Evidence map›Paper›PMID 41014152›Full record

ArticleThe oncologist2025

Intravenous haloperidol or chlorpromazine-which is more effective to improve agitation and communication in agitated delirium at the end of life?

Megumi Uchida, Tatsuya Morita, Tatsuo Akechi, Takuya Kawahara, Asao Ogawa, Kazuhiro Yoshiuchi, Naosuke Yokomichi, Akihiro Sakashita, Yoshihisa Matsumoto, Keiichi Uemura and 14 more

Abstract read
In one paragraph

Article in The oncologist, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

24 authors.

Megumi UchidaDepartment of Psychiatry and Cognitive-Behavioral Medicine, Nagoya City University Graduate School of Medical Sciences, Nagoya 467-8601, Japan.ORCID 0000-0003-2815-8400
Tatsuya MoritaDepartment of Palliative and Supportive Care, Seirei Mikatahara General Hospital, Hamamatsu 433-8558, Japan.
Tatsuo AkechiDepartment of Psychiatry and Cognitive-Behavioral Medicine, Nagoya City University Graduate School of Medical Sciences, Nagoya 467-8601, Japan.ORCID 0000-0003-1100-7518
Takuya KawaharaClinical Research Promotion Center, The University of Tokyo Hospital, Bunkyo-ku 113-8655, Japan.
Asao OgawaDepartment of Psycho-Oncology Service, National Cancer Center Hospital East, Kashiwa 277-8577, Japan.
Kazuhiro YoshiuchiDepartment of Stress Sciences and Psychosomatic Medicine, Graduate School of Medicine, The University of Tokyo, Bunkyo-ku 113-0033, Japan.
Naosuke YokomichiDepartment of Palliative and Supportive Care, Seirei Mikatahara General Hospital, Hamamatsu 433-8558, Japan.
Akihiro SakashitaDivision of Palliative Medicine, Department of Internal Medicine, Hyogo Prefectural Harima-Himeji General Medical Center, Himeji 670-8560, Japan.
Yoshihisa MatsumotoDepartment of Palliative Medicine, National Cancer Center Hospital East, Kashiwa-Shi, Chiba 277-8577, Japan.ORCID 0000-0003-3112-4818
Keiichi UemuraDepartment of Psychiatry, Tonan Hospital, Sapporo 060-0004, Japan.
Rika NakaharaDepartment of Psycho-Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan.
Satoru IwaseDivision of Palliative Medicine, Saitama Medical University Hospital, Irima 350-0495, Japan.
Megumi UchidaDepartment of Psychiatry and Cognitive-Behavioral Medicine, Nagoya City University Graduate School of Medical Sciences, Nagoya 467-8601, Japan.ORCID 0000-0003-2815-8400
Tatsuya MoritaDepartment of Palliative and Supportive Care, Seirei Mikatahara General Hospital, Hamamatsu 433-8558, Japan.
Tatsuo AkechiDepartment of Psychiatry and Cognitive-Behavioral Medicine, Nagoya City University Graduate School of Medical Sciences, Nagoya 467-8601, Japan.ORCID 0000-0003-1100-7518
Takuya KawaharaClinical Research Promotion Center, The University of Tokyo Hospital, Bunkyo-ku 113-8655, Japan.
Asao OgawaDepartment of Psycho-Oncology Service, National Cancer Center Hospital East, Kashiwa 277-8577, Japan.
Kazuhiro YoshiuchiDepartment of Stress Sciences and Psychosomatic Medicine, Graduate School of Medicine, The University of Tokyo, Bunkyo-ku 113-0033, Japan.
Naosuke YokomichiDepartment of Palliative and Supportive Care, Seirei Mikatahara General Hospital, Hamamatsu 433-8558, Japan.
Akihiro SakashitaDivision of Palliative Medicine, Department of Internal Medicine, Hyogo Prefectural Harima-Himeji General Medical Center, Himeji 670-8560, Japan.
Yoshihisa MatsumotoDepartment of Palliative Medicine, National Cancer Center Hospital East, Kashiwa-Shi, Chiba 277-8577, Japan.ORCID 0000-0003-3112-4818
Keiichi UemuraDepartment of Psychiatry, Tonan Hospital, Sapporo 060-0004, Japan.
Rika NakaharaDepartment of Psycho-Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan.
Satoru IwaseDivision of Palliative Medicine, Saitama Medical University Hospital, Irima 350-0495, Japan.

Funding

Japan Society for the Promotion of Science 15ck0106059h0002
6 · The paper itself

Abstract

backgroundDelirium frequently occurs in terminally ill patients with cancer. The purpose of this study was to determine whether intravenous haloperidol or chlorpromazine is more effective in improving agitation and communication in agitated delirium at the end of life. PATIENTS AND

methodsAll terminally ill patients with delirium treated in 39 specialized palliative care services were enrolled via the web. Delirium diagnosis and severity (Delirium Rating Scale-revised-98<DRS-R98>) were evaluated at the start of treatment (T0) and 72 h later (T1), and the psychotropic drugs used concomitantly at T1 were investigated. We evaluated whether there was an improvement in DRS-R98 agitation-related item scores and DRS-R98 communication-related item scores at T1 in patients with agitated cancer who received intravenous haloperidol or chlorpromazine from T0, and whether a significant difference existed between the two groups.

resultsOf 818 enrolled participants, 424 experienced agitation at T0, comprising 183 in the haloperidol group and 68 in the chlorpromazine group. The concomitant benzodiazepine rates were 52% and 54% in the haloperidol and chlorpromazine groups, respectively. In both groups, improvement in DRS-R98 agitation item scores was observed at T1, but there was no significant difference in improvement between the two groups. Worsening in DRS-R98 communication item scores was observed in both groups at T1, but there was no significant difference in worsening scores between the two groups.

conclusionIntravenous haloperidol and chlorpromazine are not statistically different for terminal agitation. These results should be validated in clinical trials.

Indexed as

Antipsychotic AgentsChlorpromazineDeliriumHaloperidolNeoplasmsPsychomotor AgitationAdministration, IntravenousAgedAged, 80 and overCommunicationFemaleHumansMaleMiddle AgedPalliative CareTerminal CareAntipsychotic AgentsChlorpromazineHaloperidolagitationcancercommunicationdeliriumend of lifepalliative care

Identifiers

PMID41014152
PMCPMC12618195

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.