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Reference values for intracranial pressure and lumbar cerebrospinal fluid pressure: a systematic review



Although widely used in the evaluation of the diseased, normal intracranial pressure and lumbar cerebrospinal fluid pressure remain sparsely documented. Intracranial pressure is different from lumbar cerebrospinal fluid pressure. In addition, intracranial pressure differs considerably according to the body position of the patient. Despite this, the current reference values do not distinguish between intracranial and lumbar cerebrospinal fluid pressures, and body position-dependent reference values do not exist. In this study, we aim to establish these reference values.


A systematic search was conducted in MEDLINE, EMBASE, CENTRAL, and Web of Sciences. Methodological quality was assessed using an amended version of the Joanna Briggs Quality Appraisal Checklist. Intracranial pressure and lumbar cerebrospinal fluid pressure were independently evaluated and subdivided into body positions. Quantitative data were presented with mean ± SD, and 90% reference intervals.


Thirty-six studies were included. Nine studies reported values for intracranial pressure, while 27 reported values for the lumbar cerebrospinal fluid pressure. Reference values for intracranial pressure were −  5.9 to 8.3 mmHg in the upright position and 0.9 to 16.3 mmHg in the supine position. Reference values for lumbar cerebrospinal fluid pressure were 7.2 to 16.8 mmHg and 5.7 to 15.5 mmHg in the lateral recumbent position and supine position, respectively.


This systematic review is the first to provide position-dependent reference values for intracranial pressure and lumbar cerebrospinal fluid pressure. Clinically applicable reference values for normal lumbar cerebrospinal fluid pressure were established, and are in accordance with previously used reference values. For intracranial pressure, this study strongly emphasizes the scarcity of normal pressure measures, and highlights the need for further research on the matter.


Measurements and analysis of intracranial pressure (ICP) are used to provide information for treating and managing patients with numerous neurological diseases, e.g., traumatic brain injury, acute intracranial hemorrhages, idiopathic intracranial hypertension, and hydrocephalus [1,2,3,4]. However, values for normal ICP measured intracranially remain sparsely documented, and the currently used reference interval (7 to 15 mmHg [5]) is based on studies in which lumbar cerebrospinal fluid opening pressure (LCSFop) is used as a surrogate parameter for ICP or is extrapolated from patients with a suspected ICP disorder [5,6,7,8,9,10].

In the 1920s and 30 s, it was assumed that ICP measured intracranially was equal to LCSFop measured at a lumbar spine level [11, 12]. This has, in recent years, been subject to much debate [13,14,15,16,17], and where some studies have documented similar values for intracranial measurements and lumbar measurements [13, 15], others found considerable differences between the two measurement-sites [14, 16, 17]. The reason for a difference might be due to ICP being measured in the brain parenchyma, thus not being measured in the same intracranial space as LCSFop. Thus, ICP measured ventricular might similar to LCSFop, although this has yet to be thoroughly investigated. The comparison of these studies is further hampered by differences in study design, particularly dissimilarities in body position during the measurement and the range of included study participants [13,14,15,16, 18, 19]. It is well known that ICP changes with body position [8, 18,19,20,21], e.g., ICP is lower in the vertical position compared to the horizontal position [8, 19, 21]. Also, ICP increases significantly with the body placed in lateral recumbent position compared to supine position [18, 22,23,24]. Based on this, different reference values for ICP should be established for different body positions. This systematic review aims to (1) determine reference values for normal ICP and LCSFop, and (2) examine how ICP depends on measurement-site and body position.


Prior to initiating this systematic review, the protocol was registered at PROSPERO (October 30, 2019, identification code: CRD42019143018). The review has been conducted in accordance with the PRISMA guidelines, and a completed PRISMA checklist is available in Additional file 1: Appendix 1.

Eligibility criteria

All included studies had to provide (1) measurements conducted in humans, (2) original values for either ICP or LCSFop, and (3) ICP measured either intracranially (parenchymal, intraventricular, epidural, subdural, or subarachnoid) or LCSFop measured during a lumbar puncture. All age-groups were included. Patients with intracranial pathology that potentially could alter ICP dynamics (e.g., hydrocephalus, idiopathic intracranial hypertension, intracranial hemorrhage, arteriovenous malformation, intracranial tumor, intracranial abscesses or other significant space-occupying processes within the brain) were excluded.

Since measurement of ICP requires invasive measurement methods, the included studies of ICP are based on “pseudo-healthy” patients, which we define as patients requiring neurosurgery for reasons unrelated to ICP, who were considered healthy in terms of ICP and CSF-dynamics.

Data search

On July 16st 2019, we conducted a search in MEDLINE Ovid (1946 to July 2019), Embase Ovid (1974 to July 2019), Cochrane Central Register of Controlled Trials (CENTRAL) in the Cochrane Library and Science Citation Index Expandex (1900 to July 2019), and Conference Proceeding Citation Index–Science (Web of Science) (1990 to July 2019). There was no restriction on the publication period. We included all peer-reviewed published studies without consideration for publication status or study design. The search was conducted in English, and studies with a non-English title or abstract were thus excluded. Non-English manuscripts, with an English title and abstract, were translated by a native speaker. The search strategy is attached in Additional file 2: Appendix 2. If published data in the included studies were insufficient, the authors were contacted to retrieve raw data. The systematic search was supplemented by a manual reference-search of included studies. Finally, an expert in the field (MJ) was asked to identify any obviously missing studies.

Study selection and data extraction

Four investigators (CSR, MHO, NHN, SHP) reviewed the studies for eligibility. Two different investigators assessed each study for the title, abstract and full-text screening. Discrepancies were initially resolved between the four investigators, and if this was not possible, an expert (MJ) had the deciding vote. The screening was conducted via Covidence (Covidence systematic review software, Veritas Health Innovation, Melbourne, Australia). Study design, demographics, and information regarding ICP-monitoring were extracted from each study. Study data were extracted from Covidence by NHN and verified by MHO. Disagreements were resolved by discussion.

Quality assessment

The methodological quality of the studies was independently assessed by two investigators (MHO, NHN). No intervention-based studies were included, and thus, traditional assessment methods for systematic reviews could not be used. Instead, a quality assessment method was created inspired by the Joanna Briggs Institute Critical Appraisal Tool [25]. Two parts of the tool were, however, irrelevant in the assessment of study type and therefore replaced; (1)“Was the exposure measured in a valid and reliable way?” was replaced with “Was the measurement method described in details?” and (2) “Were the outcomes measured in a valid and reliable way?” was replaced with “Was the included population without current or previous intracranial pathology that could alter ICP dynamics?”.

Data synthesis

All statistical analyses were performed in RStudio (R 3.6.2, R Development Core Team (2019), Vienna, Austria). Since all included studies were observational, and the primary purpose of this review was to determine a reference interval for ICP, a conventional meta-analysis was not applicable. Instead, included studies were pooled into two groups, (1) studies in which ICP was measured, and (2) studies in which LCSFop was measured. Raw data were assessed for normality and presented as mean ± standard deviation (SD), 95% confidence intervals (CI), and coherent reference intervals (defined as 5th to 95th percentile) [5]. If statistical values other than SD were presented (e.g., 95% confidence intervals or reference intervals), SD was manually calculated based on the given statistical data according to the Cochrane Handbook of Systematic Reviews [26]. For studies where only the median and interquartile range (IQR) were presented, the median was directly transformed to a mean, while SD was estimated from IQR by SD = IQR/1.35, as recommended in the Cochrane Handbook of Systematic Reviews [26]. Finally, if pressure values were reported in other units (e.g., mmH2O or cmH2O) it was converted to mmHg.

Normal ICP and LCSFop were subdivided into different body positions stratified by study and presented in a forest plot, including mean values and 95% CI. The corresponding weighted reference intervals for the different body positions were subsequently presented in a table for ICP and LCSFop. Pressure measurements are presented in both mmHg and cmH2O. The different body positions were compared using a two-tailed Students t-test, and P-values were presented. Due to multiplicity, we chose to Bonferroni-correct in comparison of body positions and thereby lowering the risk of type 1 errors. P-values < 0.05 were considered significant. The included studies provided insufficient data to perform a meaningful multivariate analysis adjusting for age, gender, monitoring equipment, neck position, and zero point for ICP measurement-site.


The search strategy identified a total of 2516 studies. Of these, six were found from other sources than our search string. All these six studies were found by manually searching reference list of included studies. After the removal of duplicates, 1791 studies remained. The abstract and title screening left 127 studies, and based on full-text screening, 44 studies were included (Fig. 1). Study characteristics are presented in Table 1.

Fig. 1

Flowchart of study selection process. The section “insufficient data” covers studies did not report sufficient statistical data to be included in statistical analysis. Thus, no standard deviations, confidence intervals or reference intervals were reported in these studies. The included articles “Other sources” were found by manual searching the reference list of included studies

Table 1 Characteristics of included studies

The majority of studies reported a mean value with coherent SD or a mean value with either 95% CI or reference intervals, from which SD could be calculated (n = 32). In a few studies, only median and IQR were reported (n = 4). Studies that only reported a range or a mean and no further statistical data could be provided from the authors were omitted from analysis (n = 8). Thus, 36 studies remained in the data analysis.

Reference intervals for ICP and LCSFop

Reference intervals differed significantly between body positions (e.g., lateral recumbent position LCSFop versus supine LCSFop (P = 0.04), and upright ICP versus supine ICP (P < 0.01)). Details are shown in Table 2 for both ICP and LCSFop. Nine studies provided values for ICP measured intracranially. Reference intervals were subdivided into four groups based on body position: (1) supine position with a mean ICP of 8.6 mmHg (SD 4.7, reference interval 0.9 to 16.3 mmHg), (2) upright position with a mean ICP of 1.0 mmHg (SD 4.3, reference interval − 5.9 to 8.3 mmHg), (3) continuous daytime measurement with a mean ICP of − 0.1 mmHg (SD 7.4, reference interval − 12.0 to 12.2 mmHg), and (4) continuous nighttime measurement with a mean ICP of 6.3 mmHg (SD 13.3, reference interval − 15.8 to 28.2) (Fig. 2, Table 2).

Table 2 Reference vales for intracranial pressure and lumbar cerebrospinal fluid pressure in different body positions
Fig. 2

Forest plot of lumbar cerebrospinal fluid pressure and intracranial pressure. Two forest plots describing the weighted average of lumbar cerebrospinal fluid pressure (LCSFop) and intracranial pressure (ICP) reported in each included study. The LCSFop is presented to the left and grouped into different body positions: lateral recumbent position and supine position. ICP is presented to the right, and also sub-grouped into different body positions: daytime, nighttime, supine and upright position

Twenty-seven studies provided values for LCSFop measured by lumbar puncture. LCSFop was subdivided into two groups: (1) the supine position with a mean LCSFop of 10.7 mmHg (SD 3.0, reference interval 5.7 to 15.5 mmHg), and (2) the lateral recumbent position with a mean LCSFop of 11.9 mmHg (SD 2.9, reference interval 7.2 to 16.8 mmHg) (Fig. 2, Table 2). There was a statistical difference between ICP values in the supine position and LCSFop values in the supine position (P = 0.03). There was no statistical difference between reference intervals for LCSFop based solely on the healthy population compared to reference intervals for LCSFop based on the pseudo-healthy population. The difference between healthy individuals and pseudo-healthy individuals in lateral recumbent position was 1.4 mmHg (P = 0.34) and in supine position 1.0 mmHg (P = 0.73).

Quality of included studies

The overall methodological quality of the study designs was moderate, see Additional file 3: Appendix 3. Out of seven, the average score of the included studies was 4.5. None of the studies in which ICP was measured were based on completely healthy individuals, and in only two studies, the primary aim was to determine reference intervals for ICP. For the studies in which ICP was measured, the overall methodological study quality was moderate (average study quality = 4/7). In the group of LCSFop, the overall study quality was generally higher (average study quality = 5/7) and a few studies included completely healthy individuals (n = 13) [5, 6, 23, 27,28,29,30,31,32,33,34,35]. In general, studies with LCSFop consisted of a significantly higher number of study participants (Table 1).


This systematic review aimed to establish reference intervals for normal ICP and LCSFop. Through an extensive literature search, 44 studies examining either ICP or LCSFop in pseudo-healthy or normal individuals were identified, and of these, 36 provided sufficient pressure values and statistical data to calculate reference intervals. Nine studies reported ICP values, while 27 reported LCSFop values. The overall study quality was moderate. For ICP, the study material was scarce, and the reference intervals were based on small sample sizes. Data on LCSFop were, in comparison, comprehensive in both lateral recumbent position and supine position. Finally, the reference intervals for both ICP and LCSFop were found to differ significantly between body positions, demonstrating the need for position-dependent reference intervals. After completion of the the present study, Bø et al. reported a mean CSFop of 17.5 cmH2O (12.9 mmHg) ranging for 4–30 cmH2O (2.9–22.1 mmHg) in an prospecitvely sampled out-patient population. These results further supports our conclusions [36].

The literature further indicates that age, weight, neck position, zero point for measurement-site, and monitoring equipment are of great importance in measuring ICP and LCSFop [9, 23, 37,38,39,40,41,42]. Especially zero point is of uttermost importance when measuring ICP in upright position. In supine and lateral recumbent position, zero-point matters to the extent that it has to be in the patient’s midline, which is a clinical standard in most neurological and neurosurgical departments. However, only nine of the included studies described the zero point of measurements. In terms of the studies reporting on measurement in upright position only two out of six studies reported on zero point. Thus, for the purpose in this systematic review, this was too few, and the reference values were not corrected for zero point.

Although included studies did not provide detailed information regarding age, gender and weight and their influence on ICP, these factors’ significance has previously been investigated. Pedersen et al. found ICP to be inversely related to age with an average decrease of 0.69 mmHg per decade [39]. For LCSFop, one study found a steadily decline after 50 years, that females generally had lower LCSFop, and that a high body mass index (BMI) was associated with higher values of LCSFop.[41] Hannerz et al. and Whiteley et al. among many other studies, likewise, reported that ICP or LCSFop was higher in obese patients [9, 32, 43,44,45]. However, the clinical significance of this correlation has been subject to some debate [9, 43].

Reference intervals for ICP

Due to the still invasive nature of obtaining ICP values, it is ethically unacceptable to examine ICP in healthy normal individuals. Several non-invasive ICP measuring methods have been developed, and though they can be useful to estimate interpatient ICP differences, e.g., during follow-up, none are currently accurate enough to measure absolute ICP values [46, 47]. The studies in this review included pseudo-healthy patients [20, 48,49,50], and we identified no published studies of ICP on completely healthy individuals. A new telemetric monitoring technique has become available in the last decade, allowing for ICP measurements for several months after implantation [51,52,53]. This has resulted in ICP measurements in groups outside of the traditional patient categories with suspected ICP disorders. Andresen et al. implanted a telemetric ICP monitor in patients who had a small demarcated intracranial tumor surgically removed, thus establishing a pseudo-healthy cohort [48]. Though this cohort is not completely healthy, long-term measurements via the telemetric ICP monitor provide ICP values at a time when intracranial conditions, including ICP, can be considered normal. This is an improvement, since previous research is mainly based on patients undergoing diagnostic evaluation for a suspected ICP disorder [20, 39, 54, 55]. Future research to establish normal ICP, until quantitative non-invasive technology is developed, could benefit from this telemetric monitoring technique and, hopefully, expand the material on ICP values obtained in pseudo-healthy humans. However, there are considerable issues concerning spontaneous drift in baseline pressures with the telemetric technique. Drift may occur at any time after implantation. In a previous study, we reported the median drift to be 2.5 mmHg after a median implantation time of 241 days. This study, furthermore, suggested that especially reimplantation of a new sensor into the burr hole of a previous telemetric ICP sensor might be related to measurement errors including drift in baseline pressures [51]. Thus, in future studies on the subject, we recommend (1) a new burr hole for the telemetric ICP sensor, and (2) that the telemetric sensors are tested for zero drift after explantation.

Telemetric ICP monitoring requires implantation of a telemetric ICP sensor. The implantation is comparable to implantation of a cable-based ICP sensor. It does, however, limits the need for repeated invasive procedures (e.g. repeated ICP measurements with a cable-based ICP sensor). In future research of normal ICP, the challenge will thus be to investigate ICP in patients who are as normal as possible in terms of ICP dynamics but still require neurosurgical intervention. A possible cohort could be patients undergoing neurosurgery with removal of a benign intracranial tumor or with clipping of an unruptured aneurysm. Another cohort could be patients with a severe head trauma, who after a full recovery, can be considered without damage to CSF pathways and ICP dynamics [52, 53, 56].

In this review, we found a reference interval for ICP in the supine position from 0.9 to 16.3 mmHg, based on six studies with a total of 62 participants [20, 48, 54, 57,58,59]. The reference intervals are based on a small sample size, and do, therefore, not represent a clinically-applicable reference interval. Since most humans, and in terms of patients specifically patients with idiopathic intracranial hypertension and normal pressure hydrocephalus, spend the majority of their lives in the upright (vertical) position, a reference interval for this specific position is needed for interpreting diagnostic long-term ICP monitoring. Based on six studies with a total of 62 participants [20, 39, 48, 57,58,59], this review found a reference intervals for ICP in the upright position from − 6.2 to 8.0 mmHg. Though too wide to serve as a clinically-applicable reference interval, the data show that negative ICP values can be normal in an upright position [48, 60].

For daytime ICP, the established reference intervals were likewise based on a limited number of studies (n = 2) and study participants (n = 45) [42, 61]. Furthermore, there are large interpersonal differences in the amount of time spend in an upright position during the day. These factors probably result in the wide reference interval from − 12.0 to 12.2 mmHg. As with the reference interval for ICP in the upright position, this does not serve as a practical tool in clinical decision making. For night-time, we were able to establish a reference interval from -15.8 to 28.2 mmHg. Besides a limited number of studies (n = 3) and participants (n = 57) addressing the matter [42, 61, 62], body position during sleep may vary considerably among patients. Furthermore, the degree of sleep apnoea has also been found to highly impact ICP [42]. Combined, this could potentially cause significant variations in measured ICP and, result in the very wide and not clinically useful reference interval. Unfortunately, the included studies did not provide information on body position during sleep or sleep apnoea coherent to ICP values.

There probably is considerable interpersonal differences in normal ICP. Thus, what will be normal in a 10 year-old normal weight girl may differ from an 80 year-old obese man. Therefore, the idea of using a single value of ICP as a way to distinguish normal values from pathological values, is possibly not biologically natural. Since ICP is highly dependent on body position and activities, one needs to consider if the values are achieved from bed-bound or active patients. Included data is currently to scarce to make a model accounting for these factors. Instead, we suggest a standardized controlled setting defining “baseline ICP” in different body positions related to patient characteristics (such as age, gender and weight), e.g. 10 min measurement following 20 min supine position.

Reference intervals for LCSFop

The majority of included studies on LCSFop (81%) performed pressure measurement in a lateral recumbent position [7, 9, 22, 27, 28, 30,31,32,33,34,35, 41, 43, 63,64,65,66,67,68,69,70,71,72,73], and a reference interval in this position from 7.2 to 16.8 mmHg was established. There was no significant difference between the reference intervals in healthy individuals versus pseudo-healthy individuals. The established reference interval is similar to the reference of 7 to 15 mmHg routinely used in clinical practice [5, 17, 22, 23, 48]. Seven studies obtained LCSFop values in supine position [5, 7, 23, 29, 63, 74, 75], resulted in a reference interval from 5.7 to 15.5 mmHg. Participants in three out of the seven studies were completely healthy [5, 23, 29]. There was no significant difference between reference intervals in healthy individuals versus pseudo-healthy individuals.When comparing supine LCSFop to supine ICP, we found a difference between the means corresponding to 2.1 mmHg (P = 0.03). These results suggest that supine LCSFop is not optimal as a surrogate marker of supine ICP. To our knowledge, there are no studies that compare simultaneously measured supine ICP with supine LCSFop.

Posture-dependent pressure differences

Postural-dependent pressure changes have mainly been evaluated in studies investigating ICP [18, 58]. Andresen et al. compared lumbar recumbent position to supine position in 31 patients with intracranial ICP monitoring. They found that ICP increased approximately 5 mmHg in the lateral recumbent position, a significantly higher difference than found between LCSFop in recumbent position versus supine position in this review [18]. This postural-related difference in ICP may be caused by spine flexion and, in particular, flexion of the neck during lateral recumbent position in the study by Andresen et al. [18]. A flexed neck could theoretically compress the jugular veins, thus hindering the venous return to the heart from the head, thereby increasing ICP [40, 76,77,78]. Many studies have emphasized the importance of a neutral neck during the measurement of LCSFop [22, 23, 40, 76]. Though statistically significant, the mean LCSFop difference of 1.2 mmHg between the lateral recumbent position and supine position hardly has any clinical implications (Fig. 2). This relatively small difference might be explained by LCSFop in the lateral recumbent position having been measured with the neck in a neutral position. Unfortunately, the significant change in LCSFop caused by neck position alone has not previously been subject to much debate. Thus, only six of the included studies examining LCSFop documented that LCSFop was obtained simultaneously with a neutral neck position [6, 23, 27, 30, 33, 43]. To establish an accurate reference interval of LCSFop, the neck should be held in a neutral position during all LCSFop measurements.


In this systematic review, we aimed to establish reference intervals for ICP and LCSFop.

The data on ICP was not sufficient to establish clinically applicable reference intervals for either supine position, upright position, daytime, or night-time. Negative ICP in upright position do however seem to be normal. For LCSFop we estimated clinically-applicable reference intervals in both lateral recumbent position (6.3 to 15.9 mmHg) and supine position (5.3 to 15.1 mmHg). This systematic review highlights the need for future research within the field of reference intervals for ICP measures.

Availability of data and materials

The data set used and analysed during the current study is available from the corresponding author on reasonable request.


  1. 1.

    Sæhle T, Eide PK. Intracranial pressure monitoring in pediatric and adult patients with hydrocephalus and tentative shunt failure: a single-center experience over 10 years in 146 patients. J Neurosurg. 2015;122:1076–86.

    Article  PubMed  Google Scholar 

  2. 2.

    Schuhmann MU, Sood S, McAllister JP, Jaeger M, Ham SD, Czosnyka Z, et al. Value of overnight monitoring of intracranial pressure in hydrocephalic children. Pediatr Neurosurg. 2008;44:269–79.

    PubMed  Article  Google Scholar 

  3. 3.

    Czosnyka Z, Czosnyka M. Long-term monitoring of intracranial pressure in normal pressure hydrocephalus and other CSF disorders. Acta Neurochir. 2017;159:1979–80.

    PubMed  Article  Google Scholar 

  4. 4.

    Lilja-Cyron A, Kelsen J, Andresen M, Fugleholm K, Juhler M. Feasibility of telemetric intracranial pressure monitoring in the neuro intensive care unit. J Neurotrauma. 2018;35:1578–86.

    PubMed  Article  Google Scholar 

  5. 5.

    Malm J, Jacobsson J, Birgander R, Eklund A. Reference values for CSF outflow resistance and intracranial pressure in healthy elderly. Neurology. 2011;76:903–9.

    PubMed  Article  Google Scholar 

  6. 6.

    Gilland O, Tourtellotte WW, O’Tauma L, Henderson WC. Normal cerebrospinal fluid pressure. J Neurosurg. 1974;40:587–93.

    CAS  PubMed  Article  Google Scholar 

  7. 7.

    Ekstedt J. CSF hydrodynamic studies in man II Normal hydrodynamic variables related to CSF pressure and flow. J Neurol Neurosurg Psychiatry. 1978;41:345–53.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  8. 8.

    Loman J, Myerson A, Goldman D. Effects of alterations in posture on the cerebrospinal fluid pressure. Arch Neurol Psychiatry. 1935;33:1279–95.

    Article  Google Scholar 

  9. 9.

    Whiteley W, Al-Shahi R, Warlow CP, Zeidler M, Lueck CJ. CSF opening pressure: reference interval and the effect of body mass index. Neurology. 2006;67:1690–1.

    CAS  PubMed  Article  Google Scholar 

  10. 10.

    Ekstedt J. CSF hydrodynamic studies in man. J Neurol Neurosurg Psychiatry. 1977;40:105–19.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  11. 11.

    Hodgson JS. Combined ventricular and lumbar puncture in the diagnosis of brain tumor. J Am Med Assoc. 1928;90:1524–6.

    Article  Google Scholar 

  12. 12.

    Smyth GE, Henderson WR. Observations on the cerebrospinal fluid pressure on simultaneous ventricular and lumbar punctures. J Neurol Neurosurg Psychiatry. 1938;1:226–38.

    CAS  Article  Google Scholar 

  13. 13.

    Speck V, Staykov D, Huttner HB, Sauer R, Schwab S, Bardutzky J. Lumbar catheter for monitoring of intracranial pressure in patients with post-hemorrhagic communicating hydrocephalus. Neurocrit Care. 2011;14:208–15.

    PubMed  Article  Google Scholar 

  14. 14.

    Eide PK, Brean A. Lumbar cerebrospinal fluid pressure waves versus intracranial pressure waves in idiopathic normal pressure hydrocephalus. Br J Neurosurg. 2006;20:407–14.

    CAS  PubMed  Article  Google Scholar 

  15. 15.

    Lenfeldt N, Koskinen LOD, Bergenheim AT, Malm J, Eklund A. CSF pressure assessed by lumbar puncture agrees with intracranial pressure. Neurology. 2007;68:155–8.

    CAS  PubMed  Article  Google Scholar 

  16. 16.

    Warden KF, Alizai AM, Trobe JD, Hoff JT. Short-term continuous intraparenchymal intracranial pressure monitoring in presumed idiopathic intracranial hypertension. J Neuro-Ophthalmol. 2011;31:202–5.

    Article  Google Scholar 

  17. 17.

    Eide PK, Due-Tønnessen B, Helseth E, Lundar T. Assessment of intracranial pressure volume relationships in childhood: the lumbar infusion test versus intracranial pressure monitoring. Child’s Nerv Syst. 2001;17:382–90.

    CAS  Article  Google Scholar 

  18. 18.

    Andresen M, Hadi A, Petersen LG, Juhler M. Effect of postural changes on ICP in healthy and ill subjects. Acta Neurochir. 2014;157:109–13.

    PubMed  Article  Google Scholar 

  19. 19.

    Poca MA, Sahuquillo J, Topczewski T, Lastra R, Font ML, Corral E. Posture-induced changes in intracranial pressure: a comparative study in patients with and without a cerebrospinal fluid block at the craniovertebral junction. Neurosurgery. 2006;58:899–906.

    PubMed  Article  Google Scholar 

  20. 20.

    Chapman PH, Cosman ER, Arnold MA, Portnoy HD, Sklar F. The relationship between ventricular fluid pressure and body position in normal subjects and subjects with shunts: a telemetric study. Neurosurgery. 1990;26:181–9.

    CAS  PubMed  Article  Google Scholar 

  21. 21.

    Barami K, Sood S, Ham SD, Canady AI. Postural changes in intracranial pressure in chronically shunted patients. Pediatr Neurosurg. 2000;33:64–9.

    CAS  PubMed  Article  Google Scholar 

  22. 22.

    Ellis R. Lumbar cerebrospinal fluid opening pressure measured in a flexed lateral decubitus position in children. Pediatrics. 1994;24:622–3.

    Google Scholar 

  23. 23.

    Corbett JJ, Mehta MP. Cerebrospinal fluid pressure in normal obese subjects and patients with pseudotumor cerebri. Neurology. 1983;33:1386–8.

    CAS  PubMed  Article  Google Scholar 

  24. 24.

    Wilson TJ. Textbook of child neurology. J Neurol Neurosurg Psychiatry. 1980;43:1050–1.

    PubMed Central  Article  PubMed  Google Scholar 

  25. 25.

    The Joanna Briggs Institute. Joanna Briggs Institute Reviewer’s Manual. Joanna Briggs Inst. 2014.

  26. 26.

    Higgins J, Green S. Cochrane handbook for systematic reviews of interventions version 5.1.0. Cochrane Database Syst Rev. 2011.

  27. 27.

    Skau M, Yri H, Sander B, Gerds TA, Milea D, Jensen R. Diagnostic value of optical coherence tomography for intracranial pressure in idiopathic intracranial hypertension. Graefe’s Arch Clin Exp Ophthalmol. 2012;251:567–74.

    Article  Google Scholar 

  28. 28.

    Skipper NT, Igra MS, Littlewood R, Armitage P, Laud PJ, Mollan SP, et al. Do optic canal dimensions measured on CT influence the degree of papilloedema and visual dysfunction in idiopathic intracranial hypertension? Neuro-Ophthalmol. 2019;43:3–9.

    Article  Google Scholar 

  29. 29.

    Eklund A, Jóhannesson G, Johansson E, Holmlund P, Qvarlander S, Ambarki K, et al. The pressure difference between eye and brain changes with posture. Ann Neurol. 2016;80:269–76.

    PubMed  Article  Google Scholar 

  30. 30.

    Albeck MJ, Borgesen SE, Gjerris F, Schmidt JF, Sorensen PS. Intracranial pressure and cerebrospinal fluid outflow conductance in healthy subjects. J Neurosurg. 1991;74:597–600.

    CAS  PubMed  Article  Google Scholar 

  31. 31.

    Albeck MJ, Skak C, Nielsen PR, Olsen KS, Børgesen SE, Gjerris F. Age dependency of resistance to cerebrospinal fluid outflow. J Neurosurg. 1998;89:275–8.

    CAS  PubMed  Article  Google Scholar 

  32. 32.

    Hannerz J, Greitz D, Ericson K. Is there a relationship between obesity and intracranial hypertension? Int J Obes Relat Metab Disord. 1995;19:240–4.

    CAS  PubMed  Google Scholar 

  33. 33.

    Lakke JP, Schut D. Electromanometric examination of CSF pressure response to jugular compression. I. Determination of normal values. Psychiatr Neurol Neurochir. 1968;71:57–64.

    CAS  PubMed  Google Scholar 

  34. 34.

    Puhringer F, Hormann C, Langmayr J, Schalow S, Benzer A. The effect of alfentanil on cerebrospinal fluid pressure in human volunteers. Eur J Anaesthesiol. 1997;14:211–4.

    CAS  PubMed  Article  Google Scholar 

  35. 35.

    Shapiro K, Marmarou A, Shulman K. Characterization of clinical CSF dynamics and neural axis compliance using the pressure-volume index: I The normal pressure-volume index. Ann Neurol. 1980;7:508–14.

    CAS  PubMed  Article  Google Scholar 

  36. 36.

    Bø SH, Lundqvist C. Cerebrospinal fluid opening pressure in clinical practice – a prospective study. J Neurol. 2020;267:3696–701.

    Article  PubMed  PubMed Central  Google Scholar 

  37. 37.

    Pedersen SH, Norager NH, Lilja-Cyron A, Juhler M. Telemetric intracranial pressure monitoring in children. Child’s Nerv Syst. 2020;36:49–58.

    Article  Google Scholar 

  38. 38.

    Eide PK, Bakken A. The baseline pressure of intracranial pressure (ICP) sensors can be altered by electrostatic discharges. Biomed Eng Online. 2011;10:76.

    Article  Google Scholar 

  39. 39.

    Pedersen SH, Lilja-Cyron A, Andresen M, Juhler M. The relationship between intracranial pressure and age—chasing age-related reference values. World Neurosurg. 2018;110:119–23.

    Article  Google Scholar 

  40. 40.

    Williams A, Coyne SM. Effects of neck position on intracranial pressure. Am J Crit Care. 1993;2:68–71.

    CAS  PubMed  Article  Google Scholar 

  41. 41.

    Fleischman D, Berdahl JP, Zaydlarova J, Stinnett S, Fautsch MP, Allingham RR. Cerebrospinal fluid pressure decreases with older age. PLoS ONE. 2012;7:1–9.

    Article  CAS  Google Scholar 

  42. 42.

    Riedel CS, Martinez-tejada I, Norager NH, Juhler M. B-waves are present in patients without intracranial pressure disturbances. J Sleep Res. 2020;517. file:///C:/Oel/Artikler/PhD-Mxa-2. package (clinmon)/Riedel et al. B-waves manuscript_sleep_research_vers3.1.pdf

  43. 43.

    Bono F, Lupo MR, Lavano A, Mangone L, Fera F, Pardatscher K, et al. Cerebral MR venography of transverse sinuses in subjects with normal CSF pressure. Neurology. 2003;61:1267–70.

    CAS  PubMed  Article  Google Scholar 

  44. 44.

    Berdahl JP, Fleischman D, Zaydlarova J, Stinnett S, Rand Allingham R, Fautsch MP. Body mass index has a linear relationship with cerebrospinal fluid pressure. Investig Ophthalmol Vis Sci. 2012;53(3):1422–7.

    Article  Google Scholar 

  45. 45.

    Wakerley BR, Warner R, Cole M, Stone K, Foy C, Sittampalam M. Cerebrospinal fluid opening pressure: the effect of body mass index and body composition. Clin Neurol Neurosurg. 2020;188:105597.

    CAS  PubMed  Article  Google Scholar 

  46. 46.

    Raboel PH, Bartek J, Andresen M, Bellander BM, Romner B. Intracranial pressure monitoring: Invasive versus non-invasive methods-A review. Crit Care Res Pract. 2012;2012:3–7.

    Google Scholar 

  47. 47.

    Kawoos U, McCarron RM, Auker CR, Chavko M. Advances in intracranial pressure monitoring and its significance in managing traumatic brain injury. Int J Mol Sci. 2015;16:28979–97.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  48. 48.

    Andresen M, Juhler M. Intracranial pressure following complete removal of a small demarcated brain tumor: a model for normal intracranial pressure in humans. J Neurosurg. 2014;121:797–801.

    Article  PubMed  Google Scholar 

  49. 49.

    Petersen LG, Lawley JS, Lilja-Cyron A, Petersen JCGG, Howden EJ, Sarma S, et al. Lower body negative pressure to safely reduce intracranial pressure. J Physiol England. 2019;597:237–48.

    CAS  Article  Google Scholar 

  50. 50.

    Magnéli S, Howells T, Saiepour D, Nowinski D, Enblad P, Nilsson P. Telemetric intracranial pressure monitoring: a noninvasive method to follow up children with complex craniosynostoses. A case report. Child’s Nerv Syst Child’s Nervous System. 2016;32:1311–5.

    Article  Google Scholar 

  51. 51.

    Norager NH, Lilja-cyron A, Bjarkam CR, Duus S, Juhler M. Telemetry in intracranial pressure monitoring : sensor survival and drift. Acta Neurochir. 2018;160:2137–44.

    PubMed  Article  Google Scholar 

  52. 52.

    Norager NH, Lilja-Cyron A, Hansen TS, Juhler M. Deciding on appropriate telemetric intracranial pressure monitoring system. World Neurosurg. 2019;126:564–9.

    Article  PubMed  Google Scholar 

  53. 53.

    Antes S, Tschan CA, Heckelmann M, Breuskin D, Oertel J. Telemetric intracranial pressure monitoring with the raumedic neurovent P-tel. World Neurosurg. 2016;91:133–48.

    Article  PubMed  Google Scholar 

  54. 54.

    Purvin VA, Kawasaki A, Yee RD. Papilledema and obstructive sleep apnea syndrome. Arch Ophthalmol. 2000;118:1626–30.

    CAS  PubMed  Article  Google Scholar 

  55. 55.

    Lundberg N. Continuous recording and control of ventricular fluid pressure in neurosurgical practice. Acta Psychiatr Scand Suppl. 1960;36:1–193.

    CAS  PubMed  Google Scholar 

  56. 56.

    Antes S, Stadie A, Müller S, Linsler S, Breuskin D, Oertel J. Intracranial Pressure-Guided shunt valve adjustments with the miethke sensor reservoir. World Neurosurg. 2018;109:e642–50.

    PubMed  Article  Google Scholar 

  57. 57.

    Magnéli S, Howells T, Saiepour D, Nowinski D, Enblad P, Nilsson P. Telemetric intracranial pressure monitoring: a noninvasive method to follow up children with complex craniosynostoses. A case report. Child’s Nerv Syst. 2016;32:1311–5.

    Article  Google Scholar 

  58. 58.

    Petersen LG, Petersen JCG, Andresen M, Secher NH, Juhler M. Postural influence on intracranial and cerebral perfusion pressure in ambulatory neurosurgical patients. Am J Physiol Regul Integr Comp Physiol. 2016;310:R100–4.

    CAS  Article  PubMed  Google Scholar 

  59. 59.

    Lawley JS, Petersen LG, Howden EJ, Sarma S, Cornwell WK, Zhang R, et al. Effect of gravity and microgravity on intracranial pressure. J Physiol. 2017;595:2115–27.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  60. 60.

    Lundberg N. The mean ventricular fluid pressure. Acta Psychiatr Scand Suppl. 1960;36:1–193.

    CAS  PubMed  Google Scholar 

  61. 61.

    Chari A, Dasgupta D, Smedley A, Craven C, Dyson E, Matloob S, et al. Intraparenchymal intracranial pressure monitoring for hydrocephalus and cerebrospinal fluid disorders. Acta Neurochir. 2017;159:1967–78.

    Article  PubMed  Google Scholar 

  62. 62.

    Langvatn EA, Frič R, Due-Tønnessen BJ, Eide PK. Intracranial volume versus static and pulsatile intracranial pressure values in children with craniosynostosis. J Neurosurg Pediatr. 2019;24:66–74.

    PubMed  Article  Google Scholar 

  63. 63.

    Schwartz KM, Luetmer PH, Hunt CH, Kotsenas AL, Diehn FE, Eckel LJ, et al. Position-related variability of CSF opening pressure measurements. Am J Neuroradiol. 2013;34:904–7.

    CAS  PubMed  Article  Google Scholar 

  64. 64.

    Lee MW, Vedanarayanan VV. Cerebrospinal fluid opening pressure in children: experience in a controlled setting. Pediatr Neurol. 2011;45:238–40.

    PubMed  Article  Google Scholar 

  65. 65.

    Kaiser AM, Whitelaw AGL. Normal cerebrospinal fluid pressure in the newborn. Neuropediatrics. 1986;17:100–2.

    CAS  PubMed  Article  Google Scholar 

  66. 66.

    Kawasaki A, Purvin V. Unilateral optic disc edema following trabeculectomy. J Neuro-Ophthalmol. 1998;18:121–3.

    CAS  Google Scholar 

  67. 67.

    González-Camarena PI, San-Juan D, González-Olhovich I, Rodríguez-Arévalo D, Lozano-Elizondo D, Trenado C, et al. Dynamic changes of the intraocular pressure and the pressure of cerebrospinal fluid in nonglaucomatous neurological patients. Acta Ophthalmol. 2017;95:e138–43.

    PubMed  Article  Google Scholar 

  68. 68.

    Avery RA, Shah SS, Licht DJ, Seiden JA, Huh JW, Boswinkel J, et al. Reference range for cerebrospinal fluid opening pressure in children. N Engl J Med. 2010;363:891–3.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  69. 69.

    Sugita Y, Iijima S, Teshima Y, Shimizu T, Nishimura N, Tsutsumi T, et al. Marked episodic elevation of cerebrospinal fluid pressure during nocturnal sleep in patients with sleep apnea hypersomnia syndrome. Electroencephalogr Clin Neurophysiol. 1985;60:214–9.

    CAS  PubMed  Article  Google Scholar 

  70. 70.

    Wibroe EA, Yri HM, Jensen RH, Wibroe MA, Hamann S. Osmolality of cerebrospinal fluid from patients with idiopathic intracranial hypertension (IIH). PLoS ONE. 2016;11:e0146793.

    PubMed  PubMed Central  Article  CAS  Google Scholar 

  71. 71.

    Beck J, Fung C, Ulrich CT, Fiechter M, Fichtner J, Mattle HP, et al. Cerebrospinal fluid outflow resistance as a diagnostic marker of spontaneous cerebrospinal fluid leakage. J Neurosurg Spine. 2017;27:227–34.

    PubMed  Article  Google Scholar 

  72. 72.

    Gulbrandsen P, Dietrichs E. Cerebrospinal fluid opening pressure measurements in acute headache patients and in patients with either chronic or no pain. Acta Neurol Scand. 2010;122:6–11.

    Article  Google Scholar 

  73. 73.

    Avery RA. Interpretation of lumbar puncture opening pressure measurements in children. J Neuro-Ophthalmol. 2014;34:284–7.

    Article  Google Scholar 

  74. 74.

    Friden HG, Ekstedt J. Volume/pressure relationship of the cerebrospinal space in humans. Neurosurgery. 1983;13:351–66.

    CAS  PubMed  Article  Google Scholar 

  75. 75.

    Blomquist HK, Sundin S, Ekstedt J. Cerebrospinal fluid hydrodynamic studies in children. J Neurol Neurosurg Psychiatry. 1986;49:536–48.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  76. 76.

    Hulme A, Cooper R. The effects of head position and jugular vein compression (JVC) on intracranial pressure (ICP). A Clin Study Intracranial Press. 1976;III:259–63.

    Article  Google Scholar 

  77. 77.

    Lipe HP, Mitchell PH. Positioning the patient with intracranial hypertension: how turning and head rotation affect the internal jugular vein. Hear Lung. 1980;9:1031–7.

    CAS  Google Scholar 

  78. 78.

    Holmlund P, Eklund A, Koskinen LOD, Johansson E, Sundström N, Malm J, et al. Venous collapse regulates intracranial pressure in upright body positions. Am J Physiol Regul Integr Comp Physiol. 2018;314:R377–85.

    CAS  PubMed  Article  Google Scholar 

  79. 79.

    Martin G. Lundberg's B waves as a feature of normal intracranial pressure. Surg Neurol. 1978;9(6):347–8.

    CAS  PubMed  Google Scholar 

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The project was funded by the Rigshospitalet Research Foundation, the DMSK Foundation and the Novo Nordisk Foundation (NNF17OC0024718). The funding bodies had no role in the design of the study, the study collection, analysis, interpretation of data or in writing the manuscript.

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NHN MHO, SSP, CSR, MJ designed the study. NHN, MHO, SSP, CSR screened and extracted data from studies. NHN and MHO drafted the manuscript. All authors read and approved the final manuscript.

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Correspondence to Nicolas Hernandez Norager.

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Norager, N.H., Olsen, M.H., Pedersen, S.H. et al. Reference values for intracranial pressure and lumbar cerebrospinal fluid pressure: a systematic review. Fluids Barriers CNS 18, 19 (2021).

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  • Cerebrospinal fluid pressure
  • CSF
  • ICP
  • Intracranial pressure
  • Reference intervals
  • Reference values