Accepted Manuscript Title: Age determination of subdural hematomas with CT and MRI: a systematic review Author: Tessa Sieswerda-Hoogendoorn Floor A.M. Postema Dagmar Verbaan Charles B. Majoie Rick R. van Rijn PII: DOI: Reference:

S0720-048X(14)00153-3 http://dx.doi.org/doi:10.1016/j.ejrad.2014.03.015 EURR 6717

To appear in:

European Journal of Radiology

Received date: Accepted date:

17-1-2014 11-3-2014

Please cite this article as: Sieswerda-Hoogendoorn T, Postema FAM, Verbaan D, Majoie CB, van Rijn RR, Age determination of subdural hematomas with CT and MRI: a systematic review, European Journal of Radiology (2014), http://dx.doi.org/10.1016/j.ejrad.2014.03.015 This is a PDF file of an unedited manuscript that has been accepted for publication. As a service to our customers we are providing this early version of the manuscript. The manuscript will undergo copyediting, typesetting, and review of the resulting proof before it is published in its final form. Please note that during the production process errors may be discovered which could affect the content, and all legal disclaimers that apply to the journal pertain.

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Age determination of subdural hematomas with CT and MRI: a systematic review

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Tessa Sieswerda‐Hoogendoorn, MD, MSc 1,2  Floor A.M. Postema, MSc 3  Dagmar Verbaan, MSc, PhD4  Charles B. Majoie, MD, PhD 2  Rick R. van Rijn, MD, PhD 1,2     

Affiliations 

Corresponding author 

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1 Section of Forensic Pediatrics, Department of Forensic Medicine, Netherlands Forensic  Institute, The Hague, The Netherlands  2 Department of Radiology, Academic Medical Center/Emma Children’s Hospital,  Amsterdam, The Netherlands  3 Faculty of Medicine, University of Amsterdam, Academic Medical Center, Amsterdam, The  Netherlands  4 Department of Neurosurgery, Academic Medical Center, Amsterdam, The Netherlands   

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Tessa Sieswerda‐Hoogendoorn, MD, MSc.  Section of Forensic Pediatrics, Department of Forensic Medicine  Netherlands Forensic Institute  PO Box 24044   2490 AA The Hague  The Netherlands   E‐mail: [email protected]  Phone: +31‐20‐5669111, pager 58896    Floor Postema  AMC, Faculty of Medicine, University of Amsterdam  Meibergdreef 9  1105 AZ Amsterdam  The Netherlands  Email: [email protected]  Phone: +31‐20‐5669111    Dagmar Verbaan  AMC, Department of Neurosurgery  Meibergdreef 9  1105 AZ Amsterdam   The Netherlands 

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  Acknowledgements 

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Email: [email protected]  Phone: +31‐20‐5669111    Charles Majoie  AMC, Department of Radiology  Meibergdreef 9  1105 AZ Amsterdam  The Netherlands  Email: [email protected]  Phone: +31‐20‐5669111    Rick van Rijn  AMC, Department of Radiology,   Meibergdreef 9  1105 AZ Amsterdam  The Netherlands  Email: [email protected]  Phone: +31‐20‐5669111, pager 62690   

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We would like to thank all authors who replied to our request for additional information on  their studies. Furthermore, we would like to thank the following people for their help with  the translations: Mr. J. I.L.M. Verbeke, MD (French), Mr. T. Laméris (Japanese), Ms. W.M.  Sieswerda‐Mesman, MD (German), Mr O. Olsen, MD (Norwegian), Prof. A. Rossi (Italian), Ms.  L.P. Lin (Chinese), Ms S.G. Postema, BSc (Spanish), Mr. M. Kuzak, MSc (Polish). 

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Abstract Objectives  To systematically review the literature on dating subdural hematomas (SDHs) on CT and MRI 

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scans.   

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Methods 

We performed a systematic review in MEDLINE, EMBASE and Cochrane to search for articles 

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that described the appearance of SDHs on CT or MRI in relation to time between trauma and  scanning. Two researchers independently screened the articles, assessed methodological  quality and performed data extraction. Medians with interquartile ranges were calculated. 

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Differences were tested with a Mann‐Whitney U or Kruskal Wallis H test.   

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Results 

We included 22 studies describing 973 SDHs on CT and 4 studies describing 83 SDHs on MRI.  Data from 17 studies (413 SDHs) could be pooled. There were significant differences 

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between time intervals for the different densities on CT (p 40 days was analyzed as 40 days).     

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Statistical analysis  For the studies providing individual patient data, we performed a pooled analysis. We 

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recorded density or intensity of the SDHs in combination with the time in days between the  onset of the SDH and scanning in IBM SPSS Statistics 19. Normality was assessed using the 

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Kolmogorov‐Smirnov test. Medians with interquartile ranges (IQR) were calculated for all  time intervals, as data were non‐normally distributed. Differences between different  subgroups were tested with a Mann‐Whitney U test for two groups and a Kruskal Wallis H 

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test for more than two groups. For the studies not providing individual patient data, we  extracted the time interval for each density/ intensity for the whole group. These data were 

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presented in the measure they were presented in the original article. 

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Results   Study identification  We included 23 studies describing densities of SDHs on CT (1070 cases) 9‐11,15‐17,20‐36 and 5 

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studies describing intensities of SDHs on MRI in 126 cases 17,22,36‐38. Three studies described  both CT and MRI data, meaning that in total 25 studies were included. The flow chart of 

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study selection is illustrated in Figure 1. Study characteristics of the studies included are  described in table 1. 

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  Study quality 

All studies included in this review were retrospective or prospective observational cohort 

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studies. None of the studies defined a control group. The mean score of the studies was 4  out of 6 points on the adapted NOS, see table 2. The most common methodological problem 

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was, as expected, that none of the included studies could demonstrate that the outcome of  interest (SDH) was not already present before the trauma.   

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All studies 

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Densities and time intervals between trauma and scanning on CT 

Data of 17 studies describing 413 SDHs did provide information at individual level and could 

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be pooled 9,15,17,20,22‐24,26‐35. There were significant differences between the median time  intervals (IQR) for the different densities (p 22 days - 2 SDHs hypodense after 7-22 days - 16 SDHs hypodense after > 22 days

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Author Bradford, 201336

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individual patient data suitable for pooling

Haar, 197721

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Scotti, 197711

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Reed, 198610

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Lee, 199725

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Dias, 199816

SDH = subdural hematoma SD = standard deviation

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Table 5

Group

N

Hyperdense

Children Adults

50 37

Time interval in days, median (IQR) 2 (1-3) 3 (1-30)*

Isodense

Children Adults

4 18

2 (0-5) 46 (26-90)#

Hypodense

Children Adults

63 118

2 (0-9) 16 (8-33)

Mixed density

Children Adults

11 365

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P$ Children vs adults 0.046

0 7

6 122

0.000

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Max

0 0

0 1

122 177

0.000

2 (1-3) 0 (0-11)*

0 0

11 243

0.332

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31 18

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Density

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Table 5. Pooled analysis of time intervals for each density on CT for children and adults separately.

MWU test was used to test the differences between children and adults for each density.

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* Significant difference with isodensity (p= 0.000) and hypodensity (p= 0.000) Significant difference with hypodensity (p=0.001)

N= number IQR = interquartile range Min= minimum Max= maximum

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Table 6

Density

Group

N

Time interval

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Table 6. Pooled analysis of time intervals for each density on CT for AHT and non-AHT pediatric cases separately

Min

Max

AHT vs

median (IQR)

Hypodense

Mixed density

0

-

Non-AHT

49

2 (1-4 )*

0

AHT

-

-

-

Non-AHT

4

AHT

1

Non-AHT

7

AHT

17

Non-AHT

14

#

2 (0-5 )

0

-

non-AHT 0.08

11

6

10

0.75

36 (7-61)

2

120

2 (1-4)

0

5

1 (1-3)†

0

11

0.54

MWU test was used to test the differences between AHT and non-AHT cases for each density.

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Isodense

AHT

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Hyperdense

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in days,

p$

* Significant difference with hypodensity (p=0.000) #

Significant difference with hypodensity (p=0.024)

† Significant difference with hypodensity (p=0.001) AHT= abusive head trauma N= number IQR = interquartile range Min= minimum Max= maximum

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Table 7

Table 7. Pooled analysis of time intervals for each intensity on MRI for T1 and T2 sequences

Sequence Intensity

N

Time interval in

Min

Max

days, median

9 (5-13)

3

35

Isointense

5

4 (2-33)

2

49

Hypointense

5

90 (19-105)

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Hyperintense

14

11 (5-39)

Isointense

4

7 (4-20)

Hypointense

10

Mixed

4

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2

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14

120

90

3

23

6 (2-9)

2

35

14 (10-49)

9

120

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1

ed

T2

Hyperintense

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T1

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(IQR)

intensity

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N= number IQR = interquartile range Min= minimum Max= maximum

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Table 8

Table 8. Time intervals of SDHs of different intensities on MRI in studies that did not

Results - 6 SDHs hyperintense on T1 and hypointense on T2/ Flair after 0-5 days - 6 SDHs hyperintense on T1 and hyperintense in T2/ Flair after 2-30 days - 16 SDHs with equal volumes of mixed hyper- and hypointense on T1 and mixed hyper- and hypointense on T2/ Flair after 0-30 days - 14 SDHs with unequal volumes, mostly hypointense on T1 and hyperintense on T2/ Flair, smaller component hyperintense on T1 and hypointense on T2/ Flair after 0-30 days - 11 SDHs hypo or isointense on T1 and hypointense on T2 after average 5 days, SD 4.1 - 5 SDHs hyperintense on T1 and hyperintense on T2 after average 27.8 days, SD 20 - 1 SDH hypointense on T1 and hyperintense on T2 after 37 days - 5 SDHs mixed intensity on T1 and mixed intensity on T2 after average 17.8 days, SD 12.2

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SDH= subdural hematoma

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Kaminogo, 199938

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Author Bradford, 201336

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provide individual patient data suitable for pooling

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Age determination of subdural hematomas with CT and MRI: a systematic review.

To systematically review the literature on dating subdural hematomas (SDHs) on CT and MRI scans...
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