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Enregistrement W42718891 · doi:10.1093/pch/20.1.19

Evidence for Clinicians: Nebulized epinephrine for croup in children

2015· article· en· W42718891 sur OpenAlexaff
Atsushi Kawaguchi, Ari R. Joffe

Notice bibliographique

RevuePaediatrics & Child Health · 2015
Typearticle
Langueen
DomaineMedicine
ThématiqueOtolaryngology and Infectious Diseases
Établissements canadiensUniversity of Alberta
Organismes subventionnairesnon disponible
Mots-clésCroupEpinephrineMedicineIntensive care medicineAnesthesiaPediatrics

Résumé

récupéré en direct d'OpenAlex

For the current issue of the Journal, we asked Drs Atsushi Kawaguchi and Ari Joffe to comment on and put into context the Cochrane Review on nebulized epinephrine for reducing symptoms in children with severe croup. Croup is a common childhood illness characterized by barky cough, stridor, hoarseness and respiratory distress. Children with severe croup are at risk for intubation. Nebulized epinephrine may prevent intubation. The authors searched CENTRAL 2013, Issue 6, MEDLINE (1966 to the third week of June 2013), EMBASE (1980 to July 2013), Web of Science (1974 to July 2013), CINAHL (1982 to July 2013) and Scopus (1996 to July 2013). Randomized controlled trials (RCTs) or quasi-RCTs involving children with croup evaluated in an emergency department (ED) or admitted to hospital were included. Comparisons were: nebulized epinephrine versus placebo, racemic nebulized epinephrine versus L-epinephrine (an isomer), and nebulized epinephrine delivered by intermittent positive pressure breathing (IPPB) versus nebulized epinephrine without IPPB. The primary outcome was change in croup score post-treatment. Secondary outcomes were rate and duration of intubation and hospitalization, croup return visit, parental anxiety and side effects. Two authors independently identified potentially relevant studies by title and abstract (when available), and examined relevant studies using a priori inclusion criteria, followed by methodological quality assessment. One author extracted data while the second checked accuracy. Standard methodological procedures outlined by the Cochrane Collaboration were used. Eight studies (225 participants) were included. In general, children included in the studies were young (average age <2 years in the majority of included studies). Severity of croup was described as moderate to severe in all included studies. Six studies were performed in the inpatient setting, one in the ED and one setting was not specified. Six of the eight studies were deemed to have a low risk of bias and the risk of bias was unclear in the remaining two studies. Nebulized epinephrine was associated with improvement in croup score 30 min post-treatment (three RCTs; standardized mean difference [SMD] −0.94 [95% CI −1.37 to −0.51]; I2 statistic = 0%). This effect was not significant 2 h and 6 h post-treatment. Nebulized epinephrine was associated with significantly shorter hospital stay compared with placebo (one RCT, MD −32.0 h [95% CI −59.1 to −4.9]). Comparing racemic and L-epinephrine, no difference in croup score was found after 30 min (SMD 0.33 [95% CI −0.42 to 1.08]). After 2 h, L-epinephrine showed significant reduction compared with racemic epinephrine (one RCT, SMD 0.87 [95% CI 0.09 to 1.65]). There was no significant difference in croup score between administration of nebulized epinephrine via IPPB versus nebulization alone at 30 min (one RCT, SMD −0.14 [95% CI −1.24 to 0.95]) or 2 h (SMD −0.72 [95% CI −1.86 to 0.42]). None of the studies sought or reported data on adverse effects. Nebulized epinephrine is associated with clinically and statistically significant transient reduction of symptoms of croup 30 min post-treatment. Evidence does not favour racemic epinephrine or L-epinephrine, or IPPB over simple nebulization. The authors note that data and analyses were limited by the small number of relevant studies and total number of participants and, thus, most outcomes contained data from very few or even single studies. The full text of the Cochrane Review is available in The Cochrane Library (1). The annual incidence of croup is as high as 6% in children <6 years of age presenting to paediatricians’ offices and EDs (2,3). Although usually self-limited, with symptoms resolving by 48 h in 60% of cases, up to 5% of children presenting for medical care are admitted to hospital, and up to 3% of these children are intubated (2,3). In clinical settings, severity is categorized as mild, moderate, severe and respiratory failure; at least two-thirds present with mild, and <1% with severe croup (4–6). Children with croup should be kept as comfortable as possible; care must be taken not to frighten the child, and to avoid causing agitation, both of which can worsen the airway obstruction. Humidified air was traditionally used as a primary intervention; however, a Cochrane review concluded that it was ineffective (7). The benefits of corticosteroids and nebulized epinephrine have been evaluated in multiple well-designed prospective studies (1,8). In severe croup unresponsive to treatment, endotracheal intubation is indicated. Intubation can be difficult due to severe subglottic swelling. In addition, there are instances in which the symptoms of croup are due to other structural causes of upper airway obstruction, leading to a difficult airway. Thus, intubation of a child with croup should be performed by an anesthetist with the support of an ear, nose and throat specialist, ideally in the operating room. Given the evidence that the effects of a dose of corticosteroid can be expected only after 30 min, nebulized epinephrine should be initiated as early as possible for moderate to severe croup (7). We recommend a dose of 5 mL of 1:1000 L-epinephrine for nebulization because racemic epinephrine is often not available and one study found it to be less effective than L-epinephrine. This dose should have immediate effects and last for ≥30 min. We are not aware of any contraindications to nebulized epinephrine. A recently published RCT in intensive care assessing the effect of a single dose of L-epinephrine on postextubation stridor in children showed that patients receiving a 5 mL dose, compared with a 2.5 mL or 0.5 mL dose, experienced significantly increased blood pressure at up to 180 min, but by only a mild degree (systolic and diastolic blood pressure raised by a mean of <7 mmHg) (9). Acute angle-closure glaucoma is theoretically possible after nebulized epinephrine, although we are not aware of any reported cases (10). Severe events are likely very rare given the widespread use of nebulized epinephrine for several decades. The Cochrane review did not find studies that examined repeated doses of nebulized epinephrine. In our experience, clinicians often use more than one dose of nebulized epinephrine in a short period. Although nebulized epinephrine appears to be safe, it is unclear how often it can be repeated. There is one case report of an 11-year-old child with croup receiving three doses of nebulized racemic epinephrine in 1 h, who experienced 5 min of spontaneously resolving ventricular tachycardia and a small myocardial infarction (11), and one reported case involving a 33-day-old infant with bronchiolitis who, after three doses of nebulized L-epinephrine in >90 min, experienced ventricular tachycardia with pulses, which was converted with lidocaine (12). The lack of other reports suggests that serious adverse events from repeat doses are very rare. Based on these considerations, we believe repeated doses of epinephrine are warranted for persisting severe croup while an increased level of observation is arranged, a paediatric intensivist is consulted or arrangements for intubation are being made (4,13). When one dose of nebulized epinephrine is used with a good response, at least 2 h of observation under appropriate monitoring is recommended (4,13) because the action of nebulized epinephrine is short lived. All such children should also receive a corticosteroid. Discharge home requires resolution of stridor and respiratory distress.

Récupéré en direct depuis OpenAlex et désinversé. Les résumés ne sont pas conservés dans cette base de données : les index inversés représentent 8,6 Go des 9,3 Go de texte de la base, et le serveur dispose de 13 Go libres.

Comment cette classification a été obtenuedéplier

Prédiction machine sur la base complète

Imitation des enseignants

Ni prévalence calibrée, ni vérité terrain. Validation humaine à venir. Le volet Gemma est une étiquette directe du modèle pour chaque travail de la base, lue sur la notice réduite au titre. Le volet Codex est un classifieur appris des 10 348 étiquettes directes de Codex et calibré sur les taux pondérés de l'échantillon; les champs sans appui suffisant ne portent aucun appel Codex. Le mode candidate est l'union des deux volets; le consensus est leur intersection. Ces sorties portent le statut machine_predicted_unvalidated et ne sont pas des étiquettes humaines.

score de la tête « metaresearch » (Codex)0,032
score de la tête « metaresearch » (Gemma)0,242
Version: metacan-v3-hybrid-931329e0061cStatut de validation: machine_predicted_unvalidated
Catégories candidatesaucune
Catégories consensuellesaucune
DomaineSignal candidat: aucune · Signal consensuel: aucune
Devis d'étudeSignal candidat: Revue systématique · Signal consensuel: aucune
GenreSignal candidat: Synthèse · Signal consensuel: Synthèse
Score de désaccord entre enseignants0,032
Score d'incertitude au seuil0,171

Scores du classifieur distillé par catégorie (deux têtes)

CatégorieCodexGemma
Métarecherche0,0320,242
Méta-épidémiologie (sens strict)0,0020,002
Méta-épidémiologie (sens large)0,0050,007
Bibliométrie0,0040,005
Études des sciences et des technologies0,0020,004
Communication savante0,0050,006
Science ouverte0,0050,004
Intégrité de la recherche0,0250,018
Charge utile insuffisante (le modèle a refusé de juger)0,0070,002

Scores machine (provisoires)

Les deux têtes enseignantes du modèle étudiant, lues sur ce travail. Un score ordonne la base pour la relecture; il n'affirme jamais une catégorie, et le statut de validation accompagne chaque rangée tel quel.

Scores de référence d'un modèle non mature (critères de maturité non atteints, 7 itérations). Un score ordonne; il n'affirme jamais une catégorie.

Tête enseignante Opus0,078
Tête enseignante GPT0,386
Écart entre enseignants0,308 · la distance entre les deux têtes enseignantes sur ce seul travail
Statut de validationscore_only:v0-immature-baseline · tel quel depuis la passe de notation : score_only signifie que le nombre peut ordonner les travaux, et qu'aucune étiquette de catégorie n'en découle

Classification

machine, non validée

Prédiction automatique; un appel candidat d’une seule source (Gemma direct ou Codex distillé), pas un consensus.

Les modèles n’ont appliqué aucune catégorie : rien dans la taxonomie ne correspondait à ce travail.
Devis d'étudeRevue systématique
Domainenon disponible
GenreSynthèse

Le détail, modèle par modèle et score par score, se trouve en fin de page sous « Comment cette classification a été obtenue ».

En bref

Citations5
Publié2015
Routes d'admission1
Résumé présentoui

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