Добавил:
kiopkiopkiop18@yandex.ru t.me/Prokururor I Вовсе не секретарь, но почту проверяю Опубликованный материал нарушает ваши авторские права? Сообщите нам.
Вуз: Предмет: Файл:

Ординатура / Хирургия / @xirurgi_2025 / @xirurgi_2025 - 756 - файл

.pdf
Скачиваний:
0
Добавлен:
29.08.2026
Размер:
14 Мб
Скачать
142
https://t.me/med1917
27. Hernandez M, Birnbach DJ, Van Zundert AA. Anesthetic management of the illicit­substance- using patient. Curr Opin Anesthesiol. 2005;18(3):315. https://doi.org/10.1097/01.
aco.0000169241.21680.0b.
28. Shah S, Schwenk ES, Sondekoppam RV, etal. ASRA pain medicine consensus guidelines on the management of the perioperative patient on cannabis and cannabinoids. Reg Anesth Pain Med. 2023;3:97–117.
29. Recreational drug misuse: issues for the cardiologist|Heart. https://heart.bmj.com/con-
tent/83/6/627. Accessed 19 Jun 2023.
30. Drake LR, Scott PJH.DARK classics in chemical neuroscience: cocaine. ACS Chem Neurosci. 2018;9(10):2358–72. https://doi.org/10.1021/acschemneuro.8b00117.
31. Tella SR, Schindler CW, Goldberg SR.Cocaine: cardiovascular effects in relation to inhibi­tion of peripheral neuronal monoamine uptake and central stimulation of the sympathoadrenal system. J Pharmacol Exp Ther. 1993;267(1):153–62.
32. Smith JA, Mo Q, Guo H, Kunko PM, Robinson SE.Cocaine increases extraneuronal levels of aspartate and glutamate in the nucleus accumbens. Brain Res. 1995;683(2):264–9. https://doi.
org/10.1016/0006- 8993(95)00383- 2.
33. Kuczkowski KM.The cocaine abusing parturient: a review of anesthetic considerations. Can J Anesth. 2004;51(2):145.
34. Luft A, Mendes FF. Anestesia no paciente usuário de cocaína. Rev Bras Anestesiol. 2007;57(3):307–14.
35. Ramachandaran S, Khan AU, Dadaparvar S, Sherman MS. Inhalation of Crack Cocaine Can Mimic Pulmonary Embolism. Clin Nucl Med. 2004;29(11):756–7. https://doi.
org/10.1097/00003072- 200411000- 00028.
36. Devlin RJ, Henry JA. Clinical review: major consequences of illicit drug consumption. Crit Care. 2008;12(1):202. https://doi.org/10.1186/cc6166.
37. Oh PI, Balter MS.Cocaine induced eosinophilic lung disease. Thorax. 1992;47(6):478–9.
38. Alnas M, Altayeh A, Zaman M.Clinical course and outcome of cocaine-induced pneumomedi­astinum. Am J Med Sci. 2010;339(1):65–7. https://doi.org/10.1097/MAJ.0b013e3181c371da.
39. Sofuoglu M, Dudish-Poulsen S, Poling J, Mooney M, Hatsukami DK.The effect of indi­vidual cocaine withdrawal symptoms on outcomes in cocaine users. Addict Behav. 2005;30(6):1125–34. https://doi.org/10.1016/j.addbeh.2004.10.010.
40. Bernards CM, Teijeiro A. Illicit cocaine ingestion during anesthesia. Anesthesiology. 1996;84(1):218–20.
41. O’Donnell K, Boyle S, Abdulrahman S, O’Leary E.Unexpected intraoperative hypotension in a chronic cocaine user. Anaesth Rep. 2022;10(2):e12177. https://doi.org/10.1002/anr3.12177.
42. Saggese NP, Chang C, Cardo VA. Perioperative Management for the Cocaine-Positive Patient Undergoing Elective Surgery under General Anesthesia. J Oral Maxillofac Surg. 2019;77(5):894–5. https://doi.org/10.1016/j.joms.2019.01.016.
43. Moon TS, Gonzales MX, Sun JJ, etal. Recent cocaine use and the incidence of hemodynamic events during general anesthesia: a retrospective cohort study. J Clin Anesth. 2019;55:146–50.
https://doi.org/10.1016/j.jclinane.2018.12.028.
44. Liyen Cartelle A, Nguyen A, Desai PM, etal. Safety of upper endoscopy in patients with active cocaine use. World J Gastrointest Endosc. 2021;13(10):510–7. https://doi.org/10.4253/wjge.
v13.i10.510.
45. Rothman RB, Baumann MH, Dersch CM, et al. Amphetamine-type central nervous sys­tem stimulants release norepinephrine more potently than they release dopamine and sero­tonin. Synapse. 2001;39(1):32–41.
AID- SYN5>3.0.CO;2- 3.
46. Harris D.The bioavailability of intranasal and smoked methamphetamine. Clin Pharmacol Ther. 2003;74(5):475–86. https://doi.org/10.1016/j.clpt.2003.08.002.
47. Perez-Reyes M, White WR, McDonald SA, et al. Clinical effects of daily metham­phetamine administration. Clin Neuropharmacol. 1991;14(4):352–8. https://doi.
org/10.1097/00002826- 199108000- 00007.
https://doi.org/10.1136/rapm- 2022- 104013.
https://doi.org/10.1590/S0034- 70942007000300009.
https://doi.org/10.1097/00000542- 199601000- 00025.
https://doi.org/10.1002/1098- 2396(20010101)39:1<32::
J. P. Gallagher et al.
8 Illicit Drugs andCandidates forEndoscopy andSurgery
https://t.me/med1917
48. Cruickshank CC, Dyer KR. A review of the clinical pharmacology of methamphetamine. Addiction. 2009;104(7):1085–99.
49. Vandevenne M, Vandenbussche H, Verstraete A.Detection time of drugs of abuse in urine. Acta Clin Belg. 2000;55(6):323–33. https://doi.org/10.1080/17843286.2000.11754319.
50. Shappell SA, Kearns GL, Valentine JL, Neri DF, DeJohn CA. Chronopharmacokinetics and Chronopharmacodynamics of Dextromethamphetamine in man. J Clin Pharmacol. 1996;36(11):1051–63. https://doi.org/10.1177/009127009603601109.
51. Ramos BP, Arnsten AFT.Adrenergic pharmacology and cognition: focus on the prefrontal cor­tex. Pharmacol Ther. 2007;113(3):523–36. https://doi.org/10.1016/j.pharmthera.2006.11.006.
52. Derlet RW, Rice P, Zane Horowitz B, Lord RV.Amphetamine toxicity: experience with 127 cases. J Emerg Med. 1989;7(2):157–61.
53. Gray SD, Fatovich DM, McCoubrie DL, Daly FF. Amphetamine-related presentations to an inner-city tertiary emergency department: a prospective evaluation. Med J Aust. 2007;186(7):336–9.
54. Jacobs LJ.Reversible dilated cardiomyopathy induced by methamphetamine. Clin Cardiol. 1989;12(12):725–7. https://doi.org/10.1002/clc.4960121211.
55. Yeo KK, Wijetunga M, Ito H, et al. The Association of Methamphetamine use and Cardiomyopathy in young patients. Am J Med. 2007;120(2):165–71. https://doi.org/10.1016/j.
amjmed.2006.01.024.
56. Westover AN, McBride S, Haley RW. Stroke in young adults who abuse amphetamines or cocaine: a population-based study of hospitalized patients. Arch Gen Psychiatry. 2007;64(4):495. https://doi.org/10.1001/archpsyc.64.4.495.
57. Krogh J, Lanzillotta-Rangeley J, Paratz E, etal. Practice considerations for the anesthesia professional for methamphetamine substance use disorder patients. Anesthesia Patient Safety Foundation. 2021;36(2):67–70.
58. Safdari KM, Converse C, Dong F, et al. Hemodynamic effects of methamphet­amine and general anesthesia. Anesthesiol Res Pract. 2022;2022:7542311. https://doi.
org/10.1155/2022/7542311.
59. Githens T, DeBaun MR, Campbell ST, et al. Rates of perioperative complications among patients undergoing orthopedic trauma surgery despite having positive results for metham­phetamine. Orthopedics. 2019;42(4):192–6.
60. Hadjizacharia P, Green DJ, Plurad D, et al. Methamphetamines in trauma: effect on injury patterns and outcome. J Trauma Acute Care Surg. 2009;66(3):895. https://doi.org/10.1097/
TA.0b013e318164d085.
61. Edwards AM, Johnson EG, Bernard AC.Intraoperative vasopressor use during emergency sur­gery on injured meth users. Trauma Surg Acute Care Open. 2020;5(1):e000553. https://doi.
org/10.1136/tsaco- 2020- 000553.
62. Cornwell DQ, Thompson AR, Ivie RM, Working ZM, Friess DM, Meeker JE.Methamphetamine in Orthopaedics: considerations of an at-risk population. JBJS Reviews. 2021;9(6):e20. https://
doi.org/10.2106/JBJS.RVW.20.00229.
63. Amsterdam EA, Wenger NK, Brindis RG, etal. 2014 AHA/ACC guideline for the Management of Patients with non-ST-elevation acute coronary syndromes: a report of the American College of Cardiology/American Heart Association task force on practice guidelines. J Am Coll Cardiol. 2014;64(24):e139–228. https://doi.org/10.1016/j.jacc.2014.09.017.
64. Eilert RJ, Kliewer ML. Methamphetamine-induced rhabdomyolysis. Int Anesthesiol Clin. 2011;49(2):52. https://doi.org/10.1097/AIA.0b013e3181ffc0e5.
65. Murray EP, Mansy L, Lackey JT, etal. Methamphetamine intoxication and perioperative com­plications following Orthopaedic surgical procedures. Cureus. 2021;13(10):e19082. https://
doi.org/10.7759/cureus.19082.
66. Drewes AM, Jensen RD, Nielsen LM, etal. Differences between opioids: pharmacological, experimental, clinical and economical perspectives. Br J Clin Pharmacol. 2013;75(1):60–78.
https://doi.org/10.1111/j.1365- 2125.2012.04317.x.
67. Feng Y, He X, Yang Y, Chao D, Lazarus LH, Xia Y.Current research on opioid receptor func­tion. Curr Drug Targets. 2012;13(2):230–46.
https://doi.org/10.5694/j.1326- 5377.2007.tb00932.x.
https://doi.org/10.1111/j.1360- 0443.2009.02564.x.
https://doi.org/10.1016/0736- 4679(89)90263- 1.
https://doi.org/10.3928/01477447- 20190523- 01.
143
144
https://t.me/med1917
68. Schumacher MA, Basbaum AI, Naidu RK.Opioid Agonists & Antagonists. In: Katzung BG, editor. Basic & clinical pharmacology. 14th ed. McGraw-Hill Education; 2017. accessmedi-
cine.mhmedical.com/content.aspx?aid=1148437600. Accessed 20 Jan 2022.
69. Opiate and opioid withdrawal: MedlinePlus medical encyclopedia. https://medlineplus.gov/
ency/article/000949.htm. Accessed 20 Jan 2022.
70. Sporer KA.Acute Heroin Overdose. Ann Intern Med. 1999;130(7):584–90. https://doi.org/1
0.7326/0003- 4819- 130- 7- 199904060- 00019.
71. Hser YI, Mooney LJ, Saxon AJ, etal. High mortality among patients with opioid use disor­der in a large healthcare system. J Addict Med. 2017;11(4):315–9. https://doi.org/10.1097/
ADM.0000000000000312.
72. Colvin LA, Bull F, Hales TG.Perioperative opioid analgesia—when is enough too much? A review of opioid-induced tolerance and hyperalgesia. Lancet. 2019;393(10180):1558–68.
https://doi.org/10.1016/S0140- 6736(19)30430- 1.
73. Ward EN, Quaye ANA, Wilens TE. Opioid use disorders: perioperative Management of a Special Population. Anesth Analg. 2018;127(2):539–47. https://doi.org/10.1213/
ANE.0000000000003477.
74. Koppel BS, Tuchman AJ, Mangiardi JR, Daras M, Weitzner I. Epidural spinal infection in intravenous drug abusers. Arch Neurol. 1988;45(12):1331–7. https://doi.org/10.1001/
archneur.1988.00520360049011.
75. Harrison TK, Kornfeld H, Aggarwal AK, Lembke A. Perioperative considerations for the patient with opioid use disorder on buprenorphine, methadone, or naltrexone maintenance therapy. Anesthesiol Clin. 2018;36(3):345–59. https://doi.org/10.1016/j.anclin.2018.04.002.
76. Liang J, Olsen RW. Alcohol use disorders and current pharmacological therapies: the role of GABAA receptors. Acta Pharmacol Sin. 2014;35(8):981–93. https://doi.org/10.1038/
aps.2014.50.
77. Ungur AL, Neumann T, Borchers F, Spies C.Perioperative Management of Alcohol Withdrawal Syndrome. Visc Med. 2020;36(3):160–6. https://doi.org/10.1159/000507595.
78. dfwanes. Anesthesia and Alcohol Use- DFW Anesthesia Professionals. 2019. https://anesthe-
siologydfw.com/anesthesia- and- alcohol- use/, https://anesthesiologydfw.com/anesthesia- and­alcohol- use/. Accessed 26 June 2023.
79. Chapman R, Plaat F.Alcohol and anaesthesia. Continuing Education in Anaesthesia Critical Care & Pain. 2009;9(1):10–3. https://doi.org/10.1093/bjaceaccp/mkn045.
80. Lipari RN.Key substance use and mental health indicators in the United States: results from the 2019 national survey on drug use and health; 2019. p.114.
J. P. Gallagher et al.
Chapter 9
https://t.me/med1917
Nutritional Care inGastrointestinal Surgery
MariaWobith andArvedWeimann
Abbreviations
BIA Bioelectrical impedance analysis BMI Body mass index CT Computertomography DXA Dual-X-absorptiometry ERAS Enhanced Recovery after Surgery ESPEN European Society for Clinical Nutrition and Metabolism GCP Good clinical practice GLIM Global Leadership Initiative on Malnutrition MRI Magnitude resonance imaging NRS Nutritional risk score ONS Oral nutrition supplement PG-SGA Patient-Generated Subjective Global Assessment SGA Subjective Global Assessment SMI Skeletal muscle index 6 MWD 6-Minute Walking Distance CCI Comprehensive Complication Index 95% CI 95% Condence interval OR Odds ratio NCJ Needle catheter jejunostomy NJ Nasojejunal tube ICU Intensive care unit
M. Wobith · A. Weimann (*) Department for General, Visceral and Oncological Surgery, St. George Hospital, Leipzig, Germany e-mail: Maria.Wobith@sanktgeorg.de; Arved.Weimann@sanktgeorg.de
Switzerland AG 2024 J. Faintuch, S. Faintuch (eds.), Recent Strategies in High Risk Surgery,
https://doi.org/10.1007/978-3-031-56270-9_9
145© The Author(s), under exclusive license to Springer Nature
146
https://t.me/med1917
M. Wobith and A. Weimann
Introduction
In an overweight population, the “metabolic risk” is often underestimated, with special regard to sarcopenic obesity [15]. The impact of malnutrition and sarcopenia for the risk of postoperative complications and the length of hospital stay has been shown very often [25]. Nutritional conditioning or “prehabilitation” should be considered for those exhibiting signicant metabolic risk, in accordance with ERAS protocols [610].
Malnutrition, Sarcopenia, Sarcopenic Obesity
Malnutrition often goes along with sarcopenia. While sarcopenia means a decrease in muscle mass and function, malnutrition is characterized by a global decrease of body cell mass. Especially in geriatric patients, sarcopenia can be present without malnutrition [11, 12]. Diagnosing sarcopenia is not easy in obese patients [13], and in seriously ill older populations, up to 83% can be affected [14].
Prognostic Implications
Preoperatively impaired functionality along with impaired nutritional status is crucial for postoperative mobilization and pulmonary function [15, 16]. In gastric cancer, preoperative sarcopenia has been shown to be associated with overall survival [17].
Sarcopenic obesity is a separate risk factor, where an increased amount of fat
may hide a decrease in muscle mass [13, 18, 19].
Metabolic Risk
A well validated tool is the Nutritional Risk Score (NRS-2002) [20]. NRS3 indi­cates a risk for malnutrition, and assessment should then be initiated. Parameters of the NRS are body mass index (BMI), unintended weight loss, reduced food intake, and severity of disease. Furthermore, serum albumin can be used as preoperative predictor for the underlying risk for postoperative complications [5] in line with the Joint Consensus Statement on Nutritional Screening and Therapy within a Surgical Enhanced Recovery Pathway of the American Society for Enhanced Recovery and Perioperative Quality Initiative [21]. A high metabolic risk is dened by the ESPEN guidelines if one of the following criteria is fullled: [5]:
• BMI less than 18.5kg/m
• Involuntary weight loss of more than 10–15% within 6 months
• SGA grade C, NRS5
• Serum albumin <30g/L (no liver/renal disease, no trauma/surgery)
2
9 Nutritional Care inGastrointestinal Surgery
https://t.me/med1917
147
Malnutrition According toGLIM Criteria
Muscle mass measurement has been incorporated into the Global Leadership Initiative on Malnutrition (GLIM) criteria with (1) phenotypic criteria (low body mass index (BMI), reduced muscle mass, non-volitional weight loss and (2) etiologi­cal criteria (reduced food intake or assimilation, disease burden/inammatory condi­tion) [12]. One variable from each category conrms the suspicion of malnutrition.
Measurement ofMuscle Mass
As patients undergoing surgery for gastrointestinal cancer always undergo com­puter tomography/CT for cancer staging, CT can also be exploited to determine muscle quantity and quality. Skeletal muscle index (SMI) is highly regarded as a marker of muscle mass by GLIM criteria. In the axial scan at lumbar level 3 skeletal muscle area and density can be calculated [16, 2225].
So far, no specic GLIM cut-off values have been anticipated, however propos­als should soon emerge. GLIM criteria could be also appropriate to predict postop­erative complications, in many cancer and non-cancer settings [2630].
For patients undergoing colorectal cancer surgery, it has been suggested that low risk or no need for intensive nutritional therapy would correspond to high SMI, excluding patients with BMI≥35kg/m2. High-risk subjects would be in the oppo­site category: low SMI plus those with BMI35kg/m2 [31].
Sarcopenic Obesity
This condition features high body fat and reduced muscle mass. Clinical, functional, and imaging diagnostic methods are available and are strongly recommended for surgical services, as postoperative complications and slow recovery are likely. Stage I is not associated with comorbidities, stage II displaying metabolic, functional, or cardiopulmonary dysfunction [32].
Nutritional Assessment inthePreoperative Period
Evaluation of CT scan (preferably utilizing existing images, without new expenses and X-ray exposure), bioelectrical impedance analysis (BIA), and handgrip strength can be performed very easily, and cut-off points have been dened for such vari­ables. In case body composition from CT or BIA is not available, severe metabolic risk may be dened according to the ESPEN guideline [5].
148
https://t.me/med1917
M. Wobith and A. Weimann
Indication forNutrition Therapy
Nutritional counseling should be offered to patients undergoing gastrointestinal cancer surgery. Ideally, the perioperative trajectory will be accompanied by an experienced dietician, or by the Nutrition Support Team if available [33]. It should not be waited until overt malnutrition is present. A risk for malnutrition or an underlying metabolic derangement could underlie the start of nutrition therapy.
ESPEN guidelines [5] advise nutritional support in case of malnutrition or nutritional risk, when dietary intake is likely for more than 5 days before opera­tion, or when <50% of the necessary requirements will be consumed more than 7 days.
For severe nutritional risk 7–14days assistance is indicated, if necessary postponing surgical intervention [5, 7]. Parenteral nutrition is nowadays an exception, reserved for intolerance of the gastrointestinal tract [5] (Table9.1).
Immune Enhancement
Benets regarding infectious complications have been established [3537]. Rather similar outcomes were documented within an ERAS protocol [38]. According to ESPEN, ONS is recommended for 5–7 days before surgery when risky interven­tions are programmed, and immunomodulating supplements are suggested [5].
Prehabilitation
This technique is increasingly used in many parts of the world, notably for elderly, unt, and inadequately nourished individuals. ERAS directives endorse nutritional therapy combined with exercise (physical training) and psychological support for 4–6weeks [8, 9, 39, 40]. If severe malnutrition is diagnosed there must be an inter­disciplinary decision, if and for how long the surgical procedure may be delayed for sufcient conditioning of the patient [40].
Table 9.1 Postoperative enteral and parenteral supplementation related to anticipated oral intake [34]
Oral intake (% caloric requirement) >5days Feeding None Enteral <30–50% Enteral (possible combination with parenteral) >50% Monitoring of oral intake
9 Nutritional Care inGastrointestinal Surgery
https://t.me/med1917
149
In a recently published multicentric trial targeting non-metastasized colorectal cancer patients who underwent a 4 weeks hospital based trimodal prehabilitation versus standard care, the nutritional intervention was dietary advice aiming a pro­tein intake of 1.5g/kg body weight. Furthermore, patients were encouraged to take a whey protein supplement (30g) 1 h after in-hospital training and 1 h before sleep­ing daily. A multivitamine supplement including vitamin D was also provided. In the intervention group the rate of severe and medical complications was signi­cantly reduced, a result that coincides with other reports, however divergent results have been published as well [41, 42].
Specic evidence-based recommendations concerning nutritional therapy are lack­ing [8, 9, 4345]. Most randomized studies have been performed for a duration of 7–14days, and there is no data for a period of 4–6weeks. Preoperative immunonutrition and synbiotics may be discussed and are supported in some circumstances [35, 46].
Perioperative Nutrition Therapy
In general, even after upper gastrointestinal resections, oral intake can be started on the rst day after surgery [5]. NRS3 tends to be a predictor for low compliance to ERAS protocol and for longer stay in hospital [47]. Compliance to ERAS of less than 70% signals a higher rate of postoperative complications. Nevertheless, out­comes concerning recovery time or complications are heterogeneous [48, 49]. A scheme for clinical practice is shown in Fig.9.1 [34].
Screeningfor malnutrition
Assessment of nutritional status
Oral nutritionalsupplements 5 to 7 days before surgery
Preoperative
In-patients
After
discharge
Fig. 9.1 Nutrition therapy for gastrointestinal cancer patients during the trajectory (after dis­charge ***)
Prehabilitation 4-6 weeks
• Earlyoralfeedingconsideringtolerance
• Consider supplementation if calorieand proteinintakeis insufficientfor > 5 days  useONS, enteral, or parental nutritioninastepwise approach
• Consider placement of feeding jejunostomy in high-risk patients undergoing upper
gastrointestinal cancer surgery
• Dietarycounsellingbeforedischarge
• Monitoringof nutritional status and nutrition intake
• ONSor tube feedingincase of inadequate calorieintakeor severe weight loss
150
https://t.me/med1917
M. Wobith and A. Weimann
Enteral Feeding—Jejunostomy andNasojejunal Tube
A “bariatric effect” of upper GI operations for cancer including ghrelin deciency has been advocated. Typically these patients lose 10% or more of their body weight in the rst 6 months after the procedure, with parallel muscle wasting, a condition that adversely affects tolerance and response to cancer adjuvant treatments.
Nasojejunal feeding, and needle catheter jejunostomy when a longer period is considered, are classic recommendations in such circumstances. The tubes can be placed during surgery, whenever oral alimentation is impaired or malabsorption is anticipated, as a consequence of extensive anatomical changes induced by the oper­ation [5, 5059].
Gastrointestinal Complaints
Limited gastrointestinal tolerance should be always kept in mind [60, 61]. Diarrhea has been a serious problem during long term enteral alimentation in the past. Currently with less risk of contamination of ready-to-use liquid diets, and a variety of protein and calorie compositions to choose from, depending on individual tolerance and absorptive function, this has become a much less trou­bling condition.
Vomiting, gastroesophageal reux and abdominal distension can still precipitate aspiration pneumonitis, and are one of the reasons some prefer jejunostomy instead of nasoenteral tube, in high-risk patients.
Parenteral Nutrition
The peripheral parenteral route is safe [60] and allows complementation of enteral feeding, for those unable to achieve >50% of their caloric needs more than 7days [5] via the oral/enteral route. Nevertheless, this may be a cumbersome but reason­able option in patients with inadequate oral/enteral intake on pod 3 [61].
Supplemented Parenteral Nutrition Mixtures
Glutamine and omega-3 fatty acids have been extensively used to enrich intrave­nous dietary mixtures. However, their use remains mostly optional, as long term outcomes are not clearly improved [5, 62, 63]. Whenever possible, enteral feeding should be adopted, even if only partially, as a more complete and affordable source of a balanced diet.
9 Nutritional Care inGastrointestinal Surgery
https://t.me/med1917
151
Complicated Course/Intensive Care Unit
Measured body weight (BMI≤30kg/m2), or corrected body weight (BMI>30kg/ m2) corresponding to BMI of 22kg/m2 only, have been advised to guide routine dietary prescriptions. Indirect calorimetry is a reliable tool and should be employed especially in critically ill cases [64, 65].
Late Postoperative Period, After Discharge
After undergoing extensive cancer surgery prolonged loss of 10% or 20% of previ­ous body weight is frequently seen and can interfere not only with functional status, but also with response to chemotherapy. This reinforces the importance enteral sup­port in the subsequent months as prophylaxis, for those classied as high risk [66, 67].
Therefore, dietary counseling and follow-up may be mandatory. If appropriate additionally oral nutritional supplements (ONS) may be helpful [68].
With special regard to patients with upper gastrointestinal resections, several studies have pointed out home enteral nutrition as superior to ONS.Counseling can be employed as well, however home enteral nutrition is still endowed with more predictable outcomes, generally including body mass index and skeletal muscle mass index (SMI) [6872]. Another more simple alternative to attenuate weight loss during the rst year could be ONS providing up to 400kcal/day, but compliance of the patients may be often limited [73].
The Bariatric Effect
Pharmacologic treatment may become more important in the future. In a recent randomized trial ghrelin was postoperatively administered in patients undergoing esophagectomy. A dosage dependent benecial effect of ghrelin infusion was observed on erector spinae, a marker of muscle loss [74].
Based on the available positive data, a randomized nutritional trial may be debat­able from an ethical point of view. Patient reported outcomes (PROMS) will provide a measure for shared decision making regarding post-discharge enteral nutrition. Overall, nutritional care may be considered an essential item of perioperative man­agement in gastrointestinal cancer patients. While changes may often be “mar­ginal”, underestimated cumulative effects will impact postoperative outcome [75].
Conict of Interest Arved Weimann: Lecture fees: Abbott, B. Braun, Fresenius Kabi, Falk Foundation. Research grant: B. Braun, Mucos. Maria Wobith: Lecture fees: Fresenius Kabi. Research grant: B Braun.