metricas
covid
Buscar en
Cirugía Española (English Edition)
Toda la web
Inicio Cirugía Española (English Edition) Hospital Variation in Anastomotic Leakage After Rectal Cancer Surgery in the Spa...
Información de la revista
Vol. 94. Núm. 4.
Páginas 213-220 (abril 2016)
Visitas
2653
Vol. 94. Núm. 4.
Páginas 213-220 (abril 2016)
Original article
Acceso a texto completo
Hospital Variation in Anastomotic Leakage After Rectal Cancer Surgery in the Spanish Association of Surgeons Project: The Contribution of Hospital Volume
Variabilidad interhospitalaria de la dehiscencia anastomótica en el Proyecto del Cáncer de Recto de la Asociación Española de Cirujanos: La influencia del volumen quirúrgico
Visitas
2653
Héctor Ortiza,
Autor para correspondencia
hhortiz@telefonica.net

Corresponding author.
, Sebastiano Biondob, Antonio Codinac, Miguel Á. Cigad, José Enríquez-Navascuése, Eloy Espínf, Eduardo García-Granerog, José Vicente Roigh
a Departamento Ciencias de la Salud, Universidad Pública de Navarra, Pamplona, Spain
b Unidad de Coloproctología, Departamento de Cirugía, Hospital Universitario de Bellvitge, Barcelona, Spain
c Unidad de Coloproctología, Departamento de Cirugía, Hospital Universitario Josep Trueta, Gerona, Spain
d Unidad de Coloproctología, Departamento de Cirugía, Complejo Hospitalario de Navarra, Pamplona, Spain
e Unidad de Coloproctología, Departamento de Cirugía, Hospital Universitario Donostia, San Sebastián, Spain
f Unidad de Coloproctología, Departamento de Cirugía, Hospital Universitario Vall d’Hebron, Barcelona, Spain
g Unidad de Coloproctología, Departamento de Cirugía, Hospital Universitario La Fe, Valencia, Spain
h Unidad de Coloproctología, Hospital Nisa 9 de Octubre, Valencia, Spain
Este artículo ha recibido
Información del artículo
Resumen
Texto completo
Bibliografía
Descargar PDF
Estadísticas
Figuras (1)
Tablas (2)
Table 1. Description and Results of Univariate Analysis of the Population Sample Studied.
Table 2. Analytical Results of the 3 Models.
Mostrar másMostrar menos
Abstract
Objective

This multicentre observational study aimed to determine the anastomotic leak rate in the hospitals included in the Rectal Cancer Project of the Spanish Society of Surgeons and examine whether hospital volume may contribute to any variation between hospitals.

Methods

Hospital variation was quantified using a multilevel approach on prospective data derived from the multicentre database of all adenocarcinomas of the rectum operated by an anterior resection at 84 surgical departments from 2006 to 2013. The following variables were included in the analysis; demographics, American Society of Anaesthesiologists classification, use of defunctioning stoma, tumour location and stage, administration of neoadjuvant treatment, and annual volume of elective surgical procedures.

Results

A total of 7231 consecutive patients were included. The rate of anastomotic leak was 10.0%. Stratified by annual surgical volume hospitals varied from 9.9% to 11.3%. In multilevel regression analysis, the risk of anastomotic leak increased in male patients, in patients with tumours located below 12cm from the anal verge, and advanced tumour stages. However, a defunctioning stoma seemed to prevent this complication. Hospital surgical volume was not associated with anastomotic leak (OR: 0.852, [0.487–1.518]; P=.577). Furthermore, there was a statistically significant variation in anastomotic leak between all departments (MOR: 1.475; [1.321–1.681]; P<.001).

Conclusion

Anastomotic leak varies significantly among hospitals included in the project and this difference cannot be attributed to the annual surgical volume.

Keywords:
Rectal cancer
Anastomotic leak
Comparison of departments
Case-mix
Multicentre database
Education
Resumen
Introducción

El objetivo de este estudio observacional multicéntrico fue determinar la tasa de dehiscencia anastomótica en los hospitales que participan en el Proyecto del Cáncer de Recto de la Asociación Española de Cirujanos y evaluar si había diferencias atribuibles al volumen quirúrgico entre los hospitales que participan en él.

Métodos

La variación interhospitalaria se cuantificó mediante un estudio multinivel realizado con una base de datos prospectiva de los pacientes operados por un adenocarcinoma de recto con una resección anterior en 84 hospitales, entre marzo de 2006 y diciembre de 2013. En los análisis se incluyeron: las variables demográficas, la clasificación de la American Society of Anaesthesiologists, la utilización de un estoma de derivación, la localización y el estadio del tumour, la administración de tratamiento neoadyuvante y el volumen quirúrgico anual del hospital.

Resultados

Se analizó a 7.231 pacientes operados consecutivamente. La tasa de dehiscencia anastomótica fue del 10,0%. Los porcentajes de dehiscencia de los hospitales, estratificados por el volumen quirúrgico annual, variaron entre el 9,9 y el 11,3%. En el análisis de regresión multinivel el sexo masculino, los tumores localizados por debajo de 12cm medidos desde el margen anal y los estadios T avanzados favorecieron la aparición de la dehiscencia, mientras que la presencia de un estoma de derivación la previno. El volumen quirúrgico anual del hospital no se asoció con la dehiscencia (OR: 0,852; [0,487–1,518]; P=0,577). Además, se observó una variación significativa de la tasa de dehiscencia entre los hospitales (MOR: 1,475; [1,321–1,681]; P<0,001).

Conclusión

La dehiscencia anastomótica varía de forma estadísticamente significativa entre los hospitales incluidos en el proyecto, y esta diferencia no se puede atribuir al volumen quirúrgico anual.

Palabras clave:
Cáncer de recto
Dehiscencia anastomótica
Comparación de hospitales
Volumen quirúrgico anual
Base de datos multicéntrica
Educación médica
Texto completo
Introduction

The standard treatment for cancer of the rectum, when it is possible, is anterior resection with total mesorectal excision.1 This surgical procedure is associated with anastomotic leakage rate that varies from 10% to 15%.2,3

The contributions of several factors to the appearance of this complication have been studied. Nevertheless, research into the influence of hospital surgical volume and specialisation on the frequency of anastomotic leakage is limited and controversial.4,5 Additionally, the results of Scandinavian records,6,7 which inspired the Rectal Cancer Project of the Spanish Association of Surgeons, are also controversial.

The aim of this study was to determine the rate of anastomotic leakage in the Rectal Cancer Project of the Spanish Association of Surgeons during the period 2006–2013, and to evaluate, using a multivariate study, the influence of hospital surgical volume on anastomotic leakage in the participating hospitals.

Methods

This observational multicentre study was undertaken using the prospective database of the Rectal Cancer Project of the Spanish Association of Surgeons. This teaching initiative started in 2006 with the aim of firstly introducing mesorectal excision surgery and then extended abdominoperineal amputation to multidisciplinary groups in National Health System hospitals that requested this and fulfilled the requisite conditions: they had to have Coloproctology Units with the indispensible diagnostic technical resources and perform 12 or more colorectal resections per year, which includes the following operations: anterior resection, abdominoperineal amputation, Hartmann's procedure and proctocolectomy.

Data gathered prospectively in hospitals by the surgeons in the project were sent to a central registry. This informed each hospital every year of the results of its activity in comparison with all of the other hospitals taking part. A more detailed description of this project has already been published.8,9

Patient Inclusion and Exclusion Criteria

Patients were included who had been operated electively with anterior resection from 1 March 2006 and 31 December 2013 in the 84 hospitals included in the project.

Patients operated as emergencies were excluded, as were those who lacked the results of a relevant variable and those whose results were incongruent.

Surgical Technique

Total mesorectal excision was the standard procedure to treat tumours located 12cm or less from the anal margin. Tumours above 12cm were treated using the partial excision of the mesorectum, including the mesorectal fascia up to 5cm below the tumour, or total mesorectal excision at the decision of the surgeon. Whether or not an ileostomy was performed also depended on the surgeon's decision.

Study Variables

Leakage from the anastomosis was the outcome variable of the study. Confusion variables are divided into fixed and random ones. The following demographic variables are considered to be fixed confusion variables: age, categorised into 3 groups (<65, 65–80, >80 years old), and sex; the degree of surgical risk (measured by the ASA degree of anaesthetic risk); the location of the tumour, which was categorised in 3 groups (0–6cm, 7–12cm and 13–15cm); the use of an ileostomy; the pathological stage of the tumour; the use of neoadjuvant treatment and the individual nature of each hospital, categorised in 4 groups according to the median number of patients treated per year using anterior resection: 11, 12–23, 24–35 and >36 patients. The hospital was considered to be a random confusion variable.

Definitions

Rectal tumours (CIE20) were considered to be those located in the last 15cm measured from the anal margin by rigid rectoscopy during withdrawal or by magnetic resonance.10

The pathological tumour stage was classified using the fifth edition of the TNM classification (American Joint Committee on Cancer [AJCC] stages IIV; 5th edition).11

Leakage from the anastomosis was defined as an event of the anastomosis which required interventional radiology or a postoperative surgical operation. Pelvic abscesses without radiological evidence of leakage and early recto-vaginal fistulas are also considered to be leakages from the anastomosis. Subclinical leakages detected in the soluble contrast enema before closure of the stoma were not considered to be anastomotic leaks, as is the case in the Scandinavian records which this project imitates and with which it compares its results.12,13

As the names of the hospitals and patients included are not given, it was not considered necessary to seek the approval of the Ethics Committees of the hospitals in question, although the project had been approved by them.

Statistical Analysis

Categorical variables were analysed using the χ2 test, while non-parametrical samples were compared using Mann–Whitney's U test.

To determine the variation of the outcome variable of anastomotic leakage among the hospitals included, 3 models were constructed: one model of fixed effects included the fixed confusion variables, one complete model included the fixed confusion variables and the random hospital variable, while one null model exclusively included the random hospital variable. Logistic regression was carried out in the first model, while multilevel logistic regression was applied in the other two models.

Akaike's information criterion (AIC)14 was calculated for each model, together with the deviance test. Random variance (σ2) was calculated in the multilevel models, together with their intervals of confidence, the median odds ratio (MOR)15 and the odds ratio (OR) between the best and worst, excluding 5% of the outlier hospitals. The MOR quantifies the variation between hospitals as medians, comparing randomly selected pairs of patients with the same values of the confusion variables.16

Results

Of the 7231 patients operated electively using anterior resection in the period studied, 727 (10.0%) presented anastomotic leakage.

Table 1 describes the characteristics of the population studied and the risk of leakage expressed in OR for each one of the variables studied using univariate analysis. It shows the percentages of anastomotic leakage in the hospitals grouped into categories according to surgical volume, from 9.9% to 11.3%.

Table 1.

Description and Results of Univariate Analysis of the Population Sample Studied.

  Total  No  Yes  OR  P ratio 
  7231  No.=6504 n (%)  No.=727 n (%)     
Sex
Women  2491  2307 (92.6)  184 (7.3)  Ref.  Ref. 
Men  4740  4197 (88.5)  543 (11.5)  1.62 (1.36–1.94)  .001 
Age
<65  2961  2675 (90.3)  286 (9.6)  Ref.  Ref. 
65–80  3438  3070 (89.3)  368 (10.7)  1.12 (0.95–1.32)  .169 
>80  832  759 (91.2)  73 (8.7)  0.90 (0.68–1.17)  .445 
ASA
472  431 (91.3)  41 (8.6)  Ref.  Ref. 
II  4108  3730 (90.8)  378 (9.2)  1.06 (0.77–1.51)  .726 
III  2454  2170 (88.4)  284 (11.6)  1.37 (0.98–1.96)  .063 
IV  197  173 (87.8)  24 (12.2)  1.46 (0.84–2.48)  .172 
Tumour location (cm)
13–15  1144  1050 (91.8)  94 (8.22)  Ref.  Ref. 
7–12  4631  4157 (89.8)  474 (10.2)  1.27 (1.01–1.61)  .037 
0–6  1456  1297 (89.1)  159 (10.9)  1.37 (1.05–1.79)  .021 
Stoma
No  2910  2567 (88.2)  343 (11.8)  Ref  Ref 
Yes  4321  3937 (91.1)  384 (8.9)  0.72 (0.62–0.84)  <.001 
Neoadjuvant treatment
No  3015  2704 (89.7)  311 (10.3)  Ref.  Ref. 
Yes  4216  3800 (90.1)  416 (9.8)  0.95 (0.82–1.11)  .532 
Pathological T stage
pT1  552  513 (92.9)  39 (7.1)  Ref.  Ref. 
ypT0  820  765 (93.3)  55 (6.7)  0.94 (0.62–1.46)  .794 
pT2  1869  1664 (89.0)  205 (11.0)  1.62 (1.14–2.34)  .006 
pT3  3578  3199 (89.4)  379 (10.6)  1.55 (1.12–2.22)  .008 
pT4  412  363 (88.1)  49 (11.9)  1.77 (1.14–2.77)  .011 
Pathological N stage
pNx-0  4858  4363 (89.8)  495 (10.2)  Ref.  Ref. 
pN1-2  2373  2141 (90.2)  232 (9.8)  0.96 (0.81–1.12)  .586 
M stage
pM0  6518  5879 (90.2)  639 (9.8)  Ref.  Ref. 
pM1  713  625 (87.7)  88 (12.3)  1.30 (1.02–1.64)  .037 
Hospitals classified according to median annual surgical volume
11 patients/yeara  256  227 (88.7)  29 (11.3)  Ref.  Ref. 
12–23 patients/year  1973  1775 (90.0)  198 (10.0)  0.87 (0.58–1.34)  .514 
24–35 patients/year  2264  2036 (89.9)  228 (10.1)  0.87 (0.59–1.34)  .522 
≥ 36 patients/year  2738  2466 (90.1)  272 (9.9)  0.86 (0.58–1.32)  .473 
a

In 2 hospitals the annual median number of patients treated by anterior resection of the rectum was 11.

The results of the fixed effects models, the complete model and the null model are shown in Table 2. This shows the variables that had a significant influence on anastomotic leakage. Male sex, the distance from the tumour to the anal margin and advanced T stages made it more probable; while ileostomy prevented it. Hospital surgical volume did not influence the rates of anastomotic leakage. Additionally, the complete and null models showed that leakage from the anastomosis differed significantly between the hospitals studied.

Table 2.

Analytical Results of the 3 Models.

  Fixed OR effects model 95% CI  P ratio  Complete OR model 95% CI  P ratio  Null OR model 95% CI 
Sex
Women  1.00    1.00    – 
Men  1.604 (1.347–1.918)  .001  1.627 (1.363–1.949)  .001   
Age (years)
<65  1.00    1.00    – 
65–80  1.024 (0.862–1.217)  .788  1.012 (0.849–1.206)  .897   
>80  0.766 (0.571–1.016)  .069  0.739 (0.549–0.986)  .043   
ASA
ASA I  1.00    1.00    – 
ASA II  1.062 (0.762–1.517)  .731  1.118 (0.796–1.609)  .532   
ASA III  1.331 (0.939–1.931)  .119  1.433 (1.000–2.097)  .056   
ASA IV  1.370 (0.782–2.356)  .261  1.435 (0.809–2.501)  .208   
Tumour location (cm)
15–13  1.00    1.00    – 
12–7  1.368 (1.080–1.749)  .011  1.468 (1.153–1.886)  .002   
0–6  1.551 (1.170–2.066)  .002  1.710 (1.282–2.293)  .001   
Stoma
No  1.00    1.00     
Yes  0.55 (0.46–0.66)  .001  0.639 (0.346–0.750)  .001  – 
Neoadjuvant treatment
No  1.00    1.00    – 
Yes  0.905 (0.764–1.074)  .251  0.872 (0.000-Inf)  .129   
Pathological T stage
pT1  1.00    1.00    – 
ypT0  0.989 (0.642–1.537)  .962  0.989 (0.639–1.543)  .960   
pT2  1.700 (1.200–2.467)  .004  1.716 (1.207–2.500)  .004   
pT3  1.690 (1.204–2.435)  .003  1.705 (1.209–2.466)  .003   
pT4  2.087 (1.322–3.314)  .002  2.100 (1.322–3.355)  .002   
Pathological N stage
N0  1.00    1.00    – 
pN1-2  0.843 (0.705–1.006)  .060  0.865 (0.722–1.035)  .115   
M stage
M0  1.00    1.00    – 
pM1  1.239 (0.962–1.581)  .090  1.267 (0.979–1.623)  .067   
Hospital surgical volume (operations/year)
11  1.00    1.00    – 
12–23d  0.877 (0.587–1.354)  .538  0.836 (0.492–1.449)  .513   
24–35  0.885 (0.595–1.362)  .562  0.833 (0.485–1.455)  .511   
>36  0.859 (0.580–1.318)  .468  0.852 (0.487–1.518)  .577   
AICa  4675.0    4684.5    4631.2 
Random variance σ2 95% CI  –    0.166 (0.085–0.297)    0.189 (0.101–0.330) 
Median odds ratio (MOR)b  –    1.475 (1.321–1.681)    1.513 (1.354–1.729) 
Best vs worst hospital odds ratioc  –    2.22    2.44 
P overall  <.001    <.001    <.001 
a

Akaike's criterion.

b

Comparison of the risk of anastomotic leakage between 2 hospitals selected at random.

c

Risk of anastomotic leakage comparing the hospital with the best result and the one with the worst result, excluding those hospitals with outlier values (5%).

d

In 2 hospitals the annual median number of patients treated using rectal resection was 11.

Fig. 1 shows the differences between the hospitals.

Fig. 1.

The risk of anastomotic leakage in hospitals, obtained by multilevel logistic regression, considering the hospital variable to be a random effect to correct the non-independence of data. The hospitals are represented along the vertical axis by their project code number. The value of the random constant for each hospital is shown. The hospitals are ranked from lower to higher constant value: positive constant values show the worst results.

(0.62MB).
Discussion

The results of this study indicate that in the Rectal Cancer Project of the Spanish Association of Surgeons anastomotic leakage does not depend on hospital surgical volume, and that rates vary between the hospitals included in a statistically significant way.

The greatest weakness of this study is connected with the voluntary nature of the inclusion of data in the Colorectal Cancer Project of the Spanish Association of Surgeons, above all when it is compared with records in Scandinavian countries,17,18 where it is obligatory to include data in the registry. Nevertheless, as has already been stated in greater detail,8,9 several measures were applied to prevent voluntary or involuntary distortion in inclusion as well as in the data. Unfortunately, due to the anonymous nature of the data and the lack of other sources to compare information in our country, it is not possible to state with certainty that there are no such data. Lastly, in the worst-case scenario the data in this study indicate minimum rates of anastomotic leakage.

Another weakness of this study is that the project database does not include several variables that may influence rates of anastomotic leakage, such as obesity or albumin levels, etc. Nevertheless, the aim of the project is for hospitals to know the immediate and long-term results of their work in comparison with those of all the hospitals. As the project is implemented in 15 autonomous communities, it is improbable that there will be differences that can be attributed to socio-economic factors, as has been proven in Denmark.19

The rate of anastomotic leakage observed in this study, 10%, is between the rates found in Norway17 (7%), Sweden20 (8.7%) and Denmark18 (12.7%), according to the latest reports and studies published by these registries. It is far higher than the rate shown in the Irish programme that centralises data on this disease (4.3%).5

Three of these registries evaluated the influence of hospital surgical volume on the occurrence of leakage, with contradictory results. Univariate analyses in Ireland5 and Norway6 showed differences that could be attributed to volume, while multivariate analysis in Denmark7 showed no such differences, as is the case in this study which used multilevel statistical analysis. The discrepancy between these 4 studies may therefore be explained by the difference in statistical methodology. Furthermore, multivariate analysis which makes it possible to adjust results according to multiple variables in the sample is far more solid, together with multilevel analysis.

It is a natural tendency to use national registry data to establish activity outcome indicators, as was the case in Scandinavia, as these make it possible for hospitals to try to correct variability. Unfortunately, although the departments taking part in the Rectal Cancer Project of the Spanish Association of Surgeons have similar characteristics to those of the Scandinavian hospitals, and the size of the sample of patients analysed in this study is reasonably large, it is impossible to use it as a national outcome indicator. The reason for this, as has been found for the voluntary records of the National Bowel Cancer Project in Great Britain21 and the Belgian rectal cancer PROCARE22 project, is that when hospitals do not send in all of their data and thereby distort the information, or if they fail to take part in the registry at all, the rates of surgical mortality are higher for the patients not included in the registry than they are for those who are included. This leads to an underestimation of surgical mortality at a national level, preventing exact estimations of the activity indicators.

To conclude, the results of this study indicate that in the Rectal Cancer Project of the Spanish Association of Surgeons the rate of anastomotic leakage is similar to those of the Scandinavian registries. It also varies in a statistically significant way between the hospitals included, and this difference cannot be explained by surgical volume.

Financing

This project was financed by the following research grants: FIS number: PI11/00010 and the Board of Health, Government of Navarre: 20/11.

Conflict of Interest

The authors have no conflict of interests to declare.

Acknowledgements

The collaborating Group of the Colorectal Cancer Project of the Spanish Association of Surgeons (2006–2013).

Appendix A

Virgen de la Arrixaca (Juan Luján), Bellvitge (Doménico Fraccalvieri, Sebastiano Biondo), Complejo Hospitalario de Navarra (Miguel Á. Ciga), Clínico de Valencia (Alejandro Espí), Josep Trueta (Antonio Codina), Sagunto (María D. Ruiz), Vall d’Hebrón (Eloy Espin, F. Vallribera), La Fe (Eduardo García-Granero), Complejo Hospitalario Ourense (Alberto Parajo), Germans Trias i Pujol (Ignasi Camps, Marta Piñol), Lluís Alcanyis (Vicent Viciano), Complejo Asistencial Burgos (Evelio Alonso), Hospital del Mar (Miguel Pera), Meixoeiro (Nieves Cáceres), Complejo Asistencial Salamanca (Jacinto García), Gregorio Marañón (Marcos Rodríguez), Torrecárdenas (Ángel Reina), General de Valencia (Verónica Gumbau), Txagorritxu (José Errasti), Donostia (José A. Múgica), Reina Sofía (José Gómez), Juan Ramón Jiménez (Ricardo Rada, Mónica Orelogio), Arnau de Vilanova de Valencia (Natalia Uribe), General de Jerez (Juan de Dios Franco), Arnau de Vilanova de Lérida (José Enrique Sierra), Santa Creu i Sant Pau (Pilar Hernández), Clínico de Santiago de Compostela (Jesús Paredes), Universitario de Jaén (Gabriel Martínez), Clínico San Carlos (Mauricio García), Cabueñes (Guillermo Carreño), General de Albacete (Jesús Cifuentes), Miguel Servet (José Monzón), Xeral de Lugo (Olga Maseda), Universitario de Fuenlabrada (Daniel Huerga), Clínico y Provincial de Barcelona (Luis Flores), Joan XXIII (Fernando Gris), Virgen de las Nieves (Inmaculada Segura, Pablo Palma), Nuestra Señora de la Candelaria (José G. Díaz), Complejo Hospitalario de Badajoz (Jesús Salas), Clínico Universitario San Cecilio (Francisco Pérez, Benito Mirón), General Universitario de Alicante (Félix Lluis), Virgen Macarena (Luis Capitán, Javier Valdés), Xeral-Cies de Vigo (Nieves Cáceres), Infanta Sofía (Javier Martínez), Policlínica de Vigo (Alfredo Estévez), Virgen del Rocío de Sevilla (José Díaz, María V. Maestre), San Juan de Dios del Aljarafe (Antonio Amaya, Mónica Reig), Nuestra Señora de Sonsoles (Antonio Carmona), Universitario de Getafe (Francisco Javier Jiménez), H. Granollers (Didac Ribe), Universitario de La Paz (Isabel Prieto), Rafael Méndez (Ginés Sánchez, Sergio del Valle), General Universitario Reina Sofía (Pedro A. Parra), San Pedro de Alcántara (Francisco Romero), Torrevieja Salud (Alessandro Garcea), Santa María de Lérida (Xavier Rodamilans), Virgen del Puerto (José A. Pérez), Segovia (Guillermo Asís), Reus (Santiago Blanco), Instituto Valenciano de Oncología (Alfonso García, Rafael Estévan), Viladecans (Albert Sueiras), Cruces (Alberto Lamíquiz, José M.ª García), Ramón y Cajal (Javier Die), Manises (Amparo Solana), La Ribera Alzira (Francisco J. Blanco), Nuestra Señora del Rosell (Ana Lage), Mérida (José Domínguez), Universitario Fundación Alcorcón (Paula Dujovne), Henares Coslada (Natividad Palencia), Vinaroz (Raúl Adell), Onkologikoa de San Sebastián (Roberto Martínez), Consorci Sanitari Integral (Luis Ortiz de Zarate), Complejo Hospitalario Palencia (Ana M.ª Huidobro), Fundación Jiménez Díaz (Carlos Pastor), Torrejón (Jesús Á. Garijo), Puerto Real (M.ª del Coral de la Vega), Espíritu Santo (Manuel López).

References
[1]
S.T. Martin, H.M. Heneghan, D.C. Winter.
Systematic review and meta-analysis of outcomes following pathological complete response to neoadjuvant chemoradiotherapy for rectal cancer.
Br J Surg, 99 (2012), pp. 918-928
[2]
B.C. Paun, S. Cassie, A.R. MacLean, E. Dixon, W.D. Buie.
Postoperative complications following surgery for rectal cancer.
Ann Surg, 251 (2010), pp. 807-818
[3]
F.D. McDermott, A. Heeney, M.E. Kelly, R.J. Steele, G.L. Carlson, D.C. Winter.
Systematic review of preoperative, intraoperative and postoperative risk factors for colorectal anastomotic leaks.
Br J Surg, 102 (2015), pp. 462-479
[4]
D. Archampong, D. Borowski, P. Wille-Jorgensen, L.H. Iversen.
Workload and surgeon's specialty for outcome after colorectal cancer surgery.
Cochrane Database Syst Rev, (2012), pp. CD005391
[5]
J.P. Burke, J.C. Coffey, E. Boyle, F. Keane, D.A. McNamara.
Early outcomes for rectal cancer surgery in the Republic of Ireland following a national centralization program.
Ann Surg Oncol, 20 (2013), pp. 3414-3421
[6]
A. Wibe, M.T. Eriksen, A. Syse, S. Tretli, H.E. Myrvold, O. Søreide, et al.
Effect of hospital caseload on long-term outcome after standardization of rectal cancer surgery at a national level.
Br J Surg, 92 (2005), pp. 217-224
[7]
H. Harling, S. Bulow, L.N. Moller, T. Jorgensen.
Hospital volume and outcome of rectal cancer surgery in Denmark 1994–99.
Colorectal Dis, 7 (2005), pp. 90-95
[8]
H. Ortiz, A. Codina.
Resultados del proyecto docente y auditado del cáncer de recto de la Asociación Española de Cirujanos. Seis años desde su inicio.
[9]
H. Ortiz, S. Biondo, A. Codina, M.A. Ciga, J.M. Enríquez-Navascués, E. Garcia Granero, et al.
Proyecto del Cáncer de Recto de la Asociación Española de Cirujanos. Mortalidad postoperatoria. Variabilidad interhospitalaria e influencia del volumen quirúrgico.
[10]
D.S. Keller, R. Paspulati, A. Kjellmo, K.M. Rokseth, B. Bankwitz, A. Wibe, et al.
MRI-defined height of rectal tumours.
Br J Surg, 101 (2014), pp. 127-132
[11]
L.H. Sobin, C. Wittekind.
TNM classification of malignant tumours.
5th ed., Wiley, (1997),
[12]
C.A. Bertelsen, A.H. Andreasen, T. Jørgensen, H. Harling, on behalf of the Danish Colorectal Cancer Group.
Anastomotic leakage after curative anterior resection for rectal cancer: short and long-term outcome.
Colorectal Dis, 12 (2010), pp. e76-e81
[13]
M.T. Eriksen, A. Wibe, J. Norstein, J. Haffner, J.N. Wiig.
Anastomotic leakage following routine mesorectal excision for rectal cancer in a national cohort of patients.
Colorectal Dis, 7 (2005), pp. 51-57
[14]
F.E. Harrell.
Regression modeling strategies.
Springer Verlag, (2001),
[15]
K. Larsen, J. Merlo.
Appropriate assessment of neighborhood effects on individual health: integrating random and fixed effects in multilevel logistic regression.
Am J Epidemiol, 161 (2005), pp. 81-88
[16]
J. Merlo, B. Chaix, H. Ohlsson, A. Beckman, K. Johnell, P. Hjerpe, et al.
A brief conceptual tutorial of multilevel analysis in social epidemiology: using measures of clustering in multilevel logistic regression to investigate contextual phenomena.
J Epidemiol Community Health, 60 (2006), pp. 290-297
[17]
G. Ursin, B. Møller.
Kreftregisteret Årsrapport 2014 – Nasjonalt kvalitetsregister for tykk- og endetarmskreft, Oslo.
(2014, September),
[18]
Landsdækkende database for kræft i tyk- og endetarm. National årsrapport 2014. Available from: http://www.dccg.dk/03_Publikation/02_arsraport.html [accessed 12.10.15].
[19]
M. Osler, L.H. Iversen, A. Borglykke, S. Mårtensson, S. Daugbjerg, H. Harling, et al.
Hospital variation in 30-day mortality after colorectal cancer surgery in Denmark: the contribution of hospital volume and patient characteristics.
Ann Surg, 253 (2011), pp. 733-738
[20]
K. Kokeda, R. Johansson, N. Zar, H. Brgisson, M. Dahlberg, S. Skullman, et al.
Time trends, improvements and national auditing of rectal cancer management over an 18-year period.
Colorectal Dis, 17 (2015), pp. 168-179
[21]
A.M. Almoudaris, E.M. Burns, A. Bottle, P. Aylin, A. Darzi, O. Faiz.
A colorectal perspective on voluntary submission of outcome data to clinical registries.
Br J Surg, 98 (2011), pp. 132-139
[22]
D. Jegou, F. Penninckx, T. Vandendael, C. Bertrand, E. Van Eycken.
PROCARE. Completeness and registration bias in PROCARE, a Belgian multidisciplinary project on cancer of the rectum with participation on a voluntary basis.
Eur J Cancer, 51 (2015), pp. 1099-1108

Please cite this article as: Ortiz H, Biondo S, Codina A, Ciga MÁ, Enríquez-Navascués J, Espín E, et al. Variabilidad interhospitalaria de la dehiscencia anastomótica en el Proyecto del Cáncer de Recto de la Asociación Española de Cirujanos: La influencia del volumen quirúrgico. Cir Esp. 2016;94:213–220.

Appendix A presents a list of collaborators.

Copyright © 2015. AEC
Descargar PDF
Opciones de artículo
es en pt

¿Es usted profesional sanitario apto para prescribir o dispensar medicamentos?

Are you a health professional able to prescribe or dispense drugs?

Você é um profissional de saúde habilitado a prescrever ou dispensar medicamentos