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18 Perioperative Fluid Management andVolume Assessment
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highlight the heterogeneity of the studies, such as the devices, algorithms, hemody­namic targets, and uid type, making it difcult to compare interventions and out­comes [7678].
299
Fluid Management inSpecic Patient Populations
Liver Disease andHepatic Surgeries
Due to alterations in intravascular volume and uid shifts, this population is highly susceptible to both hypervolemia and hypovolemia. Low albumin levels, malnutri­tion, and portal hypertension can further complicate volume status, resulting in the development of ascites and edema [79]. In general, a more restrictive uid approach is preferred to avoid deleterious effects of hypervolemia. If possible, CVP and arte­rial line monitoring should be maintained through the perioperative period to con­tinually assess volume status [80]. When massive volumes of ascites are surgically drained, reinfusion could be an option to minimize protein loss and hypovolemia. However, due to high levels of cytokines in the uid and other mechanisms, fever and coagulopathy could be a danger.
Ideally ascites should be controlled with diuretics, in the preoperative period. The same tenants are generally followed for patients undergoing hepatic surgery, including transplantation, with CVP monitoring and SVV often used to guide uid administration [8183].
Cardiac Surgery
GDT has emerged as a recommended approach for uid management [84]. GDT involves using advanced hemodynamic parameters such as cardiac index and mixed venous oxygenation to guide uid therapy during the perioperative period. Furthermore, GDT can help prevent overzealous uid administration, which can lead to uid overload, impaired organ function, and increased morbidity and mortal­ity. Notably the use of GDT in cardiac surgery has been associated with reduced incidence of acute kidney injury [16, 85]. Some groups advocate measuring kidney stress biomarkers, and restricting GDT to positive cases. Such would avoid extra uid administration to those patients that do not need them.
Thoracic Surgery
In patients undergoing lung resection surgery, uid management is challenging as diseased lungs, surgical exposure, and other factors can lead to interstitial and alve­olar edema. Additionally, use of dynamic parameters for GDT may be less reliable during one lung ventilation. Again, a restrictive uid strategy is defended with
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R. Bangalore et al.
euvolemia being the goal, with special attention to avoid organ dysfunction, particu­larly kidney injury. ERAS guidelines support the use of balanced crystalloids over normal saline in these patients [15].
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34. Pinsky MR, Cecconi M, Chew MS, De Backer D, Douglas I, Edwards M, Hamzaoui O, Hernandez G, Martin G, Monnet X, Saugel B, Scheeren TWL, Teboul JL, Vincent JL.Effective hemodynamic monitoring. Crit Care. 2022;26(1):294.
35. Zhang Z, Lu B, Sheng X, Jin N.Accuracy of stroke volume variation in predicting uid responsiveness: a systematic review and meta-analysis. J Anesth. 2011;25(6):904–16.
36. Myatra SN, Prabu NR, Divatia JV, Monnet X, Kulkarni AP, Teboul JL.The changes in pulse pressure variation or stroke volume variation after a “tidal volume challenge” reliably predict uid responsiveness during low tidal volume ventilation. Crit Care Med. 2017;45(3):415–21.
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38. Cannesson M, Desebbe O, Rosamel P, et al. Pleth variability index to monitor the respira­tory variations in the pulse oximeter plethysmographic waveform amplitude and predict uid responsiveness in the operating theatre. Br J Anaesth. 2008;101(2):200–6.
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40. Monnet X, Teboul JL.Passive leg raising: ve rules, not a drop of uid! Crit Care. 2015;19(1):18.
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41. Dave C, etal. Dynamic assessment of uid responsiveness in surgical ICU patients through stroke volume variation is associated with decreased length of stay and costs: a systematic review and meta-analysis. J Intensive Care Med. 2020;35(1):14–23.
42. Gavelli F, Teboul JL, Monnet X.The end-expiratory occlusion test: please, let me hold your breath! Crit Care. 2019;23(1):274.
43. Gavelli F, Shi R, Teboul JL, Azzolina D, Monnet X.The end-expiratory occlusion test for detecting preload responsiveness: a systematic review and meta-analysis. Ann Int Care. 2020;10(1):65.
44. Wang J, Zhou D, Gao Y, Wu Z, Wang X, Lv C. Effect of VTILVOT variation rate on the assessment of uid responsiveness in septic shock patients. Medicine (Baltimore). 2020;99(47):e22702.
45. Blanco P.Rationale for using the velocity-time integral and the minute distance for assessing the stroke volume and cardiac output in point-of-care settings. Ultrasound J. 2020;12(1):21.
46. Long E, Oakley E, Duke T, Babl FE, (PREDICT) PRiEDIC.Does respiratory variation in infe­rior vena cava diameter predict uid responsiveness: a systematic review and meta-analysis. Shock. 2017;47(5):550–9.
47. Ciozda W, Kedan I, Kehl DW, Zimmer R, Khandwalla R, Kimchi A.The efcacy of sono­graphic measurement of inferior vena cava diameter as an estimate of central venous pressure. Cardiovasc Ultrasound. 2016;14(1):33.
48. Antequera Martin AM, Barea Mendoza JA, Muriel A, etal. Buffered solutions versus 0.9% saline for resuscitation in critically ill adults and children. Cochrane Database Syst Rev. 2019;7:CD012247.
49. Gottlieb M, Petrak V, Binkley C.Are balanced crystalloid solutions better than Normal saline solution for the resuscitation of children and adult patients? Ann Emerg Med. 2020;75(4):532–4.
50. Self WH, Semler MW, Wanderer JP, etal. Balanced crystalloids versus saline in noncritically ill adults. NEJM. 2018;378(9):819–28.
51. Finfer S, Micallef S, Hammond N, etal. Balanced multielectrolyte solution versus saline in critically ill adults. NEJM. 2022;386(9):815–26.
52. Young P, Bailey M, Beasley R, etal. Effect of a buffered crystalloid solution vs saline on acute kidney injury among patients in the intensive care unit: the SPLIT randomized clinical trial. JAMA. 2015;314(16):1701–10.
53. Zampieri FG, Machado FR, Biondi RS, etal. Effect of intravenous uid treatment with a balanced solution vs 0.9% saline solution on mortality in critically ill patients: the BaSICS randomized clinical trial. JAMA. 2021;326(9):1–12.
54. Semler MW, Self WH, Wanderer JP, etal. Balanced crystalloids versus saline in critically ill adults. NEJM. 2018;378(9):829–39.
55. Pfortmueller CA, Faeh L, Muller M, etal. Fluid management in patients undergoing cardiac surgery: effects of an acetate-versus lactate-buffered balanced infusion solution on hemody­namic stability (HEMACETAT). Crit Care. 2019;23(1):159.
56. He H, Liu D, Ince C.Colloids and the microcirculation. Anesth Analg. 2018;126(5):1747–54.
57. Lewis SR, Pritchard MW, Evans DJ, etal. Colloids versus crystalloids for uid resuscitation in critically ill people. Cochrane Database Syst Rev. 2018;8(8):CD000567.
58. Finfer S, Bellomo R, Boyce N, etal. A comparison of albumin and saline for uid resuscitation in the intensive care unit. NEJM. 2004;350(22):2247–56.
59. Myburgh J, Cooper DJ, Finfer S, etal. Saline or albumin for uid resuscitation in patients with traumatic brain injury. NEJM. 2007;357(9):874–84.
60. Caironi P, Tognoni G, Masson S, etal. Albumin replacement in patients with severe sepsis or septic shock. NEJM. 2014;370(15):1412–21.
61. Frenette AJ, Bouchard J, Bernier P, etal. Albumin administration is associated with acute kid­ney injury in cardiac surgery: a propensity score analysis. Crit Care. 2014;18(6):602.
62. Kingeter AJ, Raghunathan K, Munson SH, et al. Association between albumin admin­istration and survival in cardiac surgery: a retrospective cohort study. Can J Anaesth. 2018;65(11):1218–27.
63. Evans L, Rhodes A, Alhazzani W, etal. Surviving sepsis campaign: international guidelines for management of sepsis and septic shock 2021. Crit Care Med. 2021;49(11):e1063–143.
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64. Brandstrup B, Tønnesen H, Beier-Holgersen R, etal. Effects of intravenous uid restriction on postoperative complications: comparison of two perioperative uid regimens: a randomized assessor-blinded multicenter trial. Ann Surg. 2003;238(5):641–8.
65. Tambyraja AL, Sengupta F, MacGregor AB, Bartolo DC, Fearon KC.Patterns and clinical outcomes associated with routine intravenous sodium and uid administration after colorectal resection. World J Surg. 2004;28(10):1046–51.
66. Grass F, Lovely JK, Crippa J, etal. Potential association between perioperative uid manage­ment and occurrence of postoperative ileus. Dis Colon Rectum. 2020;63(1):68–74.
67. Kubo Y, Tanaka K, Yamasaki M, etal. The impact of perioperative uid balance on postopera­tive complications after esophagectomy for esophageal cancer. J Clin Med. 2022;11(11):3219.
68. Shin CH, Long DR, McLean D, etal. Effects of intraoperative uid management on postopera­tive outcomes: a hospital registry study. Ann Surg. 2018;267(6):1084–92.
69. Myles PS, Bellomo R, Corcoran T, et al. Restrictive versus liberal uid therapy for major abdominal surgery. NEJM. 2018;378(24):2263–74.
70. Messina A, Robba C, Calabrò L, etal. Perioperative liberal versus restrictive uid strategies and postoperative outcomes: a systematic review and metanalysis on randomised-controlled trials in major abdominal elective surgery. Crit Care. 2021;25(1):205.
71. Melloul E, Lassen K, Roulin D, etal. Guidelines for perioperative care for pancreatoduode­nectomy: Enhanced Recovery After Surgery (ERAS) recommendations 2019. World J Surg. 2020;44(7):2056–84.
72. Corcoran T, Rhodes JE, Clarke S, Myles PS, Ho KM.Perioperative uid management strate­gies in major surgery: a stratied meta-analysis. Anesth Analg. 2012;114(3):640–51.
73. Benes J, Giglio M, Brienza N, Michard F.The effects of goal-directed uid therapy based on dynamic parameters on post-surgical outcome: a meta-analysis of randomized controlled tri­als. Crit Care. 2014;18(5):584.
74. Pearse RM, Harrison DA, MacDonald N, etal. Effect of a perioperative, cardiac output-guided hemodynamic therapy algorithm on outcomes following major gastrointestinal surgery: a ran­domized clinical trial and systematic review. JAMA. 2014;311(21):2181–90.
75. Messina A, Robba C, Calabrò L, etal. Association between perioperative uid administration and postoperative outcomes: a 20-year systematic review and a meta-analysis of randomized goal-directed trials in major visceral/noncardiac surgery. Crit Care. 2021;25(1):43.
76. Jessen MK, Vallentin MF, Holmberg MJ, etal. Goal directed haemodynamic therapy dur­ing general anaesthesia for noncardiac surgery: a systematic review and meta-analysis. Br J Anaesth. 2022;128(3):416–33.
77. Wrzosek A, Jakowicka-Wordliczek J, Zajaczkowska R, etal. Perioperative restrictive ver­sus goal-directed uid therapy for adults undergoing major non-cardiac surgery. Cochrane Database Syst Rev. 2019;12:CD012767.
78. Ebm CC, Sutton L, Rhodes A, Cecconi M.Cost-effectiveness in goal-directed therapy: are the dollars spent worth the value? J Cardiothorac Vasc Anesth 2014;28(6):1660–6.
79. Sun Y, Yang Z, Tan H.Perioperative nutritional support and uid therapy in patients with liver diseases. Hepatobiliary Surg Nutr. 2014;3(3):140–8.
80. Muilenburg DJ, Singh A, Torzilli G, Khatri VP.Surgery in the patient with liver disease. Med Clin North Am. 2009;93(5):1065–81.
81. Morkane CM, Sapisochin G, Mukhtar AM, etal. Perioperative uid management and out­comes in adult deceased donor liver transplantation—a systematic review of the literature and expert panel recommendations. Clin Transpl. 2022;36(10):e14651.
82. Carrier FM, Chassé M, Wang HT, etal. Restrictive uid management strategies and outcomes in liver transplantation: a systematic review. Can J Anaesth. 2020;67(1):109–27.
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Chapter 19
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Perioperative Fluid Administration andComplications inEmergency Gastrointestinal Surgery
BirgitteBrandstrup andAnnMereteMøller
Introduction
The patients needing surgery in the emergency setting differ from the patients in the elective setting in several ways: They are often in a septic state; they might have massive blood, fluid, and/or electrolyte imbalances; surgery is life­saving and might need to be performed as fast as possible and at least within a few hours.
The literature on emergency surgery is often difcult to interpret, because “emergency surgery” covers a wide range of very different diagnoses and surgical procedures. Many national databases include surgery for abscesses, appendicitis, and cholecystitis in the statistical analysis, giving better survival percentages. Nowadays, the risk of death from acute appendicitis or cholecystitis is close to zero. The mortality following surgery for bowel obstruction is also relatively low (up to 10% after 30days [1, 2]) as is the risk of death from a bleeding ulcer [3, 4], while the mortality following perforations of the intestinal tract regardless whether the perforation is of the stomach or the colon continues to be high (30–40% after
B. Brandstrup (*) Department of Surgery, Holbæk Hospital, Part of Copenhagen University Hospitals, Holbæk, Denmark
Institute for Clinical Medicine, Faculty of Health, University of Copenhagen, Copenhagen N, Denmark e-mail: bbrn@regionsjaelland.dk
A. M. Møller Institute for Clinical Medicine, Faculty of Health, University of Copenhagen, Copenhagen N, Denmark
Department of Anesthesia, Herlev University Hospital, Herlev, Denmark e-mail: ann.moeller@regionh.dk
Switzerland AG 2024 J. Faintuch, S. Faintuch (eds.), Recent Strategies in High Risk Surgery,
https://doi.org/10.1007/978-3-031-56270-9_19
305© The Author(s), under exclusive license to Springer Nature
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30days [2, 5, 6]). A condition with an even higher mortality is the patients with a proximal thrombosis of the superior mesenteric artery, causing infarction of the entire small bowel and the right side of the colon. Often it is impossible to save the lives of these patients.
The inclusion or exclusion of these different patient categories and differences in the ratios between them is vital for the comparison of results—a fact that is rarely taken into account when comparing survival numbers between countries or institutions.
Furthermore, national differences are present. This has many reasons ranging from differences in distances to medical aid, the number of hospitals/health staff per capita, to whether or not healthcare is free of charge or not. All these factors are important because patients may give up beforehand to seek help, and the gen­eral health of the patients might be very different. Good access to healthcare inuences whether co-existing medical conditions are well treated or not. In many rst-world countries, on the other hand, the population is getting older, and the patients often have multiple comorbidities—with a surgical emergency on top of it all.
Another very important factor differing between countries and regions is the presence of multi resistant bacteria in the environment. The surgical interven­tion needed for perforations of the colon illustrates this. In Denmark, even medium sized perforations of the colon are well treated with laparoscopic lavage and drainage only [79], while this is sometimes insufcient in other regions [10, 11]. Scandinavian countries have a very low presence of multi-resistant bacteria in the environment, rendering low-toxicity antibiotics to be effective treatment.
B. Brandstrup and A. M. Møller
Correcting Preoperative Fluid andElectrolyte Imbalances
In a perfect world, uid and electrolyte imbalances are corrected before the surgery. However, in emergency surgical situations, one must carefully weigh the risks of delaying the surgery against the risks associated with anesthesia and surgery in the presence of imbalances. In such circumstances, it may be necessary to initiate pre­operative- and continue intraoperative correction of the condition. Especially in patients with chronic electrolyte imbalances, one has no other choice than to do the surgery and anesthesia with the imbalance present, because fast corrections are more hazardous.
Patients with bowel obstruction have combined hypovolemia and dehydration. Both can be corrected preoperatively relatively quickly. The correction of hypovo­lemia with isotonic uids has priority, but often a hypotonic uid containing glu­cose to correct the dehydration benets the patient as well.
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Hypovolemia
Hypovolemia remains a common cause of intraoperative death, and hypovolemia should therefore be corrected preoperatively whenever possible. In subacute surgi­cal conditions, correction of hypovolemia is usually unproblematic as it can be cor­rected relatively quickly. This goes for patients with bowel obstruction without risk of intestinal ischemia. Here the surgery can often be postponed several hours, if the correction of uid and/or electrolyte imbalances have priority. This illustrates why the decision to operate immediately or later is a team effort between surgeons and anesthetists, and why common decision-making is superior.
In cases of acute ongoing bleeding, the situation is challenging because volume administration can never replace surgical hemostasis. Both procedures often need to be performed simultaneously. Trauma centers prioritize to stabilize the patient’s circulatory condition to the extent that vital functions are just maintained, allowing for the patient to be transferred to the operating room (with systolic blood pressure of 90mmHg or higher) [12, 13]. Cerebral perfusion continues at lower pressures in supine patients [14].
Intensive Prehospital Treatment
In certain circumstances it increases both the complication rate and mortality, nomi­nally in thoracic gunshot wounds [15]. A likely explanation is that volume replace­ment increases blood pressure, thus “ushing out” clots from the blood vessels and causing re-bleeding before surgical hemostasis is achieved. In addition, both dilu­tion of coagulation factors and uid overload may contribute to the observed harm­ful effect.
Likewise, research suggests blood pressure should not be raised to normal values in patients with a ruptured aortic aneurysm (after animal experiments, a threshold of systolic BP <95mmHg has been set [16]) to avoid re-bleeding, however the evidence is low [17]. Re-bleeding can occur in the adventitia of the vessels (in dissecting aor­tic aneurysms), pericardium, thorax, or retroperitoneum, depending on the location of the aneurysm. Bleeding into the pericardium carries a risk of cardiac tamponade.
It is likely that intravenous uid therapy, which increases blood pressure, can cause similar re-bleeding in other conditions (pelvic fractures, liver injuries, etc.) even if temporary hemostasis has been achieved. The rule is that the higher the blood pressure, the greater the blood loss during ongoing bleeding, and the greater the risk of re-bleeding in conditions with uncertain or inadequate hemostasis.
Such an effect is not seen in trauma cases where hemostasis is possible, for example, in extremity injuries with the application of effective hemostatic pressure (placement of a tourniquet).
All this circumstances notwithstanding, uncontrolled shock can rapidly lead to organ failures and death; therefore, early uid administration is standard care for
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B. Brandstrup and A. M. Møller
patients who have lost massive amounts of blood or other uids and display mark­edly depressed hemodynamic ndings. A mean arterial pressure of 50–65mmHg should be the general aim.
Management ofAcute Ongoing Bleeding
Administration of uids during acute major bleeding should be guided by thrombo­elastography (TEG) or thromboelastometry (ROTEM) [18]. TEG- or ROTEM­guided transfusion strategies may reduce the need for blood products and improve morbidity in patients with ongoing hemorrhage.
In acute bleeding, crystalloids are administered while waiting for blood prod­ucts. Articial colloids such as hydroxyethyl starch are not recommended as they might worsen dilutional coagulopathy by their adverse effects on brin polymeriza­tion and platelet aggregation.
Subsequently, blood loss is replaced with either whole blood or “blood compo­nent packs,” with regional variations in the ratio. In our routine the number of units is
dblood cells Fresh frozen plasma FFP Platelet concent
rrate1,
equivalent to whole blood transfusion.
In addition to the TEG/ROTEM, treatment is monitored using hemoglobin, inter­national normalized ratio (INR), activated partial thromboplastin time (APTT), brinogen, and platelet concentration.
We recommend giving platelets immediately, while erythrocytes and FFP are given in separate IV lines. The strategy for replacement of blood loss during surgery is summarized in Table19.1.
Table 19.1 Replacement of blood loss [19]
Loss in % of blood volume
0–20% 0–1000mL Lactated or Acetated Ringers
20–40% 1000–2000mL Supplemental Human Albumin
40–80% 2000–4000mL Supplemental paced red blood
Thereafter For every 500mL Supplemental RBC
a
Human albumin should be used at the physician’s discretion. Current recommendations, such as Clinical Guidelines for Human Albumin Use (
uploads/2020/07/2018- Albumin- Guideline.pdf), emphasize that no studies have convincingly
shown that human albumin confers survival advantages for conventional volume expansion
Loss in mL (70–80kg person) Replacement Volume
a
solution
(HA)
cells (RBC) and HA
And fresh frozen plasma (FFP) Platelets 1 for every 3 RBC and FFP
https://www.nppeag.scot.nhs.uk/wp- content/
500–3000mL
1000mL
3–4 portions RBC (1000mL) 1000mL (HA)
1 portion (ca. 300mL) 1 portion (ca. 250mL)
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Anemia
Anemia is corrected both preoperatively and intraoperatively. Typically, a blood hemoglobin level of >4.3mmol/L (7g/L) is aimed for in “healthy” individuals, and >5.6mmol/L (9g/L) in patients with severe heart/lung disease [20].
If signicant blood loss is expected during the operation, a higher preoperative hemoglobin level may be appropriate, but there is a lack of evidence supporting this. In many institutions, transfusion is chosen when the intraoperative hemoglobin level falls below 6 mmol/L (9.6 g/L), as operative bleeding is considered severe acute bleeding.
Meeting theBasic Fluid andElectrolyte Requirements oftheBody
The basic needs of patients undergoing surgery differ from those in normal condi­tions in three aspects:
1. Patients are instructed to fast.
2. Patients may experience trauma, inammation, or metabolic stress, leading to
the release of stress hormones, including aldosterone, which causes salt and water retention. In turn cytokines in the same setting could be natriuretic, such as TNF-alpha.
3. Patients are articially ventilated with 100% humidied air, thus water loss from
the airways are diminished.
Insensible perspiration is water loss through the skin and respiratory tract and is the only pure water loss from the body. Approximately two-thirds of the volume comes from the skin, while one-third comes from the respiratory tract [21]. Thus, in patients on mechanical ventilation with 100% humidied air, the insensible perspi­ration from the respiratory tract is reduced by approximately one-third. Otherwise the insensible perspiration is not much inuenced by surgery [22].
The insensible perspiration is dependent on the skin surface. However, calculat­ing skin surface may not be practical in the daily clinical setting. Therefore an approximation to body weight is made. This is introducing the mistake of underes­timating the insensible perspiration for persons with a great skin surface relative to body weight (children) and overestimating in the opposite context (persons with a bodyweight >150kg). Knowing these limitations, the insensible perspiration is in temperate climate very consistent [21] (10mL/kg/day), and if the patient is on a ventilator using humidied air, 6.6mL/kg/day.
If the patient is not on a ventilator, an increase in body temperature (fever) leads to an elevated respiratory frequency, however, the impact is minimal.
Sensible perspiration refers to visible sweat, which consists of salt and water and is always hypotonic compared to extracellular uid. Exercise, elevated environmental