Abstract
Purpose
We evaluated the intuition of expert pancreatic surgeons, in predicting the associated risk of pancreatic resection and compared this “intuition” to actual operative follow-up. The objective was to avoid major complications following pancreatic resection, which remains a challenge.
Methods
From January 2015 to February 2018, all patients who were 18 years old or more undergoing a pancreatic resection (pancreaticoduodenectomy [PD], distal pancreatectomy [DP], or central pancreatectomy [CP]) for pancreatic lesions were included. Preoperatively and postoperatively, all surgeons completed a form assessing the expected potential occurrence of clinically relevant postoperative pancreatic fistula (CR-POPF: grade B or C), postoperative hemorrhage, and length of stay.
Results
Preoperative intuition was assessed for 101 patients for 52 PD, 44 DP, and 5 CP cases. Overall mortality and morbidity rates were 6.9% (n = 7) and 67.3% (n = 68), respectively, and 38 patients (37.6%) developed a POPF, including 27 (26.7%) CR-POPF. Concordance between preoperative intuition of CR-POPF occurrence and reality was minimal, with a Cohen’s kappa coefficient (κ) of 0.175 (P value = 0.009), and the same result was obtained between postoperative intuition and reality (κ = 0.351; P < 0.001). When the pancreatic parenchyma was hard, surgeons predicted the absence of CR-POPF with a negative predictive value of 91.3%. However, they were not able to predict the occurrence of CR-POPF when the pancreas was soft (positive predictive value 48%).
Conclusions
This study assessed for the first time the surgeon’s intuition in pancreatic surgery, and demonstrated that pancreatic surgeons cannot accurately assess outcomes except when the pancreatic parenchyma is hard.
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Katz MHG, Wang H, Fleming JB, Sun CC, Hwang RF, Wolff RA, Varadhachary G, Abbruzzese JL, Crane CH, Krishnan S, Vauthey JN, Abdalla EK, Lee JE, Pisters PW, Evans DB (2009) Long-term survival after multidisciplinary management of resected pancreatic adenocarcinoma. Ann Surg Oncol 16:836–847. https://doi.org/10.1245/s10434-008-0295-2
Farges O, Bendersky N, Truant S, Delpero JR, Pruvot FR, Sauvanet A (2017) The theory and practice of pancreatic surgery in France. Ann Surg 266:797–804. https://doi.org/10.1097/SLA.0000000000002399
Vuong B, Dehal A, Uppal A et al (2018) What are the most significant cost and value drivers for pancreatic resection in an integrated healthcare system? J Am Coll Surg. https://doi.org/10.1016/j.jamcollsurg.2018.02.015
Bassi C, Marchegiani G, Dervenis C et al (2016) The 2016 update of the International Study Group (ISGPS) definition and grading of postoperative pancreatic fistula: 11 years after. Surgery 0. https://doi.org/10.1016/j.surg.2016.11.014
Cheng Y, Briarava M, Lai M, Wang X, Tu B, Cheng N, Gong J, Yuan Y, Pilati P, Mocellin S (2017) Pancreaticojejunostomy versus pancreaticogastrostomy reconstruction for the prevention of postoperative pancreatic fistula following pancreaticoduodenectomy. Cochrane Database Syst Rev 9:CD012257. https://doi.org/10.1002/14651858.CD012257.pub2
Callery MP, Pratt WB, Kent TS, Chaikof EL, Vollmer CM Jr (2013) A prospectively validated clinical risk score accurately predicts pancreatic fistula after pancreatoduodenectomy. J Am Coll Surg 216:1–14. https://doi.org/10.1016/j.jamcollsurg.2012.09.002
Braga M, Capretti G, Pecorelli N et al (2011) A prognostic score to predict major complications after pancreaticoduodenectomy. Ann Surg 254:702–707-708. https://doi.org/10.1097/SLA.0b013e31823598fb
Sandini M, Malleo G, Gianotti L (2016) Scores for prediction of fistula after pancreatoduodenectomy: a systematic review. Dig Surg 33:392–400. https://doi.org/10.1159/000445068
Vanbrugghe C, Ronot M, Cauchy F, Hobeika C, Dokmak S, Aussilhou B, Ragot E, Gaujoux S, Soubrane O, Lévy P, Sauvanet A (2018) Visceral obesity and open passive drainage increase the risk of pancreatic fistula following distal pancreatectomy. J Gastrointest Surg Off J Soc Surg Aliment Tract 23:1414–1424. https://doi.org/10.1007/s11605-018-3878-7
Farges O, Vibert E, Cosse C et al (2014) “Surgeons’ intuition” versus “prognostic models”: predicting the risk of liver resections. Ann Surg 260:923–928-930. https://doi.org/10.1097/SLA.0000000000000961
Balzan S, Belghiti J, Farges O et al (2005) The “50-50 criteria” on postoperative day 5: an accurate predictor of liver failure and death after hepatectomy. Ann Surg 242:824–828 NaN-829
Dindo D, Demartines N, Clavien P-A (2004) Classification of surgical complications: a new proposal with evaluation in a cohort of 6336 patients and results of a survey. Ann Surg 240:205–213
Wente MN, Veit JA, Bassi C, Dervenis C, Fingerhut A, Gouma DJ, Izbicki JR, Neoptolemos JP, Padbury RT, Sarr MG, Yeo CJ, Büchler MW (2007) Postpancreatectomy hemorrhage (PPH): an International Study Group of Pancreatic Surgery (ISGPS) definition. Surgery 142:20–25. https://doi.org/10.1016/j.surg.2007.02.001
Wente MN, Bassi C, Dervenis C, Fingerhut A, Gouma DJ, Izbicki JR, Neoptolemos JP, Padbury RT, Sarr MG, Traverso LW, Yeo CJ, Büchler MW (2007) Delayed gastric emptying (DGE) after pancreatic surgery: a suggested definition by the International Study Group of Pancreatic Surgery (ISGPS). Surgery 142:761–768. https://doi.org/10.1016/j.surg.2007.05.005
Slankamenac K, Graf R, Barkun J, Puhan MA, Clavien PA (2013) The comprehensive complication index: a novel continuous scale to measure surgical morbidity. Ann Surg 258:1–7. https://doi.org/10.1097/SLA.0b013e318296c732
Cohen J (1968) Weighted kappa: nominal scale agreement with provision for scaled disagreement or partial credit. Psychol Bull 70:213–220
Sim J, Wright CC (2005) The kappa statistic in reliability studies: use, interpretation, and sample size requirements. Phys Ther 85:257–268
Landis JR, Koch GG (1977) An application of hierarchical kappa-type statistics in the assessment of majority agreement among multiple observers. Biometrics 33:363–374
Mungroop TH, van Rijssen LB, van Klaveren D et al (2017) Alternative fistula risk score for pancreatoduodenectomy (a-FRS): design and international external validation. Ann Surg. https://doi.org/10.1097/SLA.0000000000002620
Ribero D, Amisano M, Zimmitti G, Giraldi F, Ferrero A, Capussotti L (2013) External tube pancreatostomy reduces the risk of mortality associated with completion pancreatectomy for symptomatic fistulas complicating pancreaticoduodenectomy. J Gastrointest Surg Off J Soc Surg Aliment Tract 17:332–338. https://doi.org/10.1007/s11605-012-2100-6
Sugimoto M, Gotohda N, Kato Y et al (2013) Risk factor analysis and prevention of postoperative pancreatic fistula after distal pancreatectomy with stapler use. J Hepato-Biliary-Pancreat Sci 20:538–544. https://doi.org/10.1007/s00534-013-0596-0
Sa Cunha A, Carrere N, Meunier B, Fabre JM, Sauvanet A, Pessaux P, Ortega-Deballon P, Fingerhut A, Lacaine F, French Fédération de Recherche EN Chirurgie (FRENCH) (2015) Stump closure reinforcement with absorbable fibrin collagen sealant sponge (TachoSil) does not prevent pancreatic fistula after distal pancreatectomy: the FIABLE multicenter controlled randomized study. Am J Surg 210:739–748. https://doi.org/10.1016/j.amjsurg.2015.04.015
Allen PJ, Gönen M, Brennan MF, Bucknor AA, Robinson LM, Pappas MM, Carlucci KE, D'Angelica MI, DeMatteo R, Kingham TP, Fong Y, Jarnagin WR (2014) Pasireotide for postoperative pancreatic fistula. N Engl J Med 370:2014–2022. https://doi.org/10.1056/NEJMoa1313688
Ansorge C, Nordin JZ, Lundell L, Strömmer L, Rangelova E, Blomberg J, del Chiaro M, Segersvärd R (2014) Diagnostic value of abdominal drainage in individual risk assessment of pancreatic fistula following pancreaticoduodenectomy. Br J Surg 101:100–108. https://doi.org/10.1002/bjs.9362
Yamamoto Y, Sakamoto Y, Nara S, Esaki M, Shimada K, Kosuge T (2011) A preoperative predictive scoring system for postoperative pancreatic fistula after pancreaticoduodenectomy. World J Surg 35:2747–2755. https://doi.org/10.1007/s00268-011-1253-x
Roberts KJ, Hodson J, Mehrzad H, Marudanayagam R, Sutcliffe RP, Muiesan P, Isaac J, Bramhall SR, Mirza DF (2014) A preoperative predictive score of pancreatic fistula following pancreatoduodenectomy. HPB 16:620–628. https://doi.org/10.1111/hpb.12186
Wellner UF, Kayser G, Lapshyn H, Sick O, Makowiec F, Höppner J, Hopt UT, Keck T (2010) A simple scoring system based on clinical factors related to pancreatic texture predicts postoperative pancreatic fistula preoperatively. HPB 12:696–702. https://doi.org/10.1111/j.1477-2574.2010.00239.x
Assifi MM, Lindenmeyer J, Leiby BE, Grunwald Z, Rosato EL, Kennedy EP, Yeo CJ, Berger AC (2012) Surgical Apgar score predicts perioperative morbidity in patients undergoing pancreaticoduodenectomy at a high-volume center. J Gastrointest Surg Off J Soc Surg Aliment Tract 16:275–281. https://doi.org/10.1007/s11605-011-1733-1
Ansorge C, Strömmer L, Andrén-Sandberg Å, Lundell L, Herrington MK, Segersvärd R (2012) Structured intraoperative assessment of pancreatic gland characteristics in predicting complications after pancreaticoduodenectomy. Br J Surg 99:1076–1082. https://doi.org/10.1002/bjs.8784
Gaujoux S, Cortes A, Couvelard A, Noullet S, Clavel L, Rebours V, Lévy P, Sauvanet A, Ruszniewski P, Belghiti J (2010) Fatty pancreas and increased body mass index are risk factors of pancreatic fistula after pancreaticoduodenectomy. Surgery 148:15–23. https://doi.org/10.1016/j.surg.2009.12.005
Fujiwara Y, Misawa T, Shiba H, Shirai Y, Iwase R, Haruki K, Furukawa K, Futagawa Y, Yanaga K (2013) A novel postoperative inflammatory score predicts postoperative pancreatic fistula after pancreatic resection. Anticancer Res 33:5005–5010
Graham JA, Kayser R, Smirniotopoulos J, Nusbaum JD, Johnson LB (2013) Probability prediction of a postoperative pancreatic fistula after a pancreaticoduodenectomy allows for more transparency with patients and can facilitate management of expectations. J Surg Oncol 108:137–138. https://doi.org/10.1002/jso.23362
Kosaka H, Kuroda N, Suzumura K et al (2014) Multivariate logistic regression analysis for prediction of clinically relevant pancreatic fistula in the early phase after pancreaticoduodenectomy. J Hepato-Biliary-Pancreat Sci 21:128–133. https://doi.org/10.1002/jhbp.11
Jutric Z, Johnston WC, Grendar J, Haykin L, Mathews C, Harmon LK, Shen J, Hahn HP, Coy DL, Cassera MA, Helton WS, Rocha FG, Wolf RF, Hansen PD, Hammill CW, Alseidi AA, Newell PH (2016) Preoperative computed tomography scan to predict pancreatic fistula after distal pancreatectomy using gland and tumor characteristics. Am J Surg 211:871–876. https://doi.org/10.1016/j.amjsurg.2016.02.001
Arai T, Kobayashi A, Yokoyama T et al (2015) Signal intensity of the pancreas on magnetic resonance imaging: prediction of postoperative pancreatic fistula after a distal pancreatectomy using a triple-row stapler. Pancreatol Off J Int Assoc Pancreatol IAP Al 15:380–386. https://doi.org/10.1016/j.pan.2015.05.479
Nahm CB, de Reuver PR, Hugh TJ et al (2017) Intra-operative amylase concentration in peri-pancreatic fluid predicts pancreatic fistula after distal pancreatectomy. J Gastrointest Surg Off J Soc Surg Aliment Tract 21:1031–1037. https://doi.org/10.1007/s11605-017-3395-0
Shi Y, Liu Y, Gao F et al (2018) Pancreatic stiffness quantified with MR elastography: relationship to postoperative pancreatic fistula after pancreaticoenteric anastomosis. Radiology:170450. https://doi.org/10.1148/radiol.2018170450
Laaninen M, Sand J, Nordback I, Vasama K, Laukkarinen J (2016) Perioperative hydrocortisone reduces major complications after pancreaticoduodenectomy: a randomized controlled trial. Ann Surg 264:696–702. https://doi.org/10.1097/SLA.0000000000001883
Villafane-Ferriol N, Van Buren G, Mendez-Reyes JE et al (2018) Sequential drain amylase to guide drain removal following pancreatectomy. HPB. https://doi.org/10.1016/j.hpb.2017.11.008
Maeda T, Kayashima H, Imai D, Takeishi K, Harada N, Tsujita E, Tsutsui S, Matsuda H (2018) Evaluation of drain amylase level after pancreaticoduodenectomy with special reference to delayed pancreatic fistula. Am Surg 84:403–409
Eguia E, Hwalek AE, Martin B et al (2018) What are the predictors that can help identify safe removal of drains following pancreatectomy? Am J Surg. https://doi.org/10.1016/j.amjsurg.2018.03.002
Umezaki N, Hashimoto D, Nakagawa S, Kitano Y, Yamamura K, Chikamoto A, Matsumura F, Baba H (2018) Number of acinar cells at the pancreatic stump predicts pancreatic fistula after pancreaticoduodenectomy. Surg Today 48:790–795. https://doi.org/10.1007/s00595-018-1656-5
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Vanbrugghe, C., Birnbaum, D.J., Boucekine, M. et al. Prospective study on predictability of complications by pancreatic surgeons. Langenbecks Arch Surg 405, 155–163 (2020). https://doi.org/10.1007/s00423-020-01866-3
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DOI: https://doi.org/10.1007/s00423-020-01866-3