GP and primary healthcare Flashcards

1
Q

Acne vulgaris

A

Acne vulgaris is a chronic inflammatory skin conditions affecting the face, back and chest.

Characterised by the blockage and inflammation of pilosebaceous unit (hair follicle)

Presents with non-inflammatory, inflammatory lesions (or a mixture)

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2
Q

Clinical features of acne vulgaris

A
  • Non-inflammatory lesions (comedones) must be present for a diagnosis
  • Papules and pustules (< 5mm)
  • Nodules or cysts (> 5mm)

Huge variety in clinical features depending on person and severity

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3
Q

Conservative management of acne vulgaris

A

Advice:

  • Avoid over-cleaning the skin
  • Use non-alkaline synthetic detergent cleansing product
  • Avoid oil-based comedogenic products
  • Treatment might irritate the skin at the start
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4
Q

Medical management for mild to moderate acne

A

1st line: 12 week course of any 2 of the following in combination:

  • Topical benzoyl
  • Topical antibiotics (clindamycin)
  • Topical retinoids (tretinoin adapalene)
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5
Q

Medical management for moderate to severe acne

A
  • 1st line: 12 week course of same medicines as above but different doses (NICE CKS)
  • Sometimes the combo topical creams combined with oral tetracycline and doxycycline
  • COCP as alternative to systemic abx for women
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6
Q

Acute stress reaction

A

Immediate and intense psychological response following exposure to traumatic event.

Appear within minutes of exposure and lasts from 3 days - 4 weeks after traumatic event.
If >1 month = PTSD

ICD10: https://icd.who.int/browse10/2019/en#/F43.0

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7
Q

Clinical features of Acute Stress Reaction

A

ICD10 criteria:
- Patient must have been exposed to an exceptional mental/physical stressor
- Exposure followed by immediate symptom onset (<1hr):

  • Social withdrawal
  • Dissociation
  • Anger
  • Despair/hopelessness
  • Inappropriate overactivity
  • Overwhelming anxiety/grief
  • Autonomic sypmtoms: tachycardia, sweating, flushing)

ICD10 book from Sheffield uni library and quesmed

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8
Q

Mangement of Acute Stress Reaction

A

1st line: trauma focused CBT, medications e.g. benozodiazepines for symptomatic relief

Consider differentials such as PTSD and adjustment disorder

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9
Q

Iron deficiency anaemia

A

Low Hb concentration in blood

Causes:

  • Dietary insufficiency, common in children
  • Loss of iron, e.g. heavy menstruation
    Inadequate iron absorption, e.g. IBD/Coeliac
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10
Q

Anaemia: Hb and Mean Cell Volume (MCV)

A

MCV = size of RBC

Women:
- Hb: 120 – 165 g/L
- MCV: 80-100 femtolitres (fL)

Men:
- Hb: 130 -180 g/L
- MCV: 80 - 100 fL
-

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11
Q

Causes of anaemia

A
  • Microcytic anaemia (low MCV)
  • Normocytic anaemia (normal MCV)
  • Macrocytic anaemia (large MCV)
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12
Q

Mmemonic for microcytotic anaemia

A

TAILS
T – Thalassaemia
A – Anaemia of chronic disease
I – Iron deficiency anaemia
L – Lead poisoning
S – Sideroblastic anaemia

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13
Q

Causes of normocytic anaemia

A

AAAHH

A – Acute blood loss
A – Anaemia of chronic disease
A – Aplastic anaemia
H – Haemolytic anaemia
H – Hypothyroidism

Anaemia of chronic disease often in CKD due to reduced erythropoietin production. Tx = erythropoietin

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14
Q

Causes of macrocytic anaemia

A
  • Megablastic (impaired DNA synthesis > large, abnormal cells): B12, folate deficiency
  • Normoblastic macrocytic anaemia: alcohol, reticulocytosis (usually from haemolytic anaemia or blood loss), hypothyroidism, liver disease, drugs (e.g. azathioprine)
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15
Q

Clinical features of anaemia

A
  • Tiredness
  • SOB
  • Headache
  • Dizziness
  • Palpitations
  • Worsening of angina, HF, PAD
  • IDA: pica, hair loss
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16
Q

Anaemia: signs on examination

A
  • Pale skin
  • Conjunctival pallor
  • Tachycardia
  • Increased RR
  • IDA: koilonychia, angular cheilitis, atrophic glossitis (smooth tongue), brittle hair + nails
  • Haemolytic anaemia: jaundice
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17
Q

Terms in iron-deficiency anaemia blood tests

A
  • Iron = ferric ions (Fe3+) in blood
  • Transferrin = carrier
  • Total iron binding capacity (TIBC) = available space on transferrin
  • Serum Ferritin = form of iron stored in cells, raised in inflammation

Normal ranges
Serum Ferritin: 41 - 400 ug/L

Serum Iron (variable throughout the day): 12 - 30 μmol/L

TIBC: 54 – 45 - 80 μmol/L

Transferrin sat: 15 - 50%

Transferrin sat (%) = serum iron/TIBC

Transferrin & TIBC = increase in IDA

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18
Q

Investigations for anaemia

A

Depends on suspected cause

  • FBC for Hb and MCV
  • Reticulocyte count (indicates red blood cell production)
  • Blood film
  • Renal profile for CKD
  • LFT for liver disease and bilirubin (raised in haemolysis)
  • Ferritin (iron)
  • B12 and folate
  • Intrinsic factor antibodies for pernicious anaemia
  • TFT for hypothyroidism
  • Coeliac disease serology (anti-TTG)
  • Myeloma screening (e.g., serum protein electrophoresis)
  • Haemoglobin electrophoresis for thalassaemia and sickle cell disease
  • Direct Coombs test for autoimmune haemolytic anaemia

Unexplained anaemia = bone marrow biopsy for leukaemia or myeloma

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19
Q

Management for iron deficiency anaemia

A

Unexplained IDA = colonscopy and oesophagogastroduodenoscopy (OGD) for malignancy

Tx:
- Oral iron (e.g., ferrous sulphate or ferrous fumarate)
- Iron infusion (e.g., IV CosmoFer)
- Blood transfusion (in severe anaemia)

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20
Q

Management of iron-deficiency anaemia in children

A
  • Tx underlying cause e.g. dietician for dietary deficiency
  • Supplements: ferrous sulphate or fumarate (not suitable for malabsorption IDA)
  • Rarely, blood transfusiion
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21
Q

Haemorrhoids

A
  • Enlarged anal vascular cushions
  • Associated with constipation and straining, pregnancy, obesity and increased intra-abdo pressure (e.g. weightlifting)

Anal cushion are specialised submucosal tissues that help control anal continence alongside internal and external anal sphincters.

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22
Q

Classification of haemorrhoids

A
  • 1st degree: no prolapse
  • 2nd degree: prolapse when straining and return on relaxing
  • 3rd degree: prolapse when straining, do not return on relaxing, but can be pushed back
  • 4th degree: prolapsed permanently
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23
Q

Clinical features of haemorrhoids

A
  • Asymptomatic
  • Painless, bright red bleeding, not mixed with stool (think ddx)
  • Sore, itchy anus
  • Lump around/inside anus
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24
Q

Examinations for haemorrhoids

A
  • External (prolapsed) haemorrhoids - swellings covered in mucosa
  • Internal - PR exam but difficult or not possible usually
  • Prolapse might be visible if pt asked to “bear down”
  • Proctoscopy needed to confirm dx
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25
Q

Differentials for rectal bleeding

A
  • Anal fissures
  • Haemorroids
  • Diverticulosis
  • Inflammatory bowel disease
  • Colorectal cancer
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26
Q

Management of haemorrhoids

A

Topical
- Anusol/Anusol HC (+hydrocortisone)+
- Germoloid (contains lidocaine)
- Proctosedyl ointment (cinchocine + HC)+

Non-surgical tx:

  • Rubber band ligation
  • Injection sclerotherapy (phenol oil to cause sclerosis and atropy)
  • Infrared coagulation
  • Bipolar diathermy (electrical current)

+ Short-term use only

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27
Q

Surgical tx for haemorrhoids

A
  • Haemorrhoidal artery ligation - cutting off blood supply to haemorroid
  • Haemorrhoidectomy - excision

Thrombosed haemorrhoids - caused by strangulation at base, resolve within a few weeks or admission + surgery if presents <72hrs with extreme pain.

28
Q

Tx for psoriasis

A

Main one in GP

Dovobet gel

29
Q

Eczema (atopic dermatitis)

A

Inflammatory skin condition characterised by dry, pruritic skin

Chronic and replasing

Usually dx < 5yo

Acute = flare-up

Chronic = chronic inflammation e.g. lichenification

30
Q

Presentation of eczema

A

Usually in childhood
- Sore, itchy skin in flexor surfaces, face, neck

  • Caused by defects in skin barrier that allow irritants, microbes and allergens to trigger immune response
  • Part of atopy (asthma, hayfever)
31
Q

Management of ezcema

A
  • Maintenance and management of flares

Maintenance: artifical skin barrier
- Emollients to apply and in shower

Avoid triggers: e.g. cold weather, washing powders, cleaning products, stress

Flares: thicker emollients, topical steroids, “wet wraps”1

Very severe flare require: IV abx, oral steroids, zinc impregnanted bandages, phototherapy, systemic immunosuppressant e.g. methothrexate

1 applying thick emollient and coering in wrap to lock moisture

32
Q

Emollients available for eczema

A

Use as thick as tolerated

Thin: E45, diprobase cream, cetraben, oilatum

Thick,greasy: 50:50 ointment (50% liquid paraffin), diprobase or centraben ointment

33
Q

Topical steroid ladder

A

Better to use stronger steroids for shortest time than weak steroids for a long time

Thin skin e.g. eyelids/face = weak

Thick skin e.g. palms = potent

  • Mild: Hydrocortisone 0.5%, 1% and 2.5%
  • Moderate: Eumovate (clobetasone butyrate 0.05%)
  • Potent: Betnovate (betamethasone 0.1%)
  • Very potent: Dermovate (clobetasol propionate 0.05%)
34
Q

Infections of the skin in eczema

A
  • Staphylococcus aureus = admission and IV abx
  • Eczema herpeticum1 = HSV/VZV. Viral swabs and aciclovir

1 Patients are very unwell with widespread, painful, vesicular rash and fever/lethargy.

35
Q

Atrophic Vaginitis

A
  • Dryness, atrophy and loss of elasticity of vaginal mucosa due to lack of oestrogen
  • More prone to inflammation
  • Change in vaginal pH and microbial flora = infection
  • Oestrogen = thicker vaginal and urinary tract epithelial lining, more secretions, elastic
36
Q

Presentation of atrophic vaginitis

A

Postmenopausal women:
- Itching
- Dryness
- Dyspareunia
- Bleeding (inflammation)
- Recurrent UTIs
- Stress incontinence
- Pelvic organ prolapse

37
Q

Signs on examination in atrophic vaginitis

A

Examine the labia and vagina
- Pale mucosa
- Thin skin
- Reduced skin folds
- Erythema and inflammation
- Dryness
- Thinning pubic hair

38
Q

Management of atrophic vaginitis

A

Vaginal lubricants e.g. Sylk, YES

Topical oestrogen = significant symptom improvements!

  • Estriol cream (applicator at night), pessaries (inserted at night), tablets, rings (3 monthly replacement)
  • CI in breast cancer, angina, VTE, monitor at least annually, stop tx if possible
39
Q

Bell’s palsy

A

Acute, sudden-onset, unilateral facial palsy, single episode, no constitutional symptoms, keratoconjunctibitis sicca (dry eye)

Cause: maybe HSV-1

Clinical dx of exclusion

Tx is high-dose corticosteroid e.g. prednisolone, eye protection (glasses, artifical tears)

Exclude Lyme’s disease-associated facial paralysis before tx as worsen outcome

40
Q

Eyelid disorders: blepharitis

A
  • Inflammation of eyelid margins
  • Gritty, itchy and dry sensation
  • Associated with dysfunction of Meibomian glands (secrets meibum (oil) onto eye surface)
  • Can lead to styes and chalazions
  • Mx = warm compress and gentle cleaning
41
Q

Eyelid disorder: stye

A

Hordeolum externum: infection of gland of Zeis and Moll, sebaceous and sweat glands at base of eyelashes

Hordeolum internum: infection of the Meibomian glands, deeper, more painful

Mx: hot compresses, analgesia, topical abx (e.g. chloramphenicol) if conjuctivitis or persistent

42
Q

Eyelid disorder: chalazion (Meibomian cyst)

A

Meibomian gland becomes blocked and swells. Swelling in eyelid, can be tender and red but usually not!

Mx: warm compresses, massage towards eyelashes to help drainage, surgical drainage might be needed

43
Q

Eyelid disorders: entropion

A

When eyelids turn inwards and lashes press against the eye

Pain, coneal damage and ulceration

Mx: tape eyelid to prevent inward turn, then refer to ophhalmology for surgery, same-day if risk to sight

44
Q

Eyelid disorder: ectropion

A

Eyelid turns outwards, exposing inner membrane

Usually bottom eyelids = exposure keratopathy as eyeball not lubricated and protected

Mx: mild cases = lubricating eye drops, severe cases = surgery, same-day referral to opthalmology if risk to sight

45
Q

Eyelid disorders: trichiasis

A

Inward growth of eyelashes, pain, corneal damage and ulceration

Mx: remove affected eyelashes, if recurrent then electrolysis, cryotherapy or laser tx to stop regrowth. Same-day ophthalmology referral if risk to sight

46
Q

Eyelid disorders: periorbital cellulitis

A

Infection of the eyelid and skin in front of the orbital septum (in front of the eye)

Swollen, red, hot skin around eyelid and eye

Tx with systemic (oral or IV) abx, can develop into orbital cellulitis so children etc. need admission and monitoring

Key ddx is orbital cellulitis = sight and life-threatening emergency

47
Q

Eyelid disorders: orbital cellulitis

A

Infection around eyelid of the tissue behind orbital septum

Pain on eye movement, reduced eye movement, vision changes, proptosis, abnormal pupil reactions

Emergency admission to opthalmology and IV abx per local policy, surgical drainage if abscess

48
Q

Benign paroxymal positional vertigo (BPPV)

A
  • Causes recurrent episodes of vertigo triggered by head movement
  • Variety of head movements trigger vertigo, e.g. turning over in bed, lasts 20 to 60s
  • Episodes over several weeks, then resolves, then reoccurs weeks or months later
  • Peripheral cause of veritgo = inner ear cause, not the brain
  • Does not cause hearing loss or tinnitus
49
Q

Pathophysiology of BPPV

A

Calcium carbonate crystals called otoconia that become displaced in the semicircular canals.

Causes: viral infection, head trauma, aging

Distruption of the endolymph flow through canals, confusing the vestibular system. Head movement = endolymph flow = vertigo

50
Q

Diagnosis of BPPV

A

Dix-Hallpike Manoeuvre

Dix for Dx

Triggers endolymph flow through semicicular canals

Positive signs = rotational nystagmus towards affected ear and vertigo

51
Q

BPPV treatment

A

Epley Manoeuvre to move crystals in semicircular canal to a position that does not disrupt endolymph flow.

52
Q

Benign Prostatic Hyperplasia (BPH)

A
  • Common in men > 50
  • Hyperplasia of stromal and epithelial cells of the prostate
53
Q

Presentation of BPH

A

Lower urinary tract symptoms (LUTS), typically:

FUNI: frequency, urgency, nocturia, intermittency (flow starts/stops)

SHID: (poor) stream, hesitancy, incomplete empyting, dribbling (terminal)

International prostate symptom score (IPSS) - socre to assess LUTS severity

54
Q

Assessment in BPH

A
  • Digital rectal exam (prostate exam)
  • Abdo exam for bladder
  • Urinary frequenct volume chart
  • Urine dipstick
  • PSA (unreliable)
55
Q

Benign vs cancerous prostate on examination

A

Benign prostate: smooth, symmetrical and soft, central sulcus

Cancerous:firm/hard, asymmetrical, craggy, irregular, loss of central sulcus

56
Q

Management of BPH

A
  • Mild = conservative

Medical:
- Alpha-blockers1 (e.g. tamsulosin) relax smooth muscle for symptoms
- 5-alpha reductase inhibtor2 (finasteride) for tx of BPH

Surgery:
- MC is transurethral resection of the prostate (TURP) - remove parts of prostate from inside of urethra

1 Key SE: postural hypotension, consider tamsulosin as cause of dizziness on standing/falls in older man
2 Key SE is erectile dysfunction

57
Q

Peripheral arterial (vascular) disease (PAD)

A

Narrowing of arteries supplying limbs and peripheries

Most common in lower limbs > intermittent claudication (ischaemia in a limb during exertion, better on rest)

Chronic limb-threatening ischaemia - end-stage of PAD, inadquate blood supply to limb even at rest.

58
Q

Presentation of PAD

A

Intermittent claudication - crampy achy pain in calf, thigh or buttock muscles when walking beyond a certain distance

Chronic limb threatening ischaemia - burning pain at rest, worse at night, non-healing ulcers and gangrene

59
Q

PAD: signs on examination

A

Generally, peripheral arterial disease:
- Skin pallor
- Cyanosis
- Depedent rubor (deep red when limb is lower than body)
- Muscle wasting
- Hair loss
- Ulcer
- Poor woundhealing
- Reduced skin temp
- Reduced sensation
- CRT > 2s
- Positive Buerger’s test

60
Q

Atherosclerosis is the underlying cause of PAD, what are the risk factors of atherosclerosis?

A

Non-modifiable risk factors: older age, FHx, male

Modifiable risk factors:

  • Smoking
  • Alcohol consumption
  • Poor diet (high in sugar and trans-fat and low in fruit, vegetables and omega 3s)
  • Low exercise / sedentary lifestyle
  • Obesity
  • Poor sleep
  • Stress

Medical co-morbidities that increase the risk:
- Diabetes
- HTN
- CKD
- Inflammatory conditions e.g. RA
- Atypical antipsychotics

Tom tip: make sure to think and ask about RFs when taking a hx from someone with atherosclerotic disease: exercise, diet, PMH, FHx, occupation, smoking, alcohol, meds

61
Q

Acute limb ischaemia

A

Occurs when a thrombus blocks the arterial supply of a distal limb.

6Ps
- Pain
- Pallor
- Pulseless
- Paralysis
- Paraesthesia (abnormal sensation or “pins and needles”)
- Perishing cold

62
Q

Leriche syndrome

A

Occlusion in distal aorta or proximal common iliac artery
- Thigh/buttock claudication
- Absent femoral pulses
- Male impotence

63
Q

PAD: Buerger’s Test

A

Assesses for PAD in legs

Part one: patient lies supine, straight leg lift 45 degrees for 1 - 2 mins, PAD = pallor

Part two: patient sits up with legs dangling, in PAD:

  • Blue initially as ischaemic tissue deoxygenates blood
  • Dark red (rubor) after due to vasodilation from waste products from anaerobic respiration
64
Q

Investigations for PAD

A
  • Ankle-bracgial pressure index