Saturday, September 24, 2016

Bronchial Asthma

Bronchial Asthma - the chronic inflammatory disease of the airway
Bronchial asthma is characterised by chronic airway inflammation, bronchial hyperreactivity and reversible airway obstruction (bronchoconstriction, mucosal oedema, increased mucus production)

Status asthmaticus is a refractory state of acute severe asthma that does not respond to standard therapy

2. Asthma is more common in children but there has been a rapid increase in adult-onset asthma lately. Males are more likely to affected than females.

3. Various trigger factors contribute to asthma.
Allergens - dust mites, pollen, dander
Bronchial infection
Cold air
Exercise
Drugs - aspirin, NSAIDs, beta-blockers
Emotions and stress
Various food
Hormones
Irritants - smoke, perfumes, smell, wood dust, etc

Extrinsic (allergic) asthma develops in patients who are prone to develop IgE antibodies.

Intrinsic (non-allergic) asthma is a manifestation in response to RTI or physosocial stressors.

4. The chief complaints are typically: cough, tightness, wheezing, dyspnoea. The symptoms often worsen at night which result in frequent awakening. If etiology is present, it worsens the symptoms. There is usually a medical history of allergies or atopies. Family history of asthma or other atopy must be noted.

Patients who smoke should be advised to stop smoking.

5. Physical examination is important to determine the severity of exacerbation. The patient may present with tachypnoea, tachycardia, usage of accessory muscles and pulsus paradoxus. On chest examination, there is hyperinflation of the chest, hunch shoulders and deformities - Harrison sulcus, pectus carinatum. Auscultation of the lungs - wheezing, prolonged expiratory phase

Be aware of dangerous signs of status asthmaticus such as paradoxical abdominal and diaphragmatic movements, pulsus paradoxus, altered mental status and silent chest (absence of wheezing). The patient may be also cyanotic and febrile. At a later stage there may be bradycardia and hypotension

6. The diagnosis of bronchial asthma is done via history taking, physical examination and confirmation through spirometry. A demonstration of reversibility more than 12% post-bronchodilator administration is diagnostic of asthma.

Pulse oximetry is monitored for oxygen saturation and supplemental oxygen given, aim to achieve >90% saturation.

Blood tests like FBC may reveal leukocytosis and eosinophilia.

Severe attacks of asthma, ABG may be needed to evaluate arterial pH levels, hypoxaemia and hypercarbia. In severe attacks, there is usually acidosis secondary to hypoventilation.

Chest X-rays are not recommended unless there is suspicion of complications.

Other tests that may be of help to identify trigger factors include bronchial provocation test and skin prick test.

7. The principles of management is to choose the treatment based on the severity. A stepwise approach to managing asthma is meant to assist decision-making.

In summary,
i. SABA prn
ii. + low dose ICS
iii. + low dose ICS and LABA
iv. + medium dse ICS and LABA
v. + high dose ICS and LABA
vi. + high dose ICS, LABA and oral corticosteroid

Consider monoclonal antibodies in step 5 and above if available (omalizumab)
Alternatives may be used in lower steps - theophylline, cromolyn
In children, leukotrine antagonists such as montelukast and zafirlukast is effective.

Patients are also educated on avoidance of trigger factors, warm-up exercise or SABA administration 5 minutes pre-exercise or LABA usage prior to exercise.

About one third of the patients fail to respond to treatment because of wrong technique. All patients should be re-educated on proper usage of and techniques.

8. Status asthmaticus is a medical emergency. Upon diagnosis of severe asthma,

i. oxygen supplementation 8L/min by mask is given to maintain SpO2 above 95%.
ii. high dose salbutamol or continuous nebulized 0.5% salbutamol
iii. IV prenisolone 250mg
iv. measure ABG, CXR for complications
v. if no improvement, IV MgSO4 25-100mg/kg over 20 minutes
vi. still no improvement, intubation with PPV

9. The complications of asthma include increased risk of influenza, pneumonia, pneumothroax, pneumomediastinum, COPD and iatrogenic Cushing syndrome.



Thursday, September 8, 2016

Psoriasis and Psoriatic Arthritis

Psoriasis and Psoriatic Arthritis
Psoriasis is a chonic skin disorder characterised by excessive proliferation of keratinocytes resulting in formation of thickened scaly plaques, itching and inflammatory changes in epidermis and dermis.
Types: guttate, pustular, arthritis
2. There is a strong genetic component in the pathogenesis of psoriasis. Certain ethnicity such as Indians; HLA/MHC; Familial clustering; are associated with psoriasis.
Patients with celiac disease also have higher prevalence of psoriasis.
3. Psoriatic lesion is erythematous papule topped by loosely adherent scale.
Chronic plaques are symmetric, sharply demarcated, erythematous and silvery scale affecting the intergluteal folds, elbow, scalp, fingernails, toenails and knees.
Koebner's Phemomenon is the development of psoriatic lesion at traumatic sites (sunburn, scratch)
Auspitz sign may be demonstrated by scraping the scale which results in bleeding points.
Nail involvement is common - pitting nail plate, hyperkeratosis, onychodystrophy and onycholysis.
Patients often complain of variable pruritus, soreness and bleeding.
** The biggest impact of psoriasis is the psychosocial functioning of patients!
4. Guttate form occurs after streptococcal pharyngitis - multiple droplike lesions on the extremities and trunk.
5. Arthritic form is classified as seronegative spondyloarthritis and manifests as arthritis, dactylitis, spondylitis and enthesitis.
Arthritis is inflammatory in nature - symptoms of prolonged morning stiffness, joint erythema, warmth, swelling and joint effusion
Distribution of joint involvement: DIPJ type, symmetric type, asymmetric oligoarthritis, axial type and arthritis mutilans.
Dactylitis - diffuse swelling of digit
Enthesitis - inflammation at site of insertion of tendon into bone. Usually occurs at Archilles tendon-calcaneus. Manifests as swelling and tenderness.
Spondyloarthritis - sacroilitis, axial spine inflammation
Other manifestation - conjunctivitis and uveitis
6. Psoriasis is diagnosed clinically. Blood result and skin biopsy are rarely needed for confirnation.
Psoriatic Arthritis is diagnosed using Classification Criteria for Psoriatic Arthritis (CASPAR) - Score of 3 or higher is diagnostic
Thus laboratory workouts are tailored according to CASPAR. Acute phase reactants (ESR, CRP) is often raised. FBC may show anaemia of chronic illness. RF and ACPA is negative in 90% of the cases.
Radiological investigations of involved joints may show soft tissue swelling, joint space narrowing, subluxation, erosive changes. New bone formation such as periostitis and fusion may also occur. Digital erosive changes with adjacent heterotopic bone formation may result in "pencil in cup" deformity.
Other workouts if available include: identification of HLA B27, arthrocentesis to rule out crystal deposition disease and inflammatory synovial fluid.
7. Treatment of Psoriasis can be divided into non-pharmacological and pharmacological therapy:
Non-pharmacological therapy:
sunbathing
eliminating triggering factors
warm water bath and skin moisturisers
local hyperthermia
surgical taping or dressing
Pharmacological therapy:
topical steroids +/- aspirin cream
calcipotriene
tar product
anthralin
retinoids
oral PUVA (psoralen + exposure to UV)
methotrexate, cyclosporin, apremilast
TNF inhibitors
8. Treatment of Psoriatic Arthritis:
NSAIDs to alleviate symptoms in mild involvement
Intraarticular corticosteroid injections
DMARDs considered early in disease, if fail,
TNF inhibitors - infliximab, adalimumab, etanercept