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Operative Neurosurgery logoLink to Operative Neurosurgery
. 2023 Jun 30;25(3):216–241. doi: 10.1227/ons.0000000000000794

Recurrent Chronic Subdural Hematoma After Burr-Hole Surgery and Postoperative Drainage: A Systematic Review and Meta-Analysis

Roger Lodewijkx *,‡,, Merijn Foppen *,, Kari-Anne Mariam Slot *,, William Peter Vandertop *,, Dagmar Verbaan *,
PMCID: PMC10389757  PMID: 37387582

BACKGROUND AND OBJECTIVE:

Reported recurrence rates of chronic subdural hematoma treated by burr-hole surgery with postoperative drainage vary considerably in the literature. We performed a systematic review and meta-analysis to define the recurrence rate of burr-hole surgery with postoperative drainage.

METHODS:

PubMed and EMBASE were searched, and Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines were followed. We used the Newcastle-Ottawa scale and Cochrane risk-of-bias tool for quality assessment of included studies and the random-effects model to calculate pooled incidence rates in R with the metaprop function if appropriate.

RESULTS:

The search yielded 2969 references; 709 were screened full text, and 189 met the inclusion criteria. In 174 studies (34 393 patients), the number of recurrences was reported as per patient and 15 studies (3078 hematomas) reported the number of recurrences per hematoma, for a pooled incidence of 11.2% (95% CI: 10.3-12.1; I2 = 87.7%) and 11.0% (95% CI: 8.6-13.4; I2 = 78.0%), respectively. The pooled incidence of 48 studies (15 298 patients) with the highest quality was 12.8% (95% CI 11.4-14.2; I2 = 86.1%). Treatment-related mortality (56 patients) has a pooled incidence of 0.7% (95% CI 0.0-1.4; I2 = 0.0%).

CONCLUSION:

The recurrence rate of chronic subdural hematoma treated by burr-hole surgery and postoperative drainage is 12.8%.

KEY WORDS: Hematoma, Subdural, Chronic, Trephining, Recurrence, Mortality


ABBREVIATIONS:

aSDH

acute subdural hematoma

cSDH

chronic subdural hematoma

I2

I-squared statistic

NA

not available

PI

prediction interval.

Over the past 3 decades, the incidence of chronic subdural hematoma (cSDH) has nearly tripled for patients older than 80 years, and because of the aging population, it is expected to become the most common cranial neurosurgical condition among adults by 2030.1,2 Although burr-hole surgery is the first treatment of choice for symptomatic cSDH,3-5 this procedure inherently carries a risk of a recurrent hematoma. Reported recurrence rates vary considerably (0%-33%), probably because surgical strategies also vary widely, from 1 or 2 burr holes with or without postoperative drainage to subdural or epidural location of drains.6-8

In recent years, less invasive, nonsurgical options to treat cSDH have been explored, such as medical treatment (steroids or tranexamic acid) or embolization of the middle meningeal artery, but randomized controlled trials are still lacking or could not prove any benefit.9,10 To accurately calculate how many patients need to be included in such randomized controlled trials (RCTs), sample size calculations should be based on reliable outcome measures in the control group, treated according to modern standards.

As the use of postoperative drainage has been shown to be clearly superior to burr-hole surgery without postoperative drainage,5 we performed a systematic review and meta-analysis to define a reliable rate of recurrence after burr-hole surgery with postoperative drainage in patients with a cSDH.

METHODS

Search Strategy and Study Selection

The results of this systematic review are reported in accordance with the guidelines of the Preferred Reporting Items for Systematic Reviews and Meta-Analyses checklist.11 This review was not registered, and a protocol was not prepared. We searched Medline (ovid) and EMBASE (embase.com) on 4th June 2021 from inception, using terms on subdural hematoma and burr hole, to identify all studies from 1946 reporting on recurrent cSDH after burr-hole surgery (see Supplementary Table 1, http://links.lww.com/ONS/A922, entitled “Syntax search”).

Articles with less than 25 patients, certain publication types (letter to the editor, commentary, survey, narrative review, study protocol), or records containing other language than English, German, French, Spanish, or Dutch were excluded. Systematic reviews and meta-analyses were only taken into consideration for forward and backward snowballing to identify any additional relevant articles. Records without abstracts were automatically passed into the full-text screening phase.

Studies were eligible for inclusion if (1) patients were 18 years or older; (2) were diagnosed with a cSDH, acute-on-chronic subdural hematoma, or when a study described both cSDH and subdural hygroma; (3) treated with burr-hole surgery and postoperative drainage; and (4) the number of recurrences or recurrence rate was explicitly reported. In Figures 1-3, we present 3 images of a cSDH, acute-on-chronic subdural hematoma, and a subdural hygroma. Postoperative drainage had to be performed in a minimum of 95% of cases to be included. A definition of a cSDH recurrence was not mandatory for inclusion, but the study had to describe recurrences or reoperations. When a study consisted of multiple treatment groups with different strategies and the patient group of interest was distinguishable (burr-hole surgery with additional drainage), the data regarding the number of patients, recurrences, and postoperative drainage of that specific subgroup of patients were collected. In case a study described that patients did not receive a postoperative drain because of brain expansion during surgery, the study was included.

FIGURE 1.

FIGURE 1.

Computed tomography scan of a left-sided chronic subdural hematoma in an axial and coronal plane.

FIGURE 3.

FIGURE 3.

Computed tomography scan of a bilateral subdural hygroma in an axial and coronal plane.

FIGURE 2.

FIGURE 2.

Computed tomography scan of a right-sided acute-on-chronic subdural hematoma in an axial and coronal plane.

Exclusion criteria were (1) medical treatment for cSDH or embolization of the middle meningeal artery before, or after, burr-hole surgery; (2) other type of surgery than burr-hole surgery; (3) enlarged and endoscopy-assisted burr-hole surgery; and (4) reported structural cause for cSDH, such as arachnoid cysts or vascular malformations.

Data Extraction

Two investigators (R.L. and M.F.) independently screened title and abstract to identify potential suitable records. Differences in judgment were discussed and resolved with mutual consent. Next, both investigators independently screened full texts, based on the inclusion and exclusion criteria and independently performed forward and backward snowballing of systematic reviews and meta-analyses to identify any additional relevant articles. Systematic reviews and meta-analyses were only taken into consideration for forward and backward snowballing to identify any additional relevant articles. A third rater (W.P.V.) adjudicated any discrepancies.

Data Collection

The following preoperative characteristics were extracted: the number of patients, mean or median age, sex, antithrombotic therapy, history of trauma, Glasgow Coma Scale (GCS) score, hematoma laterality, and total number of cSDHs (bilateral hematomas counted as 2 hematomas). Regarding operative treatment the following characteristics were collected: number of burr-holes made as per standard protocol per side, number of patients receiving irrigation, type of irrigation used, number of patients receiving a postoperative drain, type of drain, number of patients not receiving a drain because of brain expansion during surgery, and postsurgical treatment. Whenever the definition of a recurrent cSDH was stated, this was noted, as well as the number of recurrences, whether the recurrence was measured per patient or per hematoma, number of recurrences treated by surgery, and number of patients in whom the recurrence was detected by computed tomography scan, or clinical symptoms. Furthermore, data on frequency and causes of mortality directly related to cSDH treatment and the occurrence of re-recurrence were collected when possible.

Quality Assessment

The Newcastle-Ottawa scale for cohort studies, which is validated for assessing the quality of observational cohort studies, was used.12 According to the assigned number of stars, the following subdivision was made: 7–9, high quality; 4–6, high risk of bias; and 0–3, very high risk of bias. In case there was no nonexposed cohort in an included study, the maximum amount of stars to be assigned was 8. Thereby, the subdivision for these studies subsequently was 6–8, high quality; 3–5, high risk of bias; and 0–2, very high risk of bias. In addition, the Cochrane risk of bias for randomized controlled trials was used for studies in which a randomization method was used.13 Risk-of-bias judgment was determined by the overall result of the 6 domains: low risk of bias (low risk of bias for all domains), some concerns (some concerns in at least 1 domain for this result but not to be at high risk of bias for any domain), or high risk of bias (high risk of bias in at least 1 domain) accordingly. Each paper was graded and assigned a score by 2 authors [R.L. and D.V.]. A subgroup analysis was performed of the studies with the highest quality, meaning studies with Newcastle-Ottawa scale score 7–9 and score 6–8 in case of the absence of a nonexposed cohort and low risk of bias judgment determined on the Cochrane risk of bias for randomized controlled trials.

Statistical Analysis

RStudio (R: A language and environment for statistical computing. R Foundation for Statistical Computing. URL https://www.R-project.org/) with the “meta” and “metafor” package was used to perform single-arm meta-analysis including 95% CI. To assess whether effect sizes were consistent across the included studies, heterogeneity was quantified. A P-value ≤.1 for the χ2 test of heterogeneity was considered to suggest significant heterogeneity. In addition, the I-squared (I2) statistic was used, which describes the percentage of variation across studies that is due to heterogeneity rather than chance. I2 values of 25%, 50%, and 75% would, respectively, assign adjectives of low, moderate, and high categories of heterogeneity.14 In case of high heterogeneity, the random-effects model was used to correctly interpret the results.15 Metaprop function in R was used to determine single-arm prevalence, whenever possible. In addition, for single-arm prevalence of recurrence, a forest plot was created, and 95% prediction interval (PI) was calculated with the metaprop function in case of at least 10 included studies.16 The prediction interval helps in the clinical interpretation of the heterogeneity by estimating what true treatment effects can be expected in future settings.17

Single-arm prevalence analyses of a variable consisting of either 0% or 100% incidences in the included studies was determined by dividing the total number of cases in the included studies by the total number of cases of this variable.

We assessed the presence of bias using a funnel plot. The funnel plot was created with the pooled incidence and random-effects model by plotting the recurrence rate against the standard error.

RESULTS

Literature Search

The online search yielded a total of 4140 records. Screening the references of 33 systematic reviews yielded 15 additional articles. Duplicates were removed and yielded 2969 articles. After screening on title and abstract, 2260 records were excluded. The full texts of the remaining 709 articles were assessed for eligibility. Of the remaining full texts, 520 were excluded. In total, 189 articles reporting on 36 971 patients were selected for further analysis (Figure 4). Most studies were of a retrospective nature (n = 166) and otherwise randomized controlled trials (n = 23).

FIGURE 4.

FIGURE 4.

Flow chart diagram of literature search and selection.

Quality Assessment

The funnel plot shows that included studies do not seem to be symmetrically ranged around the pooled incidence of recurrence (Figure 5). Smaller studies seem to cause a more scattered array of recurrence rate. The risk-of-bias scores are shown in Table 1. Regarding the Newcastle-Ottawa scale and adjusted scale for cohort studies, the highest quality was observed in 50 (30.9%) studies, high risk of bias was observed in 104 (64.2%) studies, and very high risk in 8 (4.9%) studies.

FIGURE 5.

FIGURE 5.

Funnel plot of recurrence rates reported in 189 included studies (36 971 patients) for evaluating bias. The plot shows that the included studies in this meta-analysis do not seem to be symmetrically ranged around the pooled incidence of recurrence, shown by the smaller dashed line. This could be due to the relatively high heterogeneity reported in this study.

TABLE 1.

Baseline Characteristics of the 189 Included Studies

Author and year of publication No.of patients Mean/median age (SD/IQR/range) Male sex (%) No. of patients on antithrombotic medication (%) No. of patients with a history of trauma (%) No. of patients with a history of alcohol abuse (%) No. of patients with unilateral cSDH (%) No. of patients with bilateral cSDH (%) Total no. of hematomas No. of burr-holes performed Irrigation method appliedb Postoperative drain location Postoperative drainage timec Follow-up in months No. of patients with recurrence (%) Quality assessment
Abboud et al,18 2018 201 72 (range 25-95) 140 (70) 84 (42) 85 (42) NA 183 (91) 18 (9) 219 1 Warm saline Subdural ≤48 h 6 38 (18.9) 5h
Abouzari et al,19 2007 84 56.5 (range 21-88) 59 (70) 0 (0) 0 (0) 0 (0) 84 (100) 0 (0) 84 1 Warm saline NA ≤48 h 3 9 (10.7) Highi
Adachi et al,20 2014 120 79 76 (63) 47 (39) NA 23 (19) 120 (100) 0 (0) 120 1 Other Subdural ≤24 h 6 11 (9.2) 7h
Adrian et al,21 2017 60 69 41 (68) 6 (10) NA 3 (5) 59 (98) 1 (2) 61 1 Warm saline Subdural, subperiosteal ≤24 h 3 5 (5) 6h
Ahmed et al,22 2011 25 NA NA NA NA NA NA NA NA 1 Saline Subdural ≤48 h 1 4 (16) Highi
Ak et al,23 2017 71 NA NA NA NA NA NA NA NA 2 or 3 NA NA NA NA 8 (11.3) 2h
Amano et al,24 2020e 323 80.0 (±8.6) and 75.5 (±11.0) 209 (65) 108 (33) 222 (69) NA 209 (65) 114 (35) 437 1 Other Subdural NA 6 62 (16.5)f 5h
Aung et al,25 1999 50 62 (range 54-72) 29 (58) NA 50 (100) NA NA NA NA 2 Ringer solution/Hartmann solution Subdural ≤48 h 3 0 (0) 4h
Baechli et al,26 2004 354 68.3 (±17.0) (range 2-94) 228 (64) 144 (41) 272 (77) NA 276 (78) 78 (22) 432 1 or 2 NA Subdural ≤48 h NA 48 (13.6) 5h
Bankole et al,27 2011 73 NA NA 2 (3) 30 (41) 13 (18) 51 (70) 22 (30) 95 1 or 2 Saline Subdural ≤48 h NA 9 (12.5) 5g
Bartek et al,28 2017 1254 NA NA 555 (44) NA NA 938 (75) 316 (25) 1570 NA NA Subgaleal, subperiosteal NA 6 169 (13.5) 6h
Bartley et al,29 2020 172 74.5 (±12) and 75.1 (±13) 127 (74) 80 (47) NA NA 139 (81) 33 (19) 205 1 or 2 Warm Ringer solution Subdural ≤24 h 6 15 (8.7) 5h
Bellut et al,30 2012 113 77 (±13) and 71 (±13) 77 (68) 62 (55) NA NA 83 (73) 30 (27) 143 2 Warm saline Subdural, subperiosteal ≤48 h 3 18 (15.9) 5h
Blaauw et al,31 2020 1029 73.5 (±11) 773 (75) 571 (55) 571 (55) NA 772 (75) 257 (25) 1286 3 115 (11.2) 6h
Borger et al,32 2012 322 76 (±7.9) (range 65-94) 162 (50) 233 (72) NA 245 (76) 77 (24) 399 1 Saline Subdural NA 0.5 89 (22.3)f 4h
Carlisi et al,33 2017 35 81.3 (6.3) 22 (63) 22 (63) 22 (63) NA 29 (83) 6 (17) 41 NA NA NA ≤48 h NA 3 (8.6) 4h
Carslen et al,34 2011 206 NA NA NA NA NA NA NA NA 1 Ringer solution/Hartmann solution Subdural, subgaleal ≤24 h 6 29 (14.1) 5g
Castro-Rodriguez et al,35 2016 200 88.5 (±3.2) 107 (54) 71 (36) 114 (57) 3 (2) 167 (84) 33 (17) 233 2 Saline Subdural ≤72 h 3 26 (13) 6h
Certo et al,36 2019 30 77.1 (range 57-87) and 76.4 (range 61-91) 19 (63) NA NA NA NA NA NA 1 Saline Subdural ≤72 h 16 1 (3.3) 4g
Chan et al,37 2017 149 74 (range 42-95) 116 (78) 46 (31) NA 13 (9) 149 (100) 0 (0) 149 2 NA NA ≤48 h 6 13 (8.7) 7g
Chang et al,38 2020 122 73.6 (±11.6) (range 36-95) 83 (68) 71 (58) 73 (60) 9 (7) 79 (65) 43 (35) 165 6 14 (11.5) 7h
Chandran et al,39 2017 52 33.7 (range 18-40) 32 (62) 2 (4) 48 (92) 13 (25) 52 (100) 0 (0) 52 1 Other NA NA 1 1 (1.9) 2h
Chen et al,40 2020 171 66.0 (range 59-75) 137 (80) 22 (13) 99 (58) NA 138 (81) 33 (19) 204 6 13 (6.4)f Highi
Cheng et al,41 2014 342 77.2 (±11.4) 235 (69) 51 (15) 201 (59) NA 269 (79) 73 (21) 415 NA Saline Subdural ≤120 h 3 41 (11.9) 5h
Choi et al,42 2016 502 67 (±13) 341 (68) NA 302 (60) NA NA NA NA 1 or 2 NA NA NA NA 37 (7.4) 4h
Choi et al,43 2020 230 69.4 (±13.1) 164 (71) 36 (16) NA 34 (15)9 144 (63) 86 (37) 316 NA 49 (21.3) 5h
Chon et al,44 2012 420 67.3 (range 37-92) 334 (80) 151 (36) 237 (56) NA 352 (84) 68 (16) 488 1 NA NA ≤72 h 3 92 (21.9) 6h
Choudhury et al,45 1994 44 65 37 (84) 4 (9) 31 (70) NA 37 (84) 7 (16) 51 2 Saline Subdural ≤72 h 3 1 (2.3) 5h
Dobran et al,46 2019 50 92.4 (range 90-100) 32 (64) 35 (70) 27 (54) 3 (6) 34 (68) 16 (32) 66 6 7 (14) 4h
D'Oria et al,47 2020 210 66.5 (±6) and 67.2 (±7.1) 115 (55) 55 (26) NA 13 (6) 210 (100) 0 (0) 210 1 or 2 Saline Subdural ≤48 h 30 31 (14.8) 5h
Djientcheu et al,48 2011 195 55 (range 21-89) 155 (79) 3 (2) 159 (82) 25 (13) 156 (80) NA NA 1 or 2 Saline Subgaleal ≤48 h 9 6 (3.1) 4h
Dran et al,49 2007 198 75 (±13) (range 33-98) 142 (72) 58 (29) 150 (76) 13 (7) 169 (85) 29 (15) 227 1 Saline Subdural ≤48 h 17.5 16 (8) 6h
Drapkin,50 1991 53 Range 16-97 29 (55) 5 (9) 27 (51) NA 50 (94) 3 (6) 59 2 Saline Subdural Other NA 10 (19) 5h
Edem et al,51 2019 74 70 (range 24-96) 57 (77) 0 (0) NA NA 74 (100) 0 (0) 74 NA NA NA NA 6 16 (21.6) 6g
Eggert et al,52 1984 100 NA NA 19 (19) NA NA NA NA NA NA NA NA NA 17 11 (11) 3h
Eppel et al,53 1999 50 67.3 and 70.3 (range 27-96) 35 (70) 9 (18) 50 (100) 8 (16) 42 (84) 8 (16) 58 1 or 2 Other Subdural ≤120 h 28 8 (16) 5h
Ernestus et al,54 1997 94 NA NA NA NA NA NA NA NA NA Saline Subdural ≤96 h NA 17 (18.1) 4h
Erol et al,55 2005 35 NA NA NA NA NA 32 (91) 3 (9) 38 1 or 2 Saline Subdural ≤48 h 1 5 (14.3) Highi
Flint et al,56 2017 659 76 (range 67-83) 464 (70) NA NA NA NA NA NA 1 NA Subdural ≤48 h 6 60 (9.1) 6g
Flores et al,57 2017 220 59 167 (76) NA NA NA 220 (100) 0 (0) 220 2 Saline Subdural ≤24 h 12 13 (5.9) 4h
Frati et al,58 2004 35 69.4 24 (69) NA 35 (100) 0 (0) 30 (86) 5 (14) 40 1 Saline Subdural ≤72 h 12 5 (14.3) 4h
Fujisawa et al,59 2021 208 74 (IQR 66-83), 74 (IQR 66-81) 153 (74) 32 (15) 130 (63) 12 (5) NA NA NA 3-6 19 (9.1) Highi
Gabarros et al,60 2000 83 66.5 (range 17-86) 59 (71) 1 (1) NA NA 78 (94) 5 (6) 88 2 Saline NA ≤48 h 12 10 (12) 6g
Gelabert Gonzalez et al,61 2005 1000 72.7 (±11.4) 628 (63) 122 (12) 617 (62) 132 (13) 903 (90) 97 (10) 1097 NA Saline Subdural ≤120 h NA 61 (6.1) 4h
Gernsback et al,62 2016 215 66 155 (72) 157 (73) NA NA 195 (91) 33 (15) 261 1 or 2 NA Subdural ≤24 h NA 16 (6.1)f 3h
Gilsbach et al,63 1980 51 58.7 and 54.8 37 (73) NA NA NA 45 (88) 6 (12) 57 1 Ringer solution/Hartmann solution Subdural NA NA 9 (17.7) 4h
Glancz et al,64 2019 577 78 (IQR 98-85) 394 (68) 245 (42) 361 (63) NA 386 (67) 177 (31) 740 1 or 2 NA Subdural, subgaleal ≤72 h 2 45 (7.8) 7h
Gonugunta a Buxton,65 2001 184 68 and 72 86 (47) 34 (18) NA NA NA NA NA 1 Other Subdural NA 6 (minimum) 27 (14.7) 4h
Goto et al,66 2015 414 77.3 279 (67) 84 (20) NA NA 323 (78) 91 (22) 505 6 37 (8.9) 7h
Gurelik et al,67 2007 42 58.4 28 (67) NA 7 (17) 0 (0) NA NA NA 1 or 2 Warm saline Subdural ≤48 h 8 8 (19) Highi
Hamilton et al,68 1993 29 64 NA NA NA NA NA NA NA 1 NA Subdural NA 4 3 (10.3) 3g
Han et al,69 2009 180 62.2 (±14.3) 131 (73) NA 180 (100) NA 155 (86) 25 (14) 205 1 or 2 Warm saline Subdural ≤120 h 1 (minimal) 10 (5.6) 5h
Hani et al,70 2019 361 72.6 (±11.0) + 74.8 (±11.0) 244 (68) 191 (53) NA NA NA NA NA 2 NA Subdural, subgaleal ≤48 h 6 83 (23) 6h
Harders et al,71 1982 100 61.6 and 62.9 70 (70) 19 (19) 62 (62) 7 (7) 92 (92) 8 (8) 108 2 Ringer solution/Hartmann's solution Subdural Other 17 24 (24) 3h
Hennig & Kloster,72 1999 90 NA NA NA NA NA 82 (91) 8 (9) 98 2 Gentamicin-induced irrigation Subdural ≤48 h NA 7 (7.1)f 3g
Heringer et al,73 2017 96 NA NA NA NA NA 74 (77) 22 (23) 96 1 or 2 Saline Subdural NA 7.6 15 (15.6) 5g
Hirai et al,74 2021 320 77.3 (±10.9) 228 (71) 94 (29) NA NA 274 (86) 46 (14) 366 3 37 (10.6)f 8h
Hori et al,75 2018 92 81.9 (±8.5) and 77.5 (±8.9) 63 (68) 25 (27) 61 (66) 1 (1) 77 (84) 15 (16) 107 NA NA Subdural NA 3 15 (16.3) 6h
Hsieh et al,76 2016 75 71.9 (±12.5) 53 (71) 20 (27) 38 (51) 19 (25) 52 (69) 23 (31) 98 1 Saline Subdural NA 8 (mean) 7 (9.3) 5h
Huang et al,77 2013 98 69.3 (±12.8) 81 (83) 15 (15) 73 (74) 14 (14) 73 (74) 25 (26) 123 1 or 2 Other Subdural NA 10.6 (mean) 14 (14.3) 5h
Huang et al,78 2020 140 68.7 (±12.7) 114 (81) 91 (65) NA NA NA NA 1 NA Subdural ≤48 h 3 12 (8.6) 4h
Iftikar et al,79 2016 34 66.7 (±14.0) 28 (82) NA NA NA NA NA NA NA Saline Subdural ≤48 h 1-10 (min-max) 6 (17.6) 6g
Ishfaq,80 2017 62 72 (range 55-85) 41 (66) NA 33 (53) NA 52 (84) 10 (16) 72 1 or 2 NA Subdural, subgaleal ≤96 h NA 7 (11.3) Highi
Ishibashi et al,81 2011 34 79.1 (10) 19 (56) 5 (15) NA NA 31 (91) 3 (9) 36 1 Warm saline Subdural ≤48 h NA 1 (2.9) Highi
Jang et al,82 2015 30 68 (range 58-78.5) 21 (70) 5 (17) NA 6 (20) NA NA NA 2 Saline Subdural NA 3 3 (10) 9g
Jang et al,83 2020 291 71.8 (±11.8) 208 (71) 93 (32) NA 125 (43) 175 (60) 116 (40) 407 1 or 2 Saline NA ≤72 h 2 29 (10) 7h
Janowski & Kunert,84 2012 45 66 (range 24-86) 30 (67) NA NA NA 42 (93) 3 (7) 48 NA NA Subdural ≤24 h NA 7 (15.6) 5h
Jeong et al,85 2014 125 69.4 (±12.3) 92 (74) 35 (28) 81 (65) NA 96 (77) 29 (23) 154 NA Warm saline NA NA 3 8 (6.4) 3h
Jukovic et al,86 2014 35 NA NA NA NA NA NA NA NA NA Warm saline Subdural ≤48 h 6 0 (0) 5g
Jung et al,87 2015 182 68.1 131 (72) 46 (25) 125 (69) 65 (36) 147 (81) 35 (19) 217 1 or 2 Ringer solution/Hartmann solution Subdural ≤72 h 12 25 (13.7) 7h
Kale et al,88 2017 90 55.61 (±18.7) 54 (60) 12 (13) 75 (83) NA 75 (83) 15 (17) 105 1 or 2 Saline Subdural ≤96 h 6 9 (8.6)f 5h
Kaliaperumal et al,7 2012 50 Range 17-91 33 (66) 25 (50) 29 (58) NA 42 (84) 8 (16) 58 2 Warm saline Subdural, subperiosteal ≤48 h 6 0 (0) Highi
Kang et al,89 2007 302 236 (78) NA NA NA 267 (88) 35 (12) 337 NA NA ≤48 h 3 24 (7.9) 4h
Kaminogo et al,90 1999 38 69.3 (±12.0) 34 (89) NA 25 (66) NA 32 (84) 6 (16) 44 1 Saline Subdural ≤24 h 6 4 (9.1)f 5h
Kanyi et al,91 2018 119 61.3 (range 19-94) 95 (80) 0 (0) 65 (55) 41 (34) 95 (80) 23 (19) 141 2 Saline Subdural ≤48 h 0.5 6 (5) 4h
Kareem & Adams,92 2018 36 79 (range 55-95) 26 (72) 24 (67) 34 (94) NA 30 (83) 6 (17) 42 1 Warm Ringer solution Subperiosteal ≤48 h 3 4 (11) 3h
Katayama et al,93 2018 88 75.8 (±9.5) 67 (76) 10 (11) NA NA 77 (88) 11 (13) 99 NA Saline Subdural ≤24 h 3 11 (12.5) Highi
Khan et al,94 2019 60 62 (±13.7) (range 38-94) 40 (67) 0 (0) NA NA 53 (88) 7 (12) 67 1 or 2 Other Subdural NA NA 14 (23.3) Highi
Kim et al,95 2011 259 63.7 (±16.9) 191 (74) NA 167 (64) 15 (6) NA NA NA 1 or 2 NA NA ≤72 h 6 23 (8.9) 3g
Kim et al,96 2014 114 67.6 (±11.5) 88 (77) NA 51 (45) NA 114 (100) 0 (0) 114 NA Saline NA ≤72 h 3 28 (24.6) 6g
Kim et al,97 2016 100 70.4 (±12.6) 62 (62) 36 (36) 100 (100) NA NA NA NA 1 Saline NA ≤48 h 6 26 (26) 9g
Kim,98 2017 246 68.6 (±12.2) 173 (70) 59 (24) 187 (76) NA 183 (74) 63 (26) 309 1 or 2 NA Subdural NA 6 31 (12.6) 7h
Kiymaz et al,99 2007 29 62.7 (±3.2) 24 (83) NA 18 (62) 2 (7) NA NA NA 2 Warm saline Subdural ≤96 h NA 2 (6.9) 4g
Klein et al,100 2021 407 74.7 (±13.2) and 76.6 (±8.2) 280 (69) 209 (51) NA NA 317 (78) 90 (22) 497 32.7 ± 16.1 72 (17.7) 7h
Kocaman & Yilmaz,101 2019 30 78 (range 64-92) 20 (67) NA NA NA 30 (100) 0 (0) 30 2 Warm saline Subdural NA 6 5 (16.7) 4h
Kotwica & Brzezinski,102 1991 131 Range 18-82 101 (77) 0 (0) 93 (71) 45 (34) NA NA NA 2 Saline Subdural ≤48 h 24 (minimum) 3 (2.3) 3h
Kristof et al,103 2008 75 73 38 (51) NA 48 (64) NA 58 (77) 17 (23) 92 NA Ringer solution/Hartmann solution Subdural ≤96 h NA 17 (22.7) 6g
Krupp & Jans,104 1995 214 65 (±15) 128 (60) 13 (6) 28 (13) 15 (7) 167 (78) 45 (21) 257 1 or 2 Other Subdural ≤72 h NA 53 (25) 5h
Kurabe et al,105 2010 182 77.3 (range 65-98) 123 (68) 38 (21) NA 40 (22) 148 (81) 34 (19) 216 1 NA Subdural ≤48 h 3 14 (7.7) 5h
Kuroki et al,106 2001 45 67.3 (range 43-88) 32 (71) NA NA NA 40 (89) 5 (11) 50 1 Saline Subdural ≤120 h 44 5 (11.1) 6h
Kutty & Johny,107 2014 70 NA 55 (79) 25 (36) NA NA 53 (76) 17 (24) 87 1 Saline Subdural ≤72 h 3 2 (2.9) Highi
Kwon et al,108 2000 145 59.3 (range 23-89) 104 (72) NA NA NA 115 (79) 30 (21) 175 1 Saline Subdural ≤120 h 6 6 (4.1) 5h
Lee et al,109 2004 38 70 25 (66) NA NA 6 (16) NA NA NA 2 Saline Subdural ≤72 h NA 6 (16) 6g
Lee et al,110 2009 32 65.3 (±12.1) 25 (78) NA NA NA NA NA NA 2 Saline NA ≤120 h NA 7 (22) 5g
Lee & Park,111 2014 114 77.9 81 (71) 30 (26) 70 (61) 33 (29) 86 (75) 28 (25) 142 NA Saline Subdural ≤72 h 3 19 (16.7) 5h
Lee et al,112 2018 131 68 (±17) 85 (65) 35 (27) 71 (54) NA NA NA NA 1 Warm saline Subdural ≤72 h 6 7 (5.3) 5h
Lepic et al,113 2021 55 72.8 (±11.5) 37 (67) NA NA NA 36 (65) 19 (35) 67 1 3 (5.5) 3h
Leung et al,114 2001 46 NA NA NA NA NA NA NA NA NA Saline NA NA NA 3 (6.5) 6h
Liliang et al,115 2002 75 65.3 (range 16-92) 63 (84) NA 53 (71) 7 (9) 59 (79) 16 (21) 91 1 or 2 Saline NA ≤48 h 30 3 (4) 6h
Li et al,116 2017 115 68.3 (±5.1) 76 (66) 16 (14) NA NA 103 (90) 24 (21) NA 6 11 (9.6) 6h
Lin,117 2011 270 62.3 (±24.5) 218 (81) NA NA NA NA NA NA 1 Saline Subdural ≤72 h NA 32 (11.9) 6g
Liu et al,118 2010 398 58.1 (±18.1) 338 (85) 6 (2) 275 (69) 12 (3) 304 (76) 94 (24) 492 1 Saline NA ≤120 h NA 15 (3.8) 3h
Liu et al,119 2019 328 65.1 (±13.8) (range 22-93) 281 (86) 17 (5) 170 (52) NA 267 (81) 61 (19) 389 1 Other NA ≤48 h 6 8 (2.4) 8h
Lo et al,120 2013 98 69.3 (±12.8) (range 29-93) 81 (83) 15 (15) 73 (74) 14 (14) 73 (74) 25 (26) 123 1 or 2 Saline Subdural NA 3 14 (14.3) 5h
Lu et al,121 2018 87 68.4 (±6.5) (range 55-82) 71 (82) NA 72 (83) NA 87 (100) 0 (0) 87 2 Warm saline Subdural NA 6-12 4 (4.6) 5h
Maldaner et al,122 2019 253 75 190 (75) 106 (42) NA NA 180 (71) 73 (29) 326 2 NA Subperiosteal ≤48 h 3 40 (15.8) 7h
Markwalder,123 2000 32 61.4 22 (69) NA 26 (81) NA 27 (84) 5 (16) 37 2 NA Subdural ≤48 h 1.5 1 (3.1) 3h
Martinez Perez et al,124 2020 90 76.4 (±11.2) 71 (79) 42 (47) NA NA 78 (87) 12 (13) 102 2 NA Subdural ≤48 h 6 17 (18.9) 8h
Mellergard & Wisten,125 1996 218 70.5 (range 11-93) 155 (71) 22 (10) 135 (62) 32 (15) 193 (89) 25 (11) 243 1 Saline Subdural ≤48 h 1.5 30 (12.3)f 4h
Mersha et al,126 2020 195 57.6 137 (70) NA 124 (64) NA 147 (75) 48 (25) 243 1 Warm saline Subdural ≤24 h 4 13 (6.6) 6h
Mezue et al,127 2011 116 NA NA 26 (22) 91 (78) NA NA NA NA 1 or 2 NA NA NA NA 9 (7.8) 3h
Miah et al,128 2020 60 73 (range 34-95) 49 (82) 31 (52) 45 (75) NA 39 (65) 21 (35) 81 1 or 2 Warm Ringer solution Subdural ≤48 h 6 13 (22) 7g
Miki et al,129 2019 277 78.6 (±11.1) 181 (65) 70 (25) 193 (70) NA 234 (84) 43 (16) 320 1 Other Subdural ≤48 h 3 50 (18.1) 7h
Missori et al,130 2000 31 38 (range 20-50) 24 (77) NA 24 (77) 2 (6) 27 (87) 4 (13) 35 1 Other NA ≤24 h 2 2 (6) 4h
Morales-Gomez et al,131 2020 155 65.9 (±16.6) (range 18-95) 127 (82) 8 (5) 101 (65) 14 (9) 124 (80) 31 (20) 186 2 18 (11.6) 5h
Mori & Maeda,132 2001 500 67.3 (±15.3) and 71.3 (±14.2) 359 (72) 26 (5) 286 (57) 32 (6) 412 (82) 88 (18) 588 2 Saline Subdural ≤48 h 3 49 (9.8) 4h
Motoie et al,133 2018 787 79 (IQR 72-85) 559 (71) 199 (25) NA 195 (daily alcohol consumption)d (25) 671 (85) 116 (15) 903 NA Other Subdural NA NA 96 (12.2) 6h
Munoz-Bendix et al,134 2017 112 NA 63 (56) 63 (56) NA NA 88 (79) 24 (21) 136 1 25 (22.3) 3h
Nakagawa et al,135 2019 381 NA NA NA NA NA NA NA NA 1 Saline Subdural ≤24 h 6 71 (18.6) 4h
Nakaguchi et al,136 2001 106 67 82 (77) 0 (0) 63 (59) NA 86 (81) 20 (19) 126 1 Saline NA ≤48 h 3 21 (17)f 5h
Nunta-Aree et al,137 2017 75 60.7 (66 median) 79 (hematoma's) (NA) 35 (47) 31 (41) 2 (3) 48 (64) 27 (36) 102 2 Other NA NA 2 10 (13.3) 4h
Okano et al,138 2014 448 71.1 (range 19-97) 314 (70) 18 (4) 225 (50) NA 344 (77) 104 (23) 552 1 Saline Subdural NA 42 40 (8.9) 7h
Oral et al,139 2015 78 68.1 and 66.1 (median) 57 (73) 9 (12) 58 (74) NA 73 (94) 5 (6) 83 1 or 2 Warm saline Subdural, subgaleal ≤72 h 3 4 (5.1) 5h
Penchet et al,140 1998 236 71.7 146 (62) 57 (24) 182 (77) 18 (8) 195 (83) 41 (17) 276 1 or 2 Saline NA ≤48 h 3 10 (4.2) 3h
Piotrowski & Krombholz-Reindl,141 1996 200 67.5 150 (75) 45 (23) 109 (55) 6 (3) 163 (82) 37 (19) 237 1 NA Subdural NA 16 (8) 3h
Poulsen et al,142 2014 177 NA NA NA NA NA NA NA NA 1 Warm Ringer solution Subdural, subperiosteal NA 3 28 (15.8) Highi
Qian et al,143 2017 242 66.3 (±10.9) (range 36-93) 148 (61) 54 (22) 145 (60) 79 (33) 242 (100) 0 (0) 242 1 Warm Ringer solution Subdural ≤120 h 6 39 (16.1) 7h
Raghavan et al,144 2020 153 72.2 (±13.1) 93 (61) 41 (27) 82 (54) 26 (17) 105 (69) 48 (31) 201 1 NA Subdural NA 1 24 (15.7) 6g
Ram et al,145 1993 37 70.8 (±10) 25 (68) NA NA NA 33 (89) 4 (11) 41 2 Saline Subdural ≤48 h 1 5 (13.5) Highi
Regan et al,146 2015 61 72 (range 52-98) 36 (59) 29 (48) 38 (62) 9 (15) NA NA 80 1 or 2 or 3 Other Subdural NA NA 4 (6.6) 5g
Ridwan et al,147 2019 197 NA NA NA NA NA NA NA NA 1 or 2 NA Subdural ≤72 h 2 37 (18.8) 6g
Rohde et al,148 2002 376 64 242 (64) NA NA NA NA NA NA 1 Ringer solution/Hartmann solution Subdural NA NA 119 (31.6) 5h
Rovlias et al,149 2015 986 69 (range 29-96) 650 (66) 237 (24) 503 (51) 132 (13) 907 (92) 79 (8) 1065 2 Other Subdural Other 3 117 (11.9) 6h
Ryu et al,150 2018 187 67 (range 22-93) 135 (72) 76 (41) 93 (50) NA 187 (100) 0 (0) 187 1 Saline Subdural ≤48 h 3 22 (11.8) 6h
Sah & Rawal,151 2018 102 NA NA NA NA NA 80 (78) 22 (22) 124 NA NA Subdural NA NA 9 (8.8) 5g
Santarius et al,5 2009 108 74.4 (46-94) 83 (77) 49 (45) NA NA 87 (81) 21 (19) 129 2 Warm Ringer solution Subdural ≤48 h 6 10 (9) Highi
Sarnvivad et al,152 2011 97 60.5 (±20.1) 66 (68) 21 (22) NA NA 76 (78) 21 (22) 118 1 Saline NA NA NA 15 (16) 4g
Schoedel et al,153 2016 697 70.1 (range 1-97) 461 (66) 226 (32) 317 (45) NA NA NA NA NA NA Subdural NA NA 155 (22.2) 5g
Schwarz et al,154 2015 193 71.4 (±13.6) 137 (71) 87 (45) 143 (74) 9 (5) 138 (72) 55 (28) 250 NA Other Subdural ≤24 h 3 35 (18.1) 8h
ShafiqAlam et al,155 2017 428 NA NA NA NA NA NA NA NA NA Saline NA NA NA 53 (12.4) 5h
Shah et al,156 2014 25 NA 15 (60) NA NA NA NA NA NA 1 Warm saline Subdural ≤48 h 6 3 (12) Highi
Shen et al,157 2019 457 68.8 (range 23-92) 376 (82) 28 (6) 235 (51) NA 311 (68) 146 (32) 603 1 Saline Subdural ≤72 h 3 69 (15.1) 8h
Shim et al,158 2019 60 74.5 (range 67-90) 44 (73) 0 (0) 30 (50) NA NA NA NA 1 Saline Subdural NA NA 8 (13.3) 5g
Singh et al,159 2011 52 61.2 47 (90) NA NA NA 52 (100) 0 (0) 52 1 Gentamicin-induced irrigation Subdural NA 1 1 (2) Highi
Singh et al,160 2014 100 NA NA 24 (24) 72 (72) 34 (34) 87 (87) 13 (13) NA 1 or 2 Saline Subdural ≤48 h 6 9 (9) Highi
Sjavik et al,161 2017 1260 73 (±11) and 74 (±13) and 74 (±13) 878 (70) 222 (18) NA NA 1005 (80) 217 (17) 1439 1 Gentamicin-induced irrigation Subdural, subgaleal ≤24 h 6 169 (13.4) 6h
Song et al,162 2014 97 70 (range 15-93) 64 (66) NA 61 (63) NA 94 (97) 3 (3) 100 1 Other Subdural ≤48 h 3 16 (16.5) 6h
Sousa et al,163 2013 778 64.3 (±15.9) (range 14-93) 643 (83) NA 470 (60) NA 604 (78) 174 (22) 952 1 Saline Subdural ≤48 h 3 (minimum) 42 (5.4) 5h
Stanisic et al,164 2013 107 72.1 (±12.8) 72 (67) NA NA NA 84 (79) 23 (21) 130 1 Saline Subdural ≤24 h 7 17 (15.9) 7h
Sucu & Akar,165 2014 119 65.7 (±16.9) NA NA NA NA 84 (71) 35 (29) 154 1 or 2 NA NA ≤48 h 1 4 (3.4) 2h
Suzuki et al,166 1998 67 NA NA NA NA NA NA NA NA 1 Warm saline Subdural ≤72 h NA 2 (3) 4g
Tagle et al,167 2003 100 77 (±13) 77 (77) 21 (21) 43 (43) NA 84 (84) 16 (16) 116 1 or 2 Other NA ≤72 h 66 13 (13) 2h
Takei et al,168 2021 277 82 (range 76-89) and 87 (range 76-92) 211 (76) 79 (29) NA NA 247 (89) 30 (11) 307 3 35 (11.4)f 8h
Tahsim-Oglou et al,169 2012 247 75 (±13) and 77 (±8) 165 (67) NA NA NA 193 (78) 54 (22) 281 2 Warm Ringer solution Subdural ≤48 h 1 62 (25.1) 7h
Tailor et al,170 2017 123 75.6 88 (72) 30 (24) NA NA 97 (79) 26 (21) 149 1 or 2 NA Subdural NA 6 10 (8.1) 4g
Tanikawa et al,171 2001 33 69.3 (±14.9) NA NA NA NA NA NA NA 2 Saline Subdural ≤72 h 6 4 (12.1) Highi
Taussky et al,172 2008 76 69 (±12) (range 38-89) 54 (71) 53 (70) NA NA 55 (72) 21 (28) 97 1 or 2 Ringer solution/Hartmann solution NA ≤48 h 1 13 (13.4)f 5h
Thavara et al,173 2019 63 61.4 (±13.2) 48 (76) 9 (14) 31 (49) 6 (10) 63 (100) 0 (0) 63 1 Saline Subdural ≤24 h NA 1 (1.6) 5g
Toi et al,174 2019 342 77 (65-80) and 78 (65-79) 248 (73) 57 (17) 223 (65) NA 342 (100) 0 (0) 342 1 Other Subdural Other 3 39 (11.4) Highi
Tomita et al,175 2018 102 77.2 (±10.7) 66 (65) 21 (21) 76 (75) 4 (4) 89 (87) 13 (13) 115 1 Saline Subdural NA NA 8 (7.8) 4h
Tommiska et al,176 2019 71 78 (range 57- 93) 50 (70) 48 (68) 62 (87) NA 55 (77) 15 (21) 85 1 Warm Ringer solution Subdural ≤48 h 6 4 (5.6) 7g
Torihashi et al,177 2008 337 75.5 (range 28-96) 228 (68) 24 (7) 81 (24) NA 268 (80) 69 (20) 406 1 Saline Subdural NA 1 61 (18.1) 7h
Tosaka et al,178 2015 46 NA NA NA NA NA NA NA 46 NA Saline Subdural NA 1.5 5 (10.9)f 4g
Tsai et al,179 2010 129 71 (range 22-97) 100 (78) 11 (9) 90 (70) 6 (5) 84 (65) 45 (35) 174 2 Saline Subdural NA NA 12 (9.3) 4h
Tugcu et al,180 2014 292 61.9 (±17.8) (range 1-96) 200 (68) 56 (19) 160 (55) 4 (1) 210 (72) 82 (28) 374 2 Warm saline NA ≤96 h 1 43 (14.7) 7h
Vasella et al,181 2018 28 70.4 (±16.1) 24 (86) NA NA NA 19 (68) 9 (32) 37 2 Warm saline Subdural, subperiosteal ≤48 h 9 1 (3.6) 2h
Wan et al,182 2017 31 73.6 (range 61-83) 18 (58) 1 (3) 26 (84) NA 31 (100) 0 (0) NA 1 Saline Subdural ≤120 h 3 13 (41.9) 4g
Wang et al,183 2016 53 66.7 (±13.1) 44 (83) 0 (0) 45 (85) 8 (15) 61 1 Saline Subdural ≤72 h 1 9 (17) 5g
Wang et al,184 2017 45 67.3 (±12.9) 38 (84) 6 (13) 26 (58) 0 (0) 45 (100) 0 (0) 45 1 Saline Subdural Other 3 5 (11.1) 6g
Wang et al,185 2017 (1) 88 65.5 (±7.8) 53 (60) NA NA NA 88 (100) 0 (0) 88 1 Warm saline NA ≤72 h 12 6 (6.8) 5g
Wang et al,186 2017 (2) 57 64.6 52 (91) 0 (0) 47 (82) NA NA NA NA 1 Warm saline Subdural ≤72 h 6 0 (0) 6g
Wang et al,187 2020 653 72 (IQR 64-80) 561 (86) NA NA 234 (current drinking)d (36) 504 (77) 149 (23) 802 3 96 (14.7) 8h
Weigel et al,188 2015 93 75.6 (±12.9) and 72.6 (±13) NA 0 (0) NA NA 73 (78) 20 (22) 113 1 or 2 Other Subdural ≤72 h 3 13 (11.5)f 5h
Weng et al,189 2019 190 68 (range 27-86) 118 (62) NA 161 (85) NA 190 (100) 0 (0) 190 1 Other Subdural NA 6 17 (8.9) 4h
Won et al,190 2021 176 75 (range 65-80) and 74.5 (range 62-80) 126 (72) 87 (49) NA NA 120 (68) 56 (32) 232 3 40 (22.7) Highi
Wu et al,191 2020 331 NA 285 (86) 22 (6) 239 (72) 95 (29) 268 (81) 63 (19) 394 3 30 (9.1) 6h
Yadav et al,192 2016 140 53 (±22.1) (range 18-75) 101 (72) NA 140 (100) NA 140 (100) 0 (0) 140 1 Warm saline Subgaleal NA 21 5 (3.6) 6g
Yagnick et al,193 2019 60 64.3 51 (85) 21 (35) 20 (33) NA 42 (70) 18 (30) 78 2 Other Subdural NA 8 0 (0) 5h
Yamada et al,194 2018 1080 72.1 (±14.3) (range 13-101) 711 (66) 124 (11) 827 (77) 5 (0) 883 (82) 197 (18) 1227 1 Other Subdural ≤48 h NA 119 (11) 5h
Yamada & Notori,195 2020 193 78.8 (±0.8) and 78.2 (±9.8) and 79.2 (±8.7) 160 (83) 72 (37) NA 48 (25) 85 (44) 108 (56) 232 1 Other Subdural ≤24 h 3 16 (6.9)f Highi
Yamamoto et al,196 2003 105 71.4 (±9.6) and 71.4 (±10.5) 73 (70) 4 (4) 78 (74) 41 (39) 82 (78) 23 (22) 128 1 or 2 Warm saline NA ≤48 h 6 11 (10.5) 7h
Yan et al,197 2017 52 66.4 (±9.4) 37 (71) 12 (23) NA NA 41 (79) 11 (21) 63 1 Saline Subdural ≤72 h 12 7 (13.7) 4g
Yan et al,198 2018 231 NA 188 (81) 0 (0) 0 (0) NA 201 (87) 30 (13) 261 NA Other NA ≤48 h 3 33 (14.3) 5h
You et al,199 2018 226 65.1 (±13.4) 184 (81) 14 (6) 161 (71) NA 160 (71) 66 (29) 292 1 or 2 Saline Subdural ≤48 h 12 34 (15) 8h
Yu et al,200 2009 97 67 (range 14-93) 82 (85) NA NA 11 (11) 74 (76) 24 (25) 121 1 Saline Subdural Other 3 8 (8.2) 5h
Zakaraia et al,201 2008 40 59.7 29 (73) 0 (0) NA NA NA NA NA 2 Saline Subdural ≤72 h 6 4 (10) Highi
Zhang et al,202 2018 31 75.1 22 (71) 13 (42) 24 (77) 9 (29) 29 (94) 2 (6) 33 2 Warm saline Subdural NA 6 8 (25.1) 6g
Zhang et al,203 2019 570 71 (IQR 62-79) 422 (74) 123 (22) 380 (67) 52 (9) 333 (58) 237 (42) 807 1 or 2 Gentamicin-induced irrigation Subdural, subperiosteal ≤48 h 6 70 (12.3) 7h
Zumofen et al,204 2009 147 71.5 (range 42-93) 113 (77) 41 (28) 117 (80) 12 (8) 111 (76) 36 (24) 183 2 Saline Subperiosteal ≤48 h 3 22 (15) 5h
Pooled incidence (95% CI, I2) 71.9% (70.6-73.2; 84.3%) 23.6% (21.3-26.0; 98.5%) 64.2% (55.1-73.3; 99.8%) 12.3% (10.4-14.1; 95.8%) a See Table 5 See Table 6 See Table 6 See Results section See Results section

CSF, cerebrospinal fluid; cSDH, chronic subdural hematoma; I2, I-squared statistic; NA, not available.

a

A single burr-hole per side was made in 55.8%, a double burr-hole per side in 19.3% of cases, and in 24.9% it was reported that either a single burr-hole or a double burr- hole was used, and these could not be separated.

b

Labeled according to 6 categories we established: Saline, warm saline, Ringer solution/Hartmann solution, warm Ringer solution, Gentamicin-induced irrigation and other. Category “saline” was abbreviated, full name: saline/normal saline/isotonic saline/physiological saline. “other” included: unknown (described in included studies as: irrigation/washout/rinsing), normal saline or artificial CSF, artificial CSF, or irrigation with ARTCEREB.

c

Labeled according to 6 categories we established: ≤24 h, ≤48 h, ≤72 h, ≤96 h, ≤120 h, and other. “Other” included different drainage periods described in studies: 24–144 h, 192 ± 96 h, 48–144 h, 8 h until <5 mL per hour draining volume, and 24–216 h.

d

Excluded in calculating history of alcohol abuse proportion.

e

Only 71 patients with a bilateral cSDH underwent operation.

f

Study which calculates the recurrence rate as proportion of the total number of hematomas.

g

Quality assessment performed using the Newcastle-Ottawa scale.

h

Quality assessment performed using the adjusted Newcastle-Ottawa scale.

i

Quality assessment performed using the Cochrane risk-of-bias tool for randomized trials. High means high risk of bias.

Recurrence Rate and Mortality

Baseline characteristics of the 189 included studies reporting the number of recurrences are shown in Table 1. The pooled incidence of 174 studies with 34 393 patients reporting 4208 recurrences per number of patients was 11.2% (95% CI: 10.3-12.1; I2 = 87.7%; 95% PI: 0.0-22.0). In addition, the pooled incidence of 15 studies with 3078 hematomas reporting 370 recurrences per number of hematomas was 11.0% (95% CI: 8.6-13.4; I2 = 78.0%, 95% PI: 2.0-20.0). Forest plots are shown in the Supplementary Fig. 1, http://links.lww.com/ONS/A923 and Supplementary Fig. 2, http://links.lww.com/ONS/A924.

The pooled incidence of reported recurrence rates at 3 months (25 articles) was 12.7% (95% CI: 10.7-14.7; I2 = 86.1%) and 9.8% (95% CI: 7.6-11.9; I2 = 89.0%) at 6 months (21 articles). The pooled incidence of recurrence in patients treated by 1 burr-hole was 12.2% and in patients treated by 2 burr-holes was 12.8%.

Pooled mortality incidences are displayed in Table 2. Mortality related to cSDH treatment was seen in 56 patients with a pooled incidence of 0.7% (95% CI 0.0-1.4; I2 = 0.0%) (Table 3).

TABLE 2.

Pooled Incidence of Mortality per Time Period

Mortality period Number of studies Number of patients Pooled incidence (95% CI; I2)
In-hospital mortality 39 188 1.3% (0.9-1.7; 78.9%)
30-d mortality 29 229 2.5% (1.7-3.2; 86.6%)
3-mo mortality 9 256 3.6% (1.9-5.3; 90.0%)
6-mo mortality 15 493 6.5% (3.6-9.4; 97.2%)
Mortality without time period indication 45 199 2.0% (1.4-2.5; 73.6%)

I2, I-squared statistic.

All calculated with random-effects model.

TABLE 3.

Studies Reporting Mortality Causes Related to cSDH Treatment

Author and year Mortality cause(s) related to cSDH treatment (number of cases)
Bartley et al,29 2020 Intracerebral hematoma (n = 1), basal ganglion infarction (n = 1)
Bellut et al,30 2012 Postoperative intraparenchymal hematoma (n = 1)
Carlisi et al,33 2017 Postoperative (n = 1)
Chen et al,40 2020 Recurrent cSDH (n = 2)
Choi et al,42 2016 After taking anticoagulants (n = 3)
Djientcheu et al,48 2011 Brain herniation (n = 1), inhalation pneumonia in comatose patients with delayed treatment (n = 3)
Eppel et al,53 1999 Postoperative brain hemorrhage (n = 1)
Gabarros et al,60 2000 Recurrent bleeding (n = 1)
Hennig et al,72 1999 Infection (n = 1), rebleed after first operation (n = 1)
Kotwica et al,102 1991 Large ischemic stroke of the hemisphere compressed by the hematoma (n = 1), purulent meningitis, followed by subdural empyema (n = 1)
Lepic et al,113 2021 Sequence of rebleeding episodes and clinical worsening (n = 1)
Liu et al,119 2019 Recurrence of cSDH for which consent for repeat surgery was not given (n = 1)
Mellergard et al,125 1996 Subdural empyema after third recurrence operation (n = 1)
Mezue et al,127 2011 Secondary infection (n = 1)
Missori et al,130 2000 Acute subdural hemorrhage (n = 1)
Morales-Gomez et al,131 2020 aSDH (n = 1), parenchymal hematoma (n = 1)
Penchet et al,140 1998 Empyema (n = 1), aSDH (n = 1)
Piotrowski et al,141 1996 Cerebral decompensation which were comatose before operation (n = 6)
Ridwan et al,147 2019 Cerebrovascular accidents (n = 2)
Rohde et al,148 2002 Intracerebral bleeding (n = 4)
Schoedel et al,153 2016 Acute secondary hemorrhage (n = 5)
Shen et al,157 2019 Spontaneous ventricular hemorrhage after operation (n = 1), postoperative acute epidural hemorrhage (n = 1)
Sucu et al,165 2014 Subdural empyema (n = 1), aSDH (n = 1)
Suzuki et al,166 1998 Extreme disturbance of consciousness did not improve postoperatively and pneumonia supervened (n = 1)
Tagle et al,167 2003 Recurrence of cSDH (n = 1)
Tsai et al,179 2010 aSDH (n = 2)
Zhang et al,203 2019 Because of removal of the drain after which aSDH developed, the patient died 45 d later in the hospital because of pneumonia (n = 1)
Zumofen et al,204 2009 Continued to bleed acutely from subdural membranes despite trepanation, refrained from second intervention (n = 2)

aSDH, acute subdural hematoma; cSDH, chronic subdural hematoma.

Treatment Modalities

Pooled incidences and recurrence rates per irrigation method, type of postoperative drainage, and drainage time are shown in Tables 4-6, respectively. Ringer solution (also titled Hartmann solution) showed a recurrence rate of 21.4%, and irrigation fluid at room temperature (22 °C) showed a recurrence rate of 12.0%.

TABLE 4.

Pooled Incidence of Irrigation Method

Irrigation method No.of studies No. of patients Pooled incidence Recurrence rate Recurrence rate combined (95%CI; I2)b
Saline/normal saline/isotonic saline/physiological saline 75 13.364 47.8% 11.1% 12.0%
Ringer solution/Hartmann solution 9 1292 4.6% 21.4%
Gentamicin-induced irrigation method 4 1972 7.0% 12.5%
Warm saline 28 2893 10.4% 9.7% 11.5%
Warm Ringer solution 8 1113 4.0% 15.7%
Othera 28 7313 26.2% Not determined Not determined

I2, I-squared statistic.

a

Other includes Hartmann solution with gentamicin, normal saline or artificial CSF, artificial CSF, irrigation with ARTCEREB and those describing only irrigation/washout/rinsing.

b

Saline/normal saline/isotonic saline/physiological saline and Ringer solution/Hartmann solution are combined to determine the recurrence rate, and warm saline and warm Ringer solution are combined to investigate the effect of normal vs warm irrigation method.

Calculated by dividing the number of patient per group by the total number of patients in which the irrigation method was described.

TABLE 6.

Pooled Incidence of Postoperative Drainage Time

Drainage time in hoursa No. of studies No. of patients Pooled incidence Recurrence rate
≤24 h 17 4577 16.7% 11.4%
≤48 h 57 12 619 46.0% 11.2%
≤72 h 28 5500 20.0% 13.3%
≤96 h 5 657 2.4% 14.5%
≤120 h 11 2465 9.0% 8.3%
Otherb 6 1623 5.9% Not determined
a

When a drainage time range was given in a study, the maximum drainage time was accounted for and calculated with in the corresponding variable.

b

Other includes different drainage time periods described in studies: 24–144 h, 192 ± 96 h, 48–144 h, 8 h until <5 mL per hour draining volume, and 24–216 h.

Calculated by dividing the number of patients per group by the total number of patients in which postoperative drainage time was described.

TABLE 5.

Pooled Incidence and Recurrence Rate per Type of Postoperative Drain Location Used

Location of postoperative drain No. of studiesa No. of patients Pooled incidence Recurrence rateb
Subdural 139 24 965 80.9% 12.8%
Subperiosteal 7 780 2.5% 13.6%
Subgaleal 8 1596 5.2% 9.9%
Other 13 3536 11.4% Not determined
a

In 9 studies, more than 2 drain locations were reported and could be separated per location and was calculated additionally.

b

In 42 studies of which drain location was unknown, the first author was emailed to retrieve the drain location. Hereby, we determined 9 drain locations extra.

Calculated by dividing the number of patients per group by the total number of patients in which postoperative drain location was described.

“Other” includes studies reporting 2 or more drain locations which could not be separated.

Subgroup Analyses

We performed a subgroup analysis of the 50 studies with the highest quality regarding risk-of-bias judgment, of which 48 (15 298 patients) described the number of recurrences (2019 recurrences) as per the patient, and 2 studies (597 patients) described the recurrences (72 hematomas) as per the number of hematomas. Pooled incidence of recurrences were 12.8% (95% CI 11.4-14.2; I2 = 86.1%; 95% PI 2.0-25.0) and 12.0% (95% CI 9.4-14.7; I2 = 0.0%), respectively (see Supplementary Fig. 3 for forest plot, http://links.lww.com/ONS/A925). The pooled incidence of patients on antithrombotic medication, history of trauma, and history of alcohol abuse is 28.2% (95% CI 23.4-33.1; I2 = 98.2%), 64.4% (95% CI 55.5-73.3; I2 = 99%), and 15.3% (95% CI 10.8-19.8; I2 = 97.2%), respectively. Recurrence rates in high-quality studies per the irrigation method were as follows: saline/normal saline/isotonic saline/physiological saline, 13.8%, Ringer solution/Hartmann solution, 9.6%; gentamicin-induced irrigation method, 9.6% (determined in 1 study); warm saline, 10.7%; and warm Ringer solution of 10.0% (determined in 1 study). For the type of drainage method in high-quality studies, recurrence rate for a subdural drain was 13.6% and for subperiosteal drain was 15.8% (determined from 1 study), and a subgaleal drain was not used in high-quality studies. Regarding the duration of postoperative drainage times ≤24 hours, ≤48 hours, ≤72 hours, ≤96 hours, and ≤120 hours, the respective recurrence rates are 14.1%, 12.6%, 13.0%, 13.4% (determined in 1 study), and 13.6%.

Definitions of Recurrence Used

In 167 articles, a definition of a recurrent cSDH was stated. In 66 of these articles, reoperation was the sole definition of recurrence. In 57 articles, a combination of clinical, radiological factors and a reoperation was regarded as recurrence; in 28 articles, clinical and radiological factors defined recurrence. In 2 articles, solely clinical symptoms were regarded as a recurrence and in 14 articles only radiological features. We determined the recurrence rates per definition, which are 10.5%, 12.4%, 13.9%, 14.0%, and 9.4%, respectively. In 29 articles, a period of 3 months was used for the recurrence definition and in 24 articles a period of 6 months. In the subgroup of 50 studies with the highest quality, 23 articles used a combination of clinical, radiological factors and a reoperation as definition of recurrence. In 9 articles clinical and radiological factors determined a recurrence and in 4 articles only radiological factors. Furthermore, 17 of these high-quality studies used a period of 3 months and 7 used a period of 6 months. We analyzed the pooled incidences and recurrence rates of treatment modalities of the studies using a combination of clinical, radiological factors and a reoperation as recurrence definition (Supplementary Tables 2-4, http://links.lww.com/ONS/A926, http://links.lww.com/ONS/A927, and http://links.lww.com/ONS/A928).

DISCUSSION

This systematic review shows a pooled incidence of recurrence of 12.8% after burr-hole surgery and postoperative drainage in patients with a chronic subdural hematoma. Because this recurrence rate has been accurately determined, it can serve as an outcome measure for power calculations to determine sample sizes for future randomized clinical trials.

Most of the included studies were of a retrospective nature, the majority was judged to carry a high to very high risk of bias, and the RCTs were all considered to be of low quality. The overall pooled incidence is 11.2%. In our subgroup analysis of only those studies of the highest quality, the pooled incidence of recurrence was remarkably higher at 12.8%, which could infer that studies with poor quality systematically underestimate the recurrence rate. Therefore, the most reliable pooled incidence of recurrence is 12.8%. Our analyses of the pooled incidence of recurrence at 3 and 6 months shows that both periods do not accurately approach the overall recurrence rate of cSDH, possibly because of the low number of studies of which data could be derived from.

Recurrence of a cSDH leads to rehospitalization and reoperation, resulting in worse clinical outcome, loss of independency in these often very frail patients, and a significant increase in health care costs.205-208 Prevention of recurrences is therefore important, and various nonsurgical treatments are now being explored in randomized clinical trials, including medication (tranexamic acid).9,209 In a recent RCT, the use of dexamethasone vs placebo demonstrated that fewer recurrences occurred but that less favorable outcomes and more adverse events were noted in the dexamethasone group.10

This systematic review also provided information on recurrence rates depending on the method of irrigation used. Ringer solution (also titled Hartmann solution) showed a relatively high recurrence rate, as did irrigation fluid at room temperature (22 °C) when compared with irrigation at body temperature (37 °C), which is in line with a recent study.210 The pooled recurrence rate of subgaleal drainage was lower compared with subdural and subperiosteal drainage, although subgaleal drainage was used in only 8 studies, making it hard to draw firm conclusions. In the literature, recurrence rates after burr-hole surgery do not appear to be affected by drain location.211 However, 2 recent systematic reviews and meta-analysis showed that the insertion of a subperiosteal drain resulted in a significantly lower recurrence rate compared with a subdural drain but did not take into account a subgaleal drain.212,213 Furthermore, we researched whether patient characteristics or treatment modalities could be of influence on the high-quality recurrence rate by performing subgroup analyses. Only the irrigation method, saline/normal saline/isotonic saline/physiological saline, seems to be associated with recurrence because this rate is higher compared with the other determined rates in between treatment modalities. The pooled incidences of recurrence in the high-quality group could therefore be regarded as more stable and should be used as most reliable recurrence rates.

Limitations

A relatively high statistical heterogeneity was observed for nearly all calculated pooled incidences in the current systematic review and meta-analysis. This could be due to clinical heterogeneity because clinical diversity in studies, despite the strict inclusion and exclusion criteria, is inevitable. A difference in baseline characteristics of included studies was observed. Some studies for example applied certain age restrictions, and some only included unilateral hematomas or patients with antithrombotic therapy, and across studies, different treatment methods regarding number of burr-holes, type of irrigation, and location of the postoperative drain and different definitions of recurrence were used. Moreover, methodological heterogeneity also attributes to the statistical heterogeneity because retrospective and prospective studies and RCTs are included. When measuring prevalence of a phenomenon in diverse environments, it is expected that highly heterogeneous studies are assembled.214 Because all included studies present a recurrence rate and therefore essentially measure the same parameter, we think it is worth summarizing despite clinical and methodological heterogeneity. Furthermore, in the literature, a wide range of recurrence rates are used, and the current study is a first step to accurately provide one overall recurrence rate. A subgroup analysis of studies with the highest quality was performed and still showed high heterogeneity meaning that even in these studies clinical and methodological differences are present and cannot be avoided.

Prediction interval calculation of studies with the highest quality showed that the recurrence rate in 95% of future studies is expected to range from 2% to 25%. This wide prediction interval is likely caused by the high heterogeneity of studies because the prediction interval is a summary of the spread of underlying effects in the studies included in the random-effects meta-analysis.16 The created forest plots show a considerable in-between study difference regarding recurrence rate, even in the studies with the highest quality. Consequently, the calculated pooled recurrence rate should be interpreted with some caution.

Fortunately, randomized controlled trials are being increasingly conducted in neurosurgery. However, for power calculations to determine sample size, it is crucial to use accurate outcome measures. The current study provides the most accurate known recurrence rate for cSDH treated by burr-hole surgery and postoperative drainage. Therefore, we propose to use the recurrence rate calculated in this study for future sample size calculations. Furthermore, to compare the results of these clinical studies, consistency in terms and definitions is essential, whereas definitions for a recurrent cSDH vary considerably in the literature. We would like to recommend using the following standardized definition of a recurrent cSDH in future studies: A recurrent cSDH is defined as recurring or aggravated clinical symptoms, caused by a radiologically proven, ipsilateral reaccumulation of cSDH within 6 months of prior surgical treatment, for which additional treatment is necessary. It then still remains debatable whether a recurrence on the contralateral side is a recurrence or a newly diagnosed cSDH.

CONCLUSION

The overall recurrence rate of chronic subdural hematoma after burr-hole surgery and postoperative drainage is 12.8%. This rate should be interpreted with some caution because observed heterogeneity of included studies is high. A unified definition of cSDH recurrence after surgical treatment is advocated to ensure reliable comparison between future studies.

Supplementary Material

ons-25-216-s001.pdf (75.9KB, pdf)
ons-25-216-s002.pdf (88.4KB, pdf)
ons-25-216-s003.pdf (239.6KB, pdf)
ons-25-216-s004.pdf (92KB, pdf)
ons-25-216-s005.pdf (122.5KB, pdf)
ons-25-216-s006.pdf (119.4KB, pdf)
ons-25-216-s007.pdf (142.6KB, pdf)

Footnotes

Supplemental digital content is available for this article at operativeneurosurgery-online.com.

Contributor Information

Merijn Foppen, Email: m.foppen@amsterdamumc.nl.

Kari-Anne Mariam Slot, Email: k.slot@amsterdamumc.nl.

William Peter Vandertop, Email: wp.vandertop@amsterdamumc.nl.

Dagmar Verbaan, Email: d.verbaan@amsterdamumc.nl.

Funding

This study did not receive any funding or financial support.

Disclosures

The authors have no personal, financial, or institutional interest in any of the drugs, materials, or devices described in this article.

SUPPLEMENTAL DIGITAL CONTENT

Supplemental Content Table 1. Syntax search.

Supplementary Fig 1. Forest plot and prediction interval of pooled incidence of recurrences per number of patients.

Supplementary Fig 2. Forest plot and prediction interval of pooled incidence of recurrences per number of hematomas.

Supplementary Fig 3. Forest plot and prediction interval of pooled incidence of recurrences of studies with the highest quality.

Supplemental Content Table 2. Pooled incidence and recurrence rate of irrigation methods in studies using a definition of clinical and radiological factors and a reoperation.

Supplemental Content Table 3. Pooled incidence and recurrence rate of postoperative drain location used in studies using a definition of clinical and radiological factors and a reoperation.

Supplemental Content Table 4. Pooled incidence and recurrence rate of postoperative drainage time used in studies using a definition of clinical and radiological factors and a reoperation.

COMMENTS

This systematic review and meta-analysis provide valuable insights into the recurrence rates of chronic subdural hematoma (cSDH) after burr-hole evacuation with postoperative drainage. While several reviews and meta-analyses have been published on this topic, this study stands out for its focus on recurrence rates and its unique analysis of the impact of irrigation solutions.

The review's findings suggest that the recurrence rate of cSDH after burr-hole evacuation with postoperative drainage is 12.8%, providing neurosurgeons with important information to inform their decision-making processes. Moreover, the study's examination of the effects of different irrigation solutions on recurrence rates provides additional insight into potential interventions that could improve patient outcomes.

Overall, this review underscores the importance of ongoing research into the management of cSDH and the need for clinicians to carefully consider the specific factors that may impact recurrence rates when making treatment decisions. The study's rigorous methodology and clear reporting of results make it a valuable contribution to the current literature on this topic.

Jason H. Huang

Temple, Texas, USA

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Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

Supplemental Content Table 1. Syntax search.

Supplementary Fig 1. Forest plot and prediction interval of pooled incidence of recurrences per number of patients.

Supplementary Fig 2. Forest plot and prediction interval of pooled incidence of recurrences per number of hematomas.

Supplementary Fig 3. Forest plot and prediction interval of pooled incidence of recurrences of studies with the highest quality.

Supplemental Content Table 2. Pooled incidence and recurrence rate of irrigation methods in studies using a definition of clinical and radiological factors and a reoperation.

Supplemental Content Table 3. Pooled incidence and recurrence rate of postoperative drain location used in studies using a definition of clinical and radiological factors and a reoperation.

Supplemental Content Table 4. Pooled incidence and recurrence rate of postoperative drainage time used in studies using a definition of clinical and radiological factors and a reoperation.


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