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Separation from mechanical ventilation and survival after spinal cord injury: a systematic review and meta-analysis

Abstract

Background

Prolonged need for mechanical ventilation greatly impacts life expectancy of patients after spinal cord injury (SCI). Weaning outcomes have never been systematically assessed. In this systematic review and meta-analysis, we aimed to investigate the probability of weaning success, duration of mechanical ventilation, mortality, and their predictors in mechanically ventilated patients with SCI.

Methods

We searched six databases from inception until August 2021 for randomized-controlled trials and observational studies enrolling adult patients (≥ 16 years) with SCI from any cause requiring mechanical ventilation. Titles and abstracts were screened independently by two reviewers. Full texts of the identified articles were then assessed for eligibility. Data were extracted independently and in duplicate by pairs of authors, using a standardized data collection form. Synthetic results are reported as meta-analytic means and proportions, based on random effects models.

Results

Thirty-nine studies (14,637 patients, mean age 43) were selected. Cervical lesions were predominant (12,717 patients had cervical lesions only, 1843 in association with other levels’ lesions). Twenty-five studies were conducted in intensive care units (ICUs), 14 in rehabilitative settings.

In ICU, the mean time from injury to hospitalization was 8 h [95% CI 7–9], mean duration of mechanical ventilation 27 days [20–34], probability of weaning success 63% [45–78] and mortality 8% [5–11]. Patients hospitalized in rehabilitation centres had a greater number of high-level lesions (C3 or above), were at 40 days [29–51] from injury and were ventilated for a mean of 97 days [65–128]; 82% [70–90] of them were successfully weaned, while mortality was 1% [0–19].

Conclusions

Although our study highlights the lack of uniform definition of weaning success, of clear factors associated with weaning outcomes, and of high-level evidence to guide optimal weaning in patients with SCI, it shows that around two-thirds of mechanically ventilated patients can be weaned in ICU after SCI. A substantial gain in weaning success can be obtained during rehabilitation, with additional duration of stay but minimal increase in mortality. The study is registered with PROSPERO (CRD42020156788).

Background

Spinal cord injury (SCI) is a dramatic and life-changing event. The prevalence of traumatic SCI was reported to be between 236 and 4187 (with a most likely estimate around 500) cases per million worldwide[1, 2]. More than 75% of these traumatic injuries occur in subjects under 45 years of age, the majority of which being between the age of 16 and 30 [3, 4]. When the origin is non-traumatic, the most common causes are age-related conditions, including tumors, vascular/inflammatory diseases, and degenerative affections [5, 6].

It is estimated that more than 90% of all traumatic cervical SCIs require intubation, a majority of them require a tracheostomy, and up to 40% of the patients with complete cervical lesions remain ventilator-dependent [7, 8]. Despite many advances in the management of patients with SCI, mortality for individuals who are ventilator-dependent remains very high [9, 10]. Life expectancy largely depends on the possibility to wean them off the ventilator, as do health care expenses and quality of life [4, 11, 12].

Despite the crucial role of mechanical ventilation, studies looking at specific approaches to weaning from mechanical ventilation in SCI are scarce and published research on the topic mainly consists of retrospective observational studies and small case series [13]. The existing guidelines on respiratory management after SCI are mainly focused on non-critically ill patients [14, 15]. The probability of weaning success remains difficult to predict; no previous systematic review or meta-analysis has been conducted on the topic, and no societal guidelines or recommendations on weaning are available for this population [16].

Our aim was to investigate the probability of weaning success, duration of mechanical ventilation, mortality, and their predictors in mechanically ventilated adult patients with SCI.

Methods

We conducted this review in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses [17]. The protocol was registered in the International Prospective Register of Systematic Reviews (PROSPERO; CRD42020156788). Ethics approval was not required because all study data had been previously published and, in this study, we did not include any individual patient data.

Eligibility criteria, literature search, study selection

We conducted a systematic literature search from inception to August 2021 to identify studies enrolling adult patients (≥ 16 years of age) with SCI (at any level and from any cause, including traumatic and non-traumatic) who required mechanical ventilation, and evaluating at least one of the 3 following key outcomes: probability of weaning success, duration of mechanical ventilation, or mortality. Studies enrolling both ventilated and non-ventilated subjects were included if characteristics and outcomes of ventilated subjects could be extracted separately, or if non-ventilated subjects represented a minority (< 20%) of the study population. Case reports and case series with fewer than 10 participants were excluded. Studies enrolling > 20% of subjects under 16 years of age whose outcomes were not separable from the remaining study population were also excluded, according to usual recommendations [18].

The following six electronic bibliographic databases were searched using a comprehensive search strategy developed by one of the authors (DL), an information specialist who has expertise in database searching: OVID Medline, CINAHL, the Cochrane Central Register of Controlled Trials and the Cochrane Database of Systematic Reviews, Ovid Embase and Scopus (Additional file 1: Appendix S1).

Outcomes

The primary outcome was the probability of weaning success (complete and partial liberation from the ventilator). The secondary outcome was either time to reach liberation from the ventilator or duration of mechanical ventilation, according to each study analysis. Additional secondary outcomes included mortality at any time point, intensive care unit (ICU) or rehabilitation unit lengths of stay (according to each study setting), hospital length of stay, and probability of tracheostomy and decannulation. Factors associated with the probability of weaning-related outcomes (weaning success and duration of mechanical ventilation) were also assessed.

Studies conducted in ICUs and studies conducted in rehabilitation units were analyzed separately, given the differences in these study settings.

Data extraction and quality assessment

Each title and abstract were screened independently by two reviewers. Full texts of all the articles identified as relevant by either reviewer were then assessed for eligibility. Pairs of authors, independently and in duplicate, reviewed and selected studies meeting inclusion criteria and extracted data using a standardized data collection form (Additional file 2: Appendix S2). Consensus on extracted data was reached by discussion, and disagreements were resolved by arbitration with a third author. The same authors evaluated the quality of included studies using the Newcastle–Ottawa Scale [19, 20].

Statistical analysis

The complete statistical analysis is detailed in the Supplemental Digital Content.

For each study mean values and standard deviations (SDs) were preferred where available. In their absence, available measures including medians, ranges and 1st–3rd quartile intervals (Q1-Q3) were used to estimate sample means and SDs [21, 22]. For studies reporting values for subgroups only, the overall estimates were computed according to the Cochrane handbook guidelines [23].

The R package “meta” was used for all meta-analytic computations and plotting [24]. Synthetic results are reported as meta-analytic means for continuous variables, and both as crude proportions and meta-analytic proportions, for categorical variables. To incorporate between-study heterogeneity [25], all analyses were performed using random effects models [26].

A 95% study confidence interval (95% CI) was evaluated for all characteristics and outcomes through the standard normal distribution for meta-analytic means and according to the Clopper–Pearson method for meta-proportions [27]. Study weights were generated using the inverse variance method. Heterogeneity among studies was assessed by visual inspection of the forest plots, using the I2 statistic (threshold level for significant heterogeneity: ≥ 50%), Cochran’s Q and the Chi-squared test for homogeneity (significance level for heterogeneity: p < 0.1)[28].

Predefined subgroup analysis (significance level α = 0.05) was performed dividing studies conducted in ICUs vs rehabilitative settings.

All statistical analyses were performed using R (version 4.0.3) [29].

Results

Literature search and study characteristics

The search strategy identified 4443 records that were screened for eligibility. Eighty-two full-text articles were assessed and 43 were excluded (Fig. 1). Thirty-nine studies were finally included in the systematic review.

Fig. 1
figure 1

Flowchart of the study selection process according to PRISMA (www.prisma-statement.org)

The characteristics of the studies are reported in Additional file 1: Tables S1 and S2. The majority of the studies (26, 67%) were published in SCI or trauma journals, 7 (18%) in surgical journals, 4 (10%) in rehabilitative and 3 (8%) in critical care/general medicine journals. Six studies were multicentric [30,31,32,33,34,35], 33 were conducted at a single site [8, 12, 36,37,38,39,40,41,42,43,44,45,46,47,48,49,50,51,52,53,54,55,56,57,58,59,60,61,62,63,64,65,66]. Most studies were conducted either in Level I [8, 37, 42, 46, 57, 61, 63, 66] or in unspecified trauma/SCI treatment centers [12, 31, 35, 36, 38, 39, 41, 43, 47, 48, 50,51,52, 55, 59, 62, 65]. Twenty-five studies were run in ICUs [12, 30,31,32,33, 35,36,37,38,39,40,41,42,43,44, 46, 57, 59,60,61,62, 64,65,66], 14 in rehabilitative settings [34, 45, 47,48,49,50,51,52,53,54,55,56, 58, 61] (Additional file 1: Table S1). In 8 studies the cause of the injury was not specified [33, 43, 47, 49, 51, 53, 54, 58], all the remaining studies enrolled traumatic SCI patients, 2 of them [55, 61] enrolled both traumatic and a few non-traumatic patients, whose outcomes were not separable. Among the studies focusing on traumatic SCI, 6 excluded patients with concomitant traumatic brain injury [30, 32, 40, 60, 62, 66], 1 excluded patients with multiple spinal cord lesions [65] and 1 excluded patients with concomitant extra-spine lesions [33].

Quality of included studies is reported in Additional file 1: Table S3.

A total of 14,637 patients were enrolled (13,763 in ICU, 874 in rehabilitation units), 80% of them were male and their mean age was 43 years [95% CI 41–45]. The mean time from injury to hospitalization was 8 h [95% CI 7–9] for studies conducted in ICU, 40 days [95% CI 29–51] for studies performed in rehabilitative units (Additional file 1: Tables S1, S4). Compared to patients hospitalized in ICU, patients admitted to rehabilitation units were more frequently male (84% vs 79%, p = 0.029), had more assault lesions (11% vs 1%, p < 0.0001), and more high-level (C3 or above compared to C4 or below) lesions (55% vs 14%, p = 0.0003). Other baseline characteristics of patients enrolled in each ICU or rehabilitative study are summarized in Additional file 1: Table S4.

Primary outcome: probability of weaning from mechanical ventilation after SCI

Twenty-four studies (10 conducted in ICU and all the 14 studies conducted in rehabilitative wards) assessed the probability of complete liberation, and 6 the probability of partial liberation from the ventilator (Additional file 1: Table S2). The crude and meta-analytic proportions of complete and partial weaning are reported in Table 1 and Fig. 2. 63% [45–78%] of the patients hospitalized in ICU were completely separated from the ventilator; 72% [51–86%] of the patients admitted to a rehabilitative ward were completely, and 82% [70–90%] were either completely or partially liberated from the ventilator.

Table 1 Main outcomes after injury
Fig. 2
figure 2

Forest plots for the outcome of complete liberation from the ventilator (left panel) and for the outcome of partial or complete weaning after rehabilitation (right panel). Studies are presented according to setting classification (intensive care units vs rehabilitation units): both overall and subgroup estimates are reported. Number of events and total number of patients at risk are reported for each study. The computation process has been described in the Methods. CI: confidence interval

Most studies provided no definition of weaning success/failure, and studies that reported it widely differed in their criteria; when the definition of partial weaning was provided, analogous variability was also present (Additional file 1: Table S5). The majority of the studies did not mention the use of any weaning protocol [8, 12, 31, 33, 34, 42, 47, 49, 52, 57, 61]; two studies mentioned the use of a protocol without specifying it [48, 64]. For the remaining 10 studies, the most frequently weaning protocol was a progressive increase in ventilator-free breathing, with mild variations among the studies, including unassisted breathing until tired or graded time off the ventilator [45, 50, 58, 65]; unassisted breathing alternated to periods of intermittent mandatory ventilation, continuous positive airway pressure [43] or pressure support ventilation [46, 51, 56]; non-invasive ventilation with the tracheostomy sealed [53,54,55,56]. Only 2 studies provided information on the number of patients requiring one/two or more than two weaning attempts [16, 65], and only 3 studies reported the number of patients failing extubation [31, 57, 65].

The application of rehabilitation protocols was mentioned in 5 studies and involved respiratory and physical rehabilitation [46, 56, 60], respiratory therapy [65] and respiratory muscle training [45].

Secondary outcomes

The number of mechanical ventilation days was assessed in 14 ICU and 8 rehabilitative studies; the probability of tracheostomy in 27 studies (19 in ICU, 8 in rehabilitation), of which 10 (3 in ICU) assessed the probability of decannulation. Incidence of pneumonia was evaluated in 14 ICU and in 7 rehabilitation studies, mortality in 25 (20 ICU and 5 rehabilitation) studies (Additional file 1: Table S2).

In ICU, the mean duration of mechanical ventilation was 27 days, length of stay 23 days, hospital stay 44 days. 81% of patients were tracheostomized and 30% of them were decannulated. Incidence of pneumonia and mortality were 40% and 8%, respectively (Figures 3 and 4, Additional file 2: Figure S1, Additional file 3: S2, Additional file 4: Figure S3, Additional file 5: Figure S4. Additional file 6: Figure S5, Table 1).

Fig. 3
figure 3

Forest plot for the outcome of duration of mechanical ventilation in intensive care units and rehabilitation units (upper panel). Studies are presented according to setting classification (intensive care units vs rehabilitation units): both overall and subgroup estimates are reported. Forest plots for the outcome of duration of mechanical ventilation for rehabilitation units (including the time to admission to rehabilitation) (lower panels). Weight refers to the relative contribution of each study to the meta-analytic estimate and is generated using the inverse variance method. CI:  confidence interval

Fig. 4
figure 4

Forest plot for mortality. Studies are presented according to setting classification (intensive care units vs rehabilitation units): both overall and subgroup estimates are reported. CI: confidence interval

Patients hospitalized in rehabilitation centres were ventilated for a mean of 97 days (including duration of mechanical ventilation prior to admission and during the stay in rehabilitation, Fig. 3) and stayed in the unit for 78 days. All patients were tracheostomized and 83% of them were decannulated; 36% developed pneumonia, and less than 1% died (Fig. 4, Additional file 2: Figure S1, Additional file 3: S2, Additional file 3: Figure S3, Additional file 5: Figure S4. Additional file 6: Figure S5, Table 1).

Predictors of weaning and duration of mechanical ventilation

Variables identified as predictors of weaning failure and duration of mechanical ventilation across the studies are reported in Additional file 1: Tables S6 and S7, respectively. Among all the variables considered as predictors in the different studies, we reported those that we considered clinically relevant to the outcome. A high number of comorbidities, high Injury Severity Score, high-level lesions (C1–C3 vs C4–C7), elevated heart rate, and presence of tracheostomy appeared to be associated with increased odds of weaning failure. Shorter time to admission to a specialized SCI center, high-level lesions (C1–C4 vs C5–C8), complete lesion, low tidal volume and high positive end-expiratory pressure within 24 h from admission, and presence of tracheostomy were associated to a longer duration of mechanical ventilation.

Heterogeneity and sensitivity analysis

Data regarding heterogeneity among studies and in each subgroup are reported in Additional file 1: Table S8.

The post hoc sensitivity analysis excluding the two largest studies (Branco et al. [32], 5256 patients and Anand et al. [35], 5980 patients) did not show any difference in the duration of mechanical ventilation, proportion of tracheostomy, ICU or hospital length of stay, or mortality (Table 1, Additional file 7: Figures S6, Additional file 8: Figure S7, Additional file 9: Figure S8, Additional file 10: Figure S9, Additional file 11: Figure S10).

Due to a lack of studies reporting separate outcome data, we were unable to perform additional subgroup analyses considering the level and cause (traumatic vs non-traumatic) of spine lesion to predict the outcomes of interest. However, among the overall patients included in our study, 12,717 (87%) were retrieved by studies dealing with cervical lesions only, and of the remaining patients with mixed lesions, 1365 out of 1843 still had cervical lesions (Additional file 1: Table S4). Therefore, a potential analysis including only patients with cervical SCI was hardly expected to yield results substantially different from the overall analysis.

Discussion

In this systematic review and meta-analysis, we found that around 63% of patients were completely weaned from mechanical ventilation in ICU after SCI, and up to 82% of the previously unweaned patients were either completely or partially liberated from the ventilator during rehabilitation. This further gain in weaning required a longer time on the ventilator and tracheostomy, but was achieved without an increased risk of pneumonia or mortality.

Probability of weaning in ICU

The proportion of patients that were weaned in ICU varied widely among the studies, ranging from 16% [46] to more than 97% [65]. The blurred and heterogeneous definitions of weaning success across the studies make the interpretation of these findings complex. Factors likely to impact on this variability include SCI level and completeness of injury, presence of multiple spinal cord lesions, and concomitant traumatic brain injury [7]. The role of these factors is supported by the fact that some studies showing a high probability of weaning success did not include patients with SCIs higher than C3 [65], while studies reporting lower probabilities included them [8, 42, 46]. A role of these factors is also consistent with the exclusion of patients with multiple SCIs and traumatic brain injury in the studies that resulted in better weaning outcomes [65] and fewer ventilator days [30, 32, 66]. A lack of disaggregated subgroup data prevents from further investigation of these associations and identification of predictors of weaning outcomes. Univariate and multivariate regression analyses performed in some of the included studies [30, 31, 36, 37, 46, 63,64,65] also suggest a possible role of the severity of the lesion/trauma (reflected by the presence of a complete lesion, a high-level lesion and high Injury Severity Score), of a late transfer to a specialized acute SCI center, of clinical conditions on ICU admission (elevated heart rate, low tidal volume and high positive end-expiratory pressure values—the latter two probably reflecting a more protective strategy of ventilation), of pre-existing clinical conditions (number of comorbidities), and of the presence of tracheostomy in reducing the odds of weaning or increasing the time required to achieve it. However, studies that performed regression analyses were only a minority, the selected variables were not consistent among them, and the pooled estimates that we obtained were in most cases the result of only one or two studies. Therefore, the conclusion that can be drawn in terms of predictors of weaning outcomes are limited. Further studies are needed to better explore the association of clinical variables with weaning outcomes, and to attempt building and validating prediction models for weaning success.

Probability of weaning in rehabilitative units

The probability of partial or complete weaning success in rehabilitation reached 82%, in some cases even attaining the totality of the patients [50, 51]. This elevated probability of successful liberation was achieved despite a greater number of patients with high-level lesions and no difference in the number of complete lesions compared to ICU studies (Additional file 1: Table S4).

There are several potential explanations for the different weaning success probabilities between acute care and rehabilitation units.

First, rehabilitation units may have selected a different population of patients transferred for late mechanical ventilation liberation. The high weaning success rate in rehabilitation units may reflect isolated high cervical SCIs, which are weaned late after resolution of acute flaccid paralysis induced by denervation, and after diaphragm training [3, 67, 68], or lower cervical and thoracic SCI lesions, which may also require prolonged mechanical ventilation, due to impaired pulmonary clearance from loss of abdominal muscle function.

Second, other concomitant injuries hindering weaning success in ICU, such as traumatic brain injury, need to recover before a patient could be transferred to rehabilitation facilities.

Third, the development of ICU-acquired weakness, potentially worsening the effect of the previous two factors, has a possible further additive role in delaying weaning until rehabilitation is started.

Finally, the application of specific rehabilitation and treatment techniques, including mechanical insufflation–exsufflation, aimed at training the respiratory muscles spared by the lesion and clearing secretions, could also favor weaning in rehabilitation units [69, 70].

Secondary outcomes

The proportion of tracheostomy was heterogeneous, reaching unexpectedly low values in a few of the ICU studies [32, 40, 57, 66]. This is surprising considering that these studies enrolled patients with high-level lesions or older than 60 years of age [40], and because patients with SCI, due to a loss of sympathetic and expiratory muscle innervations [71], experience difficulty to clear secretions. The lack of published data and consensus regarding the optimal timing of tracheostomy in patients with SCI could explain the heterogeneity among studies. Concerns regarding the possibility of cross-contamination between tracheostomy and cervical spine fixation surgery sites have historically led to delays in tracheostomy performance [72, 73]. Not surprisingly, tracheostomized patients were found to fail weaning more and have a longer duration of mechanical ventilation. This is consistent with the finding that almost all patients admitted to rehabilitation facilities were tracheostomized.

Heterogeneity was also present in the probability of decannulation (11% to 62% in ICU and 25% to 100% in rehabilitation). This finding probably reflects the lack of published evidence and standardized criteria for decannulation in patients with SCI. Small studies and case series mainly convey the message that decannulation should be assessed on individualized basis, as these patients may never meet the traditional criteria for decannulation [74, 75].

Overall mortality was 6%, 8% when considering only patients admitted within 8 h from the injury, and less than 1% in patients admitted to rehabilitation facilities. This is low, considering life expectancy of ventilator-dependent patients after SCI [9]. One-year survival for ventilated patients with SCI was previously found to be 50%, and 25% for those admitted within 24 h from the injury [9]. Patients’ selection may explain the reduced mortality during rehabilitation since they survived the initial high-risk period in ICU [9], and rehabilitation techniques favoring weaning and reducing respiratory complications might hopefully affect mortality [69].

Incidence of pneumonia in ICU studies was in line with previous data in the acute phase of SCI [71], and was very low in rehabilitation considering the higher number of patients with C3 or above lesions and the longer duration of mechanical ventilation [69, 71].

This systematic review and meta-analysis has several strengths. It is the first systematic review to address the crucial topic of weaning in SCI and to analyze its trend separately, in ICU and during rehabilitation. It relies on a pre-registered protocol, it is based on a comprehensive literature search from inception, and it is based on a high number of patients with relatively low missing data of baseline variables. Limitations include the scarcity of randomized-controlled trials, the heterogeneity in terms of definition of weaning success/failure in the different studies and in whether they applied a weaning or rehabilitation protocol, and the lack of disaggregate data from the included studies that prevented us from performing a number of subgroup analyses.

Conclusions

Approximately two-thirds of the patients admitted to ICU after SCI can be completely weaned off the ventilator. Weaning success can be further enhanced for patients that are admitted to rehabilitation facilities, reaching more than 80% of the previously unweaned cases, with additional days of mechanical ventilation, but no additional infectious respiratory complications or mortality. These findings support the potential usefulness of rehabilitation facilities for ventilator-dependent SCI patients, even with high cervical injuries and after a prolonged ventilation time.

This study also highlights the need to better understand the epidemiology of weaning outcomes in this category of patients, harmonize definitions, and standardize weaning procedures. This would help to elucidate the factors associated with weaning outcomes and better evaluate the role of rehabilitation. In fact, even if the application of rehabilitative techniques in specialized SCI centers, in the acute phase, is an appealing solution to improve weaning outcomes, further data are needed to support it, and to clarify the best timing, setting, and even techniques to adopt in this unique category of patients.

Availability of data and materials

The datasets analyzed during the current study are available from the corresponding author on reasonable request.

Abbreviations

CI:

Confidence interval

ICU:

Intensive care unit

Q1–Q3:

1st–3rd quartile intervals

SCI:

Spinal cord injury

SD:

Standard deviation

References

  1. Lee BB, Cripps RA, Fitzharris M, Wing PC. The global map for traumatic spinal cord injury epidemiology: Update 2011, global incidence rate. Spinal Cord. 2014;52(2):110–6.

    Article  CAS  PubMed  Google Scholar 

  2. Kang Y, Ding H, Zhou H, Wei Z, Liu L, Pan D, et al. Epidemiology of worldwide spinal cord injury: a literature review. J Neurorestoratology. 2017;6:1–9.

    Article  CAS  Google Scholar 

  3. Winslow C, Rozovsky J. Effect of spinal cord injury on the respiratory system. Am J Phys Med Rehabil. 2003;82(10):803–14.

    Article  PubMed  Google Scholar 

  4. DeVivo MJ, Krause JS, Lammertse DP. Recent trends in mortality and causes of death among persons with spinal cord injury. Arch Phys Med Rehabil. 1999;80(11):1411–9.

    Article  CAS  PubMed  Google Scholar 

  5. New PW, Sundararajan V. Incidence of non-traumatic spinal cord injury in Victoria, Australia: a population-based study and literature review. Spinal Cord. 2008;46(6):406–11.

    Article  CAS  PubMed  Google Scholar 

  6. New PW, Rawicki HB, Bailey MJ. Nontraumatic spinal cord injury: Demographic characteristics and complications. Arch Phys Med Rehabil. 2002;83(7):996–1001.

    Article  PubMed  Google Scholar 

  7. Claxton AR, Wong DT, Chung F, Fehlings MG. Predictors of hospital mortality and mechanical ventilation in patients with cervical spinal cord injury. Can J Anaesth. 1998;45(2):144–9.

    Article  CAS  PubMed  Google Scholar 

  8. Como JJ, Sutton ERH, McCunn M, Dutton RP, Johnson SB, Aarabi B, et al. Characterizing the need for mechanical ventilation following cervical spinal cord injury with neurologic deficit. J Trauma - Inj Infect Crit Care. 2005;59(4):912–6.

    Article  Google Scholar 

  9. DeVivo MJ, Ivie CS. Life expectancy of ventilator-dependent persons with spinal cord injuries. Chest. 1995;108(1):226–32.

    Article  CAS  PubMed  Google Scholar 

  10. Shavelle RM, DeVivo MJ, Strauss DJ, Paculdo DR, Lammertse DP, Day SM. Long-term survival of persons ventilator dependent after spinal cord injury. J Spinal Cord Med. 2006;29(5):511–9.

    Article  PubMed  PubMed Central  Google Scholar 

  11. Charlifue S, Apple D, Burns SP, Chen D, Cuthbert JP, Donovan WH, et al. Mechanical Ventilation , Health , and Quality of Life Following Spinal Cord Injury. 2011;92(March).

  12. Watt JWH, Wiredu E, Silva P, Meehan S. Survival after short-or long-term ventilation after acute spinal cord injury: a single-centre 25-year retrospective study. Spinal Cord. 2011;49(3):404–10.

    Article  CAS  PubMed  Google Scholar 

  13. Sheel AW, Welch JF, Townson A. Respiratory Management Following Spinal Cord Injury - Spinal cord injury Rehabilitation Evidence. www.scienceproject.com. 2019;Version 6.:1–72.

  14. Consortium for Spinal Cord Medicine. Respiratory management following spinal cord injury: a clinical practice guideline for health-care professionals. J Spinal Cord Med. 2005;28(3):259–93.

    Article  Google Scholar 

  15. McKim DA, Road J, Avendano M, Abdool S, Côté F, Duguid N, et al. Home mechanical ventilation: a Canadian Thoracic Society clinical practice guideline. Can Respir J. 2011;18(4):197–215.

    Article  PubMed  PubMed Central  Google Scholar 

  16. Füssenich W, Hirschfeld Araujo S, Kowald B, Hosman A, Auerswald M, Thietje R. Discontinuous ventilator weaning of patients with acute SCI. Spinal Cord. 2018;56:461–8.

    Article  PubMed  Google Scholar 

  17. Moher D, Liberati A, Tetzlaff J, Altman DG. Preferred reporting items for systematic reviews and meta-analyses: The PRISMA statement. BMJ. 2009;339(7716):332–6.

    Google Scholar 

  18. Avram A, Matei O, Pintea CM, Pop PC, Anton CA. How Noisy and Missing Context Influences Predictions in a Practical Context-Aware Data Mining System. In: Herrero Á, Cambra C, Urda D, Sedano J, Quintián H, Corchado E, editors. 15th International Conference on Soft Computing Models in Industrial and Environmental Applications (SOCO 2020) [Internet]. Springer Nature; 2021. p. 30. Available from: https://doi.org/10.1007/978-3-030-57802-2_3

  19. Lo CKL, Mertz D, Loeb M. Newcastle-Ottawa Scale: Comparing reviewers’ to authors’ assessments. BMC Med Res Methodol. 2014;14(1):1–5.

    Article  Google Scholar 

  20. Sterne JA, Hernán MA, McAleenan A, Reeves BC, Higgins JP. Assessing risk of bias in a non-randomized study. In: Higgins JP, Thomas J, editors. Cochrane Handbook for Systematic Reviews of Interventions - Version 62 [Internet]. 2021. https://training.cochrane.org/handbook/current/chapter-25

  21. Hozo SP, Djulbegovic B, Hozo I. Estimating the mean and variance from the median, range, and the size of a sample. BMC Med Res Methodol. 2005;5:1–10.

    Article  Google Scholar 

  22. Wan X, Wang W, Liu J, Tong T. Estimating the sample mean and standard deviation from the sample size, median, range and/or interquartile range. BMC Med Res Methodol. 2014;14(1):1–13.

    Article  Google Scholar 

  23. Higgins J, Li T, Deeks JJ. Chosing effect measures and computing estimates of effect. In: Cochrane Handbook for Systematic Reviews of Interventions. 2020. p. 1–58.

  24. Balduzzi S, Rücker G, Schwarzer G. How to perform a meta-analysis with R: A practical tutorial. Evid Based Ment Health. 2019;22(4):153–60.

    Article  PubMed  Google Scholar 

  25. Borenstein M, Hedges LV, Higgins JPT, Rothstein HR. A basic introduction to fixed-effect and random-effects models for meta-analysis. Res Synth Methods. 2010;1(2):97–111.

    Article  PubMed  Google Scholar 

  26. DerSimonian R, Laird N. Meta-analysis in clinical trials revisited. Contemp Clin Trials. 2015;45:139–45. https://doi.org/10.1016/j.cct.2015.09.002.

    Article  PubMed  PubMed Central  Google Scholar 

  27. Clopper CJ, Pearson E. S. Biometrika Trust The Use of Confidence or Fiducial Limits Illustrated in the Case of the Binomial Author ( s ): C . J . Clopper and E . S . Pearson Published by : Oxford University Press on behalf of Biometrika Trust Stable URL : http://www.jstor.org/stab. Biometrika. 1934;26(4):404–13.

  28. Higgins JPT, Thompson SG, Deeks JJ, Altman DG. Measuring inconsistency in meta-analyses. Br Med J. 2003;327(7414):557–60.

    Article  Google Scholar 

  29. R Core Team. R: A language and environment for statistical computing [Internet]. R Foundation for Statistical Computing. 2020. Available from: https://www.r-project.org/

  30. Roquilly A, Seguin P, Mimoz O, Feuillet F, Rosenczweig E, Chevalier F, et al. Risk factors for prolonged duration of mechanical ventilation in acute traumatic tetraplegic patients—a retrospective cohort study. J Critic Care. 2014;29:313.

    Google Scholar 

  31. Kornblith L, Kutcher M, Callcut R, et al. Mechanical ventilation weaning and extubation after spinal cord injury: a western trauma association multuicenter study. J Trauma Acute Care Surg. 2013;75(6):1–20.

    Article  Google Scholar 

  32. Branco BC, Plurad D, Green DJ, Inaba K, Lam L, Cestero R, et al. Incidence and clinical predictors for tracheostomy after cervical spinal cord injury: a national trauma databank review. J Trauma Inj Infect Crit Care. 2011;70(1):111–5.

    Article  Google Scholar 

  33. Raurich JM, Rialp G, Llompart-Pou JA, Ayestarán I, Pérez-Bárcena J, Ibáñez J. Respiratory CO2 response in acute cervical spinal cord injury (CO2 response in spinal cord injury). Spinal Cord. 2014;52(1):39–43.

    Article  CAS  PubMed  Google Scholar 

  34. Fuhrer MJ, Carter RE, Donovan WH, Rossi CD, Wilkerson MA. Postdischarge outcomes of ventilator-dependent quadriplegics. Arch Phys Med Rehabil. 1987;68:353–6.

    CAS  PubMed  Google Scholar 

  35. Anand T, Hanna K, Kulvatunyou N, Zeeshan M, DItillo M, Castanon L et al. Time to tracheostomy impacts overall outcomes in patients with cervical spinal cord injury. J Trauma Acute Care Surg. 2020;89(2):358–64.

  36. Choi HJ, Paeng SH, Ph D, Kim ST, Lee KS, Kim MS, et al. The effectiveness of early tracheostomy (within at least 10 days ) in cervical spinal cord injury patients. J Korean Neurosurg Soc. 2013;54:220–4.

    Article  PubMed  PubMed Central  Google Scholar 

  37. Leelapattana P, Fleming JC, Gurr KR, Bailey SI, Parry N, Bailey CS. Predicting the need for tracheostomy in patients with cervical spinal cord injury. J Trauma Acute Care Surg. 2012;73(4):880–4.

    Article  PubMed  Google Scholar 

  38. Ganuza JR, Forcada AG, Gambarrutta C, Buigues EDDLL, Gonzalez VEM, Fuentes FP, et al. Effect of technique and timing of tracheostomy in patients with acute traumatic spinal cord injury undergoing mechanical ventilation. J Spinal Cord Med. 2011;34(1):76–84.

    Article  PubMed  PubMed Central  Google Scholar 

  39. Romero J, Vari A, Gambarrutta C, Oliviero A. Tracheostomy timing in traumatic spinal cord injury. Eur Spine J. 2009;18(10):1452–7.

    Article  PubMed  PubMed Central  Google Scholar 

  40. Higashi T, Eguchi H, Wakayama Y, Sumi M, Saito T, Inaba Y. Analysis of the risk factors for tracheostomy and decannulation after traumatic cervical spinal cord injury in an aging population. Spinal Cord. 2019;57(10):843–9. https://doi.org/10.1038/s41393-019-0289-x.

    Article  PubMed  Google Scholar 

  41. Alizo G, Sciarretta JD, Gibson S, Muertos K, Holmes S, Denittis F, et al. Multidisciplinary team approach to traumatic spinal cord injuries: a single institution’s quality improvement project. Eur J Trauma Emerg Surg. 2018;44(2):245–50.

    Article  PubMed  Google Scholar 

  42. Jones TS, Burlew CC, Johnson JL, Jones E, Kornblith LZ, Biffl WL, et al. Predictors of the necessity for early tracheostomy in patients with acute cervical spinal cord injury: a 15-year experience. Am J Surg. 2015;209(2):363–8. https://doi.org/10.1016/j.amjsurg.2014.07.016.

    Article  PubMed  Google Scholar 

  43. Gardner BP, Watt JWH, Krishnan KR. The artificial ventilation of acute spinal cord damaged patients: a retrospective study of forty-four patients. Paraplegia. 1986;24(4):208–20.

    CAS  PubMed  Google Scholar 

  44. Beom JY, Seo HY. The need for early tracheostomy in patients with traumatic cervical cord injury. CiOS Clin Orthop Surg. 2018;10(2):191–6.

    Article  PubMed  Google Scholar 

  45. Gundogdu I, Ozturk EA, Umay E, Karaahmet OZ, Unlu E, Cakci A. Implementation of a respiratory rehabilitation protocol: weaning from the ventilator and tracheostomy in difficult-to-wean patients with spinal cord injury. Disabil Rehabil. 2016;39:8288.

    Google Scholar 

  46. Richard-Denis A, Feldman D, Thompson C, Albert M, Mac-Thiong JM. The impact of a specialized spinal cord injury center as compared with non-specialized centers on the acute respiratory management of patients with complete tetraplegia: an observational study. Spinal Cord. 2018;56(2):142–50.

    Article  PubMed  Google Scholar 

  47. Chiodo AE, Scelza W, Forchheimer M. Predictors of ventilator weaning in individuals with high cervical spinal cord injury. J Spinal Cord Med. 2008;31(1):72–7.

    Article  PubMed  PubMed Central  Google Scholar 

  48. Zakrasek E, Nielson J, Kosarchuk J, Crew J, Fergusoon A, Mckenna S. Pulmonary outcomes following specialized respiratory management for acute cervical spinal cord injury: a retrospective analysis. Spinal Cord. 2017;55(6):559–65.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  49. Kim TW, Yang JH, Huh SC, Koo B, Yoon JA, Lee JS, et al. Motor and sensory function as a predictor of respiratory function associated with ventilator weaning after high cervical cord injury. Ann Rehabil Med. 2018;42(3):457–64.

    Article  PubMed  PubMed Central  Google Scholar 

  50. Atito-Narh E, Pieri-Davies S, Watt JWH. Slow ventilator weaning after cervical spinal cord injury. Br J Intensive Care. 2008;18(3):95–102.

    Google Scholar 

  51. Peterson WP, Barbalata L, Brooks CA, Gerhart KA, Mellick DC, Whiteneck GG. The effect of tidal volumes on the time to wean persons with high tetraplegia from ventilators. Spinal Cord. 1999;37(4):284–8.

    Article  CAS  PubMed  Google Scholar 

  52. Wicks AB, Menter RR. Long-term outlook in quadriplegic patients with initial ventilator dependency. Chest. 1986;90(3):406–10.

    Article  CAS  PubMed  Google Scholar 

  53. Toki A, Nakamura T, Nishimura Y, Sumida M, Tajima F. Clinical introduction and benefits of non-invasive ventilation for above C3 cervical spinal cord injury. J Spinal Cord Med. 2019. https://doi.org/10.1080/10790268.2019.1644474.

    Article  PubMed  PubMed Central  Google Scholar 

  54. Kim DH, Kang SW, Choi WA, Oh HJ. Successful tracheostomy decannulation after complete or sensory incomplete cervical spinal cord injury. Spinal Cord. 2017;55(6):601–5.

    Article  CAS  PubMed  Google Scholar 

  55. Wong S, Shem K, Crew J. Specialized respiratory management for acute cervical spinal cord injury: a retrospective analysis. Top Spinal Cord Inj Rehabil. 2012;18(4):283–90.

    Article  PubMed  Google Scholar 

  56. Bach JR. New Approaches In The Rehabilitation Of The traumatic High Level Quadriplegic. Am J Phys Med Rehabil. 1991;70(1):13.

    Article  CAS  PubMed  Google Scholar 

  57. Call MS, Kutcher ME, Izenberg RA, Singh T. Spinal cord injury: outcomes of ventilatory weaning and extubation. J Trauma Inj Infect Crit Care. 2011;71(6):1673–9.

    Article  Google Scholar 

  58. Wallbom AS, Naran B, Thomas E. Acute ventilator management and weaning in individuals with high tetraplegia. Top Spinal Cord Inj Rehabil. 2005;10(3):1–7.

    Article  Google Scholar 

  59. Shah G, Dhakal GR, Gupta A, Hamal PK, Dhungana S, Poudel S. Outcome of cervical spine trauma patients admitted to the intensive care unit at a tertiary government referral trauma center in Nepal. Glob Spine J. 2021. https://doi.org/10.1177/2192568220980703.

    Article  Google Scholar 

  60. Cinotti R, Demeure-Dit-Latte D, Mahe PJ, Langlais P, Grillot N, Bouras M, et al. Impact of a quality improvement program on the neurological outcome of patients with traumatic spinal cord injury: a before-after mono-centric study. J Neurotrauma. 2019;36(24):3338–46.

    Article  PubMed  Google Scholar 

  61. Füssenich W, Hirschfeld Araujo S, Kowald B, Hosman A, Auerswald M, Thietje R. Discontinuous ventilator weaning of patients with acute SCI. Spinal Cord. 2018;56(5):461–8.

    Article  PubMed  Google Scholar 

  62. Fenton JJ, Warner ML, Lammertse D, Charlifue S, Martinez L, Dannels-Mcclure A, et al. A comparison of high vs standard tidal volumes in ventilator weaning for individuals with sub-acute spinal cord injuries: a site-specific randomized clinical trial. Spinal Cord. 2016;54(3):234–8. https://doi.org/10.1038/sc.2015.145.

    Article  CAS  PubMed  Google Scholar 

  63. Flanagan CD, Childs BR, Moore TA, Vallier HA. Early tracheostomy in patients with traumatic cervical spinal cord injury appears safe and may improve outcomes. Spine. 2018;43(16):1110–6.

    Article  PubMed  Google Scholar 

  64. Yu WK, Ko HK, Ho LI, Wang JH, Kou YR. Synergistic impact of acute kidney injury and high level of cervical spinal cord injury on the weaning outcome of patients with acute traumatic cervical spinal cord injury. Injury. 2015;46(7):1317–23.

    Article  PubMed  Google Scholar 

  65. Liebscher T, Niedeggen A, Estel B, Seidl RO. Airway complications in traumatic lower cervical spinal cord injury: A retrospective study. J Spinal Cord Med. 2015;38(5):607–14.

    Article  PubMed  PubMed Central  Google Scholar 

  66. McCully BH, Fabricant L, Geraci T, Greenbaum A, Schreiber MA, Gordy SD. Complete cervical spinal cord injury above C6 predicts the need for tracheostomy. Am J Surg. 2014;207(5):664–9.

    Article  PubMed  Google Scholar 

  67. De Troyer A, Heilporn A. Respiratory mechanics in quadriplegia. The respiratory function of the intercostal muscles. Am Rev Respir Dis. 1980;122(4):591–600.

    PubMed  Google Scholar 

  68. Estenne M, De TA. The effects of tetraplegia on chest wall statics. Am Rev Respir Dis. 1986;134(1):121–4.

    CAS  PubMed  Google Scholar 

  69. Berney S, Bragge P, Granger C, Opdam H, Denehy L. The acute respiratory management of cervical spinal cord injury in the first 6 weeks after injury: a systematic review. Spinal Cord. 2011;49(1):17–29.

    Article  CAS  PubMed  Google Scholar 

  70. Gutierrez CJ, Harrow J, Haines F. Using an evidence-based protocol to guide rehabilitation and weaning of ventilator-dependent cervical spinal cord injury patients. J Rehabil Res Dev. 2003;40(5 SUPPL. 2):99–110.

    Article  PubMed  Google Scholar 

  71. Jackson AB, Groomes TE. Incidence of respiratory complications following spinal cord injury. Arch Phys Med Rehabil. 1994;75(3):270–5.

    Article  CAS  PubMed  Google Scholar 

  72. Northrup BE, Vaccaro AR, Rosen JE, Balderston RA, Cotler JM. Occurrence of infection in anterior cervical fusion for spinal cord injury after tracheostomy. Spine (Phila Pa 1976). 1995 Nov;20(22):2449–53.

  73. O’Keeffe T, Goldman RK, Mayberry JC, Rehm CG, Hart RA. Tracheostomy after anterior cervical spine fixation. J Trauma. 2004;57(4):855–60.

    Article  PubMed  Google Scholar 

  74. Ross J, White M. Removal of the tracheostomy tube in the aspirating spinal cord-injured patient. Spinal Cord. 2003;41(11):636–42.

    Article  CAS  PubMed  Google Scholar 

  75. Bach JR, Alba AS. Noninvasive options for ventilatory support of the traumatic high level quadriplegic patient. Chest. 1990;98(3):613–9. https://doi.org/10.1378/chest.98.3.613.

    Article  CAS  PubMed  Google Scholar 

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AFS and JG had full access to all the data and take responsibility for the integrity of the data and the accuracy of the data analysis. Concept and design: AFS, KB, JOF, LJB. Acquisition, analysis, or interpretation of data: AFS, JG, FV, YHL, DS, JMS, LJB. Drafting of the manuscript: AFS, JG, LJB. Critical revision of the manuscript for important intellectual content: AFS, JG, FV, YHL, DS, AR, KB, JOF, JMS, LJB. Statistical analysis: AFS, JG. Administrative, technical, or material support: AFS, JG, DL. Supervision: KB, JOF, JMS, LJB. All authors read and approved the final manuscript.

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Supplementary Information

Additional file 1:

Appendix S1. Search strategy and terms used in the electronic bibliographic databases. Appendix S2. Standardized Data Collection Form used to extract data. Table S1. Baseline characteristics of included studies reporting study design, number of patients analyzed and included in each study, type of patients (traumatic/non-traumatic) and spine lesion level, type of ward and hospital, mean age, and mean time from injury to hospitalization. Table S2. Baseline characteristics of included studies II reporting inclusion and exclusion criteria of each study, assessed outcomes and presence of regression analysis. Table S3. The Newcastle–Ottawa Scale for assessing the quality of nonrandomized studies. Table S4. Baseline characteristics of the patients enrolled in each study. Table S5. Summary of definitions: complete weaning, partial weaning. Table S6. Predictors for the outcome of weaning failure. Logistic regression analyses performed across the studies are reported. Beta coefficients are pooled according to the inverse variance method; univariate and multivariate regression model coefficients are pooled together in order to obtain a robust estimate (see Complete Statistical Analysis of the Supplemental Digital Content for further details). Table S7. Predictors for the outcome of duration of mechanical ventilation. Linear regression analyses performed across the studies are reported. Beta coefficients are pooled according to the inverse variance method; univariate and multivariate regression model coefficients are pooled together in order to obtain a robust estimate (see Complete Statistical Analysis of the Supplemental Digital Content for further details). Table S8. Heterogeneity among all studies and in each subgroup (ICU and rehabilitation). Relevant heterogeneity statistics and estimate ranges are reported for characteristics at baseline, characteristics of the lesion and main outcomes after the injury.

Additional file 2:

Figure S1. Forest plot for the probability of tracheostomy. Studies are presented according to setting classification (Intensive Care Units vs Rehabilitation Units): both overall and subgroup estimates are reported. CI = confidence interval.

Additional file 3:

Figure S2. Forest plot for the probability of decannulation after tracheostomy. Studies are presented according to setting classification (Intensive Care Units vs Rehabilitation Units): both overall and subgroup estimates are reported. CI = confidence interval.

Additional file 4:

Figure S3. Forest plot for Intensive Care Unit or Rehabilitation Unit lengths of stay. Studies are presented according to setting classification: both overall and subgroup estimates are reported. Weight refers to the relative contribution of each study to the meta-analytic estimate and is generated using the inverse variance method. ICU = Intensive Care Unit, CI = confidence interval.

Additional file 5:

Figure S4. Forest plot for hospital length of stay in Intensive Care Unit setting (no data are available for Rehabilitation Units). Weight refers to the relative contribution of each study to the meta-analytic estimate and is generated using the inverse variance method. CI = confidence interval.

Additional file 6:

Figure S5. Forest plot for the probability of pneumonia. Studies are presented according to setting classification (Intensive Care Units vs Rehabilitation Units): both overall and subgroup estimates are reported. CI = confidence interval.

Additional file 7:

Figure S6. Sensitivity analysis: Forest plot for the outcome of duration of MV (complete liberation from the ventilator) excluding the two largest studies (Branco et al. [32] and Anand et al. [35]). CI = confidence interval.

Additional file 8:

Figure S7. Sensitivity analysis: Forest plot for the probability of tracheostomy excluding the two largest studies (Branco et al. [32] and Anand et al. [35]). CI = confidence interval.

Additional file 9:

Figure S8. Sensitivity analysis: Forest plot for Intensive Care Unit or Rehabilitation Unit lengths of stay excluding the two largest studies (Branco et al. [32] and Anand et al. [35]). ICU = Intensive Care Unit, CI = confidence interval.

Additional file 10:

Figure S9. Sensitivity analysis: Forest plot for hospital length of stay excluding the two largest studies (Branco et al. [32] and Anand et al. [35]). CI = confidence interval.

Additional file 11:

Figure S10. Sensitivity analysis: Forest plot for mortality excluding the two largest studies (Branco et al. [32] and Anand et al. [35]). CI = confidence interval.

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Schreiber, A.F., Garlasco, J., Vieira, F. et al. Separation from mechanical ventilation and survival after spinal cord injury: a systematic review and meta-analysis. Ann. Intensive Care 11, 149 (2021). https://doi.org/10.1186/s13613-021-00938-x

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