk of bacterial contamination compared to other types of blood product

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12
Q

What is adult immune thrombocytopenia (ITP)?

A

immune related reduction in platelet

spetechiae
bleeding (epistaxis or gum bleeding)

isolated thrombocytopenia

full blood count
blood film

–> oral prednisolone but no treatment in children

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13
Q

How can you understand iron studies?

A

causes of macrocytic anaemia = B12 and folate deficiency, alcohol excess

microcytic anaemia = iron deficiency (ID) and anaemia of chronic disease (ACD)

iron studies shows the difference between these two ^
ID = transferrin and TIBC increases
ACD = transferrin and TIBC decreases

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14
Q

What scoring tool is used to assess frailty in the elderly?

A

PRISMA-7

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15
Q

What is haemochromatosis?

A

autosomal recessive of iron accumulation (HFE gene)

fatigue
erectile dysfunction
arthralgia (hands mostly)
bronze skin
diabetes

management:
1st line - venesection (monitor transferrin and serum ferritin)
2nd line - desferrioxamine

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16
Q

What is pernicious anaemia?

A

B12 deficiency

-fatigue
-dyspnoea
-pins and needles
-confusion, memory loss, poor concentration
-mild jaundice: combined with pallor results in a ‘lemon tinge’

‘test for anti intrinsic factor antibodies

** increased risk of gastric cancer**

3 injections per week for 2 weeks followed by 3 monthly treatment of vitamin B12 injections

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17
Q

What are the symptoms of sickle cell and differentials?
What are the investigations and management for sickle-cell anaemia?

A

Anaemia
Growth restriction
Splenomegaly
Recurrent infections
Jaundice

Rule out: thalassaemia, sepsis, autoimmune haemolytic anaemia

Blood film AND haemoglobin electrophoresis

acute:
pain relief
rehydrate
oxygen
blood transfusion
potential abx

chronic:
hydroxyurea
pneumococcal polysaccharide vaccine every 5 years

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18
Q

If a elderly patient with a history of Parkinson’s is admitted with confusion due to a UTI, what can be given to treat the confusion?

A

IM lorazepam (usually haloperidol but not here as the patient has Parkinson’s and same with lewy body dementia)

19
Q

How can you tell the difference between dementia with lewy bodies and parkinson’s disease dementia (PDD)?

A

it is more likely to be PDD if the patient has had parkinson’s for at least 1 year before cognitive decline

opposite for LBD

20
Q

What is frontotemporal dementia also known as and expalin it.

A

A= frontotemporal dementia
B= normal

“Pick’s disease”
-onset usually before 65
-change in personality
-impaired social conduct

atrophy on frontal and temporal lobes
tau protein (silver staining)

no treatment but can use antipsychotics (quetiapine) and antidepressants

**antipsychotics can increase mortality in dementia patients”

21
Q

What is polycythaemia vera?

A

-mutation in JAK2
-increase in red cells, platelets and neutrophils
-splenomegaly
-pruritus after hot baths

can progress to AML

–> aspirin and venesection

22
Q

What does dementia with Lewy bodies present like and how is it treated?

A

caused by accumulation of a-synuclein

-visual hallucinations
-cognitive decline WITH PERIODS OF LUCIDNESS
-parkinsons

DAT scan
clinical diagnosis

treatment:
-donepezil/rivastigmine (acetylcholinesterase inhibitors)
-memantine (NMDA antagonist)
-AVOID antipsychotics

23
Q

What blood tests should be done in a patient who is thought to have dementia?

A

a blood screen is usually sent to exclude reversible causes (e.g. Hypothyroidism).

NICE recommend the following tests: FBC, U&E, LFTs, calcium, glucose, ESR/CRP, TFTs, vitamin B12 and folate levels

24
Q

When can you not give acetylcholinesterase inhibitors e.g. donepezil, galantamine and rivastigmine?

A

asthma/COPD or if cardiac arrhythmias

25
Q

When can you not give NMDA antagonisst e.g. memantine?

A

in epilepsy

26
Q

What can cause acute confusion in the elderly?

A

-infection e.g. UTI
-constipation
-dehydration
-change in environment
-metabolic e.g. glucose/calcium levels

27
Q

What tools are used to recognise and manage medications safely?

A

STOPP - used to see risks vs benefits

START - used to suggest what medication may provide benefit

28
Q

What is mixed dementia?

A

vascular dementia and Alzheimer’s

29
Q

Lymph node pain when drinking alcohol?

A

Hodgkin’s lymphoma

30
Q

How do you treat Alzheimer’s?

A

group cognitive stimulation therapy or group reminiscence therapy and cognitive rehabilitation

Pharmacological management:
three acetylcholinesterase inhibitors:(donepezil, galantamine and rivastigmine)

Donepezil
is relatively contraindicated in patients with bradycardia

31
Q

What blood tests are included in a confusion screen?

A

TFT, B12, Folate & Glucose

32
Q

What type of psychological symptoms are seen with Alzheimer’s?

A

BPSD

behavioural and psychological symptoms of dementia

-depression
-agitation
-psychosis

33
Q

What is Von Willebrand’s disease?

A

Most common inherited bleeding disorder
Autosomal dominant

Prolonged bleeding time
APTT prolonged

—> tranexamic acid, desmopressin, factor 8 concentrate

34
Q

What is haemophilia?

A

X-linked recessive disorder
Haemophilia A = deficiency in factor 8
Haemophilia B (Christmas disease) = deficiency in factor 9

Normal bleeding time (prologned in VWD)
Prolonged APTT

35
Q

What is Hodgkin’s lymphoma/how to stage?

A

Risk factors: HIV and Epstein-Barr virus

Lymphadenopathy (neck)
Alcohol induced lymph node pain
‘B symptoms’:
Weight loss
Night sweats
Fever
Pruritus

High eosinophils
Anaemia
LDH raised
Lymph node biopsy (Reed-Sternberg cells)

Lugano classification/ Ann-Arbor staging

Chemo
Radiotherapy
Hematopoietic cell transplantation

36
Q

What is myeloma?

A

haematological malignancy: B-lymphocytes differentiate into mature plasma cells.

The median age at presentation is 70 years old.

Use the mnemonic CRABBI:
-Calcium: hypercalcaemia
-Renal: dehydration and increasing thirst
-Anaemia: fatigue and pallor
-Bleeding: thrombocytopenia
-Bones: increases the risk of pathological fractures
-Infection

Investigations:
-FBC, blood film, U+Es, bone profile
-Bone marrow aspiration: plasma cells is significantly raised
-Whole-body MRI
-X-rays: ‘rain-drop skull’

37
Q

What is the difference between Haemolytic uraemic syndrome, alpha thalassaemia and autoimmune haemolytic anaemia?

A

HUS:
-children with AKI, thrombocytopenia, haemolytic anaemia
-supportive treatment: fluid, blood transfusion, dialysis

Alpha thalassaemia:
-anaemia
-too much iron
-screening in pregnancy and newborn heel prick
-treatment: blood transfusions

Autoimmune haemolytic anaemia:
-anaemia, raised LDH
-positive Coombs’ test
-treatment: steroids +/- rituximab

38
Q

What type of cells are seen on blood films of hyposplenism, iron deficiency and myelofibrosis?

A

Hyposplenism: target cells, Howell-Jolly bodies

Iron deficiency: target cells, ‘pencil’ poikilocytes

Myelofibrosis: ‘tear-drop’ poikilocytes

39
Q

What are the symptomatic differences between myeloma and myleofibrosis?

A

myelofibrosis include:
Paleness
Shortness of breath
A feeling of fullness
Stomach pain
Itchy skin

myeloma:
Bone pain
Weakness or numbness in the arms or legs
Nausea or vomiting
Confusion

40
Q

What is thrombotic thrombocytopenic purpura (TTP)?

A

rare, typically adult females
fever
fluctuating neuro signs (microemboli)
microangiopathic haemolytic anaemia
thrombocytopenia
renal failure

Causes
post-infection e.g. urinary, gastrointestinal
pregnancy
drugs: ciclosporin, oral contraceptive pill, penicillin, clopidogrel, aciclovir
tumours
SLE
HIV

plasma exchange with high-dose corticosteroid therapy

41
Q

How do you treat folate deficiency anaemia?

A

Treat cause (diet/alcohol/pregnancy/coeliac’s/drugs) and give FOLIC acid supplements

If they also have a B12 deficiency then treat the B12 FIRST!!

42
Q

What are the 4 drugs that can cause LOW NEUTROPHILS?

A

4Cs

Carbamazepine
Clozapine
Colchicine
Carbimazole

43
Q

What could the differentials for Parkinson’s be?

A

-Parkinson’s disease
-parkinson’s drug induced
-lewy body dementia
-alzheimers
-PSP
-MSA

44
Q

What could be the differentials for alzheimer’s?

A

-dementia
-delerium
-vasulcar dementia
-frontotemporal demenia