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Enregistrement W2795703779 · doi:10.1111/acem.13422

Hot Off the Press: Topical Tranexamic Acid Compared With Anterior Nasal Packing for Treatment of Epistaxis in Patients Taking Antiplatelet Drugs

2018· letter· en· W2795703779 sur OpenAlexaff
Justin Morgenstern, Sahaana Rangarajan, Corey Heitz, Christopher Bond, William K. Milne

Notice bibliographique

RevueAcademic Emergency Medicine · 2018
Typeletter
Langueen
DomaineMedicine
ThématiqueVascular Anomalies and Treatments
Établissements canadiensWestern UniversityUniversity of CalgaryMarkham Stouffville Hospital
Organismes subventionnairesnon disponible
Mots-clésMedicineTranexamic acidNasal packingAnesthesiaRandomized controlled trialSurgeryHemostasisLidocaineNoseBlood loss

Résumé

récupéré en direct d'OpenAlex

Epistaxis is a common presenting complaint in the emergency department (ED), with a variety of possible management options including pressure, vasoconstricting medications, cautery, and nasal packing.1, 2 The use of antiplatelet medications can make epistaxis more difficult to control.3 Tranexamic acid (TXA) is an antifibrinolytic agent useful in a wide variety of hemorrhagic conditions. A prior randomized control trial by the authors of this study demonstrated improved epistaxis control with topical TXA compared to anterior nasal packing.4 However, the literature is not consistent, and no prior study has focused on patients taking antiplatelet medications.5 This study aimed to compare topical TXA and anterior nasal packing in the management of anterior nasal epistaxis in patients on antiplatelet therapy. This is a nonblinded, randomized controlled trial comparing topical TXA and anterior nasal packing in the treatment of anterior epistaxis in patients on antiplatelet medications whose bleeding persisted despite 20 minutes of pressure. Patients were randomized to either TXA (a cotton pledget soaked with 500 mg of TXA and inserted into the affected nostril until hemostasis was achieved) or anterior nasal packing (pretreatment with a cotton pledget soaked in epinephrine and 2% lidocaine for 10 minutes followed by anterior nasal packing with tetracycline ointment left in situ for 3 days). Among the 124 patients included, bleeding at 10 minutes was better controlled in the TXA group (an absolute risk reduction of 44%; 95% confidence interval [CI] = 26%–57%; p < 0.001). The TXA group also had less recurrent bleeding in the first week, a shorter ED length of stay, and higher patient satisfaction. This is a well-conducted prospective, randomized control trial with a few minor threats to validity. The patients and treating clinicians were unblinded, which could bias the results. However, the outcome assessors were blinded. This trial is also as risk of selection bias, as although they tried to include consecutive patients, 92 of the 384 patients approached were excluded because of lack of consent. The choice to use bleeding at 10 minutes as the primary outcome may result in an unfair comparison, as traditional anterior packing requires time to allow a clot to stabilize. However, secondary outcomes looking at bleeding at 24 hours and 1 week also favored TXA, and earlier cessation of bleeding may be an important outcome for our patients. The authors report a shorter ED length of stay in the TXA group, but do not report the actual time spent in the ED in each group, so it is unclear if this difference was clinically significant. As there are many treatment options for epistaxis, potential confounders exist, and unfortunately the use of other treatment options such as cautery, vasoconstrictors, and commercial packing devices is not commented upon. Furthermore, the use of traditional anterior packing compared to the more widely used commercial packing devices may limit the applicability of the results. Finally, in this study anterior packing was primarily done by trainees (PGY2s and PGY3s), so it is possible that the results will not generalize to more experienced clinicians. There were 62 patients in the TXA group and 62 patients in the anterior nasal packing group. Hemostasis was achieved by 10 minutes in 73% of the TXA group and 29% of the anterior packing group (an absolute risk reduction of 44%; 95% CI = 26%–57%; p < 0.001). Recurrent nasal hemorrhage in the first week was reported in 5% of subjects who received TXA versus 21% who received anterior packing (p = 0.007). Discharge from the ED in <2 hours was accomplished in 97% of TXA group versus 21% anterior packing group (p < 0.001). Patients allocated to the TXA group reported higher levels of satisfaction compared to those allocated to anterior nasal packing. There was no significant difference in complications between the two treatment groups. This study supports the use of topical TXA in the management of anterior epistaxis in patients on antiplatelet therapy, as it results in earlier hemostasis, decreased recurrent bleeding at 1 week, and higher patient satisfaction. It is unclear how TXA would compare to commercial packing devices. It is also unclear exactly where TXA should fit into the epistaxis management algorithm. Although there was no difference in complications noted, and TXA seems quite safe in other contexts,6, 7 this trial is too small to make definitive conclusions about adverse events. Paper in a Pic infographic by Kristy Challen: @CHeitzMD: This has completely changed my practice. Get out the clot, Afrin and txa, pressure and I have a > 80% success rate #SGEMHOP. @TheSGEM: Changed my practice too. Using TXA regularly for epistaxis. @KristyChallen: It hasn't changed mine as I was already using TXA! 1st line if simple squeezing doesn't work. This randomized controlled trial demonstrated that topical TXA resulted in more rapid bleeding cessation, less risk of rebleeding, shorter ED length of stay, and higher patient satisfaction in patients taking antiplatelet medications. Topical TXA, without or without other therapies, is a reasonable management option for patients with epistaxis.

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)0,001
score de la tête « metaresearch » (Gemma)0,003
Version: metacan-v3-hybrid-931329e0061cStatut de validation: machine_predicted_unvalidated
Catégories candidatesaucune
Catégories consensuellesaucune
DomaineSignal candidat: aucune · Signal consensuel: aucune
Devis d'étudeSignal candidat: Essai non randomisé · Signal consensuel: aucune
GenreSignal candidat: Empirique · Signal consensuel: Empirique
Score de désaccord entre enseignants0,009
Score d'incertitude au seuil0,030

Scores du classifieur distillé par catégorie (deux têtes)

CatégorieCodexGemma
Métarecherche0,0010,003
Méta-épidémiologie (sens strict)0,0010,000
Méta-épidémiologie (sens large)0,0030,002
Bibliométrie0,0000,000
Études des sciences et des technologies0,0000,001
Communication savante0,0010,001
Science ouverte0,0000,000
Intégrité de la recherche0,0010,002
Charge utile insuffisante (le modèle a refusé de juger)0,0090,000

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 Opus0,047
Tête enseignante GPT0,322
Écart entre enseignants0,275 · 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'étudeEssai non randomisé
Domainenon disponible
GenreEmpirique

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

En bref

Citations2
Publié2018
Routes d'admission1
Résumé présentoui

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