The Eyeball Test

  • Ochsner Journal
  • June 2023,
  • 23
  • (2)
  • 100-103;
  • DOI: https://doi.org/10.31486/toj.23.5035

THE RECOMMENDATION FOR INTRAVENOUS FLUIDS DURING SURGERY BEGINS IN NEW ORLEANS

The administration of intravenous fluids, crystalloids and colloids, has been an integral part of care for most surgical procedures, yet the replacement volume needed to maintain intravascular normovolemia continues to be a daily issue for most anesthesiologists.1 Although surgical procedures advanced following the introduction of ether anesthesia in the 1860s,2 intravenous fluids were only first proposed for surgery in 1924 by Dr Rudolph Matas of New Orleans to “restore the vascular equilibrium and rally the patient until the defensive cardiovascular mechanism has had time to assert itself….3 In Matas’ day, the common methods for rehydrating patients unable to tolerate oral fluids were proctoclysis or hypodermoclysis, methods that were not always successful. Matas recommended the venoclysis route, with the intravenous infusion continued guttatim for as long as circulatory doubt existed.3 However, case descriptions of intravenous hydration included patients developing congestion of the lungs and heart when fluid was rapidly administered, hence Matas’ recommendation of a “drop by drop” rate of infusion.3-5 These early descriptions were observed in critically ill patients, and the understanding of ischemia-reperfusion syndrome may not have been known.3-5

THE DEBATE CONTINUES: WET OR DRY?

What is the right fluid balance for pulmonary resection procedures or for surgical procedures in general? The study of perioperative fluid therapy has increased in recent years as studies show that a fluid administration strategy can influence postoperative outcomes.6-12 Historically, the development of postpneumonectomy pulmonary edema as originally described by Zeldin, Normandin, and colleagues13 demonstrated higher complication rates when associated with excessive intravenous fluid therapy. Consequently, Zeldin et al and others recommended restricting the administration of intravenous fluids during pulmonary surgery.13-17 Other researchers, however, could not associate postpneumonectomy pulmonary edema with excessive intravenous fluid administration.18 In contrast, restricting fluid therapy risks inadequate organ perfusion with worse postoperative outcomes.19 Although the goal is to maintain intravascular normovolemia,20,21 the classic measures of intraoperative systemic hemodynamics and urine output do not provide satisfactory measures of intravascular normovolemia.22 Furthermore, investigations with the use of complex monitoring instruments to measure perioperative intravascular volume status have not answered this need,22 hence the continued use of guidelines rather than individualization measures to maintain intravascular normovolemia during the surgical procedure.15-17

THE USE OF VOLUMETRIC CURVES TO STUDY OUTCOMES

Bellamy20 and Bundgaard-Nielsen, Secher, and Kehlet21 proposed using volumetric dose-response curves to associate perioperative fluid administration with the incidence of postoperative morbidities. We agree with that concept. The authors proposed that the volumetric curves would be shaped in the form of a U, with the limbs of the U representing increased morbidities and the optimum fluid administration range located at the bottom of the U.20,21 The approach in our study was to examine the dose-response relationships to previously reported adverse events to determine the optimum intraoperative fluid administration rates23 and then compare these findings to other lung resection studies that reported their analyses with conventional summation statistics.24-27

In our study, the associations of the intraoperative crystalloid administration rate (mL/kg/hr) to previously reported adverse events were in the shapes of J-curves (see Figures 1 through 7 in our paper “Rate of Intraoperative Crystalloid Administration During Thoracic Surgery Is Causal in Reducing Postoperative Hospital Length of Stay,” doi.org/10.31486/toj.22.0113)23 rather than the hypothesized U-curves.20,21 J-curves are not a new concept, as they have been used in the medical literature to optimize blood pressure therapy28-31; to examine relationships between alcohol intake and noncardiogenic strokes,32,33 between plasma low-density lipoprotein concentrations and recurrent coronary events,34 and between pediatric serum lead levels and intellectual development35-37; and to investigate the role of body mass index on the incidences of cancer, hip fractures, and mortality.38-41

Figure 1.

Knotted spline graph showing the duration of postoperative hospital length of stay relative to the intraoperative crystalloid administration rate (mL/kg/hr).

CAN THE SHAPE OF CURVES ALLOW PREDICTION?

In our study, postoperative hospital length of stay was fitted to intraoperative crystalloid administration rate (Figure 1 in our paper “Rate of Intraoperative Crystalloid Administration During Thoracic Surgery Is Causal in Reducing Postoperative Hospital Length of Stay,” doi.org/10.31486/toj.22.0113).23 However, when using a different statistical fitting tool, knotted splines on this same association, a different fit is obtained (Figure 1 in this editorial). This fitted line is now under less summation constraints, and 3 patterns begin to emerge. In the intraoperative crystalloid administration rate range 0 to 10 mL/kg/hr, a higher mean of postoperative hospital length of stay is observed and the highest number of outliers (defined below). A second group between 10 to 20 mL/kg/hr has a lower fitted mean and a lower number of outliers with fewer extreme values when compared to the 0 to 10 mL/kg/hr group. A third group develops once the fitted line crosses into the intraoperative crystalloid administration of 20 mL/kg/hr. The associations viewed with knotted splines analysis suggest ideal administration rates of 20 to 30 mL/kg/hr, as no further reduction in postoperative hospital length of stay was observed: an eyeball test.42 However, these observations need further investigation.

We can also examine the range of postoperative hospital length of stay with another statistical tool, the outlier plot (Figure 2 in this editorial). According to this histogram/outlier plot, the outliers begin to develop when the postoperative hospital length of stay is >10 days. When the outlier values from the histogram/outlier plot are highlighted on the knotted spline graph, all outliers are below the 20 mL/kg/hr intraoperative crystalloid administration rate (Figure 3 in this editorial) with no outliers above 20 mL/kg/hr.

Figure 2.

Histogram with outlier box plot of postoperative hospital length of stay in 222 consecutive patients following thoracic surgery. d, days.

Figure 3.

Knotted spline graph showing the postoperative hospital length of stay outliers relative to the intraoperative crystalloid administration rate (mL/kg/hr).

CONCLUSION

The use of dose-response curves allows investigators to visualize optimal intraoperative crystalloid infusion rates and use these results to develop intraoperative fluid management guidelines for this patient population. This approach provides clinical information that cannot be determined when data are solely presented as summations. This method provides an additional tool to improve our understanding of perioperative medicine.

ACKNOWLEDGMENTS

The author has no financial or proprietary interest in the subject matter of this article.

©2023 by the author(s); licensee Ochsner Journal, Ochsner Clinic Foundation, New Orleans, LA. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (creativecommons.org/licenses/by/4.0/legalcode) that permits unrestricted use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.

REFERENCES

  1. 1.
    MalbrainMLNG, LangerT, AnnaneD, Intravenous fluid therapy in the perioperative and critical care setting: executive summary of the International Fluid Academy (IFA). Ann Intensive Care. 2020;10(1):64. doi: 10.1186/s13613-020-00679-3
  2. 2.
    StoneME, MeyerMR, AlstonTA. Elton Romeo Smilie, the not-quite discoverer of ether anesthesia. Anesth Analg. 2010;110(1):195-197. doi: 10.1213/ane.0b013e3181af7f9a
  3. 3.
    MatasR. The continued intravenous “drip”: with remarks on the value of continued gastric drainage and irrigation by nasal intubation with a gastroduodenal tube (jutte) in surgical practice. Ann Surg. 1924;79(5):643-661. doi: 10.1097/00000658-192405000-00001
  4. 4.
    BaileyH, CarnowJM. Continuous intravenous saline. Br Med J. 1934;1(3809):11-13. doi: 10.1136/bmj.1.3809.11
  5. 5.
    HendonGA. Venoclysis. JAMA. 1930;95(16):11751178. doi: 10.1001/jama.1930.02720160035011
  6. 6.
    HolteK, SharrockNE, KehletH. Pathophysiology and clinical implications of perioperative fluid excess. Br J Anaesth. 2002;89(4):622-632. doi: 10.1093/bja/aef220
  7. 7.
    VercueilA, GrocottMP, MythenMG. Physiology, pharmacology, and rationale for colloid administration for the maintenance of effective hemodynamic stability in critically ill patients. Transfus Med Rev. 2005;19(2):93-109. doi: 10.1016/j.tmrv.2004.11.006
  8. 8.
    GrocottMPW, MythenMG, GanTJ. Perioperative fluid management and clinical outcomes in adults. Anesth Analg. 2005;100(4):1093-1106. doi: 10.1213/01.ANE.0000148691.33690.AC
  9. 9.
    HolteK, KehletH. Compensatory fluid administration for preoperative dehydration—does it improve outcome? Acta Anaesthesiol Scand. 2002;46(9):1089-1093. doi: 10.1034/j.1399-6576.2002.460906.x
  10. 10.
    HolteK, KehletH. Fluid therapy and surgical outcomes in elective surgery: a need for reassessment in fast-track surgery. J Am Coll Surg. 2006;202(6):971-989. doi: 10.1016/j.jamcollsurg.2006.01.003
  11. 11.
    ChappellD, JacobM, Hofmann-KieferK, ConzenP, RehmM. A rational approach to perioperative fluid management. Anesthesiology. 2008;109(4):723-740. doi: 10.1097/ALN.0b013e3181863117
  12. 12.
    BrandstrupB. Fluid therapy for the surgical patient. Best Pract Res Clin Anaesthesiol. 2006;20(2):265-283. doi: 10.1016/j.bpa.2005.10.007
  13. 13.
    ZeldinRA, NormandinD, LandtwingD, PetersRM. Postpneumonectomy pulmonary edema. J Thorac Cardiovasc Surg. 1984;87(3):359-365.
  14. 14.
    MøllerAM, PedersenT, SvendsenPE, EngquistA. Perioperative risk factors in elective pneumonectomy: the impact of excess fluid balance. Eur J Anaesthesiol. 2002;19(1):57-62. doi: 10.1017/s0265021502000091
  15. 15.
    AssaadS, PopescuW, PerrinoA. Fluid management in thoracic surgery. Curr Opin Anaesthesiol. 2013;26(1):31-39. doi: 10.1097/ACO.0b013e32835c5cf5
  16. 16.
    SearlCP, PerrinoA. Fluid management in thoracic surgery. Anesthesiol Clin. 2012;30(4):641-655. doi: 10.1016/j.anclin.2012.08.009
  17. 17.
    ŞentürkM, Orhan SungurM, SungurZ. Fluid management in thoracic anesthesia. Minerva Anestesiol. 2017;83(6):652-659. doi: 10.23736/S0375-9393.17.11760-8
  18. 18.
    TurnageWS, LunnJJ. Postpneumonectomy pulmonary edema. A retrospective analysis of associated variables. Chest. 1993;103(6):1646-1650. doi: 10.1378/chest.103.6.1646
  19. 19.
    SlingerP. Fluid management during pulmonary resection surgery. Ann Card Anaesth. 2002;5(2):220-224.
  20. 20.
    BellamyMC. Wet, dry or something else? Br J Anaesth. 2006;97(6):755-757. doi: 10.1093/bja/ael290
  21. 21.
    Bundgaard-NielsenM, SecherNH, KehletH. 'Liberal' vs. 'restrictive' perioperative fluid therapy—a critical assessment of the evidence. Acta Anaesthesiol Scand. 2009;53(7):843-851. doi: 10.1111/j.1399-6576.2009.02029.x
  22. 22.
    Bundgaard-NielsenM, HolteK, SecherNH, KehletH. Monitoring of peri-operative fluid administration by individualized goal-directed therapy. Acta Anaesthesiol Scand. 2007;51(3):331-340. doi: 10.1111/j.1399-6576.2006.01221.x
  23. 23.
    SmithMT, PeairsAD, NossamanBD. Rate of intraoperative crystalloid administration during thoracic surgery is causal in reducing postoperative hospital length of stay. Oschsner J. 2023;23(2). doi: 10.31486/toj.22.0113
  24. 24.
    LickerM, de PerrotM, SpiliopoulosA, Risk factors for acute lung injury after thoracic surgery for lung cancer. Anesth Analg. 2003;97(6):1558-1565. doi: 10.1213/01.ANE.0000087799.85495.8A
  25. 25.
    LickerM, DiaperJ, VilligerY, Impact of intraoperative lung-protective interventions in patients undergoing lung cancer surgery. Crit Care. 2009;13(2):R41. doi: 10.1186/cc7762
  26. 26.
    MatotI, DeryE, BulgovY, CohenB, PazJ, NesherN. Fluid management during video-assisted thoracoscopic surgery for lung resection: a randomized, controlled trial of effects on urinary output and postoperative renal function. J Thorac Cardiovasc Surg. 2013;146(2):461-466. doi: 10.1016/j.jtcvs.2013.02.015
  27. 27.
    ArslantasMK, KaraHV, TuncerBB, Effect of the amount of intraoperative fluid administration on postoperative pulmonary complications following anatomic lung resections. J Thorac Cardiovasc Surg. 2015;149(1):314-321.e1. doi: 10.1016/j.jtcvs.2014.08.071
  28. 28.
    AhluwaliaM, BangaloreS. Management of hypertension in 2017: targets and therapies. Curr Opin Cardiol. 2017;32(4):413-421. doi: 10.1097/HCO.0000000000000408
  29. 29.
    DudenbostelT, OparilS. J Curve in Hypertension. Curr Cardiovasc Risk Rep. 2012;6(4):281-290. doi: 10.1007/s12170-012-0246-0
  30. 30.
    CruickshankJ. The J-curve in hypertension. Curr Cardiol Rep. 2003;5(6):441-452. doi: 10.1007/s11886-003-0105-1
  31. 31.
    The J-curve phenomenon and the treatment of hypertension. JAMA. 1991;266(1):64-66.
  32. 32.
    ShiotsukiH, SaijoY, OgushiY, KobayashiS; Japan Standard Stroke Registry Study Group. Relationships between alcohol intake and ischemic stroke severity in sex stratified analysis for Japanese acute stroke patients. J Stroke Cerebrovasc Dis. 2019;28(6):1604-1617. doi: 10.1016/j.jstrokecerebrovasdis.2019.02.034
  33. 33.
    WandelerG, KrausD, FehrJ, The J-curve in HIV: low and moderate alcohol intake predicts mortality but not the occurrence of major cardiovascular events. J Acquir Immune Defic Syndr. 2016;71(3):302-309. doi: 10.1097/QAI.0000000000000864
  34. 34.
    SacksFM, MoyéLA, DavisBR, Relationship between plasma LDL concentrations during treatment with pravastatin and recurrent coronary events in the Cholesterol and Recurrent Events trial. Circulation. 1998;97(15):1446-1452. doi: 10.1161/01.cir.97.15.1446
  35. 35.
    JuskoTA, HendersonCR, LanphearBP, Cory-SlechtaDA, ParsonsPJ, CanfieldRL. Blood lead concentrations < 10 microg/dL and child intelligence at 6 years of age. Environ Health Perspect. 2008;116(2):243-248. doi: 10.1289/ehp.10424
  36. 36.
    LanphearBP, HornungR, KhouryJ, Low-level environmental lead exposure and children's intellectual function: an international pooled analysis [published correction appears in Environ Health Perspect. 2019 Sep;127(9):99001]. Environ Health Perspect. 2005;113(7):894-899. doi: 10.1289/ehp.7688
  37. 37.
    CanfieldRL, HendersonCRJr, Cory-SlechtaDA, CoxC, JuskoTA, LanphearBP. Intellectual impairment in children with blood lead concentrations below 10 microg per deciliter. N Engl J Med. 2003;348(16):1517-1526. doi: 10.1056/NEJMoa022848
  38. 38.
    NafiuOO, KheterpalS, MouldingR, The association of body mass index to postoperative outcomes in elderly vascular surgery patients: a reverse J-curve phenomenon. Anesth Analg. 2011;112(1):23-29. doi: 10.1213/ANE.0b013e3181fcc51a
  39. 39.
    HongS, YiSW, SullJW, HongJS, JeeSH, OhrrH. Body mass index and mortality among Korean elderly in rural communities: Kangwha Cohort Study. PLoS One. 2015;10(2):e0117731. doi: 10.1371/journal.pone.0117731
  40. 40.
    HongJS, YiSW, YiJJ, HongS, OhrrH. Body mass index and cancer mortality among Korean older middle-aged men: a prospective cohort study. Medicine (Baltimore). 2016;95(21):e3684. doi: 10.1097/MD.0000000000003684
  41. 41.
    KimSH, YiSW, YiJJ, KimYM, WonYJ. Association between body mass index and the risk of hip fracture by sex and age: a prospective cohort study. J Bone Miner Res. 2018;33(9):1603-1611. doi: 10.1002/jbmr.3464
  42. 42.
    WelkeKF. The eyeball test: can the blind leading the blind see better than the statistician? Circ Cardiovasc Qual Outcomes. 2014;7(1):11-12. doi: 10.1161/CIRCOUTCOMES.113.000760
Loading
Loading
Loading
  • Print
  • Download PDF
  • Email Article
  • Citation Tools