EFFECTIVE TREATMENT OF DELIRIUM IS DIFFICULT BUT NOT IMPOSSIBLE
Notice bibliographique
Résumé
To the Editor: Aside from drug trials, there are few rigorous studies of treatment of full-blown delirium.1-5 We want to congratulate Marcantonio and colleagues for conducting such an ambitious trial in this difficult field.5 Their pragmatic, randomized trial was implemented in postacute skilled nursing facilities, and the intervention consisted of important elements to abate the consequences of delirium: recognition of delirium, assessment and correction of treatable causes, prevention of complications, and restoration of function. Still, the overall outcome of the intervention was disappointing. Although delirium was recognized more often in the intervention than in the control facilities, the intervention had no effect on persistence of delirium or on mortality. However, the important steps of delirium management were not fully executed, although the investigators made great effort to train the staff in the intervention facilities. Paradoxically, treating the causes of delirium seemed to succeed even worse in the intervention than in the control settings. We agree with Marcantonio and colleagues5 that prevention of delirium is currently more effective than treatment of full-blown delirium, but we disagree with the statement that no model would succeed in shortening the duration of delirium. There are several reasons to believe that the management of delirium has developed during the last few years. Canadian studies suggested that a geriatrician's consultation improved cognition of patients with delirium more rapidly than usual care,1 although hard end points such as institutionalizations or mortality were not affected.1, 2 A trial in Finland showed that comprehensive geriatric assessment and treatment can shorten the duration of delirium and improve patients' cognition and quality of life without increasing costs.3, 6 That trial did not affect mortality or institutionalizations either. A Swedish study showed shortened delirium duration and hospital stay and less mortality, although the good results may be due to the preventive nature of this particular study.4 Further development of interventions requires several dimensions. The treatment should be based on comprehensive geriatric assessment and a fully trained geriatric team, which has been shown to be effective in several contexts.7 Sole consultations without a trained geriatric team may be insufficient.1, 2 Despite well-trained geriatricians in the previous trial, the variations in geriatric teams implementing the intervention in different wards were wide, possibly diminishing effectiveness.3, 6 Both well-trained team and geriatrician may have been instrumental for the good results in the Swedish study. It may be that patients prone to delirium need a special ward with trained staff and possibilities for emergency actions, because the environment of ordinary emergency units with their noise and bustle may be especially detrimental. Development of valid triage tools is also needed to evaluate which of these patients benefit from active treatment and which should have palliative care. Many patients are frail, and recognition of their special requirements is important. These critically ill patients are often cared for in various settings where they have been admitted by chance. Delirium indicates a truly poor prognosis; one in three is deceased within 1 year.8 The important elements of treating delirium are those that Marcantonio and colleagues suggest,5 but basing the treatment of these demanding patients solely on nursing staff is not enough, because diagnostic and prognostic skills are vital for effective medical management of complicated syndromes such as delirium.9 Marcantonio's and previous studies3, 6 suffered from similar obstacles—constant staff turnover, understaffing, lack of facility leadership, and use of agency personnel—which can make the implementation of intervention for delirium frustrating. Conflict of Interest Disclosures: The authors report professional cooperation with various companies which, to our knowledge, contribute no conflict of interest relevant to this paper. Dr. Pitkälä reports having professional cooperation including lecturing fees from pharmaceutical and other healthcare companies (including Janssen-Cilag, Leiras, Lundbeck, MSD Finland, Novartis, Pfizer, Nestle) and having participated in clinical trials funded by pharmaceutical companies. Dr. Strandberg reports having professional cooperation including consulting and lecturing fees from pharmaceutical and other healthcare companies (including AstraZeneca, Boehringer Ingelheim, Leiras, MSD Finland, Novartis, Pfizer, and Servier) and having participated in clinical trials funded by pharmaceutical companies. Dr. Tilvis has received lecturing fees from AstraZeneca, Boehringer Ingelheim, Jansen-Cilag, Lundbeck, MSD Finland, Novartis, Orion Pharma, Pfizer, and Sanofi-Aventis. Dr. Laurila reports having received consulting or lecturing fees from Janssen-Cilag, Lundbeck, Mundipharma, MSD Finland, Pfizer, and Sanofi-Aventis. Author Contributions: This was a comment letter to a previous article in this journal. It does not include data. Drafting or critically revising the manuscript for important intellectual content: KHP, TES, RST, JVL. Approval of the final manuscript: KHP, TES, RST, JVL. KHP is the guarantor. Sponsor's Role: The Finnish delirium trial was supported by the Lions Organization (Punainen Sulka—Red Feather), Helsinki University Central Hospital, Helsinki City, and the Academy of Finland (Grant 48613). The sponsors did not have any role in the study design or analysis or interpretation of data, in writing the report, or in the decision to submit this article for publication. The authors were independent researchers not associated with the funders.
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 enseignantsNi 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.
Scores du classifieur distillé par catégorie (deux têtes)
| Catégorie | Codex | Gemma |
|---|---|---|
| Métarecherche | 0,012 | 0,067 |
| Méta-épidémiologie (sens strict) | 0,003 | 0,001 |
| Méta-épidémiologie (sens large) | 0,003 | 0,002 |
| Bibliométrie | 0,002 | 0,001 |
| Études des sciences et des technologies | 0,003 | 0,004 |
| Communication savante | 0,005 | 0,008 |
| Science ouverte | 0,005 | 0,001 |
| Intégrité de la recherche | 0,017 | 0,042 |
| Charge utile insuffisante (le modèle a refusé de juger) | 0,007 | 0,005 |
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.
score_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 découleClassification
machine, non validéePrédiction automatique; un appel candidat d’une seule source (Gemma direct ou Codex distillé), pas un consensus.
Le détail, modèle par modèle et score par score, se trouve en fin de page sous « Comment cette classification a été obtenue ».