Abstract
Touch and other types of patient stimulation are necessary in critical care and generally presumed to be beneficial. Recent pre-clinical studies as well as randomized trials assessing early mobilization have challenged the safety of such routine practices in patients with acute neurological injury such as stroke. We sought to determine whether patient stimulation could result in spreading depolarization (SD), a dramatic pathophysiological event that likely contributes to metabolic stress and ischemic expansion in such patients. Patients undergoing surgical intervention for severe acute neurological injuries (stroke, aneurysm rupture, or trauma) were prospectively consented and enrolled in an observational study monitoring SD with implanted subdural electrodes. Subjects also underwent simultaneous video recordings (from continuous EEG monitoring) to assess for physical touch and other forms of patient stimulation (such as suctioning and positioning). The association of patient stimulation with subsequent SD was assessed. Increased frequency of patient stimulation was associated with increased risk of SD (OR = 4.39 [95%CI = 1.71–11.24]). The overall risk of SD was also increased in the 60 min following patient stimulation compared to times with no stimulation (OR = 1.19 [95%CI = 1.13–1.26]), though not all subjects demonstrated this effect individually. Positioning of the subject was the subtype of stimulation with the strongest overall effect on SD (OR = 4.92 [95%CI = 3.74–6.47]). We conclude that in patients with some acute neurological injuries, touch and other patient stimulation can induce SD (PS-SD), potentially increasing the risk of metabolic and ischemic stress. PS-SD may represent an underlying mechanism for observed increased risk of early mobilization in such patients.
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INTRODUCTION
The role of therapeutic touch in medicine is one that is both increasingly supported by evidence of objective benefit[1] and is central to providing humanistic care to suffering patients. As medicine becomes increasingly holistic, patients are appropriately seen as part of their social network and as individuals rather than as a “manifestation of disease”. This has led to improved understanding of the importance of family presence and human interactions, particularly during times of severe illness. Specifically, controlled trials have increasingly demonstrated benefits of family presence[2] as well as early mobilization in intensive care unit (ICU) patients[3] across a variety of conditions by decreasing complications related to immobility. It is within this context that cautionary observations both from pre-clinical work[4] and clinical trials in patients with acute neurological injuries[5] suggest that some patients may actually be harmed by these interactions.
While tactile stimulation has been proposed to potentially represent a therapeutic strategy in ischemic stroke by increasing collateral circulation to the brain[6], such an approach may in fact be harmful under some circumstances where spreading depolarization (SD) is induced[7]. Spreading depolarization is a massive, slow-moving wave of brain depolarization, resulting in transient loss of neuronal signaling and depression of normal high frequency activity[8, 9]. In stroke and other neurological injuries, SDs occur in repeated, cycling patterns around an ischemic core and can be accompanied by waves of spreading ischemia. SD is strongly implicated in exacerbation of metabolic stress, edema, and infarction in vulnerable penumbral tissue[10, 11]. In a recent pre-clinical study of middle cerebral artery (MCA) stroke[4], limb somatosensory stimulation resulted in additional SDs, which in turn were linked to infarct expansion. In that model, SDs were initiated only when the stimulated cortical brain region was in vulnerable penumbra adjacent to the infarct core. No such effect of excess SD was observed when the stimulated region was in the ischemic core itself or in normally perfused brain[4]. The fact that additional SDs induced by peripheral touching were associated with increased injury in mice raises the question of whether similar effects occur in clinical settings.
It is noteworthy that a recent randomized controlled trial (RCT) of very early mobilization after hemorrhagic and ischemic stroke reported the surprising finding of significantly decreased risk of good outcomes in patients randomized to mobilization within 24 h compared to standard care[12]. Even more concerningly, those randomized to very early mobilization demonstrated increased risk of stroke expansion[13]. Possible explanations for these effects included impaired autoregulation[14], making patients tired and slumping in their chairs[14], orthostatic hypotension[15], and upward head position[16]. These may be plausible contributors; however, the above-mentioned pre-clinical work strongly suggests that induced SD due to patient stimulation may in fact be a prominent underlying mechanism.
In the present study, we sought to determine whether routine patient stimulation early after acute neurological injuries could result in induced SD. We present an exemplary case, illustrating this plausible connection. We then assess the association of more frequent stimulation with SD in a larger group of subjects with various acute neurological injuries. Finally, we assess the temporal priority of stimulation with subsequent SD. These data, coupled with published mechanistic plausibility[4], assess the key causality factors regarding whether patient stimulation can induce SD (PS-SD). Our observations could serve as a possible mechanistic explanation for the findings of worse outcomes with mobilization and suggest new targeted therapeutic approaches such as limiting stimulation during SD vulnerable times.
RESULTS
Exemplary case with clinical stimulation increasing the risk of subsequent SD
A 29-year-old female presented with a left carotid occlusion related to cervical dissection with an NIH stroke scale score of 22. IV rt-PA was administered at 3 h 30 min from last know well (LKW). She was then taken for mechanical thrombectomy which was complicated due to need for multiple stent-retriever passes and cervical stent placement. A TICI (thrombolysis in cerebral infarction) 2b revascularization was achieved at 5 h 39 min from LKW. She nonetheless still developed a large area of infarct in the left hemisphere with early signs of herniation and so a decompressive craniectomy was performed. She was enrolled in the current study (UNM HRPO 10–159), allowing for intra-operative placement of a subdural electrocorticography (ECoG) recording electrode in a cortical region adjacent to the infarct core. She remained minimally responsive with a poor neurological exam and so was monitored with continuous EEG. Per protocol, the ECoG data were not reviewed for SD during the monitoring time, but was used to guide seizure management. The electrode strip was removed at bedside after approximately 5 days of monitoring when the neurological examination began to improve. She was eventually discharged to inpatient rehabilitation. Her 90-day modified Rankin Scale (mRS) was 4 with residual hemiparesis and aphasia. At 2 years, her mRS had improved to 3 with mild residual aphasia and significant hemiparesis, but is ambulatory and able to take care of her own affairs.
Review of ECoG data revealed that 40 recurrent SDs were detected by the electrode strip during the acute post-operative days (Fig. 1A). A significant, repeating association of standard clinical stimulation and SD was noted, with an approximately 9-min latency between stimulation and SD (Fig. 1B). We used logistic regression to estimate the risk of SD after clinical stimulation. For each minute, we found that stimulation significantly increased the odds of SD being measured 9 min later (OR = 2.85, 95% CI = 1.5–5.37, 5536 observations) (Fig. 1C). Manual ECoG review indicated that the first measurement site of SD consistently occurred in electrode lead 6 (Fig. 1A). Using the known propagation rate of SD as ~ 3 mm/min[17, 18], we sought to determine whether a potential initiation site would be in regions that would be activated by patient stimulation. A rough estimate of the distance traveled by SD in 9 min would thus be 27 mm, and this distance was mapped onto a fused image of the CT demonstrating the electrode strip location with the pre-operative MRI, demonstrating the anatomical location (Fig. 1D). We recognize that this does not consider the complex gyriform geometry of the cortex, so serves only as a rough estimate which could overestimate the linear distance. However, this plausible region of initiation very reasonably includes both the sensory cortex, motor cortex, and supplemental motor area (SMA). This is particularly relevant in that SMA is known to have bilateral input[19] and would be expected to be activated during many types of patient stimulation. The SMA is represented in a relatively large cortical region anterior to the motor cortex, so even if the proposed initiation site is closer to the electrode due to complex SD propagation patterns, it would still be within the SMA.
We then sought to determine whether it would be expected that this proposed initiation zone be anatomically located within vulnerable penumbra. The diffusion weighted MRI was therefore fused with the post-operative CT, demonstrating that the edge of the core infarct was extending into the anterior part of the SMA, strongly suggesting that this region would be vulnerable penumbra. Finally, infarct volume was measured using semi-automated segmentation[20] segmentation between the initial MRI and the CT one week later after removal of the recording electrode. There was a marked increase in final infarct volume, nearly doubling (244 cc to 416 cc) (Fig. 1D).
This case illustrates all of the core principles of our hypothesis that patient stimulation may induce SD due to cortical activation in vulnerable penumbra. In turn, these recurrent SD would be expected, based on previous data[4, 9] to cause ongoing metabolic stress in compromised tissue, leading to infarct expansion (Fig. 2). We sought to rigorously test this hypothesis across a larger group of patients with stroke and brain injury in order to determine whether these associations and temporal relationships between stimulation and SD are generalizable.
Demographics and scoring reliability
Recordings and analyses were made from 13 subjects: 2 with malignant hemispheric stroke (MHS), 8 with aneurysmal subarachnoid hemorrhage (aSAH), and 3 with severe TBI. Five additional subjects had complete data sets (scored SD and video data); however these did not have overlapping times of video and ECoG data that contained more than 1 SD. Subject demographics and outcomes are summarized in Table 1. All subjects had > 48 h of recordings with both ECoG and video recordings. Total SD counts in individual subjects ranged from 2–103. Interobserver reliability testing for stimulation scoring on video (any stim versus no stim) between two independent reviewers demonstrated a median Kappa statistic of 0.78 across included subjects (standard deviation = 0.06, range = 0.70–0.92).
Association of SD with increased stimulation frequency
Descriptive analysis: Comparing the frequency distribution between 60-min bins containing SD versus those without SD demonstrates a significant shift toward more patient stimulation in bins with more SD (Fig. 3). In Fig. 3A, this rightward shift in the frequency distribution of bins containing SD primarily emphasizes the lower proportion of bins with very low frequency of patient stimulation (0 or 1) in bins with SD compared to bins without SD (Kolmogorov–Smirnov test p = 0.0010). In order to assess if this difference was limited to a shift in low frequencies of stimulation, we also displayed the relative frequency of bins across the distribution of touch frequencies (Fig. 3B). This display emphasizes that there are more bins with SD with higher touch frequency. Note specifically that the SD bins (blue) have a larger relative frequency for nearly every touch number > 5 compared to No SD bins (orange) (Fig. 3B).
Inferential analysis: To assess for a possible “dose-dependent” effect of patient stimulation, we assessed the odds of SD with increasing stimulation frequency (up to 30) in 60-min bins. Very high frequencies of stimulation were uncommon (as can be seen in Fig. 3), so only values up to 30/hour were assessed. Given that we used a one-minute sampling unit for stimulation scoring, this would correspond to 30 min with stimulation in a given one hour bin. The effect of increased stimulation frequency in these non-overlapping 60-min bins was significantly associated with an increased risk of SD with increasing stimulation frequency (Fig. 4). This risk increased up to a maximum at 16–20 stimulation per hour and remained stable up to 26–30 stimulation per hour. Increasing stimulation was associated with increased risk of SD, particularly in the range of 6–10 stimulation/hour compared to 16–20 stimulation/hour. Data represent pooled analysis across subjects using logistic regression with mixed effect modeling.
Patient stimulation precedes SD
Having established 1) an empirical association between stimulation and SD (Figs. 3 and 4) and 2) a biologically plausible mechanism(Fig. 2 and Reference [4]), we now sought to test the temporal priority of the independent variable (stimulation) in order to support or refute a causal relationship[21, 22]. As discussed above (Fig. 1), an important consideration is the slow propagation rate of SD (~ 3 mm/minute[17, 18]) and thus the recording electrode may be remote from the initiation site. It would therefore be expected that if stimulation caused SD initiation, that there would be a patient specific, but internally consistent latency of several minutes between stimulation and SD detection.
Descriptive analysis: First, we assessed for this temporal relationship on an individual patient basis, since location of injury (and relationship to recording strip) varies among the 13 subjects. Our hypothesis was that patient stimulation would be associated with subsequent SD. In order to test this time dependency, we performed correlation analysis after introducing negative “lag” across the entire data stream for each subject. This allowed assessment of a possible latency time to detection of SD if the initiation location was remote from the monitoring electrode (i.e. “correcting” for the slow travel time between SD initiation and measurement, as shown in Fig. 2). Positive lag serves as an internal control to test the null (and biologically implausible) hypothesis that SD would be associated with subsequent patient stimulation. We noted robust effects of patient stimulation with subsequent SD, including in subject MHS1 at maximum 9 min of lag (also shown graphically in Fig. 1B) and SAH3 at 1 min of lag (Fig. 5A). On pooled analysis, we noted overall increased correlation of stimulation and SD for up to 50 min prior to SD, with no similar increased association with shift with positive (control) lag (Fig. 5B). Such a duration would correlate to a propagation distance of up to 15 cm, which is consistent with SD observed in previous clinical studies[23, 24].
Inferential analysis: To further assess the temporal priority of patient stimulation on the risk of subsequent SD, the odds of SD in the 60 min following stimulation was assessed in each subject and overall (Fig. 6). Overall, in grouped analysis using mixed effect modeling, there was a significantly increased risk of SD after stimulation (OR = 1.19, 95% CI = 1.13–1.26). Most subjects demonstrated a positive association of stimulation with subsequent SD. Two notable exceptions were subject MHS2 and SAH7 where a possible inhibitory effect of stimulation on subsequent SD was noted. The implications of these observations are discussed below (Discussion).
Effects of type of stimulation on SD
In order to assess whether different subtypes of patient stimulation had different magnitudes of effect, we repeated a similar assessment as above, focusing only on individual types of stimulation. See Table 2 for summary of different stimulation types. “Positioning” (e.g. turning, boosting up in bed, changing to sitting position, etc.) exerted the strongest effect on risk of subsequent SD with an OR of 4.92 (95%CI = 3.74–6.47). “Light touch” (e.g. isolated hand holding, etc.) also demonstrated a significant effect with an OR of 1.59 (95% CI = 1.46–1.74). “Suctioning” trended in the same direction with an OR of 1.68 (95% CI = 0.28–10.06) but was not significant due to wide confidence intervals, possibly due to the lower number of observations of this type of patient interaction. Finally, we wanted to determine whether there was a different effect of contralateral versus ipsilateral isolated light touch. While both were significantly associated with SD, surprisingly the effect of ipsilateral touch was stronger than contralateral touch (respectively OR = 1.98, 95% CI = 1.76- 2.23 and OR = 1.28, 95%CI = 1.12–1.46). The reason for this result is unclear, but it is possible that if more proximal signaling pathways are interrupted by stroke then the direct sensory pathways would not be in continuity to the cortex. Contralateral cortical stimulation with cross-hemispheric signaling through the SMA or other association areas could therefore be the mechanism for the significant effect of ipsilateral touch inducing SD. Overall the prominent effect of positioning, however, is the most notable finding in this analysis, as this would be the type of stimulation most closely related to “mobilization” as practiced in the AVERT II clinical trial[12].
DISCUSSION
Our results show that in subjects with acute neurological injuries who require craniotomy, touch and other physical stimulation is associated with increased risk of subsequent SD. Our data also support a causal relationship of PS-SD based on accepted criteria for causal inference[21, 22], most prominently, 1) association, 2) time dependency, and 3) a biologically plausible mechanism. Our observations provide the first test in human subjects of a hypothesis proposed from a preclinical study in mice[4] and provide strong mechanistic observational data to question the safety of aggressive early stimulation and mobilization practices in specific patient populations with acute neurological injuries. Further, our observations are consistent with SD as a mechanism of delayed ischemia which has been well established in pre-clinical models[4, 9, 25]. In addition, RCTs of very early mobilization suggest that such practices can result in worse neurological outcomes and larger infarct burden [5, 12, 13]. For these reasons, we agree with a recent systematic review[5] arguing for caution with early aggressive stimulation in patients with severe acute neurological injuries at risk of ischemia, until the safety of such practices can be better established.
The proximate mechanism of SD initiation in PS-SD is presumed to be related to supply–demand mismatch[4]. Specifically, when focal regions with impaired metabolic reserve (such as ischemic penumbra) are subjected to the increased demand of cortical activation with stimulation, the expected local vasodilatory response is absent[4, 26]. Similarly hyperthermia (which also results in increased metabolic demand) has also been associated with increased risk of SD[27]. In addition to metabolic compromise and impaired neurovascular coupling, other factors such as local blood brain barrier disruption[28] and decreased levels of nitric oxide [29] may also lower the threshold for initiation of SD[28].
Some hypotheses can be generated regarding which patients may be most at risk for PS-SD based on mechanisms and patterns of SD in pre-clinical and clinical studies. SD has been detected nearly universally after acute ischemic stroke, in the majority of severe aneurysmal subarachnoid hemorrhage patients, and in around half of intracerebral hemorrhage and traumatic brain injury patients[9, 30]. Some degree of tissue damage or stroke is probably a prerequisite for SD in these cases[31]. The time course of SD is particularly important, with an initial spike in the frequency of SD typically occurring at the time of injury followed by a delayed secondary peak occurring over days to weeks[32, 33]. Previous studies have suggested that this represents a secondary phase where therapeutic intervention targeting SD may be of benefit[33]; however, our data supports the possibility that this may also represent a secondary vulnerable period to PS-SD in patients with ongoing regions of penumbra or compromised brain. Clinically, such delayed injury phases correlate well with the swelling noted after large ischemic strokes[34], edema progression after TBI and ICH[35], and “vasospasm” or delayed cerebral ischemia observed after aneurysmal subarachnoid hemorrhage[36]. All of these phenomena may plausibly be explained by the effects of recurrent SD[37]. In our analyses, we identified example subjects with each of these injury types with PS-SD, suggesting that this phenomenon is not limited to ischemic stroke.
The type and degree of stimulation also deserves consideration. While the preclinical study by Von Bornstadt[4] provides a model emphasizing a narrow window of ischemia being the key determinant of SD generation, we suggest that the clinical relevance of this is much more complicated. While some cortical regions such as the somatosensory or calcarine cortex have been proposed as more vulnerable to SD based on the neuronal density[38], in ischemia, it is plausible that any region with the appropriate supply–demand mismatch of ischemia and excitation could be at risk of PS-SD. We illustrate this in an exemplary patient who may have had sensorimotor stimulation within a known ischemic region with appropriate latency to SD detection with a possible SMA or sensorimotor initiation site. In addition, if visual, auditory, or other association regions are stimulated and have an appropriate degree of ischemia, it is possible that SD may be induced in other regions as well. This could have implications for common clinical activities such as pupillary light reflex examination, television, neurologic assessment and other non-tactile stimuli. Supporting this hypothesis, we found that patient positioning was the most robust subtype of patient interaction we assessed, which would be expected to be a more prolonged and diffuse cortical activation compared to isolated light touch given that such interventions typically involve stimulation over at least many minutes. Ischemia in aSAH and TBI patients can occur in patchy and variable regions, and thus we were not able to directly hypothesize a potential cortical stimulation site within an ischemic region (as the in the case in Fig. 1); however we identified significant associations of stimulation and SD in more than half of our aSAH and TBI subjects.
While these data appear consistent with a hypothesized pre-clinical physiology and separate clinical trials which failed to demonstrate safety of very early mobilization, there are limitations to our study. SD was only assessed in a small cortical region at the site of the electrode strip and so it is possible that additional unmeasured PS-SD or stronger associations could be present in some subjects. We also did not have a method to assess for regional areas of ischemia or changes in ischemic risk over the observation time (such as development of DCI in aSAH). Further studies with perfusion imaging or focal probes in high-risk regions may be of benefit. The type of stimulation we observed may also under-estimate true stimulation occurring in the complex ICU environment. Other sources such as auditory or visual stimulation (for example if the television was on) could not be accounted for with the video analysis. All these critiques, however, suggest that we actually may be underestimating the true magnitude of PS-SD. On the other hand, we acknowledge that these data focus on a heterogeneous but high-risk group, all of whom required surgical treatment. While this diverse patient population supports the hypothesis that this is a generalizable mechanism may be present across several disease types, it is unknown if PS-SD are present in cases of minor or subcortical stroke or less severe aSAH cases without large hematomas that are typically treated endovascularly in modern practice. Finally, though positioning events may be the most similar to the type of mobilization in AVERT II, the AVERT II mobilization included sitting, standing, and walking at least three times per day. These clinical interventions were probably even more stimulating than the repositioning events in our subjects.
Finally, the data suggesting a possible protective effect of stimulation in two subjects deserves brief attention. Physiologically, this seems plausible, given that in some regions with adequate perfusion, somatosensory stimulation could increase blood flow[7]. Further, mounting data suggest that the harmful effects of SD may be most prominent in metabolically compromised tissue, while could theoretically have protective mechanisms remote from the injury and ischemia[39]. Additional studies coupling perfusion measurements with ECoG could help determine whether there are some subjects where stimulation increases local tissue perfusion.
These observations have significant and concerning implications for standard practices in the care of patients with neurological injuries. While large-scale practice changes should not be made based on small case series, our observations are supported by strong pre-clinical and clinical data regarding ischemic progression mechanisms as well as pragmatic trials which resulted in a call for caution in early mobilization of ischemic stroke patients. It therefore seems prudent at the very least, for clinicians to express some degree of uncertainty regarding the safety of early frequent stimulation in acute stroke and brain injury patients if not medically necessary for clinical care. Further mechanistic, clinical, and outcome data are urgently needed to assess the implications of the current study for acute neurological care and determine whether targeted pharmacologic approaches[40, 41] could minimize such risk.
MATERIALS AND METHODS
Study population
Subjects were prospectively enrolled in an observational study focused on the role of SD in acute neurological injuries using previously published criteria[42]. (UNM HRPO 10–159) Informed consent from the patient or legally authorized representative was obtained for all subjects, which included discussion of the nature of the study and possible consequences. Briefly, inclusion criteria were any adult patient undergoing craniotomy or craniectomy for hemorrhagic or ischemic stroke (including aneurysm rupture) or traumatic brain injury (TBI) who were expected to require at least 72 h of neuro-intensive care monitoring. Consent was sought prospectively from a legally authorized representative in most cases (unless the subject themselves were able to consent). Some of these subjects also underwent continuous EEG monitoring at the clinical discretion of the neuro-intensivist and neurosurgeon, and this was considered a second inclusion criteria for the current analysis.
ECoG and VideoEEG recordings
The methodology for recording and analysis of ECoG for SD has been published[42]. Briefly, at the conclusion of the intradural portion of the procedure, a 1 × 6 subdural platinum recording electrode (Auragen, IntegraLife: Plainsboro, NJ) was placed over the region thought to be at highest risk of injury expansion (for example, adjacent to infarct in MHS and in the region at highest risk of vasospasm after aneurysm clipping). After return to the ICU, ECoG was recorded using a full spectrum DC coupled amplifier[43]. DC ECoG was reviewed post hoc. In all subjects, continuous standard EEG and ECoG recordings with video were also collected. Video EEG recording and management was performed using standard 10–20 EEG montage and AC coupled amplifier with at least daily review by a board certified epileptologist. These data were used to guide care regarding antiseizure medications if required. The strip electrode was then removed at the bedside using gentle traction, similar to a surgical drain, when further invasive monitoring was no longer thought to be needed by the critical care team.
SD and stimulation scoring
SD was scored offline after data collection was complete—it was not incorporated into clinical management so as not to introduce any potential bias. The EEG analysis described above incorporates the high frequency ECoG data; however, it is not possible to assess for SD using these data. Separate ECoG recordings were acquired using a full spectrum DC amplifier coupled with the Component Neuromonitoring System (Moberg ICU solutions: Ambler PA) and archived in a hospital server. Data were exported to LabChart (ADInstruments: Colorado Springs, CO) for formal scoring using standardized approaches and criteria[42] with scoring by expert reviewers (APC and CWS). SD was defined as a DC shift, usually with associated transient depression of high frequency (0.5-50 Hz) filtered data unless occurring on a baseline of suppressed activity (which was then defined as isoelectric spreading depolarization [ISD]). In addition, spread to adjacent electrodes and stereotypical repeating patterns[44] are additional criteria to aid in scoring. Only subjects with > 1 SD were included for further analysis. SD times were then exported in spreadsheet files for each subject to a central server.
Continuous video recordings used for EEG were then reviewed by a separate panel of reviewers. Each file was reviewed in its entirety by two independent reviewers with no knowledge of the SD scoring and no EEG interpretation experience (to ensure that no EEG findings would be incorporated into the video review). The video files were reviewed continuously for the entire monitoring period at up to 20 × playback speed. Scoring was performed on a minute by minute basis and scored as to valid video recording (yes/no) and stimulation versus no stimulation. Stimulation was further divided into light touch (ipsilateral/ contralateral), suctioning, positioning, or other interventions. Scoring was assessed for inter-rater reliability using the kappa statistic. Stimulation scoring was combined into a single column where both raters agreed on touch and touch type to ensure the highest standard of rigor.
SD and video files for each subject were then linked into continuous time-series files. Data were reviewed for accuracy and continuity of monitoring start and stop dates and times to ensure standardization between data sets. Absent data was recorded as NaN to maintain continuity of the time series. See Fig. 7 for summary of the data acquisition and linking.
Illustrative case methods
After standard clinical data were extracted, additional image analysis was performed. Infarct volumes were extracted using semi-automated segmentation (ITK SNAP 3.8.0[20]). The pre-operative MRI with diffusion weighted (DWI) sequence was used for the baseline measurement and the first head CT performed the day after strip electrode removal was used for the final measurement. These measurements were used for descriptive purposed only. In order to assess the anatomic relationship of the strip electrode to both cortical structures and to the infarct, the pre-operative MRI (DWI) and T2 sequences were used. Image fusion was performed using automated software (StealthStation S7, Medtronic: Minneapolis, MN) and validated with manual review. DICOM measurement references were preserved in order to perform subsequent distance measurements.
Analysis and statistics
No formal power analysis or sample size was conducted as the ability to detect any effect within subjects or between subjects was entirely unknown. We limited the sample to the subjects enrolled prior to separate efforts that incorporate SD analysis into clinical management of patients, so that there would be no potential confounding effect of medications being tested for SD [40, 41] or of clinical interventions targeting SD [45].
Multiple potential confounders exist in testing our hypothesis that stimulation could trigger SD[4]. Specific concerns include the fact that the position of the electrode strip relative to either a vulnerable region or a potential initiation site are unknown. Due to this, the predicted latency from initiation to measurement is unknown, even if a strong association exists. In addition, we expected that more stimulation duration (i.e. more stimulation in a certain interval) would be necessary as compared to isolated stimulation. For all these reasons, we used multiple methods to try to prove or disprove our hypothesis.
First, we assessed the overall proportion of 60-min bins that contained at least one SD and compared the number of manipulations within those bins. Since we used a one-minute sampling period, this can also be thought of as assessing the number of minutes with at least some type of manipulation. These were non-overlapping consecutive bins. Only bins with complete data for both variables were included. These two frequency distributions were compared using the Kolmogorov–Smirnov two sample test. This approach was performed to assess whether more frequent stimulation was associated with increased risk of SD. In the study by Von Bornstadt[4], SD was only initiated after several minutes of continuous stimulation. The effect of more stimulation burden would be expected to have a larger impact compared to more isolated stimulation events.
In order to attempt to generate an inference of the effect of more manipulation, we used logistic regression to assess the risk of SD with increased frequency of manipulation within non-overlapping 60-min bins. Mixed effect modeling was used, treating each subject as an independent variable in order to account for bias related to repeated within-subject measures.
In order to assess the possibility of time latency from stimulation to subsequent triggered SD, shifting cross-correlation analysis was performed. For each subject, the time series data manipulation stream (video scoring) was lagged in one-minute intervals and the correlation between SD and stimulation at that latency was assessed. Shifting the SD in the negative direction would “correct” for a possible latency from stimulation to subsequent, triggered SD only if they occurred in a predictable, repeating pattern after stimulation. Shifting in the positive direction serves as an internal control (i.e. ruling out that any association could be due to SD occurring before stimulation). We assessed the Pearson correlation coefficient per subject and overall for each shifted interval and displayed the results using a heat map.
This approach provided relevant descriptive data in order to perform subsequent inferential assessment. Given that the effect of increased correlation appeared to last for nearly one hour (Fig. 3), we chose this time as a reasonable sampling time to determine whether there was an increased risk of SD after stimulation. For each subject we used each minute of data and determined if there was stimulation versus no stimulation (independent variable). For each minute, we then assessed the risk of SD (dependent variable) in the subsequent 60 min using logistic regression. Though inter-observer reliability was very good, we sought to further increase the rigor of this approach by assessing only stimulation times that were scored by both reviewers compared to times scored as no stimulation by both reviewers. In other words, the discordant times were not factored into this analysis. This still left > 2000 observations in all subjects due to the prolonged monitoring times. To combine data between subjects, we used mixed effect modeling. Using this approach, we can assess whether or not there is an increased risk of SD after stimulation compared to no stimulation and also assess the weather stimulation could be protective against subsequent SD.
In order to assess the effects of individual subtype of stimulation, the types of stimulation as assessed above were reviewed. In order to be the most restrictive of subtype, we considered only times when both reviewers scored the stimulation subtype. As above, we performed logistic regression for each minute to assess the risk of SD in the following 60 min using mixed effect modeling. In this analysis, we only assessed homogeneously scored subtype versus no stimulation. For example “both reviewers scored suction versus no stimulation”. We repeated this analysis for “positioning”, “suction”, “any light touch”, “ipsilateral light touch”, and “contralateral light touch” (both of these relative to the side of the electrode strip and craniotomy.)
Data handling and display was performed with MATLAB (vR2020b). Statistical analysis was performed using SAS (v9.4).
Availability of data and materials
Data available upon reasonable request, subject to institutional and IRB oversight policies
Change history
19 May 2022
A Correction to this paper has been published: https://doi.org/10.1007/s12975-022-01037-0
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Acknowledgements
Adarsh Vangala, Breannan Howell, Saul Fernandez, Emma Brandt, and Zainab Cheema for video scoring. Li Luo and Mark Krasberg for developmental statistical analysis Yiliang Zhu, Richard A Campbell for advisory support. Medical Illustration by Yvonne Wylie Walston.
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National Institutes of Health grant P20 GM109089 (APC, CWS); National Institutes of Health grant NS 102978, 104742 (KCB).
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Carlson, A.P., Davis, H.T., Jones, T. et al. Is the Human Touch Always Therapeutic? Patient Stimulation and Spreading Depolarization after Acute Neurological Injuries. Transl. Stroke Res. 14, 160–173 (2023). https://doi.org/10.1007/s12975-022-01014-7
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DOI: https://doi.org/10.1007/s12975-022-01014-7