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3MG TRIAL MAGNESIUM’S ROLE IN THE TREATMENT OF ASTHMA
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BACK GROUND OF ASTHMA GUIDELINES BTS guidelines 2012 for asthma categorizes presentation into severity and helps guide treatment with regards to the category
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BTS - MODERATE EXACERBATION ASTHMA increasing symptoms PEF >50-75% best or predicted No features of acute severe asthma
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BTS - ACUTE SEVERE ASTHMA Any one of following; PEF 33-50% best or predicted respiratory rate ≥25/min heart rate ≥110/min inability to complete sentences in one breath
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LIFE THREATENING EXACERBATION OF ASTHMA In a patient with acute severe asthma with any one of PEF <33% best or predicted SpO2 <92% PaO2 <8 kPa normal PaCO2 (4.6-6.0 kPa) silent chest/cyanosis/poor respiratory effort Arrhythmia/exhaustion/altered conscious level
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NEAR FATAL ASTHMA Raised PaCO2 Requiring mechanical ventilation with raised inflation pressures
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BTS GUIDELINES FOR TREATMENT - NEBULISERS Give supplementary oxygen to all hypoxaemic patients with acute asthma to maintain an SpO2 level of of 94-98% Nebulised β2 agonist bronchodilators should be driven by oxygen. Use high dose inhaled β2 agonists as first line agents in acute asthma and administer as early as possible. Reserve intravenous β2 agonists for those patients in whom inhaled therapy cannot be used reliably In patients with severe asthma that is poorly responsive to an initial bolus dose of β2 agonist, consider continuous nebulisation with an appropriate nebuliser
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BTS GUIDELINES FOR TREATMENT- STEROIDS Give steroids in adequate doses in all cases of acute asthma. Continue prednisolone 40-50 mg daily for at least five days or until recovery.
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BTS GUIDELINES FOR TREATMENT – MG++ Consider giving a single dose of IV magnesium sulphate for patients with: acute severe asthma who have not had a good initial response to inhaled bronchodilator therapy life threatening or near fatal asthma. IV magnesium sulphate (1.2-2 g IV infusion over 20 minutes) should only be used following consultation with senior medical staff.
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BTS GUIDELINES - ANTIBIOTICS Routine prescription of antibiotics is not indicated for patients with acute asthma.
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BTS GUIDELINES – ITU REFERRAL Refer any patient: requiring ventilatory support with acute severe or life threatening asthma, failing to respond to therapy, evidenced by: - deteriorating PEF - persisting or worsening hypoxia - hypercapnea + - ABG analysis showing pH or H - exhaustion, feeble respiration - drowsiness, confusion, altered conscious state - - -respiratory arrest
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THE TREATMENT OF INTEREST FOR THIS PODCAST; MG++ As the BTS guidelines states; ‘Consider giving a single dose of IV magnesium sulphate for patients with: acute severe asthma who have not had a good initial response to inhaled bronchodilator therapy life threatening or near fatal asthma’
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THE PAPER Entitled ‘Intravenous or nebulised magnesium sulphate versus standard therapy for severe acute asthma (3Mg trial); a double blind, randomised control trial Published Lancet June 2013 Lead author – Steve Goodacre
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AUTHORS REASON FOR CONDUCTING THE TRIAL Stepwise approach to exacerbations of asthma including, O2, nebulisers, steroids They note the delay in onset of action of corticosteroids and pondered if magnesium could bridge the gap from minutes of action delivered with nebs to the hours due to steroids
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AUTHORS DILEMA RE. NEBULIZED VS IV MAGNESIUM FOR ASTHMA Neb Pro’s Quicker onset of action Decreased side effects No i.v. access required Neb Con’s Reduced dose delivery
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AUTHORS REASON FOR CONDUCTING THE TRIAL Current evidence draws differing conclusions on the effectiveness of treatment and none had directly compared the effect of nebulised vs intravenous administrations
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THE PAPER P>15 years old attending the ED with acute severe asthma (PF 25bpm, HR> 110 bpm, inability to complete sentences in 1 breath Exclusions – life threatening features, CI’s to the treatment (pregnancy, hepatic/renal failure, heart block or known hypermagnesaemia. Unable to consent, previous enrollment in the 3Mg study, previous use of Mg in the past 24 hour I Double blinded, multicentre, randomised placebo controlled trial across 34 UK ED’s of just over 1100 patients. Patients received either 2g i.v. Mg ++ (over 20 minutes)/ 1.5g nebulised Mg++ (7.5ml) at 20 minute intervals/placebo. In the first 2 groups placebos were also given being nebulised N saline and i.v. N Saline over the same timeframe. Patients also received standard BTS therapy for acute severe asthma. Data was collected until 2 hours after randomisation. Patients, staff and researchers were blinded to treatment allocations. C 2 primary outcomes; proportion of patients admitted to hospital on that ED visit or within 7 days & breathlessness measured on a 100 mm VAS in the 2 hours after initiation of the treatment OHospital admission was not affected in a statistically significant manner between active treatments and placebo (i.v. Mg++ OR 0.84 95% CI 0.61-1.15, neb Mg++ OR 0.76 95% CI 0.53-1.10) Mean improvements in VAS did not differ between active treatments and placebo (i.v. Mg++ 2.6mm 95% CI -1.6 to 6.8mm and nebulised Mg++ -2.6mm 95% CI -7.0 to 1.8mm) (NB a positive value reflects a greater improvement than placebo)
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PAPER Strengths Double blinded RCT Multicentre Received current gold standard of treatment Weaknesses Study sample was under powered
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HOW WILL THIS PAPER AFFECT MY PRACTICE In the adult patient presenting with acute severe asthma there is no evidence to suggest benefit either in symptomatic relief as measured on the VAS or likelihood of hospital admission Beware that in acute severe asthma when the BTS guidelines state ‘consider mg++ in patients with acute severe asthma who have not had a good initial response to inhaled bronchodilator therapy’ that there may not be a good response/any at all
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REFERNECES https://www.brit-thoracic.org.uk/document-library/clinical- information/asthma/btssign-asthma-guideline-quick- reference-guide/ Goodacre, Steve et al. Intravenous or Nebulised Magnesium Sulphate Versus Standard Therapy for Severe Acute Asthma (3Mg Trial): a Double-Blind, Randomised Controlled Trial. The Lancet Respiratory Medicine 1, no. 4 (June 2013): 293–300. doi:10.1016/S2213-2600(13)70070-5. doi:10.1016/S2213-2600(13)70070-5.
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