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Record W4404914197 · doi:10.1097/ana.0000000000001013

Abstracts From the 52nd Annual Meeting of the Society for Neuroscience in Anesthesiology and Critical Care, September 12-14, 2024

2024· article· en· W4404914197 on OpenAlexaboutno aff

Bibliographic record

VenueJournal of Neurosurgical Anesthesiology · 2024
Typearticle
Languageen
FieldNeuroscience
TopicAnesthesia and Neurotoxicity Research
Canadian institutionsnot available
Fundersnot available
KeywordsMedicineAnesthesiologyNeuroscienceAnesthesiaPsychology

Abstract

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Risk Factors for Chronic Dysphagia after Anterior Surgical Decompression for Degenerative Cervical Myelopathy: Results of the Multicenter, Randomized, Controlled, Phase III, CSM-Protect Clinical Trial Alex B. Bak, Ali Moghaddamjou, Michael G. Fehlings University of Toronto, Toronto, Canada Introduction: Early dysphagia is a common complication after anterior cervical surgery for degenerative cervical myelopathy (DCM). However, factors associated with the development of chronic postoperative dysphagia remain unclear. Chronic dysphagia can have devastating effects on patient quality-of-life, satisfaction, and contribute to malnutrition. The goal of this study was to evaluate the natural history of dysphagia after anterior surgery for DCM and to identify factors associated with chronic postoperative dysphagia. Methods: This ambispecitve cohort study included adult patients who received anterior decompressive surgery for DCM between 2012 to 2017 across 16 university-affiliated sites as part of the prospective, randomized CSM-Protect clinical trial. Presence and severity of dysphagia was assessed with the Bazaz scale, which grades patients’ dysphagia as none, mild, moderate, or severe based on frequency and type of food or liquid ingested. Latent class trajectory modelling (LCTM) was applied to classify patients into distinct trajectories based on their logitudnial Bazaz scale scores over the initial 1yr after surgery with time points at baseline, 1mo, 6mo, and 1yr. Predictors of recovery trajectories were identified using descriptive statistics and multivariate logistic regression with odds ratios (ORs) and 95% confidence intervals (CIs) on demographic and surgical variables. Results: From a total of 290 patients, 132 subjects met the eligibility criteria. Preoperatively, 11.4% of patients had moderate dysphagia, which peaked to 19.7% at 1mo with 7.6% developing severe dysphagia. This rate decreased to 11.4% of moderate and 3.8% of severe dysphagia at 6mo and further to 10.6% and 3.0%, respectively at 1yr. From this raw data, two distinct cubic trajectories for postoperative dysphagia were identified. Their polynomial course was classified as: 1) resolved early dysphagia (n=112, 84.9%), described by an early development of mild dysphagia by 1 month and rapid, complete resolution of symptoms by 6mo; and 2) chronic dysphagia (n=20, 15.1%), described by a development of mild to moderate dysphagia by 1mo and continued or worsening symptoms at 1yr. Demographically, older patients and male sex were associated with the resolved early dysphagia trajectory. Conversely, pertaining to comorbidities, patients with a history of psychiatric disorders such anxiety and depression was associated with chronic dysphagia trajectory. Additionally, presenting with gait impairment and having a stenotic cause due to hypertrophied ligamentum flavum was associated with unresolved dysphagia at 1yr. Conclusions: More than one in eight DCM patients that underwent anterior cervical surgery reported unresolved dysphagia of moderate or greater severity at one year. Younger patients and those with pre-existing anxiety and depression were more likely to report subjective long-term symptoms of dysphagia. Our findings lend support to the existence of a heterogenous group of patients wherein the customarily reported pattern of resolved early postoperative dysphagia may not apply. Relationship Between Pain and Functional and Health-related Outcome Measures in Degenerative Cervical Myelopathy: Results of a Prospective, Multicenter Dataset of 914 Patients Alex B. Bak, Ali Moghaddamjou, Michael G. Fehlings University of Toronto, Toronto, Canada Introduction: While pain is increasingly regarded as a top recovery priority by patients living with degenerative cervical myelopathy (DCM), this outcome has been under-recognized and understudied. Pain can be a driver to seek surgical intervention particularly in individuals with mild DCM. To address this gap, we examined the relationship between pain and other functional and health-related outcome measures in DCM. Methods: We identified patients who underwent surgical decompression for DCM from the prospective, multicenter AOSpine CSM-NA, CSM-I, and CSM-Protect trials. Outcomes were modified Japanese Orthopedic Association (mJOA) score, Nurick classification, Short Form 36 (SF36) Physical Component Summary (SF36-PCS), and SF36 Mental Component Summary. Pain was prospectively assessed using Neck Disability Index Pain Intensity (NDI-PI) score preoperatively, and at 6mo and 1yr follow up. Pain intensity was categorized as minimal (NDI-PI=0 or 1), moderate (NDI-PI=2), and severe (NDI-PI>2). Correlation between pain intensity as a continuous variable and outcome measures at each timepoint, as well as their changes at 1yr from baseline was described with Spearman’s ρ and P values. Correlation between change in pain and rate of minimum clinically important difference (MCID) for mJOA, SF36-PCS, and SF36-MCS was described with Pearson’s correlation coefficient r and P values. Results: Of 914 eligible DCM patients, 32.2% had severe preoperative pain, 29.1% moderate pain, and 38.7% had minimal pain. Pain intensity was poorly correlated with mJOA and Nurick preoperatively and all follow-up time points. SF36-PCS and SF36-MCS was significantly and moderately correlated with pain at all time points. Changes in mJOA was poorly correlated with changes in pain (ρ=−0.12; P<0.001) as was Nurick grade (ρ=0.15; P<0.001). Changes in patient-reported outcomes of SF36-PCS was significantly and fairly correlated with changes in pain (ρ=−0.37; P<0.001) as was SF36-MCS (ρ=−0.26; P<0.001). Changes in pain was poorly correlated with reaching MCID of mJOA (r=−0.10; P=0.152), but moderately correlated with reaching MCID for SF36-PCS (r=−0.29; P<0.001) and MCS (r=−0.22 P=0.001).In a subset of 156 mild DCM patients, 23.1% reported severe preoperative pain, 29.5% reported moderate pain, and 47.4% had minimal pain. The pain groups did not differ in demographic, medical, or procedural variables. Patients with greater pain was associated with lower self-reported preoperative mental health and physical functioning, but not preoperative Nurick or mJOA scores. Correlation trends were similar to the total DCM cohort. Conclusion: There is a high prevalence of preoperative pain in DCM patients who undergo surgery. The clinician-administered mJOA and Nurick classification are poorly correlated with pain and insensitive to changes in pain, postoperatively. Patient-reported outcomes of the Mental and Physical Component Summaries of the SF36 were moderately and significantly correlated with pain and changes in pain, postoperatively. Plasma GFAP and GAD65-Ab: new biomarkers for attention deficit hyperactivity disorder pathology Li-Min Zhang1, Hui-Tao Miao1, Yu-Dong Shan1, Ting-Ting Liu1, Dong-Xue Zhang2, Wei-Juan Gao3 1Hebei Province Cangzhou Hospital of Integrated Traditional and Western Medicine, Cangzhou, China. 2Cangzhou Central Hospital, Cangzhou, China. 3Hebei University of Chinese Medicine, Shijiazhuang, China Background Attention deficit hyperactivity disorder (ADHD) is a prevalent neurodevelopmental disorder in children of school age. In mice with ADHD, glial fibrillary acidic protein (GFAP) levels were significantly higher, whereas glutamic acid decarboxylase 65 (GAD65) levels were lower. The goal of this study is to look at the potential function of GFAP and GAD65 antibodies (GAD65-Ab) in mice and children with ADHD by assessing GFAP and GAD65-Ab levels in the blood. Methods An ADHD model was established in pregnant mice with 15 mg/kg of S-ketamine administration using intraperitoneal injection for 5 days from G14 to G18. Children were enrolled if they met in ADHD Rating Scale (ARS) in DSM-5 criteria for ADHD based on clinical interviews. Venous blood was obtained from children and mice under aseptic conditions and the serum was centrifuged and preserved. Clear supernatants from mice and children were processed simultaneously in duplicate, side by side, for ELISA assay with the calibrators supplied in the GFAP and GAD65-Ab kit. Results In mice with ADHD-like behaviors, there was a strong positive connection between serum GFAP levels and open-arm times in the elevated plus maze, which corresponded with the association between serum GFAP levels and hyperactivity-impulsivity ratings The of serum GFAP levels as an for of ADHD was to be based on the a of and a of the under the was Additionally, we that in mice ADHD-like behaviors, a in time was to an in blood GAD65-Ab an of there was a between scores and serum GAD65-Ab levels r The support the that elevated blood levels of GFAP and GAD65-Ab may be in the of ADHD in children and that levels may be correlated with the severity of ADHD in of of and blood of and surgical of with have been to lower This report of a patient with of and and the of with a underwent The was by of the and and an of and were of with a high of was and the was elevated to using The patient was to the for and the elevated a was as the and was continued to of was and was in the of two of other of to The but to to and the blood was with a of the which the of for The and were and respectively and the to 5 and the surgery. The patient and was to the was from the had lower physical other after of and has not been In to and is to lower and of are in and an to other of which may time to by the is This was part of a to after of and the of have been and for surgical time is of the measures to but are not to of the and the of other of are may be more in in mild in mice of Hui-Tao Miao1, Li-Min Zhang1, Dong-Xue 1Hebei Province Cangzhou Hospital of Integrated Traditional and Western Medicine, Cangzhou, China. Cangzhou, China. Hospital of China. Central Hospital, Cangzhou, China that depression is a common mental health In a we identified that changes in a model of and However, there is of the potential of in depression under This study to and potential in such between Methods: mild in We assessed and changes at and using severity scores and potential Results: Our findings that with and significantly to the of and Additionally, that in and in in the with findings the potential of the of in under greater effects in mice to Conclusion: a in mice to mild to the of the in with the of The of and on Outcomes in of Medicine, University of Western and of Clinical University of Western and Canada Introduction: is a and on patient surgical and the individuals the surgery. is as a in surgical has the of on patient the of understudied. We a cohort study to the of on in surgery. Methods we included all adult patients who underwent surgery at the from to was from the and and were examined as The outcome was logistic regression was to the association with of patients’ surgical and The outcomes included patient recovery measures such as pain score, time to of and Results: total of with complete were included for and surgical were in total of were in The of the is in 1 and a from to year. a and high were associated with in The odds were P<0.001) and Conversely, and of and The of high in was more in than their as in In to the in patients by and a The were and patients who were and to the those under the of criteria score significantly with an coefficient of to and of were to the Conclusion: In this study the of and to a in in surgery. Our is to and the of having a with high study based on the of one in and for as a may further and potential in clinical for Introduction: Methods of are with the However, the of patients we obtained from a of patients presenting with who underwent Our was functional outcome as by at Our included at time to time to total score, of total of time blood of and of severe Methods: of an of patients presenting to the University of with who underwent between and were patients were included in the Results: Patients in each group were similar in of and were in the group to the group In times in the group were to the to time to time and total procedural time were for patients who underwent as were total times were not significantly between the two groups were not significantly between the two groups scores were similar between the two groups the of as a score of or was in the group of blood and of severe blood were significantly in the group and were to be of but type was The type of at for a is after between the and the We that the baseline of and were similar between the and was greater in patients for baseline of and we that there was difference in of at to we there was difference in or at We that were to had a time to as well as a total This is to other that patients under to and were to be in the to or we this was in the We that patients under were significantly more likely to be or the patients had a more and blood However, a of difference in long-term we that are a is a from in a clinical as well as individuals in The have an and to be There is a for of for and on the part of are for in of are a with for and by a for with are a of health to the have been in such The important is which to a by of of and The for an important between to the and patient with the of difference in between is by the of that can for and The this other by a of of in are or of and the of The in development and after as a strong of and the of for This was established in of and the by was in and the group a of in at the time of this was a of this have had in the as and a This is of in their In the for the in was with an to the of a In to in clinical and in and This as the which the for development in was this but the has had from this were who as a to be in and a in their of have their of development in of the not as and but in the Conclusion: development and of is an important as of by in if this was not the for the the of for of and in Patients of Medicine, Introduction: and is a common surgical such as and has have been across surgical to for such is a Our study at the of in patients who underwent at and received preoperative for Methods: This study the of patients who underwent were into two group and The groups were score based on history of and groups were for outcomes of in after surgery. outcomes included type of and of in postoperative was using logistic and regression for and continuous Results: We identified patients that met the criteria in group and in and were similar between the two groups history of and administration which were to be in group However, were not to be of Our that group had a decreased of in the was not The of was between the two groups which was significantly decreased in the group In study the of did not to a in the of or of the of for of in patients but the of study are similar to those was with or was with and and with a of and prospective, be to if or more are in patients of early after for a cohort study and Hospital, Introduction: that the rate of early after between The in of patients in to this early is for patient the of and and may to postoperative the to identify for early after clinical and and surgical blood of early The that in clinical of and course of the may the to early after more than Methods: a follow-up to the we to a cohort We that the of of early after in is and to be In the study to the is the rate of early after are the and surgical factors associated with early after logistic regression be to groups using a of on and a of with of early be identified using logistic regression The to the under the Conclusion: The of this of is to identify and surgical of early after in The findings of study be to multicenter on this The of on the of after surgery in patients with a of and Pain Medicine, University Hospital, Introduction: have that may blood in patients with surgery. This study the potential association between and of postoperative in adult patients with Methods: We and of adult patients with who underwent surgery between and In patients were included in the The was to and multivariate logistic regression were to identify factors for postoperative Results: The rate of postoperative was of was associated with an of postoperative with of and of 95% confidence odds 95% 95% and a history of and 95% were identified as factors Conclusions: In patients with administration is associated with an of postoperative the of the of in patients with a for surgery in patients with changes for The of of and Introduction: We in the of is the we other the and in surgical We be an part of the In this prospective, we to the changes in blood using of in by in The study has been in the Clinical of the the of the of in The was by the and demographic patients of to physical were for the The and were at the time points in the the of the the of a 1), was at after but at of after but The time of from was with other as the study Results: The of for was There was a in and after This after of the The of patients with an in of more than a from There was correlation between the of and and minimum Conclusion: of as a for the to the recovery from after randomized are to 1 in this of a with a cervical University of Introduction: The of surgery in is of and for be further in that intervention to We the of a with an cervical and of This the of and we a to and that patient outcome at with a history of worsening and pain, and of the in with and of a from to the of the symptoms and a and to with under was to in for or with and the due to for with new and of a The an to cervical and the The of included worsening symptoms or to and the of for included an goal for and a total to and and were and after and surgery. after an the patient underwent a surgical time of was with and surgical to of The included an with goal but and with and the patient had and of but in all was on postoperative 5 with continued This patient had a outcome in the of a cervical points the of in the of this cervical and and under using and that can identify functional to into the the of Additionally, there were between and that were the and the that the elevated Our a to this for and that was by on effects after in of and University of Medicine, and all to after an of of the may be has been reported that to functional outcome in mice after In this the effects of after of in on outcome and were Methods: were with in and to The were to and groups by The was to group and was 15 after for were to from after The were for rate and outcome using a 2) at and days after were outcome at days was assessed by and and levels on the after were using of in each by an assay was between and to from were by are as and was by the was to Results: in the group for the and of in the group did not score on the in the group to be lower than that in the group scores at days and total were similar in the two groups 16 in the group was of that in the group in the group was of that in the group However, the difference was not and of and were similar in the two groups Conclusion: significantly the rate in However, and outcomes were not significantly the of to may but be to functional of for Patients with University of Canada Introduction: is as a for due to of of and The Hospital in patients with we report of for patients with a look at patient and complication Methods: This was under a from the We a of adult patients with of or greater who have surgery for of or under between and Patients who had intervention or such as for a were from this We baseline demographic clinically of such for of and The were for postoperative and Results: Between and a total of patients were with an of of patients had a greater than of the patients had a at the time of surgery. patients received a of and for patients received as patients received which were by the in the of a modified or patients the of or the to the surgery. patients intervention in the or to or patients their one due to worsening of their the other days in of their of Conclusion: of in patients with are to To the of this of patients with using is the of The rate of intervention of and to in is similar or lower to the described in the for for patients Our findings that patients with can undergo under and that in and of not be a for this of the of and using the of Introduction: is common in patients with or However, conditions reported with of such as with and for is This patient groups with and in patients, and as well as that may we identify patients that may from a Methods: was with from with were identified by the of for or were that of a or and that is to if were and were identified with and of were The of in this was by the for patients with from the of those with included The of patients in this group was patients were male and identified as with and other The the demographic across the that with than using for we on that included or Of was as the common and were to patients with were reported in of all with that the a for was reported in The total of with is which to patients with associated with of The total of for patients is with and in an associated with of on this an of In to and we with of which may the of such as Conclusions: the of this that in the there are which the and patient associated with Our of the that the conditions may be for Patients from as well as patients with may be for early In the and that may from development of an and be a to conditions and of on of in Trial of and Background is the complication of of to to Our was to evaluate the of on in patients with by and adult patients with were enrolled over one in this prospective, In group was to a of for of 5 In group was to a of were for Patients were for or of and levels of serum were Outcomes were assessed using at and at 1 and Results The of and was in group as to In the patients who did the with more severe was in the group of were in the was significantly in group at Outcomes at and and were in the The of was lower in those who received the of in is a and intervention in patients with of in in Introduction: are for continuous in the and in patients, for blood and The common are the and is a with is one of which in patients with is a for Methods: We report a of a a to a and a was under as the on were for the at on the side and on the side, with on the on we the who the of the with in the and The was and a was a and of the of by the was days and the patient was in a blood blood for and for in surgery and severe and of and are to to patients and factors such as and be to disorders and that may at the is a clinical conditions not but and and surgical at the using a can the and The is the for with reported and to the the has a lower of Additionally, and may in but their in the or is and are that can with due to a of is a for in particularly in patients with who to have a due to the of the by the between the and may be in patients with decreased or or In may can be by in to using as in this Conclusion: with and of the on the in patients with and in a with Introduction: and for particularly in patients with a history of and can have similar clinical can be to from each other or from The of to as well as are and a is of We a with such Methods: We report a of with history of and was for of a for pain in the To the of were and total was In to included Index to not evaluate of but by the to the and were The surgery and the patient was is an disorder associated with by to and or to due to from the in and and and can or The for is the be from conditions such as or symptoms are to those in in a more Patients with history of and may In an study of

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How this classification was reachedexpand

Full frame distilled prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.

metaresearch head score (Codex)0.001
metaresearch head score (Gemma)0.004
Version: codex-gemma-dda1882f352aValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Bench or experimental · Consensus signal: none
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.770
Threshold uncertainty score0.694

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0010.004
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0010.001
Bibliometrics0.0000.000
Science and technology studies0.0000.002
Scholarly communication0.0000.000
Open science0.0010.000
Research integrity0.0000.001
Insufficient payload (model declined to judge)0.0000.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.050
GPT teacher head0.328
Teacher spread0.277 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one teacher head, not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designBench or experimental
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

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Published2024
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