The association of acute hypercarbia and plasma potassium concentration during laparoscopic surgery: a retrospective observational study
BMC Surgery volume 21, Article number: 31 (2021)
It is uncertain whether increases in PaCO2 during surgery lead to an increase in plasma potassium concentration and, if so, by how much. Hyperkalaemia may result in cardiac arrhythmias, muscle weakness or paralysis. The key objectives were to determine whether increases in PaCO2 during laparoscopic surgery induce increases in plasma potassium concentrations and, if so, to determine the magnitude of such changes.
A retrospective observational study of adult patients undergoing laparoscopic abdominal surgery was perfomed. The independent association between increases in PaCO2 and changes in plasma potassium concentration was assessed by performing arterial blood gases within 15 min of induction of anaesthesia and within 15 min of completion of surgery.
289 patients were studied (mean age of 63.2 years; 176 [60.9%] male, and mean body mass index of 29.3 kg/m2). At the completion of the surgery, PaCO2 had increased by 5.18 mmHg (95% CI 4.27 mmHg to 6.09 mmHg) compared to baseline values (P < 0.001) with an associated increase in potassium concentration of 0.25 mmol/L (95% CI 0.20 mmol/L to 0.31 mmol/L, P < 0.001). On multiple regression analysis, PaCO2 changes significantly predicted immediate changes in plasma potassium concentration and could account for 33.1% of the variance (r2 = 0.331, f(3,259) = 38.915, P < 0.001). For each 10 mmHg increment of PaCO2 the plasma potassium concentration increased by 0.18 mmol/L.
In patients receiving laparoscopic abdominal surgery, there is an increase in PaCO2 at the end of surgery, which is independently associated with an increase in plasma potassium concentration. However, this effect is small and is mostly influenced by intravenous fluid therapy (Plasma-Lyte 148 solution) and the presence of diabetes.
Trial registration Retrospectively registered in the Australian New Zealand Clinical Trials Registry (Trial Number: ACTRN12619000716167).
Increased partial pressure of arterial carbon dioxide (PaCO2) (hypercarbia) is common in the setting of mechanical ventilation and surgery [1, 2]. The effect of hypercarbia and respiratory acidosis on plasma potassium concentrations ([K+]p) is unclear with some studies showing an increase in concentration and others showing no effect [3,4,5,6,7,8,9,10]. Further, a body of longstanding evidence indicates that the hyperkalaemia-acidaemia relationship is more complex than the relatively simplistic, but commonly accepted notion that hyperkalaemia develops due to an increase in extracellular acidity and subsequent exchange of extracellular hydrogen ions for intracellular potassium ions . Challenging this theory, early studies have shown that the directional flux of potassium during acute acid–base disorders is not uniform among various tissues [11,12,13]. During acute respiratory acidosis, potassium was shown to move extracellularly in skeletal muscle [12, 14, 15] and liver tissue [16, 17], but intracellularly in cardiac tissue [11, 15, 18, 19]. Whilst mild hyperkalaemia intraoperatively is usually asymptomatic, high plasma levels of potassium may result in cardiac arrhythmias, muscle weakness or paralysis. Understanding this relationship has specific implications for the prevention of severe hyperkalaemia and the immediate monitoring and management of hyperkalaemia in the intra- and postoperative periods, as timely recognition and treatment of complications that arise from hyperkalaemia is imperative.
These conflicting findings, together with a lack of information from large scale studies concerning the quantitative and temporal relationships between changes in PaCO2 and [K+]p have clinical relevance during anaesthesia. Accordingly, a retrospective study was performed to describe the association between changes in PaCO2 and acute changes in [K+]p in patients undergoing laparoscopic surgery. Laprascopic surgery is a well-described model of carbon dioxide absorption and subsequent hypercarbia during anaesthesia [1, 2, 20,21,22]. The following hypotheses were made. First, in alignment with the current literature [1, 2], patients undergoing laparoscopic surgery would develop acute respiratory acidosis. Second, the development of any respiratory acidosis would cause acute respiratory acidaemia. Finally, there would be an acute rise in [K+]p in response to the respiratory acidaemia. To test these hypotheses, patients undergoing extraperitoneal and intraperitoneal laparoscopic surgery were restrospectively studied in a university hospital.
The Austin Health Human Research Ethics Committee approved this study (LNR/19/Austin/41) and provided a waiver for participant consent. Between February 2015 and February 2019, data was collected from the medical records of all patients undergoing extraperitoneal and intraperitoneal laparoscopic abdominal surgery at university hospital. Patients were included if they underwent surgery of greater than two hours duration, received an arterial line as part of anaesthesia care and were hospitalised for at least one postoperative night. To accurately compare changes in PaCO2 and [K+]p during surgery to baseline values, data was collected from patients who had an arterial blood gas sampled within 15 min of induction of anaesthesia and a subsequent arterial blood gas sampled within 15 min of completion of surgery. The study was registered the study with the Australian New Zealand Clinical Trials Registry (Trial number ACTRN12619000716167; registered 13th May 2019; available at http://www.anzctr.org.au/Trial/Registration/TrialReview.aspx?id=377303&showOriginal=true&isReview=true).
Conduct of anaesthesia, was at the discretion of the treating anaesthetist and in accordance with existing protocols for patients undergoing major laparoscopic surgery at our institution. All patients received balanced crystalloid fluid therapy with the buffered fluid Plasma-Lyte 148 solution (Baxter Healthcare, Toongabbie, Australia). The physiochemical and electrolyte composition of Plasma-Lyte 148 is similar to human plasma, with a pH of 7.4 and a potassium concentration of 5 mmol/L.
During surgery, the handling and transportation of blood gas aspirates were performed using a standard hospital sampling protocol. A 3–5 mL sample of arterial blood was slowly aspirated into a 5 mL discard syringe minimising any force or strain during the aspiration process. Then, 1.0 mL of arterial blood was aspirated from the arterial line over a 2 s period and placed into a safePICO™ blood gas aspirator (Radiometer Medical Aps, Brenshel, Denmark) containing 80 IU electrolyte balanced heparin. This blood sampling technique is designed to minimise any in-vitro haemolysis, which can falsely increase values of plasma constituents, especially potassium. The safePICO aspirator has a clear 1.0 mL label designed for accurate blood sampling, which is necessary to produce reliable results.
The blood sample syringe was transported horizontally and at standard operating room temperature (22 °C) to an automated blood gas analyser (ABL800, Radiometer, Denmark). [K+]p, PaCO2, and pH were measured directly by the analyser and automatically entered into the patient’s electronic medical record. The same blood gas analyser was used for all measurements with regular calibration performed to ensure consistency in sample analysis. As a result, high analytical performance in the measurement of pH, PaCO2, [K+]p and oximetry parameters were obtained. The system uses an automatic mixing system to obtain a homogenous sample for correct results thereby avoiding vigorous manual mixing, which can also lead to a haemolysed blood gas sample. The analyser prewarmed all samples to 37 °C prior to measurement, and the alpha-stat model was applied for all blood gases analyses.
The primary aim of the study was to describe the relationship between PaCO2 and [K+]p. To investigate the independent association between acute hypercarbia and hyperkalaemia, we collected the following preoperative patient variables: age (years), gender, body mass index (kg/m2), current smoker status, ASA physical status classification, history of obstructive pulmonary lung disease, presence of other comorbidities, and surgery urgency. Intraoperative variables collected included the type of laparoscopic surgery, duration of surgery and amount of intraoperative fluid administered. We also collected the ARISCAT score, adjusted for the laparoscopic surgery, which predicts the risk of pulmonary complications after surgery [23, 24].
Inferential statistics were performed with IBM SPSS Statistics for Windows, version 23 (IBM Corp., Armonk, NY, USA). Missing value assessments were performed with R software 3.5.2 (R Development Core Team, Vienna, Austria, 2018) using “mice” and “missMDA” packages. Figure 1 was created using MS Word 365 (16.0.13127.20402) and Fig. 2 was created using SigmaPlot for Windows version 12.0 (Systat Software Inc., 2011, U.S.A).
For all continuous variables, data exploration for outliers and missing values was performed. If there were extreme outliers, winsorization was applied. Only two values from each of baseline [K+]p and pH at the end of surgery were extreme outliers and were replaced with the most adjacent values. If the missing value rate was below 5%, we planned a complete case analysis. Normality assumptions were examined with a visual check of the quantile–quantile (Q-Q) plot. Variables of apparent violated normality assumption were treated with non-parametric statistical analysis methods.
Baseline characteristics were presented using descriptive statistics. Values at baseline and at the end of surgery were compared using the paired t-test. To investigate the relationship between the magnitude of PaCO2 changes, [K+]p changes, and patient characteristics, correlation analysis was performed. For the relationship between the magnitude of PaCO2 changes and [K+]p changes, visual checking of the scatter plot and curve-fit analysis using regression were performed with various types of equations. Based on these results, linear regression was performed to clarify the relationship between the magnitude of PaCO2 changes and [K+]p changes, and other patient characteristics.
To establish the final model, the stepwise selection method was used, and assumptions of linear regression were tested with a histogram and a Q-Q plot for multivariate normality, correlation matrix and variance inflation factors for multicollinearity, Durbin-Watson statistics for autocorrelation, and visual checking of the scatter plot for each independent variable for homoscedasticity. Regression diagnostics were performed with the normality test of residuals. Finally, the characteristics of patients who presented with hypercarbia were also evaluated to enhance the understanding of risk factors for intraoperative CO2 retention. All data were presented with mean ± SD, number (percentile), or median (IQR). The statistically inferred values were expressed as mean (95% confidence intervals [CI]) with corresponding effect sizes, and P values. A two-tailed P value of below 0.050 was considered statistically significant.
A graphical representation of patients undergoing surgery during the study period is presented in Fig. 1. Overall, 1889 patients underwent laparoscopic surgery. Of these, 1596 patients were excluded (no arterial line: n = 984, no blood gas analysis performed: n = 347, blood gas sampled at incorrect times: n = 265). Two hundred and ninety-three patients fulfilled the study inclusion criteria. Four patients were excluded due to duplication of data from the records. A total of 289 patients were included in the final statistical analysis (Additional file 1: De-identified database).
The mean (SD) age of patients was 63.2 ± 11.5 years; 176 (60.9%) patients were male, and the mean (SD) body mass index was 29.3 ± 6.8 kg/m2. The mean (SD) corrected ARISCAT score was 29.5 ± 11.8, and 51 (17.6%) patients were current smokers. Patient comorbidities and baseline characteristics are presented in Table 1. Most surgeries were elective, and the median (IQR) duration of surgery was 184 min (137.3 min to 240.0 min). For all 6 patients who underwent emergency surgery, the admission diagnosis was acute lower gastrointestinal bleeding. No patient had acute peritonitis and all patients underwent definitive surgery after inpatient optimisation.
Intraoperatively, no patient received intraoperative potassium supplementation except for that contained in Plasma-Lyte 148. The median (IQR) volume of Plasma-Lyte 148 solution administered was 2.0 L (1.0 L to 2.1 L), with an approximate estimated infusion rate of 11 mL/min. Nine patients (3.8%) received an intraoperative blood transfusion. The median (interquartile range) number of packed red blood cell units transfused was 1 unit (1 unit to 3 units). No patient received a massive blood transfusion. The maximum number of red blood units transfused was three.
Comparisons of pH, PaCO2 and [K+]p at baseline and at the end of surgery are presented in Table 2. At the completion of the surgery, PaCO2 had increased by 5.18 mmHg (95%CI, 4.27 mmHg to 6.09 mmHg) compared to baseline values (P < 0.001, Cohen’s d = 1.26,). pH also decreased reciprocally to the increased PaCO2 (P < 0.001, Cohen’s d = 0.99), with a similarly large effect size observed. [K+]p increased by 0.25 (95% CI: 0.20 to 0.31) mmol/L at the end of surgery compared to baseline values (P < 0.001, Cohen’s d = 0.03). The effect size of this change was small. Before and after changes in these variables are presented graphically in Fig. 2. Bicarbonate and standard base excess values remained within normal laboratory limits at all time points (Table 2).
Correlation analysis between PaCO2 changes, [K+]p changes and other baseline patient characteristics are presented in Table 3. Increases in PaCO2 correlated weakly with increasing BMI (r = 0.12, P = 0.049), and higher [K+]p were associated with type II diabetes mellitus (rho = 0.13, P = 0.023). According to curve-fit analysis results, a linear model (R2 = 0.217, P < 0.001) was suitable because quadratic and squared models resulted in the same proportion of the variance for the [K+]p change associated with PaCO2 changes (R2 = 0.217, P < 0.001 for the quadratic and squared models).
Multiple regression analysis evaluating whether PaCO2 changes during surgery significantly predicted immediate changes in [K+]p at completion of surgery demonstrated that a final fitted regression model could predict 33.1% of the observed variance in PaCO2 (R2 = 0.331, F(3,259) = 38.915, P < 0.001). Regression analysis showed that PaCO2 changes, intraoperative Plasma-Lyte 148 administration volume, and a history of type II diabetes mellitus significantly predicted changes in [K+]p at completion of surgery (β = 0.018 (95% CI: 0.011 to 0.025), P < 0.001; β = 0.061 (95% CI: 0.031 to 0.091), P < 0.001; β = 0.154 (95% CI: 0.023 to 0.284), P = 0.021 respectively). There was no association between [K+]p and duration of surgery (P = 0.102, Table 4).
Thus, for each 10 mmHg increment of PaCO2 from baseline during surgery, [K+]p increased by 0.18 mmol/L. Furthermore, [K+]p increased by 0.061 mmol/Lfor each litre of Plasma-Lyte 148 administered, and patients with type II diabetes mellitus experienced a 0.154 mmol/L greater rise in [K+]p compared to those without.
In a single centre retrospective study describing the association of acute changes in PaCO2 with acute changes in [K+]p in patients undergoing laparoscopic surgery, CO2 pneumoperitoneum induced small but significant increases in PaCO2 and small but significant decreases in pH during surgery. Moreover, [K+]p increased slightly but significantly at the end of surgery compared to baseline. After adjustment for multiple potential confounders, for every 10 mmHg increment in PaCO2 from baseline, [K+]p increased by almost 0.2 mmol/L. Finally, changes in [K+]p were additionally positively affected by the amount of Plasma-Lyte 148 administered and the presence of type II diabetes mellitus. Given the magnitude of the changes observed, our findings imply that any acute hypercarbic or hyperkalaemic state induced by laparoscopic surgery is probably of limited clinical significance.
Our findings imply that during surgery clinicians should not ascribe large changes in [K+]p to hypercarbia. Other aetiological factors should be considered as a more likely cause of hyperkalaemia. Such differentials should include renal failure, non-renal and endocrine causes, medications and surgical factors. The main hormonal system regulating renal potassium excretion is the renin–angiotensin–aldosterone system. Medications used in the perioperative setting that inhibit this system include angiotensin converting enzyme inhibitors, angiotensin II receptor blockers, nonsteroidal anti-inflammatory drugs, and adrenergic beta-antagonists. Other common anaesthesia medications known to cause hyperkalaemia during surgery include suxamethonium, beta-blockers, digoxin, mannitol and some intravenous penicillins (high potassium content). Finally, surgical causes that can result in the release of potassium from injured cells include ischaemia–reperfusion injury, rhabdomyolysis from surgical associated muscle damage, and high-volume blood transfusion. In many patients, during surgery the cause of hyperkalaemia is multifactorial.
Our findings concur with the landmark study by Finsterer et al. , who prospectively investigated the effects of hypercarbia on [K+]p in 17 patients undergoing major abdominal surgery. The authors induced a model of hypercarbia (mean PaCO2 of 71 mmHg) by removing the soda-lime absorbers from the anaesthesia circuit, and without changing minute volume ventilation and adding CO2 to the inspiratory gas to obtain elevated end-tidal CO2 concentrations. PaCO2 rose by about 30 mmHg resulting in a decrease in pH of 0.2–0.25. A linear relationship between PaCO2 and [K+]p was observed and the authors reported that [K+]p increased by 0.30 mmol/L after 90 min of induced hypercarbia. Our findings are also aligned with others  showing that PaCO2 and [K+]p are related, even with minor degrees of hypercarbia. Hassan et al. , reported that [K+]p increased by 0.39 mmol/L per every 7.5 mmHg increase in PaCO2, a greater increase compared to the present study. Hassan’s findings were almost identical to that reported by Edwards et al. , who showed that [K+]p increased by 0.4 mmol/Lper 10 mmHg change in PaCO2, a doubling of what was observed in the present study.
Our findings however are at variance with the case series of 24 patients undergoing cardiac surgery who were exposed to a 15 min period of apnoeic or low tidal volume ventilation . Over this time period, PaCO2 increased from 43.6 mmHg at baseline to 83.9 mmHg with [K+]p increasing marginally from 4.16 mmol/L at baseline to 4.28 mmol/L at 15 min. This study was limited by a small sample size and exposure to significant hypercarbia for only a 15 min duration. Similarly, Natalani et al.  compared the acute changes in [K+]p in acutely hypercapnic patients undergoing rigid bronchoscopy. The sampling time to evaluate the effects of PaCO2 on hyperkalaemia was also of short duration (20 min), and acute respiratory acidosis did not affect [K+]p. These findings suggest that there appears to be both a quantitative and temporal relationship between changes in [K+]p and hypercarbia under anaesthesia, and that acute hypercarbia of short duration may have less of an effect on [K+]p compared to prolonged exposure. As there was no significant association between [K+]p and duration of surgery in this study, and only patients who had a surgical duration of two hours were included, it is likely that the temporal onset of [K+]p change due to a change in PaCO2 is less than two hours.
Our study has several strengths. Data on a relatively large sample size was provided and a detailed description of the acute effects of hypercarbia and its associations with [K+]p during laparoscopic surgery were analysed. PaCO2, [K+]p, bicarbonate and standard base excess values were collected directly from arterial blood samples and were not amenable to ascertainment bias or derivation. The timing of blood gases in relation to the start and completion of surgery was manually cross-checked with the patients’ medical records by two independent investigators, allowing for accurate confirmation of these data points at the start and at completion of surgery. The large dataset examines the impact of laparoscopic surgery on PaCO2 and [K+]p by directly measuring PaCO2 and [K+]p at baseline and at the completion of surgery, allowing a greater understanding of the temporal relationship of changes in [K+]p and PaCO2 to be observed.
Our study has several limitations. It was a single centre study, limiting the external validity of our findings. However, given laparoscopic surgery with CO2 insufflation is utilised worldwide, our findings are likely relevant and externally generalisable. We cannot extrapolate our results to shorter surgical times, to paediatric patients or to patients at high risk of developing hyperkalaemia (renal failure patients, rhabdomyolysis, tumour lysis syndrome etc.). However, the biological principles and physiochemical changes described are likely to apply to all hypercarbic patients undergoing general anaesthesia. As only two blood gases were sampled, the exact onset and rate of change of the findings observed cannot be evaluated. This study was not designed to determine whether there was an association between changes in PaCO2 or [K+]p and the occurrence of detrimental clinical outcomes. Similarly, we did not evaluate the association between changes in PaCO2 or [K+]p with specific medications that are known to be associated with hyperkalaemia such as preoperative use of certain antihypertensive medications e.g. angiotensin-converting enzyme inhibitors, angiotensin II receptor blockers, and/or potassium-sparing diuretics. This data was unable to be collected and we acknowledge this as a limitation of the study. However, this study was designed to evaluate the change in PaCO2 from baseline rather than the absolute value of [K+]p at baseline, which is more likely to be effected by these medications. As the anaesthesia records in our institution are hand-written, and not part of the hospital’s electronic medical record system, corresponding end-tidal CO2 values were not able to be collected retrospectively. However, the focus of this study was primarily on the association of PaCO2 and [K+]p, rather than end-tidal CO2 and acid–base responses to an increased PaCO2. For all cases the initial CO2 insufflation occurred at a rate of 1 to 5 L/min to achieve an intraabdominal pressure of 12 to 15 mmHg. We used a constant CO2 flow of approximately 200 to 400 mL/min to maintain pneumoperitoneum perioperatively. Given this standard practice for all patients, we cannot make any inferences about the relationship of intraabdominal pressure and changes in PaCO2. Finally, due to the heterogeneity of clinical precipitants for potassium disorders, and the observational nature of this study, our findings are merely associations and do not infer causation.
During laparscopic surgery, for every 10 mmHg increase in PaCO2 from baseline, [K+]p increased by almost 0.2 mmol/L. [K+]p was further elevated with the administration of the crystalloid solution Plasma-Lyte 148 and the presence of type II diabetes mellitus. Clinicians should not ascribe larger changes in [K+]p to hypercarbia in this setting and should consider other aetiological factors in their differential diagnosis.
Availability of data and materials
The deidentified datasets analysed during the current study are available from the corresponding author on reasonable request.
- PaCO2 :
Partial pressure of arterial carbon dioxide
- CO2 :
- [K+]p :
Plasma potassium concentrations
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The study was approved by the Austin Health Human Research Ethics Committee (LNR/19/Austin/41) and no additional administrative permissions were required to access the raw data. Given the retrospective design, a waiver of participant consent was granted by the ethics committee.
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Weinberg, L., Lee, DK., Gan, C. et al. The association of acute hypercarbia and plasma potassium concentration during laparoscopic surgery: a retrospective observational study. BMC Surg 21, 31 (2021). https://doi.org/10.1186/s12893-020-01034-w