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The effect of different volumes and temperatures of saline on the bladder pressure measurement in critically ill patients
Critical Care volume 11, Article number: R82 (2007)
Intra-abdominal hypertension is common in critically ill patients and is associated with increased severity of organ failure and mortality. The techniques most commonly used to estimate intra-abdominal pressure are measurements of bladder and gastric pressures. The bladder technique requires that the bladder be infused with a certain amount of saline, to ensure that there is a conductive fluid column between the bladder and the transducer. The aim of this study was to evaluate the effect of different volumes and temperatures of infused saline on bladder pressure measurements in comparison with gastric pressure.
Thirteen mechanically ventilated critically ill patients (11 male; body mass index 25.5 ± 4.6 kg/m2; arterial oxygen tension/fractional inspired oxygen ratio 225 ± 48 mmHg) were enrolled. Bladder pressure was measured using volumes of saline from 50 to 200 ml at body temperature (35 to 37°C) and room temperature (18 to 20°C).
Bladder pressure was no different between 50 ml and 100 ml saline (9.5 ± 3.7 mmHg and 13.7 ± 5.6 mmHg), but it significantly increased with 150 and 200 ml (21.1 ± 10.4 mmHg and 27.1 ± 15.5 mmHg). Infusion of saline at room temperature caused a significantly greater bladder pressure compared with saline at body temperature. The lowest difference between bladder and gastric pressure was obtained with a volume of 50 ml.
The bladder acts as a passive structure, transmitting intra-abdominal pressure only with saline volumes between 50 ml and 100 ml. Infusion of a saline at room temperature caused a higher bladder pressure, probably because of contraction of the detrusor bladder muscle.
Intra-abdominal pressure (IAP) is the pressure generated inside the abdominal cavity and depends on the degree of flexibility of the diaphragm and abdominal wall, and on the density of its contents . Intra-abdominal hypertension (IAH), defined as an abnormal increase in IAP, can be common in critically ill patients, being present in 18% to 81% of the patients depending on the cut-off level used [2–8].
Several clinical conditions such as accumulation of blood, ascites, retroperitoneal haematoma, bowel oedema, necrotizing pancreatitis, massive fluid resuscitation, packing after control laparotomy and closure of a swollen noncompliant abdominal wall may induce IAH [3, 9]. IAH has adverse effects on several organs, causing reductions in cardiac output , deterioration in gas exchange [11–13] and decreases in splachnic-renal perfusion [14–16]. In surgical , trauma  and medical  critically patients, the IAH was an independent predictor factor of hospital mortality. Although surgical decompression remains the only definitive therapy in the case of substantial IAH, and the IAP is lower after decompression, mortality remains considerable [18, 19].
Because the abdomen and its contents can be considered to be relatively noncompressive and fluid in character, behaving in accordance with Pascal's law, the IAP measured at one point is assumed to reflect the IAP throughout the abdomen . A variety of methods for measuring IAP have been proposed, which are either indirect (by transduction of bladder, gastric, or uterine pressure using a ballon catheter) or direct (using a intraperitoneal catheter) [1, 20]. However, among the different methods, the intra-bladder pressure (IBP) technique is the most commonly used because of its simplicity and low cost [4, 21].
The bladder technique, originally described by Kron and coworkers , assumes that the bladder behaves like a passive pressure membrane transducer when it is infused with a small amount of saline . However, various saline volumes for bladder priming, 50 ml up to 250 ml, have been used to estimate IBP [10, 14, 21–23]. Previous studies demonstrated that a small volume of saline (10 to 25 ml) is required to prime the bladder in order to avoid overestimating the IBP [22, 24, 25]. The International Abdominal Compartment Syndrome Consensus Conference  suggested that a maximal instillation volume of 25 ml of saline should be used. In addition the bladder – being a muscular organ – may change its elasticity in response to various external stimuli, such as an infusion of warm saline . Thus the bladder may not always behave like a passive elastic structure, leading to inaccurate estimation of IAP.
The aim of this study was to evaluate IAP estimated by bladder pressure, measured with the bladder infused with different volumes of saline at room and body temperatures, in comparison with intra-gastric pressure (IGP).
Materials and methods
Thirteen sedated, mechanically ventilated patients admitted to the intensive care unit of Ospedale Policlinico were enrolled. Exclusion criteria were contraindications to bladder pressure measurement (a recent history of bladder surgery, haematuria, trauma, or neurogenic bladder).
The study was approved by the institutional review board of our hospital, and informed consent was obtained in accordance with Italian national regulations.
The IBP was measured using a revision of the Cheatham's original technique  with disposable pressure transducer (Edward Lifesciences, Irvine, CA, USA). A 18-gauge needle was inserted into the culture aspiration port of the Foley's catheter and connected with a sterile tube to the pressure transducer using two three-way stopcocks. A standard infusion bag of normal saline was attached to one stopcock and a 60 ml syringe was connected to the second stopcock. Before taking any measurements, the system was flushed with sterile saline and the pubic symphysis was always used as zero reference point with the subject in the complete supine position.
The IBP was measured at different volumes of saline infusion (50, 100, 150 and 200 ml, with steps of 50 ml) at room temperature (18 to 20°C). The sequence of measurements was then repeated using saline infusion warmed to body temperature (35 to 37°C). At each volume of saline, the IBP was recorded 5 to 10 s after the termination of saline infusion (early recording) and 5 min later (late recording) by keeping the bladder catheter closed. After each measurement the bladder was emptied.
Each patient was studied at an external positive end-expiratory pressure of 10 cmH2O, with the other ventilatory parameters (previously selected by the attending physician) unchanged during the study. Thus, each patient underwent two randomized series of measurements.
The IGP was measured using a radio-opaque balloon (SmartCath; Bicore, Irvine, CA, USA) connected to a pressure transducer (Bentley Trantec; Bentley Laboratories, Irvine, CA, USA) . For measurement purposes, the gastric balloon was inflated with 1.0 ml air.
The IBP and IGP were measured at end-expiration and the signals were recorded on a personal computer for subsequent analysis (Colligo; Elekton, Milan, Italy).
The level of sedation before the study was evaluated using the Ramsay scale . The Simplified Acute Physiology Score II was used to assess the severity of systemic illness at study entry , whereas the Sepsis Related Organ Failure Assessment score was computed on the day of the study by considering the worst value for each organ system (respiratory, cardiovascular, renal, coagulation, liver and neurological) .
The effects of volume, temperature of saline infused and time of recording were analyzed by two-way repeated measures analysis of variance, followed by Student/Newman Keuls test for multiple comparison (SigmaStat 2.03; SPSS Inc., Chicago, IL, USA) . P < 0.05 was considered statistically significant.
The mean bias (bladder minus gastric pressure), precision (standard deviation of the bias) and limits of agreement were calculated using the Bland-Altman analysis . The percentage error was calculated in accordance with the method proposed by Crichley and coworkers .
All data are expressed as mean ± standard deviation.
The main clinical characteristics are reported in Table 1. The patients were studied after a mean of 6 ± 3.8 days from intensive care admission.
The IBP was no different with 50 and 100 ml volumes of saline (9.5 ± 3.7 mmHg and 13.7 ± 5.6 mmHg; P = 0.071), but it was significantly higher with 150 and 200 ml saline (21.1 ± 10.4 and 27.1 ± 15.5 mmHg; P < 0.001; Figure 1). Considering the IBP measured with 50 ml of saline infused as reference, we computed the agreements with the IBP measured with 100, 150 and 200 ml of saline (Table 2).
Four patients (30.7% of the population) were classified as having IAH (IAP >12 mmHg) when 50 ml saline was used. This increased to eight patients (61.5% of the population) when 100 ml saline was used.
The IBP was significantly lower 5 min after saline infusion (late recording) than just after the saline infusion (early recording), but only with the bladder infused with 200 and 150 ml of saline (21.1 ± 10.4 versus 16.2 ± 5.6 mmHg, and 27.1 ± 15.5 versus 19.3 ± 8.9 mmHg; P < 0.005; Figure 1). At each volume infused, the infusion of saline at body temperature resulted in a significantly lower IBP than did infusion of saline at room temperature (8.2 ± 4.4 versus 7.7 ± 3.7 mmHg with 50 ml saline, 11.4 ± 5.9 versus 10.2 ± 3.8 mmHg with 100 ml saline, 15.4 ± 8.8 versus 13.3 ± 5.0 mmHg with 150 ml saline, and 25.7 ± 16.5 versus 22.8 ± 17.0 mmHg with 200 ml saline; P < 0.001; Figure 2). The differences between the paired measurements of IGP and IBP (bias) are given in Table 3. The lowest bias was found for a 50 ml volume of saline, whereas the bias increased with increasing the volume of saline infused in the bladder.
The major findings of this study were as follows. First, increasing the volume of saline infused led to higher IBP. Second, the IBP was significantly lower when measured after 5 min compared with when it was measured just after the termination of the volume infusion, but only with 150 and 200 ml saline. Third, the IBP was significantly lower when measured with infusion of saline at body temperature compared with saline at room temperature. Finally, the lowest bias between the IBP and IGP was obtained with the bladder infused with 50 ml saline.
An increase in IAP is associated with various organ dysfunctions (local and systemic), which in turn are associated with significantly increased in morbidity and mortality . Despite these potential adverse clinical consequences, however, IAP is commonly measured only when there is some clinical suspicion; furthermore, there is currently no general consensus on how frequently it should be measured . Sugrue and coworkers  found that clinical examination alone was not accurate in estimating IAP, finding that the likelihood of physicians correctly identifying IAH was lower than 50%. Thus, accurate estimation of IAH is fundamental to appropriate and timely patient management .
The most widely used technique to measure the IAP is the bladder pressure technique, as proposed by Kron and coworkers . In that study the authors found that the IBP measured using saline volumes between 50 and 100 ml through a Foley catheter correlated well with pressures measured using a peritoneal dialysis catheter during several infusions of peritoneal dialysis solution. Iberti and colleagues , in a canine model of increased IAP, estimated bladder pressure with the bladder empty; they demonstrated that the IBP accurately reflected the IAP. Fusco and coworkers , using a human model in which IAP ranged between 0 and 25 mmHg during laparoscopic surgery, found that the bladder emptied (with a volume of 0 ml) yielded the most accurate estimation of IAP. However, at an IAP of 25 mmHg the bladder volume exhibiting the lowest bias was 50 ml.
In the present study, although we did not find any statistically significant difference (there was only a trend) in IBP measured using saline volumes of 50 and 100 ml, this difference could lead to a patient being incorrectly identified as having IAH if a 100 ml rather than a 50 ml of volume were used. Similarly, De Waele and colleagues  demonstrated that 12 patients were categorized as suffering from IAH when a volume of 10 ml was used, increasing to 15 and 17 patients, respectively, when 50 and 100 ml volumes were used. Previous studies conducted in adult patients [22, 24, 25] found that the increase in IBP was statistically significant with a small instillation volume, and two studies conducted in children and infants [37, 38] found that the IAP is most accurately measured by instilling into the bladder 1 ml saline per kilogram of body weight. Thus, it has been proposed that the appropriate amount of volume is that required to create a fluid column without interposed air .
Although these findings clearly indicate that the IBP can overestimate IAP when large volumes of saline are infused, the possible mechanisms involved are still not clearly understood. The bladder is a muscular membranous organ that is composed of four layers, namely mucous, adventitia, serosa and muscularis, and its elasticity decreases in response to a direct mechanical increase in stress and strain on its structure (when a large amount of saline is infused). In addition, the elasticity of bladder can also be reduced by contraction of the detrusor muscle, mediated by sensory receptors located in the bladder wall, after a rapid infusion of saline or other fluid that is not at body temperature .
A recording of bladder pressure 5 min after termination of the infusion yielded a significantly lower IBP only with a volume of saline up to 150 ml; this suggests that the bladder takes longer to reach a stable condition only when it is infused with large volumes. However, this is not relevant in current clinical practice, because the IAP is usually measured with volumes of saline lower than 150 ml.
We found that infusion of saline at body temperature, at each volume infused, also resulted in a significantly lower IBP compared with infusion of saline at room temperature. Rapid infusion of saline at a temperature lower than body temperature may activate contraction of the detrusor muscle (as mentioned above) by a reflex loop through nociceptors with C afferent fibres located in the bladder wall , causing a falsely elevated IAP recording.
Another possible cause of reduced elasticity of the bladder might be continued urine drainage through the catheter . In critically ill patients, De Waele and coworkers  observed a direct relationship between the duration of catheterization and the difference in bladder pressure measured using volumes of saline of 10 and 100 ml. This suggests that the bladder should be filled only minimally if an accurate measurement of IAP is to be obtained, especially in patients with prolonged catheterization.
In cases of bladder trauma, pelvic fractures or haematoma, or neurogenic bladder, in which the bladder pressure technique cannot be applied, the IGP technique is recommended . Compared with the IBP technique, IGP measurements do not interfere with urine output and avoid risk for infection . In critically ill patients and in patients undergoing laparoscopic cholecystectomy with the abdominal cavity inflated at a pressure of 20 mmHg, a clinically acceptable agreement between IGP and IBP was observed [41, 42]. Unexpectedly, we found much greater limits of agreement, probably because of the presence of gastric motor activity, which falsely increases 'true' estimation of IAP.
In clinical practice the IAP should be estimated using the IBP technique, infusing the bladder with only a small amount of volume of saline at body temperature to avoid overestimating the IAP. If this is not feasible, then the IGP should be measured.
In clinical practice, IAP should be estimated using the IBP technique with the bladder infused with only a small volume of saline.
The saline infused should be at body temperature to avoid overestimating the IAP.
It is recommended that sufficient equilibration time be allowed before the IAP is measured.
IGP correlates with IBP only at low volumes of saline.
Malbrain ML, Cheatham ML, Kirkpatrick A, Sugrue M, Parr M, De Waele W, Balogh Z, Leppäniemi A, Olvera C, Ivatury R, et al.: Results from the International Conference of Experts on Intra-abdominal Hypertension and Abdominal Compartment Syndrome. I. Definitions. Intensive Care Med 2006, 32: 1722-1732. 10.1007/s00134-006-0349-5
Balogh Z, McKinley BA, Holcomb JB, Miller CC, Cocanour CS, Kozar RA, Valdivia A, Ware DN, Moore FA: Both primary and secondary abdominal compartment syndrome can be predicted early and are harbingers of multiple organ failure. J Trauma 2003, 54: 848-859.
Malbrain MLNG: Abdominal pressure in the critically ill. Curr Opin Crit Care 2000, 6: 17-29. 10.1097/00075198-200002000-00003
Malbrain ML: Different techniques to measure intra-abdominal pressure (IAP): time for a critical re-appraisal. Intensive Care Med 2004, 30: 357-371. 10.1007/s00134-003-2107-2
Malbrain ML, Chiumello D, Pelosi P, Wilmer A, Brienza N, Malcangi V, Bihari D, Innes R, Cohen J, Singer P, et al.: Prevalence of intra-abdominal hypertension in critically ill patients: a multicentre epidemiological study. Intensive Care Med 2004, 30: 822-829. 10.1007/s00134-004-2169-9
Malbrain ML, Chiumello D, Pelosi P, Bihari D, Innes R, Ranieri VM, Del Turco M, Wilmer A, Brienza N, Malcangi V, et al.: Incidence and prognosis of intraabdominal hypertension in a mixed population of critically ill patients: a multiple-center epidemiological study. Crit Care Med 2005, 33: 315-322. 10.1097/01.CCM.0000153408.09806.1B
Sugrue M, Buist MD, Hourihan F, Deane S, Bauman A, Hillman K: Prospective study of intra-abdominal hypertension and renal function after laparotomy. Br J Surg 1995, 82: 235-238. 10.1002/bjs.1800820234
Sugrue M, Jones F, Janjua KJ, Deane SA, Bristow P, Hillman K: Temporary abdominal closure: a prospective evaluation of its effects on renal and respiratory physiology. J Trauma 1998, 45: 914-921.
Morken J, West MA: Abdominal compartment syndrome in the intensive care unit. Curr Opin Crit Care 2001, 7: 268-274. 10.1097/00075198-200108000-00010
Iberti TJ, Kelly KM, Gentili DR, Hirsch S, Benjamin E: A simple technique to accurately determine intra-abdominal pressure. Crit Care Med 1987, 15: 1140-1142.
Cullen DJ, Coyle JP, Teplick R, Long MC: Cardiovascular, pulmonary, and renal effects of massively increased intra-abdominal pressure in critically ill patients. Crit Care Med 1989, 17: 118-121. 10.1097/00003246-198902000-00002
Gattinoni L, Pelosi P, Suter PM, Pedoto A, Vercesi P, Lissoni A: Acute respiratory distress syndrome caused by pulmonary and extrapulmonary disease. Different syndromes? Am J Respir Crit Care Med 1998, 158: 3-11.
Ranieri VM, Brienza N, Santostasi S, Puntillo F, Mascia L, Vitale N, Giuliani R, Memeo V, Bruno F, Fiore T, et al.: Impairment of lung and chest wall mechanics in patients with acute respiratory distress syndrome: role of abdominal distension. Am J Respir Crit Care Med 1997, 156: 1082-1091.
Kron IL, Harman PK, Nolan SP: The measurement of intra-abdominal pressure as a criterion for abdominal re-exploration. Ann Surg 1984, 199: 28-30.
Diebel LN, Wilson RF, Dulchavsky SA, Saxe J: Effect of increased intra-abdominal pressure on hepatic arterial, portal venous, and hepatic microcirculatory blood flow. J Trauma 1992, 33: 279-282.
Diebel LN, Dulchavsky SA, Wilson RF: Effect of increased intra-abdominal pressure on mesenteric arterial and intestinal mucosal blood flow. J Trauma 1992, 33: 45-48.
Biancofiore G, Bindi ML, Romanelli AM, Boldrini A, Consani G, Bisà M, Filipponi F, Vagelli A, Mosca F: Intra-abdominal pressure monitoring in liver transplant recipients: a prospective study. Intensive Care Med 2003, 29: 30-36.
Cheatham ML, Malbrain ML, Kirkpatrick A, Sugrue M, Parr M, De Waele J, Balogh Z, Leppäniemi A, Olvera C, Ivatury R, et al.: Results from the International Conference of Experts on Intra-abdominal Hypertension and Abdominal Compartment Syndrome. II. Recommendations. Intensive Care Med 2007, 33: 951-962. 10.1007/s00134-007-0592-4
De Waele JJ, Hoste EA, Malbrain ML: Decompressive laparotomy for abdominal compartment syndrome: a critical analysis. Crit Care 2006, 10: R51. 10.1186/cc4870
De Waele JJ, De laet I, Malbrain ML: Rational intraabdominal pressure monitoring: how to do it? Acta Clin Belg Suppl 2007, 1: 16-25.
Cheatham ML, Safcsak K: Intraabdominal pressure: a revised method for measurement. J Am Coll Surg 1998, 186: 594-595. 10.1016/S1072-7515(98)00122-7
Fusco MA, Martin RS, Chang MC: Estimation of intra-abdominal pressure by bladder pressure measurement: validity and methodology. J Trauma 2001, 50: 297-302.
Yol S, Kartal A, Tavli S, Tatkan Y: Is urinary bladder pressure a sensitive indicator of intra-abdominal pressure? Endoscopy 1998, 30: 778-780.
De Waele J, Pletinckx P, Blot S, Hoste E: Saline volume in transvesical intra-abdominal pressure measurement: enough is enough. Intensive Care Med 2006, 32: 455-459. 10.1007/s00134-005-0062-9
Malbrain ML, Deeren DH: Effect of bladder volume on measured intravesical pressure: a prospective cohort study. Crit Care 2006, 10: R98. 10.1186/cc4962
Geirsson G, Lindström S, Fall M: The bladder cooling reflex and the use of cooling as stimulus to the lower urinary tract. J Urol 1999, 162: 1890-1896. 10.1016/S0022-5347(05)68062-7
Chiumello D, Pelosi P, Taccone P, Slutsky A, Gattinoni L: Effect of different inspiratory rise time and cycling off criteria during pressure support ventilation in patients recovering from acute lung injury. Crit Care Med 2003, 31: 2604-2610. 10.1097/01.CCM.0000089939.11032.36
Ramsay MA, Savege TM, Simpson BR, Goodwin R: Controlled sedation with alphaxalone-alphadolone. Br Med J 1974, 2: 656-659.
Le Gall JR, Lemeshow S, Saulnier F: A new Simplified Acute Physiology Score (SAPS II) based on a European/North American multicenter study. JAMA 1993, 270: 2957-2963. 10.1001/jama.270.24.2957
Vincent JL, Moreno R, Takala J, Willatts S, De Mendonca A, Bruining H, Reinhart CK, Suter PM, Thijs LG: The SOFA (Sepsis-related Organ Failure Assessment) score to describe organ dysfunction/failure. On behalf of the Working Group on Sepsis-Related Problems of the European Society of Intensive Care Medicine. Intensive Care Med 1996, 22: 707-710.
Armitage P: Statistical Method in Medical Research. Oxford, UK: Blackwell Scientific; 1971.
Bland JM, Altman DG: Statistical methods for assessing agreement between two methods of clinical measurement. Lancet 1986, 1: 307-310.
Critchley LA, Critchley JA: A meta-analysis of studies using bias and precision statistics to compare cardiac output measurement techniques. J Clin Monit Comput 1999, 15: 85-91. 10.1023/A:1009982611386
Ravishankar N, Hunter J: Measurement of intra-abdominal pressure in intensive care units in the United Kingdom: a national postal questionnaire study. Br J Anaesth 2005, 94: 763-766. 10.1093/bja/aei117
Sugrue M, Bauman A, Jones F, Bishop G, Flabouris A, Parr M, Stewart A, Hillman K, Deane SA: Clinical examination is an inaccurate predictor of intraabdominal pressure. World J Surg 2002, 26: 1428-1431. 10.1007/s00268-002-6411-8
Mayberry JC, Goldman RK, Mullins RJ, Brand DM, Crass RA, Trunkey DD: Surveyed opinion of American trauma surgeons on the prevention of the abdominal compartment syndrome. J Trauma 1999, 47: 509-513.
Davis PJ, Koottayi S, Taylor A, Butt WW: Comparison of indirect methods of measuring intra-abdominal pressure in children. Intensive Care Med 2005, 31: 471-475. 10.1007/s00134-004-2539-3
Suominen PK, Pakarinen MP, Rautiainen P, Mattila I, Sairanen H: Comparison of direct and intravesical measurement of intraabdominal pressure in children. J Pediatr Surg 2006, 41: 1381-1385. 10.1016/j.jpedsurg.2006.04.030
Ball CG, Kirkpatrick AW: 'Progression towards the minimum': the importance of standardizing the priming volume during the indirect measurement of intra-abdominal pressures. Crit Care 2006, 10: 153. 10.1186/cc4987
Hackler RH, Hall MK, Zampieri TA: Bladder hypocompliance in the spinal cord injury population. J Urol 1989, 141: 1390-1393.
Collee GG, Lomax DM, Ferguson C, Hanson GC: Bedside measurement of intra-abdominal pressure (IAP) via an indwelling naso-gastric tube: clinical validation of the technique. Intensive Care Med 1993, 19: 478-480. 10.1007/BF01711092
Sugrue M, Buist MD, Lee A, Sanchez DJ, Hillman KM: Intra-abdominal pressure measurement using a modified nasogastric tube: description and validation of a new technique. Intensive Care Med 1994, 20: 588-590. 10.1007/BF01705728
The authors declare that they have no competing interests.
DC conceived of the study, participated in its design and coordination, performed the measurements and wrote a first draft of the manuscript. FT participated in the study design and coordination, performed the measurements and to helped draft the manuscript. MC participated in the study design and coordination, and performed the measurements. FP performed the statistical analysis and helped to draft the manuscript. GLB participated in the study design and coordination, and performed the measurements. GM participated in the study design and coordination, and performed the measurements. SA participated in the study design and coordination, and performed the measurements. CC participated in the study design and coordination, and performed the measurements. LG conceived the study, participated in its design and coordination, coordinated the final analysis of collected data and revised the manuscript, writing its final version.
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Chiumello, D., Tallarini, F., Chierichetti, M. et al. The effect of different volumes and temperatures of saline on the bladder pressure measurement in critically ill patients. Crit Care 11, R82 (2007). https://doi.org/10.1186/cc6080
- Saline Infusion
- Neurogenic Bladder
- Bladder Pressure
- Sepsis Relate Organ Failure Assessment
- Peritoneal Dialysis Solution