- About this Journal ·
- Abstracting and Indexing ·
- Advance Access ·
- Aims and Scope ·
- Article Processing Charges ·
- Articles in Press ·
- Author Guidelines ·
- Bibliographic Information ·
- Citations to this Journal ·
- Contact Information ·
- Editorial Board ·
- Editorial Workflow ·
- Free eTOC Alerts ·
- Publication Ethics ·
- Reviewers Acknowledgment ·
- Submit a Manuscript ·
- Subscription Information ·
- Table of Contents
Anesthesiology Research and Practice
Volume 2012 (2012), Article ID 647258, 6 pages
Effect of Head Rotation on Cerebral Blood Velocity in the Prone Position
1Department of Anaesthesia, Sygehus Nord, 4300 Holbæk, Denmark
2Department of Diagnostic Radiology, Bispebjerg University Hospital, 2400 Copenhagen, Denmark
3Department of Anaesthesia, Bispebjerg Hospital Research Unit for Anaesthesia and Intensive Care (B.R.A.IN), Bispebjerg University Hospital, Bispebjerg Bakke 23, 2400 Copenhagen NV, Denmark
4Department of Clinical Biochemistry, Bispebjerg University Hospital, 2400 Copenhagen, Denmark
5Acute Admissions Unit, Department of Internal Medicine, Laboratory for Clinical Cardiovascular Physiology, AMC Center for Heart Failure, University of Amsterdam, 1105 AZ Amsterdam, The Netherlands
6School of Biomedical Sciences, University of Nottingham Medical School, Queen's Medical Centre, Nottingham NG7 2RD, UK
Received 30 April 2012; Revised 3 July 2012; Accepted 25 July 2012
Academic Editor: Peter Andrews
Copyright © 2012 Jakob Højlund et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Background. The prone position is applied to facilitate surgery of the back and to improve oxygenation in the respirator-treated patient. In particular, with positive pressure ventilation the prone position reduces venous return to the heart and in turn cardiac output (CO) with consequences for cerebral blood flow. We tested in healthy subjects the hypothesis that rotating the head in the prone position reduces cerebral blood flow. Methods. Mean arterial blood pressure (MAP), stroke volume (SV), and CO were determined, together with the middle cerebral artery mean blood velocity (MCA ) and jugular vein diameters bilaterally in 22 healthy subjects in the prone position with the head centered, respectively, rotated sideways, with and without positive pressure breathing (10 cmH2O). Results. The prone position reduced SV (by %; ) and CO (by %), and slightly increased MAP (from to mmHg) as well as bilateral jugular vein diameters, leaving MCA unchanged. Positive pressure breathing in the prone position increased MAP (by mmHg) but further reduced SV and CO (by % and % below baseline) while MCA was maintained. The head-rotated prone position with positive pressure breathing augmented MAP further ( mmHg) but not CO, narrowed both jugular vein diameters, and reduced MCA (by %). Conclusion. During positive pressure breathing the prone position with sideways rotated head reduces MCA ~10% in spite of an elevated MAP. Prone positioning with rotated head affects both CBF and cerebrovenous drainage indicating that optimal brain perfusion requires head centering.
Prone positioning of patients during anesthesia is required for a variety of surgical procedures . Furthermore, the prone versus supine position promotes ventilation/perfusion matching in critically ill patients with acute respiratory distress syndrome . When moving a patient into the prone position, arterial pressure usually remains stable whereas a reduction in cardiac output (CO)  is attributed to a decrease in venous return  by abdominal compression with partial inferior caval vein obstruction . Many anesthetists place the head centered in a headrest during prone positioning especially during more extended procedures, for example, spine surgery. However, since it is less cumbersome and/or the head position may not be considered important many patients are placed with the head positioned to the side. This is especially the case when laryngeal mask airways are used for surgery in the prone position, which is an increasingly used practice [5–9]. In the anesthetized patient, the positioning-related reduction in CO is amplified by positive pressure ventilation. Complications associated with prone positioning often with the head in a sideward-rotated position include occlusion of cervical arteries or veins, and injuries of the cervical spine and peripheral nerves [1, 6, 10]. Particularly, carotid and vertebral artery occlusion and dissection and middle cerebral artery (MCA) infarction have been linked to head rotation or extension . In a recent review, postoperative visual loss as a recognized complication of prone positioning has been linked to hemodynamic alterations . Positive pressure breathing in the supine position reduces cerebral blood flow . Also, prone positioning raises intracranial pressure with potentially adverse consequences for cerebral perfusion and/or cerebral venous drainage . Additional sideward rotation of the head in that position leads to venous compression with potential cerebral venous outflow impairment. In infants, prone positioning with the head rotated versus the supine position with the head centered reduces transcranial Doppler determined MCA blood velocity (MCA ) . Also, rotating of the head increases cerebral blood volume attributed to impairment of venous drainage  whereas in adults the effects of head direction during prone positioning have not been studied. We hypothesized that during positive pressure breathing in the prone position, head rotation would reduce MCA . We set out to investigate systemic hemodynamics and brain arterial and venous characteristics by following MCA as an index of cerebral blood flow and jugular vein diameter in the prone position with and without positive pressure breathing and/or head rotation.
2. Materials and Methods
22 healthy volunteers (7 women), aged years (mean ± standard deviation), height cm, weight kg participated in this investigation. All gave their informed consent prior to inclusion in the study. The study was approved by the Ethics Committee for Copenhagen and Frederiksberg (KF 01 287338) and was performed in accordance with the Helsinki Declaration.
MCA was measured using a DWL Multiflow 4X Doppler apparatus (DWL, Sipplingen, Germany). The proximal segment of the right middle cerebral artery was insonated at a depth of 45–57 mm through the “postero-temporal window.” After the optimal signal-to-noise ratio was established the probe was fixed to the head with adhesive ultrasonic gel (Tensive, Parker Laboratories Inc., Fairfield, NJ, USA) and firmly secured using a custom-made headband. A clear, soft, plastic mask (VBM Medizintechnik GmbH, Sulz, Germany) was fitted over each subject’s nose and mouth using elastic bands around the back of the head: positive pressure breathing was applied using a Whisperflow fixed flow generator using pressurized room air and Whisperflow isobaric continuous positive airway pressure (CPAP) valves with 10 cmH2O opening pressure (Caradyne, Galway, Ireland).
Finger arterial pressure was measured by a Finometer apparatus (Finapres Medical Systems, Amsterdam, The Netherlands). The cuff was applied to the midphalanx of the middle finger of the dominant hand and placed at heart level. 10 subjects had a 1.1 mm inner diameter arterial catheter placed in the radial artery of the nondominant hand. Blood gases were analyzed on an ABL 800-series apparatus (Radiometer, Copenhagen, Denmark). All variables were A/D converted, sampled at a rate of 100 Hz, 16 bit (PCI-Base 1000 hardware and NextView software (BMC Messsysteme GmbH, Berlin, Germany)) by PC and stored for off-line analysis.
The cross-sectional area of both internal jugular veins () were measured using a LOGIQ 500 pro series ultrasound machine (GE Medical Systems, Milwaukee, WI, USA) adapting the Cirovic method for measuring jugular cross-sectional area . All measurements were performed with a 9 MHz linear probe perpendicular to the skin surface at skin markings made equidistantly between the mastoid process and the jugular notch. Compression of the vein was avoided by applying abundant ultrasonic gel thus minimizing skin pressure by the probe. The ultrasonic picture was frozen at end-expiration for off-line analysis.
Following instrumentation, the subject was placed supine on an Alphamaquet 1150 operating table (Maquet, Rastatt, Germany) and rested for 30 minutes. Measurements were performed in 3 body positions in random order with and without supplementation of 10 cmH2O CPAP: (1) supine, (2) prone with the head centered, supported by the brow and cheekbones in a horseshoe headrest with supplemental padding, and (3) prone with the head rotated ~80 degrees to the right resting it on a soft pillow. Each measurement cycle consisted of 4 min of ambient pressure breathing and 4 minutes of positive pressure breathing; also in random order. Baseline was the supine position with 0 cmH2O of CPAP. Arterial blood gas samples were obtained during the last 15 seconds of each intervention. Within the last 2 minutes of each intervention, the cross-sectional areas of both internal jugular veins () were quantified.
2.2. Data Analysis
The finger arterial pressure curve was analyzed using Beatscope software (Finapres Medical Systems, Amsterdam, The Netherlands). Beat-to-beat systolic, diastolic, and mean arterial pressures (MAP), as well as stroke volume (SV), were computed from the arterial pressure pulse wave by off-line Model flow analysis . This method computes an aortic flow waveform by simulating a nonlinear, time-varying model of the aortic input impedance, thereby calculating SV. Changes in SV and CO are tracked accurately, whereas absolute values require calibration against a Fick principle method [17–19]. MAP was obtained as the integral of pressure over one beat divided by the corresponding beat length. Heart rate (HR) was the reciprocal of the interbeat interval. CO was the product of SV and HR. All variables were transformed to equidistantly resampled data at 1 Hz by polynomial interpolation and averaged over 30 second intervals just prior to the end of each intervention. Changes are reported relative to baseline.
2.3. Statistical Analysis
Data obtained as averages over a sampling period are expressed as mean ± SEM. Data from a single sampling point (jugular luminal area) are expressed as mean ± SD. The effect of positive pressure breathing and head position on cerebral and systemic outcome variables was tested using paired t-test between interventions of interest (prone versus supine; prone with the head turned versus prone; ambient versus positive pressure breathing in the different positions). A -value < 0.05 was considered to indicate a statistically significant difference.
3.1. Prone Position and Head Rotation
SV and CO decreased from supine to prone position together with an increase in MAP. MCA , PaCO2 and PaO2 remained unchanged (Table 1, Figure 1). Head rotation to the right side in the prone position increased MAP further but left SV, CO, MCA , PaCO2, and PaO2 unchanged.
3.2. Positive Pressure Breathing
In the supine position, addition of 10 cmH2O of CPAP increased MAP slightly and more so when prone. SV and CO decreased with positive pressure breathing regardless of body position. MCA decreased with positive pressure breathing in the supine position. CPAP increased PaO2 mainly in the supine position, while PaCO2 remained unchanged (Table 1, Figure 1).
3.3. Positive Pressure Breathing and Head Rotation
The reductions in SV and CO were similar to those seen in the prone position with the head centered, while MAP reached the highest values. MCA reached a nadir with positive pressure breathing in the head-rotated prone position (Table 1, Figure 1). PaCO2 remained unchanged.
3.4. Jugular Vein Diameters
In the supine position and in the prone position with the head centered, jugular vein diameter was ~40–75% larger on the right side. Prone positioning increased jugular vein diameters on both sides but decreased with rightward head rotation especially on the right side (Table 1).
The results of this study provide insight into the effects of prone positioning, head rotation and positive pressure breathing on brain perfusion and brain venous drainage. The prone position with sideways rotated head and positive breathing narrowed the ipsilateral internal jugular vein together with a ~10% reduction in MCA in spite of an elevated MAP. These results suggest that for this commonly applied anesthetic approach both cerebral blood flow and cerebrovenous drainage are optimal only with the head centered.
Transcranial Doppler ultrasound monitors blood peak flow velocity rather than volume flow, and changes in the diameter of the insonated vessel could modulate velocity independently of volume flow. During craniotomy, the diameter of the MCA remains unchanged by even large changes in arterial pressure . Constancy of the diameter of the MCA as determined with magnetic resonance imaging during changes in carbon dioxide tension and in simulated orthostasis further supports that the MCA is not involved in regulation of cerebral vascular resistance  linking changes in MCA to those in cerebral blood flow .
All Finometer and TCD variables were A/D converted and stored for off-line analysis. The off-line analysis involved detection and manually removal of artifacts with subsequent semiautomated data extraction. This semiautomated process leaves little potential for introduction of bias. Jugular vein areas were obtained off-line by manually tracking the outline of the vein. Potential for bias exist as we consider blinding impractical because the position of the head was revealed by the distortion of the structures in the ultrasonographic picture.
With prone position, we observed a small reduction in cardiac stroke volume and output (Figure 1) in accordance with an earlier report in anesthetized patients likely reflecting reduced venous return . The approximate doubling of internal jugular vein cross-sectional area when positioned below heart level suggests passive gravitational jugular vein dilation (Table 1). However, MCA was largely unaffected (Figure 1).
Head rotation in the prone position increased MAP by ~4 mmHg (Figure 1) possibly reflecting unloading of carotid baroreceptors by altered pressure from the soft tissues with a reflex increase in sympathetic nervous activity . Head-down rotation engages the otolith organs and vestibular otolith stimulation may increase sympathetic activity during baroreflex unloading . Positive pressure breathing also enhances resting muscle sympathetic activity and the reduction of urinary output and sodium excretion associated with prolonged positive pressure breathing has been attributed to cardiopulmonary receptor unloading . A contribution of enhanced sympathetic activity modulating cerebral vascular tone may be considered. The increase in MAP from supine to the prone position presumably by increased sympathetic activity was not accompanied by changes in MCA reflecting integrity of cerebrovascular autoregulation mechanisms. In contrast, positive pressure breathing reduced cardiac output together with MCA whereas MAP increased. A restricted CO that challenges MAP limits flow to the brain [27, 28], but under conditions where MAP is not challenged by a restricted CO, the influence of sympathetic stimulation on CBF is not manifested . Thus, in this study, we consider an altered cerebral venous outflow resistance rather than sympathetic activity to dominate CBF.
With the head-turned constancy of MCA was maintained notwithstanding a ~50% reduction in . The cerebral venous system is characterized by many collaterals and void of valves directing blood flow , explaining why compression of one jugular vein was of no consequence for cerebral blood flow as long as the central blood volume was maintained. Rotation per se appears to be of little influence for the cerebral blood supply since rotation of the head in the supine position leaves the diameter of the common and internal carotid artery unchanged . Our subjects had their head supported in a horseshoe headrest avoiding external pressure on the neck, and we consider compromised arterial cerebral inflow unlikely to have caused the reduction in MCA . However, carotid compression cannot be excluded in prone-positioned anesthetized patients, for example, by external compression of supporting pillows and/or inappropriate extention/rotation. Only ~40% of normal subjects have a complete Circle of Willis maintaining blood flow to the contralateral side of the brain with unilateral occlusion . Thus, variations in the Circle of Willis may have influenced cerebral hemodynamics following head rotation in the prone position. Furthermore, especially with incomplete Circle of Willis, the side of head rotation may be of importance for the hemodynamic response, but this was not investigated in our study.
During positive pressure breathing when supine MCA was reduced together with SV and CO conforming an earlier report  and reflecting a reduction of the central blood volume imposed by positive pressure breathing . Under the conditions of this study, absence of changes in PaCO2 with CPAP renders an effect of CO2 on CBF unlikely.
During positive pressure breathing in the head centered prone position MCA was maintained despite a further reduction in SV and CO. This observation is compatible with the notion that an increase in cerebral perfusion pressure in the prone position may sustain CBF (Figure 1) [34, 35].
MCA reached a nadir of ~10% below baseline in the head-rotated prone position with positive pressure breathing. This reduction is within the range observed under everyday physiological challenges, that is, standing up . By comparison a ~50% decline is associated with clinical ischemia  and syncope . As general anesthesia has a favorable supply/demand profile for cerebral oxygen flux—even during induction, where the cardiovascular depression often is largest , it could be argued that the changes induced by prone position are of little clinical relevance to most patients. However, even small reductions in cerebral blood supply could be deleterious in the setting of an already compromised cerebral perfusion, for example, in elderly subjects with vascular disease [12, 34, 35, 38].
The applied pressure of 10 cmH2O of CPAP is (on average) similar to the prevailing intrathoracic pressure when ventilating healthy patients in the prone position  whereas in the presence of lung disease or marked obesity inflation pressures may surpass this value. The reduction of the central blood volume as an accompanying effect of positive pressure breathing did reduce CO and MCA . These new findings are of clinical relevance since they indicate that CBF may be compromised by venous compression in the head-turned prone position when the central blood volume is challenged by positive pressure breathing.
In healthy awake individuals, the prone position with positive pressure breathing reduced MCA especially when the head was rotated to the side. These results may have implications for the anesthetized and ventilated patient. The hypothesis that in the prone position both CBF and cerebrovenous drainage are optimal only with the head centered should be tested in patients undergoing general anesthesia.
The authors are grateful to the staff at the Department of Clinical Physiology and the Department of Diagnostic Radiology, Bispebjerg University Hospital for lending the equipment for this study.
- H. Edgcombe, K. Carter, and S. Yarrow, “Anaesthesia in the prone position,” British Journal of Anaesthesia, vol. 100, no. 2, pp. 165–183, 2008.
- C. Guérin, “Ventilation in the prone position in patients with acute lung injury/acute respiratory distress syndrome,” Current Opinion in Critical Care, vol. 12, no. 1, pp. 50–54, 2006.
- T. Hatada, M. Kusunoki, T. Sakiyama et al., “Hemodynamics in the prone jackknife position during surgery,” American Journal of Surgery, vol. 162, no. 1, pp. 55–58, 1991.
- S. Dharmavaram, W. S. Jellish, R. P. Nockels et al., “Effect of prone positioning systems on hemodynamic and cardiac function during lumbar spine surgery: an echocardiographic study,” Spine, vol. 31, no. 12, pp. 1388–1393, 2006.
- A. Abrishami, P. Zilberman, and F. Chung, “Brief review: airway rescue with insertion of laryngeal mask airway devices with patients in the prone position,” Canadian Journal of Anesthesia, vol. 57, no. 11, pp. 1014–1020, 2010.
- J. R. Brimacombe, V. Wenzel, and C. Keller, “The ProSeal laryngeal mask airway in prone patients: a retrospective audit of 245 patients,” Anaesthesia and Intensive Care, vol. 35, no. 2, pp. 222–225, 2007.
- A. M. López, R. Valero, and J. Brimacombe, “Insertion and use of the LMA SupremeTM in the prone position,” Anaesthesia, vol. 65, no. 2, pp. 154–157, 2010.
- A. Ng, D. G. Raitt, and G. Smith, “Induction of anesthesia and insertion of a laryngeal mask airway in the prone position for minor surgery,” Anesthesia and Analgesia, vol. 94, no. 5, pp. 1194–1198, 2002.
- V. Sharma, C. Verghese, and P. J. McKenna, “Prospective audit on the use of the LMA-Supreme™ for airway management of adult patients undergoing elective orthopaedic surgery in prone position,” British Journal of Anaesthesia, vol. 105, no. 2, pp. 228–232, 2010.
- L. A. Lee, S. Roth, K. L. Posner et al., “The American society of anesthesiologists postoperative visual loss registry: analysis of 93 spine surgery cases with postoperative visual loss,” Anesthesiology, vol. 105, no. 4, pp. 652–659, 2006.
- J. H. Rasmussen, T. Mantoni, B. Belhage, and F. C. Pott, “Influence of upper body position on middle cerebral artery blood velocity during continuous positive airway pressure breathing,” European Journal of Applied Physiology, vol. 101, no. 3, pp. 369–375, 2007.
- A. Reinprecht, M. Greher, S. Wolfsberger, W. Dietrich, U. M. Illievich, and A. Gruber, “Prone position in subarachnoid hemorrhage patients with acute respiratory distress syndrome: effects on cerebral tissue oxygenation and intracranial pressure,” Critical Care Medicine, vol. 31, no. 6, pp. 1831–1838, 2003.
- F. Eichler, O. Ipsiroglu, T. Arif et al., “Position dependent changes of cerebral blood flow velocities in premature infants,” European Journal of Pediatrics, vol. 160, no. 10, pp. 633–639, 2001.
- A. Pellicer, F. Gayá, R. Madero, J. Quero, and F. Cabañas, “Noninvasive continuous monitoring of the effects of head position on brain hemodynamics in ventilated infants,” Pediatrics, vol. 109, no. 3, pp. 434–440, 2002.
- S. Cirovic, C. Walsh, W. D. Fraser, and A. Gulino, “The effect of posture and positive pressure breathing on the hemodynamics of the internal jugular vein,” Aviation Space and Environmental Medicine, vol. 74, no. 2, pp. 125–131, 2003.
- K. H. Wesseling, J. R. C. Jansen, J. J. Settels, and J. J. Schreuder, “Computation of aortic flow from pressure in humans using a nonlinear, three-element model,” Journal of Applied Physiology, vol. 74, no. 5, pp. 2566–2573, 1993.
- L. W. J. Bogert and J. J. Van Lieshout, “Non-invasive pulsatile arterial pressure and stroke volume changes from the human finger,” Experimental Physiology, vol. 90, no. 4, pp. 437–446, 2005.
- B. P. M. Imholz, W. Wieling, G. A. Van Montfrans, and K. H. Wesseling, “Fifteen years experience with finger arterial pressure monitoring: assessment of the technology,” Cardiovascular Research, vol. 38, no. 3, pp. 605–616, 1998.
- K. H. Wesseling, R. Purschke, N. T. Smith, H. J. Wust, B. de Wit, and H. A. Weber, “A computer module for the continuous monitoring of cardiac output in the operating theatre and the ICU,” Acta Anaesthesiologica Belgica, vol. 27, pp. 327–341, 1976.
- C. A. Giller, “Transcranial Doppler monitoring of cerebral blood velocity during craniotomy,” Neurosurgery, vol. 25, no. 5, pp. 769–776, 1989.
- J. M. Serrador, P. A. Picot, B. K. Rutt, J. K. Shoemaker, and R. L. Bondar, “MRI measures of middle cerebral artery diameter in conscious humans during simulated orthostasis,” Stroke, vol. 31, no. 7, pp. 1672–1678, 2000.
- S. Moritz, P. Kasprzak, M. Arlt, K. Taeger, and C. Metz, “Accuracy of cerebral monitoring in detecting cerebral ischemia during carotid endarterectomy: a comparison of transcranial Doppler sonography, near-infrared spectroscopy, stump pressure, and somatosensory evoked potentials,” Anesthesiology, vol. 107, no. 4, pp. 563–569, 2007.
- M. Biais, O. Bernard, J. C. Ha, C. Degryse, and F. Sztark, “Abilities of pulse pressure variations and stroke volume variations to predict fluid responsiveness in prone position during scoliosis surgery,” British Journal of Anaesthesia, vol. 104, no. 4, pp. 407–413, 2010.
- B. Pump, U. Talleruphuus, N. J. Christensen, J. Warberg, and P. Norsk, “Effects of supine, prone, and lateral positions on cardiovascular and renal variables in humans,” American Journal of Physiology, vol. 283, no. 1, pp. R174–R180, 2002.
- T. L. Shortt and C. A. Ray, “Sympathetic and vascular responses to head-down neck flexion in humans,” American Journal of Physiology, vol. 272, no. 4, part 2, pp. H1780–H1784, 1997.
- S. Tanaka, S. Sagawa, K. Miki, J. R. Claybaugh, and K. Shiraki, “Changes in muscle sympathetic nerve activity and renal function during positive-pressure breathing in humans,” American Journal of Physiology, vol. 266, no. 4, part 2, pp. R1220–R1228, 1994.
- N. H. Secher, T. Seifert, and J. J. Van Lieshout, “Cerebral blood flow and metabolism during exercise: implications for fatigue,” Journal of Applied Physiology, vol. 104, no. 1, pp. 306–314, 2008.
- J. J. Van Lieshout and N. H. Secher, “Last Word on Point: counterpoint: sympathetic activity does/does not influence cerebral blood flow,” Journal of Applied Physiology, vol. 105, no. 4, p. 1374, 2008.
- A. Bill and J. Linder, “Sympathetic control of cerebral blood flow in acute arterial hypertension,” Acta Physiologica Scandinavica, vol. 96, no. 1, pp. 114–121, 1976.
- E. Tobinick, “The cerebrospinal venous system: anatomy, physiology, and clinical implications,” Medscape General Medicine, vol. 8, no. 1, p. 53, 2006.
- F. P. Glor, B. Ariff, A. D. Hughes et al., “Influence of head position on carotid hemodynamics in young adults,” American Journal of Physiology, vol. 287, no. 4, pp. H1670–H1681, 2004.
- M. J. Krabbe-Hartkamp, J. Van Der Grond, F. E. De Leeuw et al., “Circle of Willis: morphologic variation on three-dimensional time-of- flight MR angiograms,” Radiology, vol. 207, no. 1, pp. 103–112, 1998.
- J. J. Van Lieshout, W. Wieling, J. M. Karemaker, and N. H. Secher, “Syncope, cerebral perfusion, and oxygenation,” Journal of Applied Physiology, vol. 94, no. 3, pp. 833–848, 2003.
- M. Nekludov, B. M. Bellander, and M. Mure, “Oxygenation and cerebral perfusion pressure improved in the prone position,” Acta Anaesthesiologica Scandinavica, vol. 50, no. 8, pp. 932–936, 2006.
- A. Thelandersson, A. Cider, and B. Nellgård, “Prone position in mechanically ventilated patients with reduced intracranial compliance,” Acta Anaesthesiologica Scandinavica, vol. 50, no. 8, pp. 937–941, 2006.
- F. Pott, J. J. Van Lieshout, K. Ide, P. Madsen, and N. H. Secher, “Middle cerebral artery blood velocity during a Valsalva maneuver in the standing position,” Journal of Applied Physiology, vol. 88, no. 5, pp. 1545–1550, 2000.
- A. T. Lovell, H. Owen-Reece, C. E. Elwell, M. Smith, and J. C. Goldstone, “Continuous measurement of cerebral oxygenation by near infrared spectroscopy during induction of anesthesia,” Anesthesia and Analgesia, vol. 88, no. 3, pp. 554–558, 1999.
- A. I. R. Maas, M. Dearden, F. Servadei, N. Stocchetti, and A. Unterberg, “Current recommendations for neurotrauma,” Current Opinion in Critical Care, vol. 6, no. 4, pp. 281–292, 2000.
- P. Pelosi, M. Croci, E. Calappi et al., “The prone positioning during general anesthesia minimally affects respiratory mechanics while improving functional residual capacity and increasing oxygen tension,” Anesthesia and Analgesia, vol. 80, no. 5, pp. 955–960, 1995.