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Good Practice in Postoperative and Procedural Pain Management ...

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necessary to ensure that the patient will have access tosuitable analgesia.Pa<strong>in</strong> after surgery is usually most severe <strong>in</strong> the first24–72 h but may persist for several days or weeks.Analgesia can be given regularly (by the clock) <strong>in</strong> theearly postoperative period <strong>and</strong> then ‘as required’accord<strong>in</strong>g to assessed pa<strong>in</strong>. Drugs to counteractunwanted effects of analgesia or other side effects ofsurgery such as PONV should also be available <strong>and</strong>adm<strong>in</strong>istered when necessary.<strong>Postoperative</strong> pa<strong>in</strong> should be assessed frequently: seesection 3.0 for further <strong>in</strong>formation. Analgesic regimensshould be sufficiently flexible to allow for <strong>in</strong>ter-<strong>in</strong>dividualdifferences <strong>in</strong> the response to analgesics <strong>and</strong> thevariation <strong>in</strong> the requirement for pa<strong>in</strong> relief that occursdur<strong>in</strong>g the postoperative period.5.2 ENT surgery5.2.1 Myr<strong>in</strong>gotomyDra<strong>in</strong>age of the middle ear, usually with <strong>in</strong>sertion of atube, is a treatment for otitis media. Myr<strong>in</strong>gotomy isusually considered to be a m<strong>in</strong>or procedure, undertakenon a day-case basis. See also section 5.1 for thegeneral pr<strong>in</strong>ciples of postoperative pa<strong>in</strong> management.<strong>Good</strong> practice po<strong>in</strong>tAs myr<strong>in</strong>gotomy is a brief procedure, oral paracetamolor NSAID should be adm<strong>in</strong>istered preoperativelyto ensure adequate analgesia at the end of surgery.RecommendationsOral paracetamol or NSAIDS (ibuprofen, diclofenac, orketorolac) <strong>in</strong> suitable doses can achieve adequate earlypostoperative analgesia: Grade B (1–4).Opioids are effective but not recommended for rout<strong>in</strong>euse because of side effects: Grade B (1,5–8).EvidenceParacetamol (oral) produces dose-related analgesia;10 mgÆkg )1 is no better than placebo (3) or is associatedwith higher supplemental requirements (8), whereas pa<strong>in</strong>scores are lower with 15–20 mgÆkg )1 (1,2,4,5,9).Ibuprofen <strong>and</strong> diclofenac appear to provide similaranalgesia to paracetamol (2,10), but the comb<strong>in</strong>ationhas not been tested.Ketorolac 1 mgÆkg )1 (<strong>in</strong>travenous) provides m<strong>in</strong>orimprovements <strong>in</strong> analgesia when compared with lowdoses of paracetamol, 10 mgÆkg )1 (3,8); paracetamol10 mgÆkg )1 + code<strong>in</strong>e 1 mgÆkg )1 (8); paracetamol15 mgÆkg )1 (but only first 10 m<strong>in</strong> there was no differenceat 20 m<strong>in</strong>) (4). See section 6.5 for recommendeddoses of ketorolac <strong>and</strong> other NSAIDS.Opioids, for example code<strong>in</strong>e, butorphanol, orfentanyl, have been associated with <strong>in</strong>creased sideeffects when compared with NSAIDs or paracetamol,without cl<strong>in</strong>ically significant improvements <strong>in</strong> analgesia;therefore, their use is not warranted for rout<strong>in</strong>emyr<strong>in</strong>gotomy:i. <strong>in</strong>creased sedation <strong>and</strong> time to discharge for oralcode<strong>in</strong>e: (1), nasal fentanyl (7) <strong>and</strong> nasal butorphanol (6)ii. <strong>in</strong>creased vomit<strong>in</strong>g with oral code<strong>in</strong>e or nasal butorphanol(8).LA block of the auricular branch of the vagus providedequivalent analgesia to <strong>in</strong>tranasal fentanyl (11).Analgesia Table 5.2.1Opioid a 1)NSAID 1)Paracetamol 1)Directevidencea Not rout<strong>in</strong>ely recommended because of side effects: see text.5.2.2 TonsillectomyTonsillectomy (±adenoidectomy) is one of the mostfrequently performed procedures <strong>in</strong> children. Chronicor recurrent tonsillitis with tonsillar hyperplasia lead<strong>in</strong>gto upper airway obstruction, for example <strong>in</strong> sleepapnea syndromes, is the most frequent <strong>in</strong>dication fortonsillectomy. The choice of analgesia, postoperativemonitor<strong>in</strong>g, <strong>and</strong> duration of hospital admission is<strong>in</strong>fluenced by the potential for serious complicationssuch as apnea, perioperative bleed<strong>in</strong>g, <strong>and</strong> postoperativenausea <strong>and</strong> vomit<strong>in</strong>g (PONV). Pa<strong>in</strong> after tonsillectomycan persist for many days. See also section 5.1for the general management of postoperative pa<strong>in</strong>.<strong>Good</strong> practice po<strong>in</strong>tAs significant levels of pa<strong>in</strong>, behavioral disturbance, sleepdisruption, <strong>and</strong> altered activity can persist for 5–8 daysfollow<strong>in</strong>g tonsillectomy, regular adm<strong>in</strong>istration of analgesiamay be necessary dur<strong>in</strong>g this period. Information forfamilies about pa<strong>in</strong> assessment <strong>and</strong> medication use follow<strong>in</strong>gdischarge is particularly important.34 ª 2012 Blackwell Publish<strong>in</strong>g Ltd, Pediatric Anesthesia, 22 (Suppl. 1), 1–79

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