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Correspondence  |   March 2018
In Reply
Author Notes
  • Montreal General Hospital, McGill University Health Center, Montreal, Quebec, Canada (G.B.). gabriele.baldini@mcgill.ca
  • (Accepted for publication November 27, 2017.)
    (Accepted for publication November 27, 2017.)×
Article Information
Correspondence
Correspondence   |   March 2018
In Reply
Anesthesiology 3 2018, Vol.128, 683-685. doi:10.1097/ALN.0000000000002051
Anesthesiology 3 2018, Vol.128, 683-685. doi:10.1097/ALN.0000000000002051
We would like to thank Bloomstone et al. for their important comments on our study.1  We certainly agree with Bloomstone et al. that fluid responsiveness should not be confused with hypovolemia. Being a fluid responder does not necessarily mean requiring additional intravenous fluids. Vice versa, fluid responsiveness should be determined before volume expansion, when clinical signs of hypovolemia suggest that patients might require additional intravenous fluids. Identifying hypovolemic patients might be challenging, however, given that standard hemodynamic parameters or biologic markers used during surgery may not be specific enough, or may fail to identify hypovolemic patients in a timely fashion. Furthermore, the majority of studies evaluating the effectiveness of goal-directed fluid therapy on postoperative outcomes, including ours, include protocols that preemptively maximize stroke volume by administering bolus of fluids based on dynamic indices or on the stroke volume response to a fluid challenge, independent of the presence of clinical signs of hypovolemia. As Bloomstone et al. also reported in their referenced and important consensus statement, stroke volume maximization has been considered “the cornerstone of most goal-directed therapy protocols.”2 
Although consensus statements and recommendations on perioperative fluid therapy (that we fully support) properly advocate to first determine whether “the patient requires hemodynamic support or augmentation of cardiovascular function”2  or to contextualize the presence of fluid responsiveness (i.e., is there a problem justifying additional fluid administration?),3  and second, to establish the presence of fluid responsiveness,2,3  it must be acknowledged that these recommendations are based on studies mainly adopting maximal stroke volume optimization protocols,4–7  rather than protocols based on stroke volume optimization when ascertained clinically.
In our study, we decided to preemptively maximize stroke volume because splanchnic hypoperfusion occurs before clinical signs of hypovolemia are manifested, even when blood losses are minimal.8  We believed that, in the absence of an accurate method or biologic marker to monitor splanchnic perfusion, preemptively maximizing stroke volume would have prevented occulted hypovolemia, and, therefore, minimized gastrointestinal dysfunction caused by splanchnic ischemia.
We would also like to thank Drs. Ripollés-Melchor and Aldecoa for their comments on our study.1  We disagree, however, with Ripollés-Melchor and Aldecoa that a similar amount of fluid was administered the day of surgery; patients in the control group overall received significantly more fluids (2,370 ml vs. 1,535 ml, P < 0.001), but less colloids (0 ml vs. 900 ml, P < 0.001) than patients in the goal-directed fluid therapy group.1  However, although a larger volume of colloids was infused in the goal-directed fluid therapy group, intravascular expansion might have been similar, possibly explaining why stroke volume and cardiac output, and probably splanchnic perfusion, were not statistically different between the two groups. In fact, it must be considered that the volume expanding effect of crystalloids infused during surgery and anesthesia is increased, while the volume expanding effect of colloid is reduced because of the inflammatory response associated with surgery.9  On the other hand, the larger volume of crystalloid administered in the control group might not have caused enough bowel edema to impair bowel function significantly, as also indicated by a marginal weight gain (less than 2.5 kg) on day 1, and by a rapid recovery of weight balance on day 2. Avoidance of splanchnic hypoperfusion and the absence of significant bowel edema in both groups, together with the other considerations reported in the discussion of the manuscript,1  might have contributed to the fact that we did not observe a lower incidence of primary postoperative ileus in the goal-directed fluid therapy group. Our findings also highlight the importance of judicious administration of intravenous fluids in the postoperative period to limit gastrointestinal dysfunction.10  In fact, only 48% and 44% of patients in the goal-directed fluid therapy group and in the control group, respectively, continued to receive intravenous fluids after day 0, limiting the risk of bowel edema and subsequent delayed recovery of bowel function.
Our study was not designed to determine the effect of goal-directed fluid therapy on overall complications, but to determine whether goal-directed fluid therapy could specifically reduce primary postoperative ileus after colorectal surgery in the context of an Enhanced Recovery Program. However, a secondary analysis pooling all data of the 128 patients included in the study was performed (submitted with the original manuscript1  and available to reviewers only). The results of univariate and multivariate regression analysis, including all perioperative factors and hemodynamic variables (stroke volume, stroke volume index, cardiac output, cardiac index, mean arterial pressure, and oxygen delivery index less than 400 ml · min–1 · m–2 at the beginning and end of surgery) that could potentially increase the risk of primary postoperative ileus, did not reveal any significant association with primary postoperative ileus (multivariate regression analysis, model statistic: discriminative power area under the curve = 0.753; Hosmer-Lemeshow goodness of fit test: P = 0.280). Similarly, we could not identify any perioperative factor or hemodynamic value independently associated with 30-day postoperative complications (multivariate regression analysis, model statistic: discriminative power area under the curve = 0.738; Hosmer-Lemeshow goodness of fit test: P = 0.664).
We agree with Ripollés-Melchor and Aldecoa that the value of goal-directed fluid therapy has been proven mainly in high-risk surgical patients,11,12  and not in the context of an Enhanced Recovery Program.13  As recommended by consensus statements and others,2,3,14  it should not be used in low-risk surgical patients, providing that rational and evidence-based physiologic principles are followed to guide fluid therapy.15  Finally, we believe that future studies are warranted to better define “high-risk” patients and surgical procedures, because this definition varies significantly among the studies evaluating the impact of goal-directed fluid therapy on postoperative outcomes. Similarly, more research is needed to determine if extending goal-directed fluid therapy to the postoperative period could improve outcomes, especially considering that on surgical floors a large proportion of patients still receive bolus of intravenous fluids, based mainly on the evaluation of inaccurate signs of hypovolemia and fluid responsiveness.
Competing Interests
Deltex Medical Ltd. (Chichester, United Kingdom) loaned the esophageal doppler monitor to Dr. Baldini. Dr. Baldini’s academic research funding was used to purchase the esophageal doppler probes. Dr. Baldini received travel funding and consulting fees from Edwards Lifesciences Inc. (Mississauga, Ontario, Canada). The other authors declare no competing interests.
Juan C. Gómez-Izquierdo, M.D., Alessandro Trainito, M.D., David Mirzakandov, R.R.T., B.Sc., Barry L. Stein, M.D., A. Sender Liberman, M.D., Patrick Charlebois, M.D., Nicolò Pecorelli, M.D., Liane S. Feldman, M.D., Franco Carli, M.D., Gabriele Baldini, M.D., M.Sc. Montreal General Hospital, McGill University Health Center, Montreal, Quebec, Canada (G.B.). gabriele.baldini@mcgill.ca
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