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12 Preoperative Endoscopy
145
abnormal ndings on endoscopy. Of the total cohort, 18.4% had changed their planned operation after endoscopy results (Table12.1).
Wiltberger etal. [20] showed alterations in 76% of preoperative EGDs. The main ndings were gastric or duodenal ulcers (53%)—mostly supercial and all deep ulcers were related to H. pylori infection; erosive esophagitis (23%)—mostly Los Angeles grade A; hiatal hernia (21%) usually small in size; gastric polyps (8%); and gastric adenocarcinoma (1%).
In a systematic review and meta-analysis, Bennett etal. [21] showed the abnor­mal ndings in routine preoperative endoscopy before bariatric surgery. The main endoscopic alterations were gastritis (37.6%), hiatal hernia (21.1%), and esophagi­tis (14.4%). H. pylori was present in 36.2% (biopsied if suspicious) and 20.2% (routine biopsies) of cases. The proportion of EGDs resulting in a change of surgical approach was 7.8%. Changes in medical management were seen in 27.5%, but after eliminating H. pylori eradication, this was found to be only 2.5% (Table12.2).
Table 12.1 Pathologic ndings in asymptomatic and symptomatic patients in the entire study cohort performed by Chang etal. [19]
Asymptomatic % Symptomatic % Total % P value
Number of patients 387 61.3 244 38.7 631 Esophagitis 91 23.5 76 31.1 167 26.5 0.034 Hiatal hernia 89 23.0 82 33.6 171 27.1 0.0035 Gastric ulcer 22 5.7 9 3.7 31 4.9 NS Duodenal ulcer 1 0.3 1 0.4 2 0.3 NS Barrett’s 16 4.1 13 5.3 29 4.6 NS Duodenal mass 3 0.8 1 0.4 0.4 0.6 NS Helicobacter pylori 33 8.5 21 8.6 54 8.6 NS Total number of abnormal
ndings
255 65.9 203 83.2 458 72.6 <0.00001
Table 12.2
ndings in routine preoperative endoscopy before bariatric surgery in the meta-analysis performed by Bennett etal. [21]
Abnormal
Number of studies
Pathology %
Gastritis 37.6 31 7.598 Hiatal hernia 21.1 39 9.723 Esophagitis 14.4 37 9.129 Bulbitis/duodenitis 5.2 20 5.974 Gastric ulcer 3.6 25 6.356 Barrett’s esophagus 2.1 19 5.802 Gastric intestinal
metaplasia Duodenal ulcer 1.8 16 3.547 Gastric cancer 0.4 12 3.586 Esophageal cancer 0.2 5 1.278 HP (biopsied if
suspicious) HP (routine biopsies) 20.2 23 5.650
reporting
2.2 5 1.126
36.2 8 1.652
Number of patients (total)
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Table 12.3
ndings in routine preoperative endoscopy before bariatric surgery in the meta-analysis performed by Parkish etal. [18]
Abnormal
EGD ndings
Gastritis 1562 34.6 Hiatal hernia 889 19.7 Helicobacter pylori 888 19.7 Esophagitis (all grades) 786 17 Duodenitis 226 5 Gastric ulcer 97 2 Duodenal ulcer 14 0.3 Barrett’s esophagus 45 0.1 Carcinoma 4 0.08
Number of patients (N=4511) %
In a systematic review and meta-analysis performed by Parikh etal. [18], the patients were grouped based on EGD ndings: Group 1—ndings that did not sig­nicantly change management; Group 2—ndings that delayed, altered, or can­celed surgery. Overall, 92.4% (n= 6.112) of the patients had a normal EGD or ndings that did not change clinical management (group 1) and 7.6% (n=504) had ndings that delayed or altered surgery (group 2) (Table12.3).
A position statement by IFSO showed that abnormal EGD ndings are likely to be found in at least 55.5% of patients prior to bariatric surgery. The most common abnormal ndings were gastritis, hiatal hernia, and esophagitis. Conditions that would lead to modication or delay of surgery were less commonly found, with
16.5% ndings that led to modication or delay of the planned procedure and 0.2% that had surgery cancelled [22].
12.2.2 Testing andTreatment ofH. pylori
There are conicting data for preoperative testing and treatment of H. pylori related to surgical outcomes.
Marginal ulceration after RYGB is diagnosed in 1% to 16% of patients and pre­operative H. pylori infection is twice as common among the patients who had mar­ginal ulceration (32%) as among those who had not (12%) (p=0.02) [23]. Patients tested for H. pylori have a lower incidence of postoperative marginal ulcers (n=5,
2.4%) than patients who do not undergo this screening (n=354, 6.8%, P<0.05) [24].
The incidence of postoperative perforation is higher in patients who do not undergo screening/treatment for H. pylori (5% vs. 0%; P=0.09) [25]. Although most studies show the benet of H. pylori screening and treatment in patients who will undergo RYGB, Papasavas et al. [26] did not show an association between H. pylori infection and marginal or gastric ulcers. The evidence is unclear regarding the benet of H. pylori eradication prior to sleeve gastrectomy [27].
12 Preoperative Endoscopy
147
ASGE suggests that testing and eradication of H. pylori before bariatric surgery should be individualized [17] and the European Association for Endoscopic Surgery (EAES) concluded that no recommendation can be made for an ordinary routine H. pylori eradication or no eradication prior to bariatric surgery on the basis of available evidence [28].
References
1. Schlottmann F, Nayyar A, Herbella FAM, Patti MG. Preoperative Evaluation in Bariatric Surgery. J Laparoendosc Adv Surg Tech A. 2018;28(8):925–9.
2. Runkel N, Colombo-Benkmann M, Huttl TP, Tigges H, Mann O, Sauerland S.Bariatric sur­gery. Dtsch Arztebl Int. 2011;108(20):341–6.
3. Mandeville Y, Van Looveren R, Vancoillie PJ, Verbeke X, Vandendriessche K, Vuylsteke P, etal. Moderating the enthusiasm of sleeve gastrectomy: up to fty percent of reux symptoms after ten years in a consecutive series of one hundred laparoscopic sleeve gastrectomies. Obes Surg. 2017;27(7):1797–803.
4. De Palma GD, Forestieri P. Role of endoscopy in the bariatric surgery of patients. World J Gastroenterol. 2014;20(24):7777–84.
5. Genco A, Soricelli E, Casella G, Maselli R, Castagneto-Gissey L, Di Lorenzo N, et al. Gastroesophageal reux disease and Barrett’s esophagus after laparoscopic sleeve gastrectomy: a possible, underestimated long-term complication. Surg Obes Relat Dis. 2017;13(4):568–74.
6. Gorodner V, Buxhoeveden R, Clemente G, Sole L, Caro L, Grigaites A.Does laparoscopic sleeve gastrectomy have any inuence on gastroesophageal reux disease? Preliminary results. Surg Endosc. 2015;29(7):1760–8.
7. Sheppard CE, Sadowski DC, de Gara CJ, Karmali S, Birch DW. Rates of reux before and after laparoscopic sleeve gastrectomy for severe obesity. Obes Surg. 2015;25(5):763–8.
8. Haenen FW, Gys B, Moreels T, Michielsen M, Gys T, Lafullarde T.Linitis plastica of the bypassed stomach 7 years after Roux-en-Y gastric bypass: a case report. Acta Chir Belg. 2017;117(6):391–3.
9. Azagury D, Dumonceau JM, Morel P, Chassot G, Huber O.Preoperative work-up in asymp­tomatic patients undergoing Roux-en-Y gastric bypass: is endoscopy mandatory? Obes Surg. 2006;16(10):1304–11.
10. Korenkov M, Sauerland S, Shah S, Junginger T.Is routine preoperative upper endoscopy in gastric banding patients really necessary? Obes Surg. 2006;16(1):45–7.
11. Zeni TM, Frantzides CT, Mahr C, Denham EW, Meiselman M, Goldberg MJ, etal. Value of preoperative upper endoscopy in patients undergoing laparoscopic gastric bypass. Obes Surg. 2006;16(2):142–6.
12. Loewen M, Giovanni J, Barba C.Screening endoscopy before bariatric surgery: a series of 448 patients. Surg Obes Relat Dis. 2008;4(6):709–12.
13. Mong C, Van Dam J, Morton J, Gerson L, Curet M, Banerjee S. Preoperative endoscopic screening for laparoscopic Roux-en-Y gastric bypass has a low yield for anatomic ndings. Obes Surg. 2008;18(9):1067–73.
14. Sauerland S, Angrisani L, Belachew M, Chevallier JM, Favretti F, Finer N, etal. Obesity sur­gery: evidence-based guidelines of the European Association for Endoscopic Surgery (EAES). Surg Endosc. 2005;19(2):200–21.
15. Committee SG. SAGES guideline for clinical application of laparoscopic bariatric surgery. Surg Obes Relat Dis. 2009;5(3):387–405.
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16. Mechanick JI, Youdim A, Jones DB, Garvey WT, Hurley DL, McMahon MM, etal. Clinical practice guidelines for the perioperative nutritional, metabolic, and nonsurgical support of the bariatric surgery patient-2013 update: Cosponsored by American association of clinical endo­crinologists, The obesity society, and American society for metabolic & bariatric surgery*. Obesity (Silver Spring). 2013;21(Suppl 1):S1–S27.
17. Asge Standards of Practice C, Evans JA, Muthusamy VR, Acosta RD, Bruining DH, Chandrasekhara V, et al. The role of endoscopy in the bariatric surgery patient. Surg Obes Relat Dis. 2015;11(3):507–17.
18. Parikh M, Liu J, Vieira D, Tzimas D, Horwitz D, Antony A, etal. Preoperative endoscopy prior to bariatric surgery: a systematic review and meta-analysis of the literature. Obes Surg. 2016;26(12):2961–6.
19. Chang VC, Pan P, Shah SK, Srinivasan A, Haberl E, Wan C, etal. Routine preoperative endos­copy in patients undergoing bariatric surgery. Surg Obes Relat Dis. 2020;16(6):745–50.
20. Wiltberger G, Bucher JN, Schmelzle M, Hoffmeister A, Dietrich A. Preoperative endoscopy and its impact on perioperative management in bariatric surgery. Dig Surg. 2015;32(4):238–42.
21. Bennett S, Gostimir M, Shorr R, Mallick R, Mamazza J, Neville A.The role of routine pre­operative upper endoscopy in bariatric surgery: a systematic review and meta-analysis. Surg Obes Relat Dis. 2016;12(5):1116–25.
22. Brown WA, Johari Halim Shah Y, Balalis G, Bashir A, Ramos A, Kow L, etal. IFSO position statement on the role of esophago-gastro-duodenal endoscopy prior to and after bariatric and metabolic surgery procedures. Obes Surg. 2020;30(8):3135–53.
23. Rasmussen JJ, Fuller W, Ali MR.Marginal ulceration after laparoscopic gastric bypass: an analysis of predisposing factors in 260 patients. Surg Endosc. 2007;21(7):1090–4.
24. Schirmer B, Erenoglu C, Miller A.Flexible endoscopy in the management of patients undergo­ing Roux-en-Y gastric bypass. Obes Surg. 2002;12(5):634–8.
25. Hartin CW Jr, ReMine DS, Lucktong TA. Preoperative bariatric screening and treatment of Helicobacter pylori. Surg Endosc. 2009;23(11):2531–4.
26. Papasavas PK, Gagne DJ, Donnelly PE, Salgado J, Urbandt JE, Burton KK, etal. Prevalence of Helicobacter pylori infection and value of preoperative testing and treatment in patients undergoing laparoscopic Roux-en-Y gastric bypass. Surg Obes Relat Dis. 2008;4(3):383–8.
27. Brownlee AR, Bromberg E, Roslin MS.Outcomes in patients with helicobacter pylori under­going laparoscopic sleeve gastrectomy. Obes Surg. 2015;25(12):2276–9.
28. Di Lorenzo N, Antoniou SA, Batterham RL, Busetto L, Godoroja D, Iossa A, et al. Clinical practice guidelines of the European Association for Endoscopic Surgery (EAES) on bar­iatric surgery: update 2020 endorsed by IFSO-EC, EASO and ESPCOP. Surg Endosc. 2020;34(6):2332–58.
Chapter 13
Postoperative Care
LéonieBouvet
13.1 Introduction
The experience of our group with biliopancreatic diversion with duodenal switch (BPD-DS) goes back to the early 1990s [1]. Years of experience with the care of patients undergoing malabsorptive surgery has led to the development of multiple time-tested postoperative protocols.
Even in experienced hands, laparoscopic BPD-DS has a slightly higher rate of perioperative complications when compared to sleeve gastrectomy or gastric bypass [2]. This difference is partly explained by the complexity of the technic and propor­tionally longer operative time. It also relates to the fact that such procedures are usually offered to patients with higher BMIs (>50kg/m2) and more severe comor­bidities. On the other hand, standardized postoperative pathways contribute to decrease the complication rate and allow for early recognition of complications.
Implementation of postoperative enhanced recovery protocols that take into con­sideration the particularities of BPD-DS is a central component of safe periopera­tive care. This chapter will review the different aspects of postoperative management following laparoscopic BPD-DS.
L. Bouvet (*) Department of Surgery, Quebec City Heart and Lung Institute, Laval University, Quebec City, QC, Canada
© The Author(s), under exclusive license to Springer Nature Switzerland AG 2023 A. Teixeira et al. (eds.), Duodenal Switch and Its Derivatives in Bariatric and Metabolic Surgery, https://doi.org/10.1007/978-3-031-25828-2_13
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13.2 Multidisciplinary Team
As for many aspects of the bariatric surgery process, postoperative management of patients undergoing BPD-DS is facilitated by the involvement of an experienced multidisciplinary team. It includes bariatric surgeons and dedicated nurses, dieti­cians, and pharmacists. Internal medicine specialists are also routinely implicated in the perioperative care, especially for diabetic patients.
13.3 Postoperative Unit
After undergoing laparoscopic BPD-DS, most patients can safely be discharged from the postanesthesia care unit to the regular oor on a dedicated bariatric oor. Patients with sleep apnea that are adequately treated with noninvasive positive pres­sure ventilation make no exception [3]. Use of intensive care units is exceptional and limited to particular intraoperative events, or to patients with severe cardio­pulmonary comorbidities.
13.4 Analgesia
Multimodal analgesia is a cornerstone in pain control after BPD-DS.In addition to intraoperative strategies, it contributes to reducing opioid use and their side effects. Postoperative analgesic medication protocols include regular doses of nonsteroidal anti-inammatory drugs (NSAIDs) and acetaminophen. Every patient is also pre­scribed a proton pump inhibitor (PPI) for gastric protection and control of early gastroesophageal reux symptoms.
13.5 Diet
On the day of surgery, patients are given intravenous uids and sips of water are permitted 2h after extubation. Nausea is frequent after surgery, and liberal use of intravenous antiemetic medication is routine, particularly for patients undergoing one stage BPD-DS due to the sleeve component. Clear liquids diet is initiated on postoperative day 1 and advanced to full liquids diet the next day. All patients are evaluated and counseled by a clinical dietician during their hospital stay. The impor­tance of high levels of protein intakes is reinforced and patients are counselled on different protein supplements that can be safely added to their diet even at an early stage. The different steps of postoperative diet progression are summarized in Table 13.1. Patients are also given elaborated documentation with examples of
13 Postoperative Care
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Table 13.1
diet progression
Postoperative
Type of diet Duration Step 1 Clear liquids POD 1 Step 2 Full liquids 1week Step 3 Pureed 1week Step 4 Minced 2weeks Step 5 Tender 1week Step 6 Regular Remaining
appropriate meals for every step. The same dietary progression is used either for the rst stage or second stage BPD-DS.Unsurprisingly, diet progression is easier for second stage BPD-DS patients [4] but the recent duodenoileal anastomosis warrants the same careful progression of texture. Food intolerance is rare, but failure to prog­ress to the next step should lead to reevaluation by the dietician or the bariatric surgeon to avoid early protein malnutrition.
13.6 Thromboprophylaxis
Deep venous thrombosis (DVT) and pulmonary embolism (PE) are the leading causes of major morbidity and mortality after bariatric surgery. In a study reporting 1000 consecutive cases of BPD-DS, incidence rate of PE was 0.4% following lapa­roscopic procedures and caused the only perioperative mortality (0.1%) [5]. After bariatric surgery, the majority of venous thromboembolism (VTE) events occur after the patients are discharged home, with an average time of diagnosis of
11.6days [6]. Thromboprophylaxis is therefore mandatory in the early periopera­tive period and extended postdischarge therapy for high-risk patients have been rec­ommended [7].
Sequential compression devices are initiated intraoperatively and kept until the patients resume adequate ambulation, usually on postoperative day 1. Early ambula­tion is routine and starts with the help of caregivers on the day of surgery. By post­operative day 1, patients are expected to ambulate in the hallway by themselves.
One dose of unfractionated subcutaneous heparin is given on the rst evening after surgery and low-molecular-weight heparin is started on postoperative day 1. Doses are adjusted for patient’s BMIs with the majority of patients receiving Dalteparin 7500IU daily [8]. For patients who weigh greater than 180kg, or with previous history of DVT or PE, doses are increased to 10,000IU daily. Dalteparin is preferred to other low-molecular-weight heparins because daily injections are sufcient for most high BMI patients.
Given that the great majority of BPD-DS patients will be considered high-risk for VTE on risk calculator scales, all patients at our institution are prescribed low­molecular- weight heparin upon discharge for a total of 20days. This regimen has not led to an increase in postoperative bleeding events.
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13.7 Investigations
Accordingly with enhanced recovery protocol principles, any routine use of surgical drains, urinary catheter, and nasogastric tube are avoided. Current literature states that it does not prevent perioperative complication and can delay recovery [911]. Frequent vital signs and urinary output are recorded. Usual blood work on postop­erative day 1 and 2 includes complete blood count, creatinine, and ions. Interestingly, postoperative bleeding rarely occurs following either one-stage or two-stages BPD-DS compared to sleeve gastrectomy alone. This is likely because delayed bleeding complications are associated more with the sleeve component. As the sleeve is performed at the beginning of the operation in BPD-DS, it allows for a second look of the hemostasis at the end of the procedure.
No routine leak test is done, as they do not prevent complications, can be falsely reassuring, and can cause delays in diet initiation [12]. Every patient is assessed at least once daily by an experienced bariatric surgeon. Any unexplained tachycardia or pulmonary distress should raise suspicion for anastomotic or gastric leaks. CT-scan with intravenous and oral contrast is the examination of choice to identify a leak for stable patients. Nonetheless, even with a reassuring CT scan, diagnostic laparoscopy should be performed in worsening patients.
13.8 Adjustments ofComorbidity Treatments
The improvement of obesity-related diseases after BPD-DS outstands the results of any other bariatric surgery. A meta-analysis by Buchwald etal. reported resolution of hypertension in 81%, improvement of dyslipidemia in 99%, and improvement or remission of type 2 diabetes mellitus (T2DM) in 98% [13]. Second stage BPD-DS results are similar to one-stage in regards to correction of obesity-related comorbidities.
13.9 Antihypertensive Medication
The principal mechanisms through which obesity-related hypertension occurs is excess plasma volume expansion and increased cardiac output with a concomitant decrease in natriuresis due to excess body mass. Accordingly, mechanisms through which weight loss helps resolve hypertension are well described [14]. Nonetheless, more recent data suggests that immediate postsurgical changes in gut hormones are likely to contribute to hypertension control. This is also supported by the increased remission rate of hypertension following metabolic surgeries when compared to purely restrictive procedures. Independently of weight loss, glucagon-like peptide 1 (GLP-1), ghrelin, leptin, and peptide YY (PYY) alterations seem to inuence hyper­tension remission following BPD-DS.
13 Postoperative Care
These more recent ndings further support holding or reducing anti-hypertensive therapy, starting in the immediate postoperative period. Cessation of diuretics, angiotensin-converting-enzyme inhibitors (ACE inhibitors), and angiotensin recep­tor blockers (ARBs) is done preferentially to avoid the risk of acute renal failure secondary to decreased uid intake following surgery. In patients with persistent hypertension upon discharge, calcium channel blockers (CCBs) are either contin­ued or added to reach good tension control. Known cardiac diseases also warrant the represcription of cardioprotective molecules like beta-blockers.
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13.10 Dyslipidemia Medication
BPD-DS has a sustainable effect on the metabolic syndrome, including dyslipid­emia. Marceau etal. reported a decreased total cholesterol, low-density lipoprotein cholesterol (LDL), and triglycerides, with high-density lipoprotein cholesterol (HDL) remaining stable after a mean follow-up of 7.9±4.6years [15]. This sup­ports cessation of dyslipidemia medication after BPD-DS with the exception of patients in which statins are also indicated for further treatment of known athero­sclerosis disease.
13.11 Diabetic Medication
Malabsorptive bariatric procedures improve T2DM using multiple pathways, most of them preceding signicant weight loss [1618]. These metabolic inuences are initiated immediately after surgery by caloric restriction, increased GLP-1 levels, decreased nutrient absorption, changes in bile acid, incretin effect, and modication of intestinal microbiome [19]. A recent study evaluating the early perioperative mechanisms of glycemic control after BPD-DS conrmed that caloric restriction increases insulin sensitivity and secretion [20]. Therefore, rapid resolution of hyper­glycemic state is observed in the immediate postoperative period supporting the dramatic reduction or cessation of diabetic medications. To avoid postoperative hypoglycemia, insulin secretagogues, sodium-glucose cotransporter-2 inhibitors, and thiazolidinediones are discontinued. Similarly, insulin doses should be signi­cantly reduced. To reach tight glycemic control, frequent glycemic measurements and use of subcutaneous rapid-acting insulin adjustment protocols are routine after BPD-DS.Changes in diabetes treatment at the time of discharge are made propor­tionally to the severity of T2DM.For example, patients with severe T2DM will usually resume taking metformin or incretin-based therapies once they are tolerat­ing liquid diet. Control of hyperglycemia in the early postoperative stage will some­times necessitate reintroduction of basal long-acting insulin, at reduced doses. Thus, diabetologists are implicated in the postoperative care of any patient with a more complex treatment regimen. In a study addressing long-term results for
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insulin- treated T2DM after BPD-DS, 97% of patients were off insulin and 68% were in complete remission. Mean time to reach remission was 40.4months [21]. Therefore, frequent follow-up for diabetes treatment downstaging are warranted in the weeks, months, and even years after BPD-DS.
13.12 Contraceptive Counselling
After BPD-DS, pregnancy should be postponed for at least 2years. Weight should be stabilized and nutritional parameters proven normal on routine post-bariatric blood works. Pregnancy occurring within 2years of surgery are at increased risk of gestational complications.
For female patients, fertility is increased following bariatric surgery. Furthermore, oral contraceptives are no longer reliable after BPD-DS due to malabsorption. To avoid incidental early pregnancy after surgery, discharge counselling should include recommendations for effective contraception for all female patients. Intrauterine devices are the preferred contraception methods after BPD-DS.They can be inserted before surgery without increased risk of VTE.
13.13 Vitamins
Upon discharge, patients are given a prescription for daily vitamins and mineral supplementations. They are advised to introduce these supplements 1month after surgery, allowing patients a period of adaptation to their reduced gastric volume. Importance of lifelong supplementation is again reinforced. Usual initial prescrip­tion doses are summarized in Table13.2. Vitamin B12 dosage tends to increase on long-term follow-up after BPD-DS even with low dose supplements of 20–40 mcg included within the multivitamin complex. Therefore, vitamin B12–specic supple­ments are not included in our initial postoperative prescriptions as they rarely need to be added on subsequent follow-up in our experience. Blood works are planned every 4months in the rst postoperative year. Vitamin supplements will be adjusted in time following these routine blood works.
Table 13.2
doses of vitamins and minerals supplementations
Initial daily
Multivitamin and mineral complex 2 tablets Calcium carbonate 1000mg Ferrous sulfate 300mg Vitamin D3 20,000IU Vitamin A 30,000IU