Predictive factors of severe abdominal pain during and after transarterial chemoembolization for hepatocellular carcinoma.


Journal

European radiology
ISSN: 1432-1084
Titre abrégé: Eur Radiol
Pays: Germany
ID NLM: 9114774

Informations de publication

Date de publication:
May 2021
Historique:
received: 27 05 2020
accepted: 09 10 2020
revised: 03 09 2020
pubmed: 31 10 2020
medline: 16 4 2021
entrez: 30 10 2020
Statut: ppublish

Résumé

To prospectively assess the frequency of severe abdominal pain during and after transarterial chemoembolization (TACE) for hepatocellular carcinoma (HCC) using the visual analog scale (VAS), and to identify predictive factors. Ninety-eight TACE performed in 80 patients (mean 65 ± 12 years old, 60 men) were consecutively and prospectively included. Abdominal pain was considered severe if the VAS ≥ 30/100 after treatment administration, or if opioid analgesic (grades 2-3) intake was required during hospitalization. Patient and tumor characteristics as well as technical factors associated with severe pain were identified by binary logistic regression. The criterion for severe pain was met in 41/98 (42%) of procedures (peri-procedural pain 30/98 [31%] and opioid consumption during hospitalization 24/98 [25%]). Multivariate analysis identified age (odds ratio [OR] = 0.943 (95% confidence interval 0.895-0.994), p = 0.029), cirrhosis (OR = 0.284 (0.083-0.971), p = 0.045), and alcoholic liver disease (OR = 0.081 (0.010-0.659), p = 0.019) as negative predictive factors of severe abdominal pain. Severe abdominal pain occurred in or after 1/13 (8%), 8/34 (24%), 22/41 (54%), and 10/10 (100%) TACE sessions when none, one, two, and three of the protective factors were absent, respectively (p < 0.001). The area under the ROC curve of the combination of factors for the prediction of severe abdominal pain was 0.779 (CI 0.687-0.871). Severe abdominal pain was frequent during and after TACE revealing a clinically relevant and underestimated problem. A predictive model based on three readily available clinical variables suggests that young patients without alcoholic liver disease or cirrhosis could benefit from reinforced analgesia. • Severe abdominal pain occurs in 43% of TACE for HCC. • Younger age, absence of cirrhosis, and absence of alcoholic liver disease were identified as independent predictive factors of severe abdominal pain. • A simple combination of the three abovementioned features helped predict the occurrence of severe abdominal pain.

Identifiants

pubmed: 33123789
doi: 10.1007/s00330-020-07404-5
pii: 10.1007/s00330-020-07404-5
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

3267-3275

Commentaires et corrections

Type : ErratumIn

Références

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Auteurs

Atanas Pachev (A)

Department of Radiology, APHP.Nord, Hôpital Beaujon, Clichy, Hauts-de-Seine, France.

Lucas Raynaud (L)

Department of Radiology, APHP.Nord, Hôpital Beaujon, Clichy, Hauts-de-Seine, France.

Luisa Paulatto (L)

Department of Radiology, APHP.Nord, Hôpital Beaujon, Clichy, Hauts-de-Seine, France.

Marco Dioguardi Burgio (M)

Department of Radiology, APHP.Nord, Hôpital Beaujon, Clichy, Hauts-de-Seine, France.
INSERM U1149, CRI, Paris, France.

Vincent Roche (V)

Department of Radiology, APHP.Nord, Hôpital Beaujon, Clichy, Hauts-de-Seine, France.
Université de Paris, Paris, France.

Carmela Garcia Alba (C)

Department of Radiology, APHP.Nord, Hôpital Beaujon, Clichy, Hauts-de-Seine, France.

Annie Sibert (A)

Department of Radiology, APHP.Nord, Hôpital Beaujon, Clichy, Hauts-de-Seine, France.

Matthieu Lagadec (M)

Department of Radiology, APHP.Nord, Hôpital Beaujon, Clichy, Hauts-de-Seine, France.

Juliette Kavafyan-Lasserre (J)

Department of Anaesthesiology, APHP.Nord, Hôpital Beaujon, Clichy, Hauts-de-Seine, France.

Catherine Paugam-Burtz (C)

Université de Paris, Paris, France.
Department of Anaesthesiology, APHP.Nord, Hôpital Beaujon, Clichy, Hauts-de-Seine, France.

Valérie Vilgrain (V)

Department of Radiology, APHP.Nord, Hôpital Beaujon, Clichy, Hauts-de-Seine, France.
INSERM U1149, CRI, Paris, France.
Université de Paris, Paris, France.

Maxime Ronot (M)

Department of Radiology, APHP.Nord, Hôpital Beaujon, Clichy, Hauts-de-Seine, France. maxime.ronot@aphp.fr.
INSERM U1149, CRI, Paris, France. maxime.ronot@aphp.fr.
Université de Paris, Paris, France. maxime.ronot@aphp.fr.

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