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1、儿童急性中耳炎的治儿童急性中耳炎的治疗疗第1页,共70页,编辑于2022年,星期四SOURCE INFORMATIONN Engl J Med,2011,364:105-115(had been cited by 16 articles)From the Department of Pediatrics,University of Pittsburgh School of Medicine,USA.Correspondence author:Dr.Hoberman E-mail:hobermanchp.edu.2第2页,共70页,编辑于2022年,星期四美国科学信息所(美国科学信息所(ISI)
2、公布)公布 3第3页,共70页,编辑于2022年,星期四BACKGROUNDAcute otitis media(AOM)is the most frequently diagnosed illness in children in the US.Most children have routinely been treated with antimicrobial drugs in the US.1.Tahtinen PA,et al.A placebo-controlled trial of antimicrobial treatment for acute otitis media.N
3、Engl J Med 2011;364:116-126 2.Klein JO.Is acute otitis media a treatable disease?N Engl J Med 2011;364:168-1695第5页,共70页,编辑于2022年,星期四nA watchful-waiting strategy has long been applied in several countries to minimize the use of antimicrobial drugs.-Netherlands and Scotland4,5 -USA,2004,6,7 -Canada 8
4、4.Appelman CL,et al.Otitis media acuta:NHG-standaard(eerste herziening).Huisarts Wet 1999;42:362-366 5.Scottish Intercollegiate Guidelines Network.Diagnosis and management of childhood otitis media in primary care.Guideline no.66.Edinburgh:Royal College of Physicians in Edinburgh,2003.8.Forgie S,Zha
5、nel G,Robinson J.Management of acute otitis media.Paediatr Child Health(Oxford)2009;14:457-4646第6页,共70页,编辑于2022年,星期四AOM in children aged 6 to 23 months is“nonsevere”6(mild otalgia and T 39 during the preceding 24 hours)Diagnosis of AOM is uncertain.7Indications of Watchful Waiting 6.Kaleida PH,et al
6、.Amoxicillin or myringotomy or both for acute otitis media:results of a randomized clinical trial.Pediatrics 1991;87:466-474 7.American Academy of Pediatrics Subcommittee on Management of Acute Otitis Media.Diagnosis and management of acute otitis media.Pediatrics 2004;113:1451-14657第7页,共70页,编辑于2022
7、年,星期四OBJECTIVESTo evaluate the extent to which antimicrobial treatment(Amoxicillin-clavulanate)and placebo treatment affect the course of both symptoms and signs of AOM in children aged 6 to 23 months.11第11页,共70页,编辑于2022年,星期四METHODS1.Eligibility and Enrollment2.Randomization3.Assessment of Symptoms4
8、.Otoscopic Examination,Overall Assessment,and Management5.Outcomes6.Statistical Analysis12第12页,共70页,编辑于2022年,星期四 Inclusion Criteria Eligible children(1)will be aged 6 to 23 months,(2)have received pneumococcal conjugate vaccine,and(3)have evidence of AOM defined as:A.Recent(within 48 hours),onset of
9、 signs and symptoms and a score of 3 on the AOM-SOS scale.B.Presence of middle-ear effusionC.Moderate or marked bulging of the tympanic membrane or slight bulging accompanied by either otalgia or marked erythema of the membrane.14第14页,共70页,编辑于2022年,星期四AOM-SOSThe Acute Otitis Media Severity of Sympto
10、ms(AOM-SOS)scale11,12 The AOM-SOS scale consists of seven items:tugging of ears,crying,irritability,difficulty sleeping,diminished activity,diminished appetite,and fever.As“none,”“a little,”or“a lot,”with corresponding scores of 0,1,and 2scores range from 0 to 14,with higher scores indicating greate
11、r severity of symptoms 11.Shaikh N,et al.Development and preliminary evaluation of a parent-reported outcome instrument for clinical trials in acute otitis media.Pediatr Infect Dis J 2009;28:5-8 12.Shaikh N,et al.Responsiveness and construct validity of a symptom scale for acute otitis media.Pediatr
12、 Infect Dis J 2009;28:9-12 15第15页,共70页,编辑于2022年,星期四AOM-SOS16第16页,共70页,编辑于2022年,星期四Exclusion Criteria(protocol)(1)certain signs or symptoms(e.g.,toxic appearance,otalgia 48 hours,spontaneous perforation of the tympanic membrane and drainage or temperature 105F);(2)clinical or anatomical characteristi
13、cs that might obscure response to treatment(e.g.,tympanostomy,submucous cleft palate,high-arched palate,or Downs syndrome);(3)underlying systemic problems that might obscure response to infection(e.g.,serious underlying disease e.g.,cystic fibrosis,neoplasm,juvenile diabetes),concomitant infection,k
14、nown renal insufficiency,known hepatic insufficiency,history of immune dysfunction,chronic gastrointestinal conditions,malignancy;18第18页,共70页,编辑于2022年,星期四(4)sensorineural hearing loss;(5)comedications(e.g.,systemic corticosteroids at any point while enrolled in the study,more than one dose of system
15、ic antimicrobial therapy within 96 hours,any investigational drug or vaccine;(6)hypersensitivity to penicillin,amoxicillin or amoxicillin-clavulanate,or phenylketonuria or known hypersensitivity to aspartame;(7)unable to complete the study protocol or not having access to a telephone;and(8)current e
16、nrollment in another study or previously enrolled in this study.aspartame阿司帕坦阿司帕坦;phenylketonuria苯丙酮酸尿苯丙酮酸尿19第19页,共70页,编辑于2022年,星期四2.RandomizationStratification according to history of recurrent AOM(defined as 3 episodes in 6 months or 4 episodes in 1 year)and according to their exposure or nonexpos
17、ure to three or more children for at least 10 hours per week.At each study site,within each stratum,we randomly assigned children in blocks of four,in a 1:1 ratio20第20页,共70页,编辑于2022年,星期四Amoxicillinclavulanate(Augmentin ES,GlaxoSmithKline),90/6.4mg/kg/day in 2 divided doses for 10 days.Placebo was si
18、milar to Amoxicillinclavulanate in appearance and taste.The parents were unaware of the childrens group assignments.Parents prepared acetaminophen as needed for the relief of symptoms.21第21页,共70页,编辑于2022年,星期四3.Assessment of SymptomsStructured interview by telephone every day until the first follow-u
19、p visit and in person at each visit.Parents record their childs AOM-SOS scores and other pertinent clinical information in a diary twice a day for 3 days and once a day thereafter.22第22页,共70页,编辑于2022年,星期四4.Otoscopic Examination,Overall Assessment,and ManagementOtoscopy on day 1,day 4-5,day 10-12,day
20、 21-25.SlightOtoscopic Photographs Moderate markedbulging of tympanic membrane23第23页,共70页,编辑于2022年,星期四Overall AssessmentTo categorize clinical success or clinical failure at each visit.Clinical failure at or before the day 45 visit:a lack of substantial improvement in symptoms,a worsening of signs o
21、n otoscopic examination,or both.Clinical failure at the day 1012 visit:the failure to achieve complete or nearly complete resolution of symptoms and of otoscopic signs.13.Kaleida PH.Assessment of otoscopists accuracy regarding middle-ear effusion:otoscopic validation.Am J Dis Child 1992;146:433-435
22、24第24页,共70页,编辑于2022年,星期四Management for clinical failure casesA standardized 10-day regimen of orally administered amoxicillin,at a dose of 90mg/kg/day,and cefixime,at a dose of 8mg/kg/day.Once a child had met the criteria for clinical failure,he or she remained in that category for the analyses.25第2
23、5页,共70页,编辑于2022年,星期四Relapse at the day 2125 visit:the reappearance of AOM in a child who had previously been categorized as having met the criteria for clinical success.26第26页,共70页,编辑于2022年,星期四To obtain nasopharyngeal specimens from the children for culturing,at study entry and at the day 1012 and d
24、ay 2125 visits.27第27页,共70页,编辑于2022年,星期四5.OutcomesThe primary outcome measures A.The time to resolution of symptoms:-The time to the first recording of an AOM-SOS score of 0 or 1 -The time to the second of two successive recordings of that score.B.The symptom burden over time:-The mean AOM-SOS score
25、of each day over the first 7 days of follow-up -The groups weighted mean scores for that period.28第28页,共70页,编辑于2022年,星期四The secondary outcomes:A.Overall clinical efficacyB.The occurrence of adverse eventsC.Nasopharyngeal colonization ratesD.The use of acetaminophenE.The use of health care resources.
26、29第29页,共70页,编辑于2022年,星期四RESULTS1.Study Population2.Efficacy of Treatment -Symptomatic Response -Clinical Failure -Prognostic Factors and Effect Modifiers -Relapse and Residual Middle-Ear Effusion3.Nasopharyngeal Colonization and Other Outcomes4.Complications and Adverse Events33第33页,共70页,编辑于2022年,星期
27、四1.Study Population1385 Children were assessed for eligibility887 Were not eligible498 Were eligible291 Underwent randomization207 Had parent who declined participation144 Were assigned to and received amoxicillinclavulanate147 Were assigned to and received placebo34第34页,共70页,编辑于2022年,星期四 Selected D
28、emographic and Clinical Characteristics(1)1.Age at entry 611 mo 1217 mo 1823 mo2.Sex Male Female3.Race White Black Other4.Maternal level of education Less than high school High-school graduate College graduate5.Type of health insurance Private Medicaid6.Exposure to other children Yes No36第36页,共70页,编
29、辑于2022年,星期四7.AOM-SOS score(1)Baseline score35689111214(2)Mean baseline score(SD)8.Laterality of acute otitis mediaBilateralUnilateral9.Degree of tympanic membrane bulging in worse ear SlightModerateMarked Selected Demographic and Clinical Characteristics(2)uThere were no significant differences in c
30、haracteristics between the two study groups.37第37页,共70页,编辑于2022年,星期四2.Efficacy of Treatment:2.1Symptomatic Response The proportion of children in whom symptoms had not resolved40第40页,共70页,编辑于2022年,星期四 Day2 Day4 Day7Group A 35%61%80%Group B 28%54%74%P=0.14 for the overall comparisonRates of the first
31、 recording of a score of 0 or 1Group A:children who were treated with amoxicillinclavulanateGroup B:children who were treated with placebo41第41页,共70页,编辑于2022年,星期四42第42页,共70页,编辑于2022年,星期四 Day2 Day4 Day7Group A 20%41%67%Group B 14%36%53%P=0.04 for the overall comparisonRates of two successive recordin
32、gs of a score of 0 or 1 In 54%of the instances in which scores fell to 0 or 1,a subsequent score was higher than 1.43第43页,共70页,编辑于2022年,星期四44第44页,共70页,编辑于2022年,星期四The 7-day weighted mean(SE)score was lower in the amoxicillinclavulanate group than in the placebo group(2.790.16 vs.3.420.18;P=0.01).46第
33、46页,共70页,编辑于2022年,星期四 Group A Group B P Value*Day4-5 4%23%0.001Day10-12 16%51%0.001*At or before the day(n)Rates of clinical failure at different time2.2Clinical Failure47第47页,共70页,编辑于2022年,星期四2.3 Prognostic Factors and Effect ModifiersAt day 10 to 12Childrens exposure or nonexposure,(P=0.007)Childr
34、en with higher AOM-SOS scores at entry and with lower scores(P=0.004)Children with bilateral AOM with unilateral AOM(P=0.002)Children with more bulging of the tympanic membrane and with less bulging(P0.001)50第50页,共70页,编辑于2022年,星期四2.4Relapse and Residual Middle-Ear EffusionAt the day 2125 visit.Group
35、 A Group B P ValueRelapse 19/119(16%)13/70(19%)0.56 71/141(50%)87/139(63%)0.05Middle-ear effusion54第54页,共70页,编辑于2022年,星期四3.Nasopharyngeal Colonization and Other OutcomesFrom day 1 to the day 2125 visit,there were no significant changes in either group in the rates of nasopharyngeal colonization with
36、 nonsusceptible Streptococcus pneumoniae.55第55页,共70页,编辑于2022年,星期四There were no significant differences between the study group in either the mean daily number of doses of acetaminophen administered(0.37 and 0.43,respectively;P=0.35)or the use of health care resources.56第56页,共70页,编辑于2022年,星期四4.Compli
37、cations and Adverse EventsMastoiditis developed in one child in the placebo group on day 5.Diarrhea and diaper-area dermatitis were more common among children who received amoxicillinclavulanate.Perforation of tympanic membraneOral thrush VomitingRash57第57页,共70页,编辑于2022年,星期四DISCUSSIONChildren treate
38、d with amoxicillinclavulanate had consistently more favorable short-term outcomes,including:1.A sustained symptomatic response,2.An absence of otoscopic evidence of persistent middle-ear infection,3.A reduced rate of residual middle-ear effusion.59第59页,共70页,编辑于2022年,星期四The principal side effects wer
39、e diarrhea and dermatitis in the diaper area,but the side effects were usually not severe enough to discontinue the treatment of the drugs.62第62页,共70页,编辑于2022年,星期四The differences in outcome in this trial were greater than the differences seen in most previous trials of antimicrobial agents,Not becau
40、se of better outcomes among the children treated with amxicillinclavulanate but because of higher rates of clinical failure among the children who received placebo.This finding seems to be attributable to the stringent diagnostic criteria68第68页,共70页,编辑于2022年,星期四CONCLUSIONSAmong children aged 6 to 23
41、 months with AOM,treatment with amoxicillinclavulanate for 10 days affords a measurable short-term benefit,irrespective of the initial severity.The benefit must be weighed against concern not only about the side effects of the medication but also about the contribution of antimicrobial treatment to the emergence of bacterial resistance.69第69页,共70页,编辑于2022年,星期四Supported by a grant(3U01AI066007-02S1)from the National Institute of Allergy and Infectious Diseases.Thanks70第70页,共70页,编辑于2022年,星期四
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