Новости | Магазин | Журналы | Контакты | Правила | Доставка | |
Вход Регистрация |
В настоящее время панкреатодуоденальная резекция, несмотря на большую частоту осложнений, сопровождается приемлемым уровнем послеоперационной летальности. Это, наряду с существенным увеличением выживаемости при раке поджелудочной железы, делает необходимым изучение негативных функциональных последствий операции и методов их хирургической профилактики. В обзоре литературы представлена характеристика трех основных послеоперационных синдромов: гастростаза, панкреатической экзокринной и эндокринной недостаточности. Показана зависимость проявлений указанных синдромов от патоморфологических характеристик культи поджелудочной железы, сохранения привратника, варианта панкреатодигестивного анастомоза и других особенностей реконструктивного этапа операции.
Ключевые слова:
поджелудочная железа, панкреатодуоденальная резекция, панкреатогастроанастомоз, панкреатоеюноанастомоз, гастростаз, экзокринная недостаточность, эндокринная недостаточность
Литература:
1. Котельников А.Г., Патютко Ю.И., Трякин А.А. Злокачественные опухоли поджелудочной железы. В кн. Онкология. Клинические рекомендации / под ред. М.И. Давыдова. - М.: Издательская группа РОНЦ, 2015. - 680 с.
2. Narayanan S., Martin A.N., Turrentine F.E. et al. Mortality after pancreaticoduodenectomy: assessing early and late causes of patient death. J. Surg. Res. 2018; 231: 304 - 308 https://doi.org/10.1016/j.jss.2018.05.075
3. Kawaida H., Kono H., Hosomura N. et al. Surgical techniques and postoperative pancreatic fistula after pancreatic surgery. World Journal of Gastroenterology, 2019; 25 (28): 3722 - 3737. https://doi.org/10.3748/wjg.v25.i28.3722
4. Conroy T., Hammel P., Hebbar M. et al. FOLFIRINOX or Gemcitabine as Adjuvant Therapy for Pancreatic Cancer. The New England Journal of Medicine. 2018, vol. 379, No 25, 2395 - 2406 https://doi.org/10.1056/NEJMoa1809775
5. Janssen Q.P., van Dam J.L., Doppenberg D. et al. FOLFIRINOX as initial treatment for localized pancreatic adenocarcinoma: a retrospective analysis by the Trans-Antlantic pancreatic surgery Consortium. JNCI J Natl Cancer Inst (2022) 00(0): djac 018, 1 - 9 https://doi.org/10.1093/jnci/djac018
6. Matsunaga H., Tanaka M., Takahata S. et al. Manometric evidence of improved early gastric stasis by erythromycin after pylorus-preserving pancreatoduodenectomy. World J. Surg. 2000; 24: 1236 - 1241 https://doi.org/10.1007/s002680010244
7. Jang J.Y., Kim S.W., Han J.K. et al. Randomized prospective trial of the effect of induced hypergastrinemia on the prevention of pancreatic atrophy after pancreatoduodenectomy in humans. Ann Surg. 2003; 237: 522 - 529 https://doi.org/10.1097/01.SLA.0000059985.56982.11
8. Восканян С.Э., Коротько Г.Ф. Морфофункциональная организация поджелудочной железы и острый послеоперационный панкреатит (экспериментальные и клинические аспекты). - М.: Литтерра, 2017. - 528 с.
9. Wu J.M., Kuo T.C., Yang C.Y. et al. Resolution of diabetes after pancreaticoduodenectomy in patients with and without pancreatic ductal cell adenocarcinoma. Ann Surg Oncol. 2013; 20: 242 - 249 https://doi.org/10.1245/s10434-012-2577- у
10. Muscogiuri G., Mezza T., Prioletta A. et al. Removal of duodenum elicits GLP-1 secretion. Diabetes Care. 2013; 36: 1641 - 1646 https://doi.org/10.2337/dc12-0811
11. Chang M.K., Lee J.H. Pathophysiology after pancreaticoduodenectomy. World Journal of Gastroenterology, 2015; 21 (19): 5794 - 5804 https://doi.org/10.3748/wjg.v21.i19.5794.
12. Iiazawa Y., Kato H., Kishiwada M. et al. Long-term outcomes after pancreaticoduodenectomy using pair-watch suturing technique: different roles of pancreatic duct dilatation and remnant pancreatic volume for the development of pancreatic endocrine and exocrine dysfunction. Pancreatology, 2017; 17: 814 - 821 https://doi.org/10.1016/j.pan.2017.06.008
13. Wente M.N., Bassi C., Dervenis C. et al. Delayed gastric emptying (DGE) after pancreatic surgery: a suggested definition by the International Study Group of Pancreatic Surgery (ISGPS). Surgery, 2007; 142: 761 - 768 https://doi.org/10.1016/j.surg.2007.05.005.
14. Iqbal N., Lovegrove R.E., Tilney H.S. et al. A comparison of pancreaticoduodenectomy with extended pancreaticoduodenectomy: a metaanalysis of 2822 patients. Eur J Oncol., 2009; 35: 79 - 86 https://doi.org/10.1016/j.ejso.2008.01.002
15. Matsumoto I., Shinzeki M., Asari S. et al. A prospective randomized comparison between pylorus- and subtotal stomach-preserving pancreatoduodenectomy on postoperative delayed gastric emptying occurrence and long-term nutritional status. J.Surg. Oncol. 2014; 109: 690 - 696 https://doi.org/10.1002/jso.23566
16. Kawai M., Tani M., Hirono S. Pylorus ring resection reduces delayed gastric emptying in patients undergoing pancreatoduodenectomy: a prospective, randomized, controlled trial of pylorus-resecting versus pylorus-preserving pancreatoduodenectomy. Ann Surg 2011, 253: 495 - 501 https://doi.org/10.1097/SLA.0b013e31820d98f1.
17. Коханенко Н.Ю., Павелец К.В., Ширяев Ю.Н., Радионов Ю.В., Кашинцев А.А., Петрик С.В. Имеет ли значение вариант панкреатодуоденальной резекции при оценке функциональных результатов операции? Фундаментальные исследования, 2015, № 1, с. 537 - 541
18. Cai X., Zhang M., Liang C. et al. Delayed gastric emptying after pancreaticoduodenectomy: a propensity score-matched analysis and clinical nomogram study. BMC Surgery, 2020, 20: 1 - 9 https://doi.org/10.1186/s12893-020-00809-5
19. Fahlbusch T., Luu A.M., Hohn P. et al. Impact of pylorus preserving on delayed gastric emptying after pancreaticoduodenectomy - analysis of 5000 patients based on the German StuDoQ/Pancreas-Registry. Gland Surg., 2022; 11 (1): 67 - 76 https://doi.org/10.21037/gs-21-645
20. Eshuis W.J., van Eijck C.H., Gerhards M.F. et al. Antecolic versus retrocolic route of the gastroenteric anastomosis after pancreatoduodenectomy: a randomized controlled trial. Ann Surg., 2014; 259: 45 - 51 https://doi.org/10.1097/SLA.0b013e3182a6f529.
21. Tamandl D., Sahora K., Prucker J. et al. Impact of the reconstruction method on delayed gastric emptying after pylorus-preserving pancreaticoduodenectomy: a prospective randomized study. World J Surg. 2014; 38: 465 - 475 https://doi.org/10.1007/s00268-013-2274-4
22. Imamura N., Chijiiwa K., Ohuchida J. et al. Prospective randomized clinical trial of a change in gastric emptying and nutritional status after a pylorus-preserving pancreaticoduodenectomy: comparison between an antecolic and a vertical rertocolic duodenijejunostomy. HPB (Oxford). 2014; 16: 384 - 394 https://doi.org/10.1111/hpb.12153
23. Gangavatiker R., Pal S., Javed A. et al. Effect of antecolic or retrocolic reconstruction of the gastro/duodenojejunostomy on delayed gastric emptying after pancreaticoduodenectomy: a randomized controlled trial. J Gastrointest Surg. 2011; 15: 843 - 852 https://doi.org/10.1007/s11605-011-1480-3
24. Kurahara H., Shinchi H., Maemura K. et al. Delayed gastric emptying after pancreatoduodenectomy. J Surg Res. 2011; 171: e187 - e192 https://doi.org/10.1016/j.jss.2011.08.002.
25. Chijiiwa K., Imamura N., Ohuchida J. et al. Prospective randomized controlled study of gastric emptying assessed by (13)C-acetate breath test after pylorus-preserving pancreaticoduodenectomy: comparison between antecollic and vertical retrocolicduodenojejunostomy. J Hepatobiliary Pancreat Surg. 2009; 16: 49 - 55 https://doi.org/10.1007/s00534-008-0004-3
26. Shimoda M., Kubota K., Katoh M., Kita J. Effect of billroth II or Roux-en-Y reconstruction for the gastrojejunostomy on delated gastric emptying after pancreaticoduodenectomy: a randomized controlled study. Ann Surg. 2013; 257: 938 - 942 https://doi.org/10.1097/SLA.0b013e31826c3f90
27. Ke S., Ding X.M., Gao J. et al. A prospective, randomized trial of Roux-en-Y reconstruction with isolated pancreatic drainage versus conventional loop reconstruction after pancreaticoduodenectomy. Surgery. 2013; vol.153, no. 6, pp. 743 - 752 https://doi.org/10.1016/j.surg.2013.02.008
28. Tani M., Kawai M., Hirono S. et al. Randomized clinical trial of isolated Roux-en-Y versus conventional reconstruction after pancreaticoduodenectomy. Br.J.Surg. 2014; vol.101, no.9, pp. 1084 - 1091 https://doi.org/10.1002/bjs.9544
29. Busquets J., Martin S., Fabregat J. et al. Randomized trial of two types of gastrojejunostomy after pancreatoduodenectomy and risk of delayed gastric emptying (PAUDA trial). The British Journal of Surgery, 2019, vol. 106, no.1, pp. 46 - 54 https://doi.org/10.1002/bjs.11023.
30. Ma F., Fan Y., Zhang L. et al. Roux-en-Y and Billroth II reconstruction after pancreaticoduodenectomy: a meta-analysis of complications. Volume 2020, article ID 6131968, 10 pages https://doi.org/10.1155/2020/6131968
31. Yang J., Wang C., Huang Q. Effect of Billroth II or Roux-en-Y reconstruction for the gastrojejunostomy after pancreaticoduodenectomy: meta-analysis of randomized controlled trials. Journal of gastrointestinal Surgery, 2015, vol. 19, no. 5, pp. 955 - 963 https://doi.org/10.1007/s11605-015-2751-1
32. Dominguez-Munoz J.E. Pancreatic enzyme therapy for pancreatic exocrine insufficiency. Curr. Gastroenterol. Rep., 2007, 9: 116 - 122 https://doi.org/10.1007/s11894-007-0005-4
33. Bartel M.J. et al., Pancreatic exocrine insufficiency in pancreatic cancer. A review of the literature. Dig Liver Dis., 2015, 47: 1013 - 1020 https://doi.org/10.1016/j.dld.2015.06.015
34. Pathanki A.M., Attard J.A., Bradley E. et al. Pancreatic exocrine insufficiency after pancreaticoduodenectomy: current evidence and management. World J Gastrointest Pathophysiol., 2020; 11(2): 20 - 31 https://doi.org/10.4291/wjgp.v11.i2.20
35. Roberts K.J., Bannister C.A., Schrem H. Enzyme replacement improves survival among patients with pancreatic cancer: results of a population based study. Pancreatology, 2019; 19: 114 - 121 https://doi.org/10.1016/j.pan.2018.10.010
36. Thogari K., Tewari M., Shukla S.K. et al. Assessment of exocrine function of Pancreas following pancreaticoduodenectomy. Indian Journal of Surgical Oncology, 2019, 10 (2): 258 - 267 https://doi.org/10.1007/s13193-019-00901-0
37. Lim P-W., Dinh K.H., Sullivan M. et al. Thirty-day outcomes underestimate endocrine and exocrine insufficiency after pancreatic resection. HPB, 2016, 18: 360 - 366 https://doi.org/10.1016/j.hpb.2015.11.003
38. Singh V.K., Haupt M.E., Geller D.E. et al. Less common etiologies of exocrine pancreatic insufficiency. World J.Gastroenterol., 2017, 23: 7059 - 7076 https://doi.org/10.3748/wjg.v23.i39.7059
39. Domiguez-Munoz J.E., Alvarez-Castreo A., Larino-Noia J. et al. Endoscopic ultrasonography of the pancreas as an iderect method to predict pancreatic exocrine insufficiency in patients with chronic pancreatitis. Pancreas, 2012; 41: 724 - 728 https://doi.org/10.1097/МПА.0b013e31823b5978
40. Matsumoto J., Traverso L.W. Exocrine function following the Whipple operation as assessed by stool elastase. J. Gastrointest Surg., 2006, 10: 1225 - 1229 https://doi.org/10.1016/дж.гассур.2006.08.001
41. Nakamura H., Murakami Y., Uemura K. Reduced pancreatic parenchymal thickness indicates exocrine pancreatic insufficiency after pancreatoduodenectomy. J.Surg.Res., 2011, 171: 473 - 478 https://doi.org/10.1016/j.jss.2010.03.052
42. Kwak B.J., Choi H.J., You Y.K. et al. Comparative long-term outcomes for pancreatic volume change, nutritional status, and incidence of new-onset diabetes between pancreatogastrostomy and pancreatojejunostomy after pancreaticoduodenectomy. HepatoBiliary Surg Nutr., 2020; 9 (3): 284 - 295 https://doi.org/10.21037/hbsn.2019.04.18
43. Патютко Ю.И., Котельников А.Г. Хирургия рака органов билиопанкреатодуоденальной зоны. М.: ОАО «Издательство «Медицина», 2007, 448 с.
44. Halloran C.M., Cox T.F., Chauhan S. et al. Partial pancreatic resection for pancreatic malignancy is associated with sustained pancreatic exocrine failure and reduced quality of life: a prospective study. Pancreatology, 2011; 11: 535 - 545 https://doi.org/10.1159/000333308
45. Lemaire E., O'Toole D., Sauvanet A. et al. Functional and morphological changes in the pancreatic remnant following pancreaticoduodenectomy with pancreaticogastric anastomosis. Br.J.Surg., 2000, 87: 434 - 438 https://doi.org/10.1046/j.1365-2168.2000.01388.x
46. Sikkens E.C.M. et al. Prospective assessment of the influence of pancreatic cancer resection on exocrine pancreatic function. B.J.S., 2014, 101: 109 - 113 https://doi.org/10.1002/bjs.9342
47. Lyubimova N.V., Kosyrev V.Y., Patyutko Y.I., Kushlinskii N.E. Analysis of elastase 1 for evaluation of excretory function of the pancreas after gastropancreatoduodenal resection. Bull Exp Biol Med., 2003, 135: 34 - 36 https://doi.org/10.1023/a: 1023433509956
48. Beger H.G., Poch B., Mayer B., Siech M. New onset of diabetes and pancreatic exocrine insufficiency after pancreaticoduodenectomy for benign and malignant tumors. Ann Surg., 2017, 20: 1 - 16 https://doi.org/10.1097/SLA.0000000000002422
49. Morera-ocon F.J. et al. Considerations on pancreatic exocrine function after pancreaticoduodenectomy. World J.Gastrointest. Oncol., 2014, 6: 325 - 329 https://doi.org/10.4251/wjgo.v6.i9.325
50. Rault A., SaCunha A., Klopfenstein D. et al. Pancreaticojejunal anastomosis is preferable to pancreaticogastrostomy after pancreaticoduodenectomy for longterm outcomes of pancreatic exocrine function. J.Am.Coll Surg, 2005; 201: 239 - 244 https://doi.org/10.1016/j.jamcollsurg.2005.03.026
51. Roeyen G., Jansen M., Ruyssinck L. et al. Pancreatic exocrine insufficiency after pancreaticoduodenectomy is more prevalent with pancreaticogastrostomy than with pancreaticojejunostomy. A retrospective multicenter observational cohort study. HPB (Oxford), 2016; 18: 1017 - 1022 https://doi.org/10.1016/j.hpb.2016.09.002
52. Tseng D.S.J., Molenaar I.Q., Besselink M.G. et al. Pancreatic exocrine insufficiency in patients with pancreatic or periampullary cancer. Pancreas, 2016, v.45, N 3, p. 325 - 330 https://doi.org/10.1097/МПА.0000000000000473
53. Hirata K., Nakata B., Amano R. et al. Predictive factors for change of diabetes mellitus status after pancreatectomy in preoperative diabetic and nondiabetic patients. J. Gastrointest Surg, 2014; 18: 1597 - 1603 https://doi.org/10.1007/s11605-014-2521-5
54. Fujino Y., Suzuki Y., Matsumoto I. et al. Long-term assessment after pancreaticoduodenectomy with pancreatic duct invagination anastomosis. Surg Today., 2007; 37: 860 - 866 https://doi.org/10.1007/s00595-007-3507-7
55. Lozinska L., Westr?m B., Prykhodko O. et al. Decreased insulin secretion and glucose clearance in exocrine pancreas-insufficient pigs. Exp Physiol., 101.1 (2016), pp. 100 - 112 https://doi.org/10.1113/EP085431
At present, pancreaticoduodenoctomy causes the high incidence of complications. However, it is associated with an acceptable level of postoperative mortality. With this regard and taking into consideration a significant increase in survival in pancreatic cancer, it is highly relevant to study the negative functional outcomes of surgery and develop methods for their surgical prevention. The bibliographic review focuses on the features of three main postsurgical syndromes: gastric stasis, pancreatic exocrine and endocrine insufficiency. The study shows the dependence of these syndromes on pathomorphological characteristics of pancreatic stump, preservation of the pyloric, the variant of pancreatodigestive anastomosis and other features of reconstructive stage of the surgery.
Keywords:
pancreas, pancreaticoduodenoctomy, pancreaticogastrostomy, pancreaticojejunostomy, gastric stasis, exocrine insufficiency, endocrine insufficiency