Impact of cirrhosis in patients undergoing laparoscopic liver resection in a nationwide multicentre survey.


Journal

The British journal of surgery
ISSN: 1365-2168
Titre abrégé: Br J Surg
Pays: England
ID NLM: 0372553

Informations de publication

Date de publication:
02 2020
Historique:
received: 05 07 2019
revised: 21 09 2019
accepted: 27 09 2019
pubmed: 10 1 2020
medline: 28 10 2020
entrez: 10 1 2020
Statut: ppublish

Résumé

The aim was to analyse the impact of cirrhosis on short-term outcomes after laparoscopic liver resection (LLR) in a multicentre national cohort study. This retrospective study included all patients undergoing LLR in 27 centres between 2000 and 2017. Cirrhosis was defined as F4 fibrosis on pathological examination. Short-term outcomes of patients with and without liver cirrhosis were compared after propensity score matching by centre volume, demographic and tumour characteristics, and extent of resection. Among 3150 patients included, LLR was performed in 774 patients with (24·6 per cent) and 2376 (75·4 per cent) without cirrhosis. Severe complication and mortality rates in patients with cirrhosis were 10·6 and 2·6 per cent respectively. Posthepatectomy liver failure (PHLF) developed in 3·6 per cent of patients with cirrhosis and was the major cause of death (11 of 20 patients). After matching, patients with cirrhosis tended to have higher rates of severe complications (odds ratio (OR) 1·74, 95 per cent c.i. 0·92 to 3·41; P = 0·096) and PHLF (OR 7·13, 0·91 to 323·10; P = 0·068) than those without cirrhosis. They also had a higher risk of death (OR 5·13, 1·08 to 48·61; P = 0·039). Rates of cardiorespiratory complications (P = 0·338), bile leakage (P = 0·286) and reoperation (P = 0·352) were similar in the two groups. Patients with cirrhosis had a longer hospital stay than those without (11 versus 8 days; P = 0·018). Centre expertise was an independent protective factor against PHLF in patients with cirrhosis (OR 0·33, 0·14 to 0·76; P = 0·010). Underlying cirrhosis remains an independent risk factor for impaired outcomes in patients undergoing LLR, even in expert centres. El objetivo de este estudio fue analizar el impacto de la cirrosis en los resultados a corto plazo después de la resección hepática laparoscópica (laparoscopic liver resection, LLR) en un estudio de cohortes multicéntrico nacional. MÉTODOS: Este estudio retrospectivo incluyó todos los pacientes sometidos a LLR en 27 centros entre 2000 y 2017. La cirrosis se definió como fibrosis F4 en el examen histopatológico. Los resultados a corto plazo de los pacientes con hígado cirrótico (cirrhotic liver CL) (pacientes CL) y los pacientes con hígado no cirrótico (non-cirrhotic liver, NCL) (pacientes NCL) se compararon después de realizar un emparejamiento por puntaje de propension del volumen del centro, las características demográficas y del tumor, y la extensión de la resección. Del total de 3.150 pacientes incluidos, se realizó LLR en 774 (24,6%) pacientes CL y en 2.376 (75,4%) pacientes NCL. Las tasas de complicaciones graves y mortalidad en el grupo de pacientes CL fueron del 10,6% y 2,6%, respectivamente. La insuficiencia hepática posterior a la hepatectomía (post-hepatectomy liver failure, PHLF) fue la principal causa de mortalidad (55% de los casos) y se produjo en el 3,6% de los casos en pacientes CL. Después del emparejamiento, los pacientes CL tendieron a tener tasas más altas de complicaciones graves (razón de oportunidades, odds ratio, OR 1,74; i.c. del 95% 0,92-0,41; P = 0,096) y de PHLF (OR 7,13; i.c. del 95% 0,91-323,10; P = 0,068) en comparación con los pacientes NCL. Los pacientes CL estuvieron expuestos a un mayor riesgo de mortalidad (OR 5,13; i.c. del 95% 1,08-48,6; P = 0,039) en comparación con los pacientes NCL. Los pacientes CL presentaron tasas similares de complicaciones cardiorrespiratorias graves (P = 0,338), de fuga biliar (P = 0,286) y de reintervenciones (P = 0,352) que los pacientes NCL. Los pacientes CL tuvieron una estancia hospitalaria más larga (11 versus 8 días; P = 0,018) que los pacientes NCL. La experiencia del centro fue un factor protector independiente de PHLF (OR 0,33; i.c. del 95% 0,14-0,76; P = 0,010) pacientes CL. CONCLUSIÓN: La presencia de cirrosis subyacente sigue siendo un factor de riesgo independiente de peores resultados en pacientes sometidos a resección hepática laparoscópica, incluso en centros con experiencia.

Sections du résumé

BACKGROUND
The aim was to analyse the impact of cirrhosis on short-term outcomes after laparoscopic liver resection (LLR) in a multicentre national cohort study.
METHODS
This retrospective study included all patients undergoing LLR in 27 centres between 2000 and 2017. Cirrhosis was defined as F4 fibrosis on pathological examination. Short-term outcomes of patients with and without liver cirrhosis were compared after propensity score matching by centre volume, demographic and tumour characteristics, and extent of resection.
RESULTS
Among 3150 patients included, LLR was performed in 774 patients with (24·6 per cent) and 2376 (75·4 per cent) without cirrhosis. Severe complication and mortality rates in patients with cirrhosis were 10·6 and 2·6 per cent respectively. Posthepatectomy liver failure (PHLF) developed in 3·6 per cent of patients with cirrhosis and was the major cause of death (11 of 20 patients). After matching, patients with cirrhosis tended to have higher rates of severe complications (odds ratio (OR) 1·74, 95 per cent c.i. 0·92 to 3·41; P = 0·096) and PHLF (OR 7·13, 0·91 to 323·10; P = 0·068) than those without cirrhosis. They also had a higher risk of death (OR 5·13, 1·08 to 48·61; P = 0·039). Rates of cardiorespiratory complications (P = 0·338), bile leakage (P = 0·286) and reoperation (P = 0·352) were similar in the two groups. Patients with cirrhosis had a longer hospital stay than those without (11 versus 8 days; P = 0·018). Centre expertise was an independent protective factor against PHLF in patients with cirrhosis (OR 0·33, 0·14 to 0·76; P = 0·010).
CONCLUSION
Underlying cirrhosis remains an independent risk factor for impaired outcomes in patients undergoing LLR, even in expert centres.
ANTECEDENTES
El objetivo de este estudio fue analizar el impacto de la cirrosis en los resultados a corto plazo después de la resección hepática laparoscópica (laparoscopic liver resection, LLR) en un estudio de cohortes multicéntrico nacional. MÉTODOS: Este estudio retrospectivo incluyó todos los pacientes sometidos a LLR en 27 centros entre 2000 y 2017. La cirrosis se definió como fibrosis F4 en el examen histopatológico. Los resultados a corto plazo de los pacientes con hígado cirrótico (cirrhotic liver CL) (pacientes CL) y los pacientes con hígado no cirrótico (non-cirrhotic liver, NCL) (pacientes NCL) se compararon después de realizar un emparejamiento por puntaje de propension del volumen del centro, las características demográficas y del tumor, y la extensión de la resección.
RESULTADOS
Del total de 3.150 pacientes incluidos, se realizó LLR en 774 (24,6%) pacientes CL y en 2.376 (75,4%) pacientes NCL. Las tasas de complicaciones graves y mortalidad en el grupo de pacientes CL fueron del 10,6% y 2,6%, respectivamente. La insuficiencia hepática posterior a la hepatectomía (post-hepatectomy liver failure, PHLF) fue la principal causa de mortalidad (55% de los casos) y se produjo en el 3,6% de los casos en pacientes CL. Después del emparejamiento, los pacientes CL tendieron a tener tasas más altas de complicaciones graves (razón de oportunidades, odds ratio, OR 1,74; i.c. del 95% 0,92-0,41; P = 0,096) y de PHLF (OR 7,13; i.c. del 95% 0,91-323,10; P = 0,068) en comparación con los pacientes NCL. Los pacientes CL estuvieron expuestos a un mayor riesgo de mortalidad (OR 5,13; i.c. del 95% 1,08-48,6; P = 0,039) en comparación con los pacientes NCL. Los pacientes CL presentaron tasas similares de complicaciones cardiorrespiratorias graves (P = 0,338), de fuga biliar (P = 0,286) y de reintervenciones (P = 0,352) que los pacientes NCL. Los pacientes CL tuvieron una estancia hospitalaria más larga (11 versus 8 días; P = 0,018) que los pacientes NCL. La experiencia del centro fue un factor protector independiente de PHLF (OR 0,33; i.c. del 95% 0,14-0,76; P = 0,010) pacientes CL. CONCLUSIÓN: La presencia de cirrosis subyacente sigue siendo un factor de riesgo independiente de peores resultados en pacientes sometidos a resección hepática laparoscópica, incluso en centros con experiencia.

Autres résumés

Type: Publisher (spa)
El objetivo de este estudio fue analizar el impacto de la cirrosis en los resultados a corto plazo después de la resección hepática laparoscópica (laparoscopic liver resection, LLR) en un estudio de cohortes multicéntrico nacional. MÉTODOS: Este estudio retrospectivo incluyó todos los pacientes sometidos a LLR en 27 centros entre 2000 y 2017. La cirrosis se definió como fibrosis F4 en el examen histopatológico. Los resultados a corto plazo de los pacientes con hígado cirrótico (cirrhotic liver CL) (pacientes CL) y los pacientes con hígado no cirrótico (non-cirrhotic liver, NCL) (pacientes NCL) se compararon después de realizar un emparejamiento por puntaje de propension del volumen del centro, las características demográficas y del tumor, y la extensión de la resección.

Identifiants

pubmed: 31916594
doi: 10.1002/bjs.11406
doi:

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

268-277

Informations de copyright

© 2020 BJS Society Ltd Published by John Wiley & Sons Ltd.

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Auteurs

C Hobeika (C)

Department of Hepatobiliary and Pancreatic Surgery and Liver Transplantation, Sorbonne Université, Centre de Recherche Scientifique Saint Antoine, Hôpital Pitié Salpétrière, Paris, France.

D Fuks (D)

Department of Digestive, Oncological and Metabolic Surgery, Institut Mutualiste Montsouris, University Paris Descartes, Paris, France.

F Cauchy (F)

Department of Hepatobiliary and Pancreatic Surgery and Liver Transplantation, Hôpital Beaujon, Clichy, France.

C Goumard (C)

Department of Hepatobiliary and Pancreatic Surgery and Liver Transplantation, Sorbonne Université, Centre de Recherche Scientifique Saint Antoine, Hôpital Pitié Salpétrière, Paris, France.

O Soubrane (O)

Department of Hepatobiliary and Pancreatic Surgery and Liver Transplantation, Hôpital Beaujon, Clichy, France.

B Gayet (B)

Department of Digestive, Oncological and Metabolic Surgery, Institut Mutualiste Montsouris, University Paris Descartes, Paris, France.

E Salamé (E)

Department of Digestive Surgery and Liver Transplantation, Trousseau University Hospital, Tours University, Tours, France.

D Cherqui (D)

Department of Hepatobiliary and Pancreatic Surgery and Liver Transplantation, Centre Hépato-biliaire de Paul Brousse, Villejuif, France.

E Vibert (E)

Department of Hepatobiliary and Pancreatic Surgery and Liver Transplantation, Centre Hépato-biliaire de Paul Brousse, Villejuif, France.

O Scatton (O)

Department of Hepatobiliary and Pancreatic Surgery and Liver Transplantation, Sorbonne Université, Centre de Recherche Scientifique Saint Antoine, Hôpital Pitié Salpétrière, Paris, France.

T Nomi (T)

Nara Medical University, Nara, Japan.

N Oudafal (N)

Institut Mutualiste Montsouris, Paris, France.

T Kawai (T)

Pitié Salpétrière Hospital, Assistance Publique - Hôpitaux de Paris (APHP), Paris, France.

S Komatsu (S)

Pitié Salpétrière Hospital, Assistance Publique - Hôpitaux de Paris (APHP), Paris, France.

S Okumura (S)

Pitié Salpétrière Hospital, Assistance Publique - Hôpitaux de Paris (APHP), Paris, France.

N Petrucciani (N)

Hôpital Henri Mondor, APHP, Creteil, France.

A Laurent (A)

Hôpital Henri Mondor, APHP, Creteil, France.

P Bucur (P)

Trousseau Hospital, University Hospital Centre of Tours, Tours, France.

L Barbier (L)

Trousseau Hospital, University Hospital Centre of Tours, Tours, France.

B Trechot (B)

Centre Hépato-biliaire de Paul Brousse, APHP, Villejuif, France.

J Nunèz (J)

Centre Hépato-biliaire de Paul Brousse, APHP, Villejuif, France.

M Tedeschi (M)

Centre Hépato-biliaire de Paul Brousse, APHP, Villejuif, France.

M-A Allard (MA)

Centre Hépato-biliaire de Paul Brousse, APHP, Villejuif, France.

N Golse (N)

Centre Hépato-biliaire de Paul Brousse, APHP, Villejuif, France.

O Ciacio (O)

Centre Hépato-biliaire de Paul Brousse, APHP, Villejuif, France.

G Pittau (G)

Centre Hépato-biliaire de Paul Brousse, APHP, Villejuif, France.

A Sa Cunha (AS)

Centre Hépato-biliaire de Paul Brousse, APHP, Villejuif, France.

R Adam (R)

Centre Hépato-biliaire de Paul Brousse, APHP, Villejuif, France.

C Laurent (C)

Hospital University Centre of Bordeaux, Bordeaux, France.

L Chiche (L)

Hospital University Centre of Bordeaux, Bordeaux, France.

P Leourier (P)

Hospital University Centre of Amiens-Picardie, Amiens, France.

L Rebibo (L)

Hospital University Centre of Amiens-Picardie, Amiens, France.

J-M Regimbeau (JM)

Hospital University Centre of Amiens-Picardie, Amiens, France.

L Ferre (L)

Saint Eloi Hospital, Hospital University Centre of Montpellier, Montpellier, France.

F R Souche (FR)

Saint Eloi Hospital, Hospital University Centre of Montpellier, Montpellier, France.

J Chauvat (J)

Saint Eloi Hospital, Hospital University Centre of Montpellier, Montpellier, France.

J-M Fabre (JM)

Saint Eloi Hospital, Hospital University Centre of Montpellier, Montpellier, France.

F Jehaes (F)

Croix Rousse Hospital, Hospices Civils de Lyon, Lyon, France.

K Mohkam (K)

Croix Rousse Hospital, Hospices Civils de Lyon, Lyon, France.

M Lesurtel (M)

Croix Rousse Hospital, Hospices Civils de Lyon, Lyon, France.

C Ducerf (C)

Croix Rousse Hospital, Hospices Civils de Lyon, Lyon, France.

J-Y Mabrut (JY)

Croix Rousse Hospital, Hospices Civils de Lyon, Lyon, France.

T Hor (T)

St Antoine Hospital, APHP, Paris, France.

F Paye (F)

St Antoine Hospital, APHP, Paris, France.

P Balladur (P)

St Antoine Hospital, APHP, Paris, France.

B Suc (B)

Rangueil Hospital, Hospital University Centre of Toulouse, Toulouse, France.

F Muscari (F)

Rangueil Hospital, Hospital University Centre of Toulouse, Toulouse, France.

G Millet (G)

Claude Huriez Hospital, Hospital University Centre of Lille, Lille, France.

M El Amrani (M)

Claude Huriez Hospital, Hospital University Centre of Lille, Lille, France.

C Ratajczak (C)

Claude Huriez Hospital, Hospital University Centre of Lille, Lille, France.

K Lecolle (K)

Claude Huriez Hospital, Hospital University Centre of Lille, Lille, France.

E Boleslawski (E)

Claude Huriez Hospital, Hospital University Centre of Lille, Lille, France.

S Truant (S)

Claude Huriez Hospital, Hospital University Centre of Lille, Lille, France.

F-R Pruvot (FR)

Claude Huriez Hospital, Hospital University Centre of Lille, Lille, France.

A-R Kianmanesh (AR)

Robert Debré Hospital, Hospital University Centre of Reims, Reims, France.

T Codjia (T)

Charles Nicolle Hospital, Hospital University Centre of Rouen, Rouen, France.

L Schwarz (L)

Charles Nicolle Hospital, Hospital University Centre of Rouen, Rouen, France.

E Girard (E)

Michalon Hospital, Hospital University Centre of Grenoble, Grebnoble, France.

J Abba (J)

Michalon Hospital, Hospital University Centre of Grenoble, Grebnoble, France.

C Letoublon (C)

Michalon Hospital, Hospital University Centre of Grenoble, Grebnoble, France.

M Chirica (M)

Michalon Hospital, Hospital University Centre of Grenoble, Grebnoble, France.

A Carmelo (A)

Hôpital Européen, Marseille, France.

C VanBrugghe (C)

Hôpital Européen, Marseille, France.

Z Cherkaoui (Z)

Nouvel Hôpital Civil, Hospital University Centre of Strasbourg, Strasbourg, France.

X Unterteiner (X)

Nouvel Hôpital Civil, Hospital University Centre of Strasbourg, Strasbourg, France.

R Memeo (R)

Nouvel Hôpital Civil, Hospital University Centre of Strasbourg, Strasbourg, France.

P Pessaux (P)

Nouvel Hôpital Civil, Hospital University Centre of Strasbourg, Strasbourg, France.

E Buc (E)

Hospital University Centre of Clermont-Ferrand, Clermont-Ferrand, France.

E Lermite (E)

Hospital University Centre of Angers, Angers, France.

J Barbieux (J)

Hospital University Centre of Angers, Angers, France.

M Bougard (M)

Hospital University Centre of Angers, Angers, France.

U Marchese (U)

Institut Paoli-Calmettes, Marseille, France.

J Ewald (J)

Institut Paoli-Calmettes, Marseille, France.

O Turini (O)

Institut Paoli-Calmettes, Marseille, France.

A Thobie (A)

Hospital University Centre of Caen Normandie, Caen, France.

B Menahem (B)

Hospital University Centre of Caen Normandie, Caen, France.

A Mulliri (A)

Hospital University Centre of Caen Normandie, Caen, France.

J Lubrano (J)

Hospital University Centre of Caen Normandie, Caen, France.

J Zemour (J)

Hospital University Centre of Saint-Pierre, Saint Pierre, Department of Réunion, France.

H Fagot (H)

Hospital University Centre of Saint-Pierre, Saint Pierre, Department of Réunion, France.

G Passot (G)

Hospital University Centre of Lyon Sud, Lyon, France.

E Gregoire (E)

La Timone Hospital, Hospital University Centre of Marseille, Marseille, France.

J Hardwigsen (J)

La Timone Hospital, Hospital University Centre of Marseille, Marseille, France.

Y-P le Treut (YP)

La Timone Hospital, Hospital University Centre of Marseille, Marseille, France.

D Patrice (D)

Louis Pasteur Hospital, Colmar, France.

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