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BNF for Children 2011-2012

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<strong>BNF</strong>C <strong>2011</strong>–<strong>2012</strong> 2.4 Beta-adrenoceptor blocking drugs 87Neonatal seizures (section 4.8.1). By intravenous infusionNeonate initially 2 mg/kg over 10 minutes, followedby 6 mg/kg/hour <strong>for</strong> 6 hours; reduce doseover the following 24 hours (4 mg/kg/hour <strong>for</strong> 12hours, then 2 mg/kg/hour <strong>for</strong> 12 hours)Note Preterm neonates may require lower dosesEye section 11.7Local anaesthesia section 15.2Administration <strong>for</strong> intravenous infusion, dilute withGlucose 5% or Sodium Chloride 0.9%Lidocaine (Non-proprietary) AInjection 1%, lidocaine hydrochloride 10 mg/mL, netprice 2-mL amp = 21p; 5-mL amp = 26p; 10-mL amp= 39p; 20-mL amp = 78pInjection 2%, lidocaine hydrochloride 20 mg/mL, netprice 2-mL amp = 32p; 5-mL amp = 31p; 10-mL amp= 60p; 20-mL amp = 80pInfusion, lidocaine hydrochloride 0.1% (1 mg/mL)and 0.2% (2 mg/mL) in glucose intravenous infusion5%. 500-mL containersMinijet c Lidocaine (UCB Pharma) AInjection, lidocaine hydrochloride 1% (10 mg/mL),net price 10-mL disposable syringe = £8.48; 2%(20 mg/mL), 5-mL disposable syringe = £8.182.4 Beta-adrenoceptorblocking drugsBeta-adrenoceptor blocking drugs (beta-blockers) blockthe beta-adrenoceptors in the heart, peripheral vasculature,bronchi, pancreas, and liver.Many beta-blockers are available but experience inchildren is limited to the use of only a few.Differences between beta-blockers may affect choice.The water-soluble beta-blockers, atenolol and sotalol,are less likely to enter the brain and may there<strong>for</strong>e causeless sleep disturbance and nightmares. Water-solublebeta-blockers are excreted by the kidneys and dosagereduction is often necessary in renal impairment.Some beta-blockers, such as atenolol, have an intrinsicallylonger duration of action and need to be given onlyonce daily. Carvedilol and labetalol are beta-blockerswhich have, in addition, an arteriolar vasodilating actionand thus lower peripheral resistance. Although carvediloland labetalol possess both alpha- and beta-blockingproperties, these drugs have no important advantagesover other beta-blockers in the treatment of hypertension.Beta-blockers slow the heart and can depress the myocardium;they are contra-indicated in children withsecond- or third-degree heart block. Sotalol may prolongthe QT interval, and it occasionally causes lifethreateningventricular arrhythmias (important: particularcare is required to avoid hypokalaemia in childrentaking sotalol).Beta-blockers can precipitate asthma and should usuallybe avoided in children with a history of asthma orbronchospasm. If there is no alternative, a child withwell-controlled asthma can be treated <strong>for</strong> a co-existingcondition (e.g. arrhythmia) with a cardioselective betablocker,which should be initiated with caution at a lowdose by a specialist and the child monitored closely <strong>for</strong>adverse effects. Atenolol and metoprolol have less effecton the beta 2 (bronchial) receptors and are, there<strong>for</strong>e,relatively cardioselective, but they are not cardiospecific;they have a lesser effect on airways resistance butare not free of this side-effect.Beta-blockers are also associated with fatigue, coldnessof the extremities, and sleep disturbances with nightmares(may be less common with the water-solublebeta-blockers, see above).Beta-blockers can affect carbohydrate metabolism causinghypoglycaemia or hyperglycaemia in children withor without diabetes; they can also interfere with metabolicand autonomic responses to hypoglycaemia therebymasking symptoms such as tachycardia. However, betablockersare not contra-indicated in diabetes, althoughthe cardioselective beta-blockers (e.g. atenolol andmetoprolol) may be preferred. Beta-blockers should beavoided altogether in those with frequent episodes ofhypoglycaemia.Pregnancy Beta-blockers may cause intra-uterinegrowth restriction, neonatal hypoglycaemia, and bradycardia;the risk is greater in severe hypertension. Theuse of labetalol in maternal hypertension is not knownto be harmful, except possibly in the first trimester.In<strong>for</strong>mation on the safety of carvedilol duringpregnancy is lacking. If beta-blockers are used close todelivery, infants should be monitored <strong>for</strong> signs of betablockade(and alpha-blockade with labetalol or carvedilol).For the treatment of hypertension in pregnancy,see section 2.5.Breast-feeding Infants should be monitored as thereis a risk of possible toxicity due to beta-blockade (andalpha-blockade with labetalol or carvedilol), but theamount of most beta-blockers present in milk is toosmall to affect infants. Atenolol and sotalol are presentin milk in greater amounts than other beta-blockers. Themanufacturer of esmolol advises avoidance if breastfeeding.Hypertension Beta-blockers are effective <strong>for</strong> reducingblood pressure (section 2.5), but their mode of action isnot understood; they reduce cardiac output, alter baroceptorreflex sensitivity, and block peripheral adrenoceptors.Some beta-blockers depress plasma renin secretion.It is possible that a central effect may also partlyexplain their mode of action. Blood pressure can usuallybe controlled with relatively few side-effects. In generalthe dose of beta-blocker does not have to be high.Labetalol may be given intravenously <strong>for</strong> hypertensiveemergencies in children (section 2.5); however, care isneeded to avoid dangerous hypotension or beta-blockade,particularly in neonates. Esmolol is also usedintravenously <strong>for</strong> the treatment of hypertension particularlyin the peri-operative period.Beta-blockers can be used to control the pulse rate inchildren with phaeochromocytoma (section 2.5.4).However, they should never be used alone as betablockadewithout concurrent alpha-blockade may leadto a hypertensive crisis; phenoxybenzamine shouldalways be used together with the beta-blocker.2 Cardiovascular system

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