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Micro-CT yields high image quality in human fetal post-mortem imaging despite maceration

BMC Medical Imaging volume 21, Article number: 128 (2021) Cite this article

Abstract

Background

Current clinical post-mortem imaging techniques do not provide sufficiently high-resolution imaging for smaller fetuses after pregnancy loss. Post-mortem micro-CT is a non-invasive technique that can deliver high diagnostic accuracy for these smaller fetuses. The purpose of the study is to identify the main predictors of image quality for human fetal post-mortem micro-CT imaging.

Methods

Human fetuses were imaged using micro-CT following potassium tri-iodide tissue preparation, and axial head and chest views were assessed for image quality on a Likert scale by two blinded radiologists. Simple and multivariable linear regression models were performed with demographic details, iodination, tissue maceration score and imaging parameters as predictor variables.

Results

258 fetuses were assessed, with median weight 41.7 g (2.6–350 g) and mean gestational age 16 weeks (11–24 weeks). A high image quality score (> 6.5) was achieved in 95% of micro-CT studies, higher for the head (median = 9) than chest (median = 8.5) imaging. The strongest negative predictors of image quality were increasing maceration and body weight (p < 0.001), with number of projections being the best positive imaging predictor.

Conclusions

High micro-CT image quality score is achievable following early pregnancy loss despite fetal maceration, particularly in smaller fetuses where conventional autopsy may be particularly challenging. These findings will help establish clinical micro-CT imaging services, addressing the need for less invasive fetal autopsy methods.

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Background

Conventional perinatal autopsy can determine a cause of death or diagnosis by identifying developmental abnormalities and reducing the discrepancy between the ante- and post-mortem diagnosis [1]. However, parental uptake for conventional autopsy has been in decline for several decades due to its invasive nature [2, 3]. Minimally-invasive imaging techniques which are more acceptable to parents [3,4,5] have been developed to determine the causes of miscarriage and stillbirth, and to assist in the planning of future pregnancies [6,7,8,9,10]. Most current clinically available scanning methods do not provide sufficient image resolution of smaller fetuses [9, 11], necessitating trialling higher resolution techniques [10, 12,13,14].

Micro-CT is a technique that can achieve high resolution of anatomical structures [15,16,17,18,19] and with the addition of a potassium tri-iodide (I2KI) contrast agent can provide detailed soft tissue imaging which can identify developmental abnormalities in early pregnancy where conventional autopsy is challenging [15, 16, 20,21,22,23,24]. Micro CT has been used to image human fetuses with high diagnostic accuracy [20, 25], but the optimal imaging parameters across a range of fetal size, gestation, and maceration and how these relate to image quality have yet to be determined. The aim of this study was to identify the strongest demographic or imaging-derived determinants of fetal post-mortem micro-CT imaging.

Methods

Ethical approval was granted for this retrospective, single centre study (13/LO/1994 and 17/WS/0089) with all specimens being handled according to the Human Tissue Act (2004). Parental consent was obtained for post-mortem imaging.

Patient selection

Consecutive unselected fetuses under 350 g body weight from a 3-year period (January 2017 to November 2019) underwent whole body micro-CT imaging as part of the consented autopsy examination for clinical care. Prior to imaging, all fetuses were stored in the hospital mortuary and refrigerated at 4 °C. Fetuses were immersed in a solution of 2.5% I2KI (2–13 days) to allow full iodination through diffusion of the contrast to the centre of the fetus according to established protocols [26]. We used 5 days per 100 g body weight as an estimation of time to iodination.

Post-mortem micro-CT imaging

Micro-CT imaging was completed using one of two Nikon micro-CT scanners depending on machine availability (model: Med-X or XTH 225-ST; Nikon, Tring, UK). Two micro-CT studies were performed for each fetus to allow for highest resolution and magnification imaging as possible: a dedicated head study, and combined chest abdomen pelvis study [20]. The micro-CT imaging was completed by one of three operators, each with at least 4 years of scanning experience.

Fetuses were secured within the scanner using foam supports, moisture absorbent wrapping material and Parafilm M (Bemis, Oshkosh, USA) to ensure mechanical stability [27]. Projection images acquired by the scanner were reconstructed using modified Feldkamp filtered back-projection algorithms with proprietary software (CTPro3D; Nikon Metrology, UK) and post processed using VGStudio MAX 3.4 (Volume Graphics GmbH, Heidelberg, Germany). Isotropic voxel sizes varied according to specimen size and magnification, ranging from 11.6 to 89.3 µm. We applied beam hardening correction, no noise reduction median filter or tube filtration.

Demographic data and imaging factors

Demographical data included gestational age (weeks), post-mortem weight (g), post-mortem interval (days), mode of death, and three fetal measurements in centimetres (crown-rump length (CRL), crown-heel length (CHL) and head circumference (HC) as well as whether an abnormality was detected by micro-CT (yes/no).

The timings between delivery and imaging were recorded, and comprised of:

  1. 1.

    Time to immersion (defined as the time from birth to placement in I2KI solution) and

  2. 2.

    Iodination time (defined as the time spent in I2KI solution prior to micro-CT imaging).

Specialist paediatric pathologists subjectively assessed the degree of maceration at external examination for the whole body, and derived a single score for each fetus, based on previously published work (0 = no maceration, 3 severe/established maceratio[28, 29]).

Imaging parameters were recorded for the head and chest/abdomen/pelvis examinations and fell within the following ranges: kilovoltage (60–160 kilovolts), current (78–400 µA), power (7–40 Watts), exposure time (125–1000 ms), frames per projection (1–4) projections (1066–3141) and effective pixel size (EPS) (11.6–89.3 microns).

Image analysis

Image quality assessments were completed independently by two board-certified paediatric radiologists, with 5 years (SS) and 16 years (OA) of specialist post-mortem radiology experience. All images were anonymised, and observers were blinded to the clinical history and pathological assessments.

Image quality assessments were made on 2 selected axial images per fetus, one through the head at the level of the mid-brain, and one through the thorax at the level of the heart, providing a 4-chamber cardiac view.

Each radiologist provided three different subjective image quality assessments:

  1. 1.

    Full iodination (yes, diagnostic/no, non-diagnostic) Fig. 1.

  2. 2.

    Imaging maceration score

Fig. 1
figure 1

Axial micro-CT images acquired through the head (a,b) and chest (c,d) demonstrating incomplete (a, c) and complete (b, d) iodination. The areas of lower density (i.e., black) seen within the central portion of the images (a, c) demonstrate incomplete iodine penetration through the body, and hamper diagnostic interpretation of soft tissue structures. (Axial micro-CT images acquired at 100kv, 150uA, 354 ms, 1 frames per projection) (fpp) and 3141 number of projections.)

Full size image

(Based on a scale 0–3: where 0 = none, 1 = mild cracking, distortion but images diagnostic, 2 = moderate disruption with reduction in normal tissue planes, limited diagnosis, 3 = severe maceration, non-diagnostic with severely distorted internal anatomy) Fig. 2, and

  1. 3.

    Image quality score

Fig. 2
figure 2

Axial micro-CT head images of four different fetuses demonstrating different degrees of maceration. a No maceration, b mild cracking and distortion of the image (add arrows), c moderate disruption with reduction in tissue planes (arrow), d non-diagnostic severe maceration

Full size image

(Based on a scale from 0 to 10: where 0–3 = poor image quality, very grainy images, loss of normal tissue planes; 4–6 = moderate image quality, some graininess perceptible, but major structures and tissue planes unaffected; 7–10 = high image quality, imperceptible graininess in image, excellent detail), Fig. 3. This score does not take into account iodination or maceration score.

Fig. 3
figure 3

Axial micro-CT images through the head and chest in different fetuses, demonstrating differences in image quality. Images which were grainy and tissue planes indistinct were assessed as poor quality (a), with residual image graininess in moderate quality (b), which was imperceptible in high quality (c)

Full size image

Statistical analysis

Descriptive statistics were calculated for baseline demographics, tissue preparation variables and image parameters. Inter- and intra-rater reliability was investigated through the kappa statistic (with linear weights) for maceration score and summary statistics (median, IQR) presented for the differences between image quality ratings. The average ratings between the two radiologist readers for image quality (the primary outcome) and maceration score were used as the final outcome for subsequent analyses.

Simple and multivariable linear regression models were fitted for the outcome variables of image quality and perceived maceration score, separately for head and chest images. Baseline demographics, tissue preparation variables and image parameters were considered as predictor variables in these models. A forward and backward model selection approach was adopted to minimise the model fit statistic AIC to choose the final multivariable models. All analyses were carried out in R version 3.6.1.

Results

Demographics and imaging parameters

258 fetuses underwent micro-CT with a median post-mortem weight 41.7 g (range 2.6–350), mean gestational age of 16 weeks (range 11–24). Further demographic data is provided in Table 1. The time to immersion showed a bimodal distribution with peaks < 10 days (median 3) and > 10 days (median 16 days), Fig. 4.

Table 1 Study cohort demographic data and imaging parameter range
Full size table
Fig. 4
figure 4

Bimodal distribution of time to immersion across the fetuses included in our cohort

Full size image

Approximately a quarter (68/258, 26.5%) of cases showed significant abnormality on micro-CT, the results of which have been presented elsewhere [20]. The imaging indication was mostly miscarriage 157/258 (60.9%), followed by termination of pregnancy (TOP) 69/258 (26.7%) and intrauterine death (IUD) 32/258 (12.4%). The range of imaging parameters used were the same for head and chest imaging (Table 1) with minor differences between examination areas in < 5% of cases (kilovoltage (kV), current, exposure time, power), apart from number of projections and estimated pixel size which varied to a greater degree due to anatomical area size (Table 1).

Overall image quality assessments

An image quality score of greater than 6.5 was recorded in 247/258 (95.8%) head and 251/258 (97.3%) chest imaging (i.e., 497/516 (95.9%) images overall). Image quality scores were higher for head (median = 9, range 4–10) than for chest (median = 8.5, range 5–10; p < 0.001; Fig. 5).

Fig. 5
figure 5

Difference in range in image quality scores between head and chest axial images, with head displaying greater overall image quality than chest.”

Full size image

Complete agreement between the two observers was seen in 51.2% (132/258) head images and 36% (93/258) chest images with mean score used as “image quality” for the results.

Maceration and iodination assessments

250/258 (96.9%) of all cases were classed as fully iodinated. There was high agreement of iodination status for heads 250/258 (96.8%) and chest 252/258 (97.6%).

Imaging of the brain scored greater for maceration than the chest. In just over a quarter of brain imaging cases (69/258, 26.7%) the highest maceration imaging score of 3 was provided, compared to only 3/258 (1.2%) chest images. There was an acceptable inter-rater agreement for the maceration score, with weighted Kappa = 0.56 (95% CI 0.49–0.63, p < 0.001).

Pathologists at external examination however recorded that over half of all fetuses 133/258, 51.6%) were severely macerated (i.e., score 3); a minority (14/258 (5.4%) as moderately macerated (i.e., score 2) or mildly macerate (i.e., score 1, 30 / 258, 11.6%) and approximately a third (81/258, 31.4%) as not macerated.

There was agreement of maceration score on micro-CT images and pathological assessment (within ± 0.5) for the head in 150/258 (58.1%), and chest in 107/258 (41.5%), with micro-CT images predominantly scoring less severe maceration in (64/258) 24.8% head and 138/258 (53.5%) chest imaging than external assessment.

Image quality predictors

The main predictor of image quality for both head and chest was the pathological score of maceration, with a more severe maceration score associated with lower image quality (p < 0.001), although this only accounted for 6.6% of the variation for head imaging and 11.6% for chest imaging. Increasing gestational weight was also negatively associated with image quality in the adjusted models (p < 0.001 head, p = 0.003 chest), but not in unadjusted models.

The main imaging parameter predictor of the image quality score was the number of projections acquired, which was positively associated with image quality in both head and chest models. A greater image quality score was also positively associated with frames per projection (for 2 frames, as opposed to 1 or 4 frames) in both head (p < 0.081) and chest (p < 0.001) images.

Time to immersion was also negatively associated with image quality in chest images with borderline significance (p = 0.039), although there were several missing datapoints (69/258; 26.7%) where this was not recorded in the clinical notes. EPS was also negatively associated (Table 2).

Table 2 Simple and multivariable linear regression analysis
Full size table

Discussion

In this study, a high image quality score (of over 6.5) was achieved in the clear majority (96%) of fetal head and chest micro-CT studies from a range of gestational weights. The strongest negative predictor of final image quality was the extent of fetal maceration, with decreasing image quality also associated with increasing body weight. The strongest imaging parameter predictors for image quality were the number of frames per projection and EPS.

There was some discrepancy between micro-CT imaging assessment and pathological visual assessment of the extent of fetal maceration, where pathological maceration assessment was a better predictor of poor micro-CT image quality, although poor image quality was only found in 4.1% of fetuses overall. This means that we achieved good micro-CT image quality in the overwhelming majority of cases despite several severely macerated fetuses being referred to our unit, which will help the more widespread use of high-resolution imaging in macerated cases. Therefore, micro-CT could be used as a triage tool to determine which cases might be best suited for further pathological evaluation.

Whilst we focussed on image quality in this study, a recent diagnostic accuracy study showed that maceration rendered up to 50% of imaging non-diagnostic, in particular for the brain [20] and heart [9, 30], although analysis at autopsy is equally extremely challenging. Further optimisation of micro-CT may help provide greater diagnostic yield in future.

Image quality was also rated as consistently higher for head than chest imaging. This is likely due to intrinsic differences in image quality related to anatomical shapes and ensuring full inclusion within the imaging detectors: spherical objects (such as the head) can be positioned closer to the X-ray source, enabling lower EPS, whereas more elongated shapes (such as the body) require positioning further away, enforcing a higher EPS to achieve optimal coverage. This causes an increased number of projections, optimised by the scanner automatically, related to object diameter of for the head in comparison to the body, which would explain both higher image quality for the head and a negative association between increased EPS and image resolution/quality. A few fetuses which were imaged using more frames per projection chest (4/258) 2.7%, head 6/258 (2.3%), also yielded higher image quality, which is to be expected with increased signal to noise, although these scans take significantly longer, as scan time is the sum of exposure time, frames per projection and number of projections. This may explain our findings in this retrospective study, although these should be prospectively tested in a future study.

Gestational weight was negatively associated with image quality with a higher image quality rating overall for head when compared to chest images. Both these results can be explained by lower weight fetuses and smaller anatomical areas (particularly heads), resulting in a lower EPS and a higher resolution micro-CT image. Lower gestational weights and fetuses below 20 weeks gestation have significantly poorer diagnostic accuracy and image quality using other post-mortem techniques (MRI) [11] and Ultrasound [30], and should be diverted to micro-CT. Together, these factors combined influence the development of a clinical protocol for optimal resolution on a patient-by-patient basis.

We found a bimodal time-to-immersion pattern in our patient demographics, which is likely to represent differences between referral centres and their respective consent procedures. Access to the micro-CT service was expedited where full parental consent was given on referral, but delays were encountered if further information was required, results in two peaks at median 3 and 16 days (Fig. 4). This could also explain why TOP was a statistically significant positive predictor for image quality when compared to miscarriage, as these cases are likely to be referred more rapidly, also with minimal maceration. We have since adopted dedicated consent procedures at all referring centres to reduce these delays and improve both parent and professionals understanding of the procedures.

As micro-CT can generate high quality imaging in small, macerated fetuses where perinatal autopsy is known to present considerable logistical challenges, it offers an attractive alternative to those parents who do not consent to invasive autopsy and is likely to increase the uptake of post-mortem investigations [2,3,4,5]. This gives the opportunity to offer a broader range of post-mortem techniques on an individualised basis and can be useful to triage those cases in whom invasive autopsy will be of maximal yield. Formal autopsy will be of most use where post-mortem investigations and antenatal imaging findings are not concordant [31], although following fetal loss below 18 weeks gestation it is unlikely that detailed antenatal ultrasound will have been performed.

Limitations

The main limitation was the retrospective nature of this study, where we used a relatively narrow range of imaging parameters, limited by machine capability. Were this study conducted prospectively, a wider range of imaging parameters would have been undertaken to determine optimal imaging factors, as has been performed for individual extracted organs in previous work [32]. However, this study represented “in practice” learning within our department, and we have adopted several of the key points from these results into our everyday clinical practice.

We also did not include diagnostic accuracy in this study, as several of these fetuses did not undergo comprehensive autopsy, given that our service has developed to meet a clinical demand predominantly targeted towards parents who prefer non-invasive micro-CT imaging to invasive autopsy techniques for early gestation pregnancy loss. Diagnostic accuracy has been reported elsewhere [20, 21, 25], but our results show that high image quality is possible even in severely macerated, small fetuses.

Conclusion

High micro-CT fetal image quality is achievable following early pregnancy loss despite maceration. Higher resolution is achievable in smaller fetuses, particularly where conventional autopsy may be challenging. These factors should influence the establishing of a clinical micro-CT imaging service to address the growing need for less invasive autopsy methods.

Availability of data and materials

The datasets generated and/or analysed during the current study are not publicly available due to the sensitive nature of the data but are available from the corresponding author on reasonable request.

Abbreviations

CHL:

Crown-heel length

CRL:

Crown-rump length

EPS:

Effective pixel size

FPP:

Frames per projection

HC:

Head circumference

IUD:

Intra-uterine death

I2KI:

Potassium tri-iodide

kV:

Kilovoltage

Micro-CT:

Micro-computed tomography

PMUS:

Post-mortem ultrasound

PMMRI:

Post-mortem magnetic resonance imaging

TOP:

Termination of pregnancy

References

  1. Sonnemans LJP, Vester MEM, Kolsteren EEM, Erwich JJH, Nikkels PGJ, van Rijn RR, et al. Dutch guideline for clinical foetal-neonatal and paediatric post-mortem radiology, including a review of literature. Eur J Pediatr. 2018;177:791–803.

    Article  CAS  Google Scholar 

  2. Lewis C, Hill M, Arthurs OJ, Hutchinson C, Chitty LS, Sebire NJ. Factors affecting uptake of postmortem examination in the prenatal, perinatal and paediatric setting. BJOG. 2018;125(2):172–81.

    Article  CAS  Google Scholar 

  3. Lewis C, Riddington M, Hill M, Arthurs O, Hutchinson J, Chitty L, et al. Availability of less invasive prenatal, perinatal and paediatric autopsy will improve uptake rates: a mixed -methods study with bereaved parents. BJOG. 2019;126(6):754.

    Article  Google Scholar 

  4. Lewis C, Latif Z, Hill M, Riddington M, Lakhanpaul M, Arthurs OJ, et al. “We might get a lot more families who will agree”: Muslim and Jewish perspectives on less invasive perinatal and paediatric autopsy. PLoS ONE. 2018;13(8):e0202023.

    Article  Google Scholar 

  5. Lewis C, Hutchinson JC, Riddington M, Hill M, Arthurs OJ, Fisher J, et al. Minimally invasive autopsy for fetuses and children based on a combination of post-mortem MRI and endoscopic examination: a feasibility study. Health Technol Assess. 2019;23(46):1–104.

    Article  Google Scholar 

  6. Shelmerdine SC, Sebire NJ, Arthurs OJ. Perinatal post-mortem ultrasound (PMUS): radiological-pathological correlation. Insights Imaging. 2019;10(1):81.

    Article  Google Scholar 

  7. Shelmerdine SC, Singh M, Simcock IC, Calder AD, Ashworth M, Beleza A, et al. Characterization of Bardet-Biedl syndrome by postmortem microfocus computed tomography (micro-CT). Ultrasound Obstet Gynecol. 2019;53:129–34.

    Article  Google Scholar 

  8. Shelmerdine SC, Hutchinson JC, Ward L, Sekar T, Ashworth MT, Levine S, et al. INTACT (INcision-less TArgeted Core Tissue) biopsy procedure for perinatal autopsy: initial feasibility. Ultrasound Obstet Gynecol. 2019.

  9. Shelmerdine SC, Langan D, Mandalia U, Sebire NJ, Arthurs OJ. Maceration determines diagnostic yield of fetal and neonatal whole body post-mortem ultrasound. Prenat Diagn. 2020;40(2):232–43.

    Article  Google Scholar 

  10. Shelmerdine SC, Hutchinson JC, Kang X, Suich JD, Ashworth M, Cannie MM, et al. Novel usage of microfocus computed tomography (micro-CT) for visualisation of human embryonic development-Implications for future non-invasive post-mortem investigation. Prenat Diagn. 2018;38(7):538–42.

    Article  Google Scholar 

  11. Jawad N, Sebire NJ, Wade A, Taylor AM, Chitty LS, Arthurs OJ. Body weight lower limits of fetal postmortem MRI at 1.5 T. Ultrasound Obstet Gynecol. 2016;48(1):92–7.

    Article  CAS  Google Scholar 

  12. Dawood Y, Strijkers GJ, Limpens J, Oostra RJ, de Bakker BS. Novel imaging techniques to study postmortem human fetal anatomy: a systematic review on microfocus-CT and ultra-high-field MRI. Eur Radiol. 2019.

  13. Kang X, Carlin A, Cannie M, Sanchez TC, Jani JC. Fetal postmortem imaging: an overview of current techniques and future perspectives. American Journal of Obstetrics and Gynecology. 2020.

  14. Kang X, Cannie MM, Arthurs OJ, Segers V, Fourneau C, Bevilacqua E, et al. Post-mortem whole-body magnetic resonance imaging of human fetuses: a comparison of 3-T vs. 1.5-T MR imaging with classical autopsy. Eur Radiol. 2017;27(8):3542–53.

    Article  Google Scholar 

  15. Lombardi CM, Zambelli V, Botta G, Moltrasio F, Cattoretti G, Lucchini V, et al. Postmortem microcomputed tomography (micro-CT) of small fetuses and hearts. Ultrasound Obstet Gynecol. 2014;44(5):600–9.

    Article  CAS  Google Scholar 

  16. Lombardi S, Scola E, Ippolito D, Zambelli V, Botta G, Cuttin S, et al. Micro-computed tomography: a new diagnostic tool in postmortem assessment of brain anatomy in small fetuses. Neuroradiology. 2019;61(7):737–46.

    Article  Google Scholar 

  17. Li KZ, Gao Y, Zhang R, Hu T, Guo B. The effect of a manual instrumentation technique on five types of premolar root canal geometry assessed by microcomputed tomography and three-dimensional reconstruction. BMC Med Imaging. 2011;11:14.

    Article  Google Scholar 

  18. Al Faraj A, Shaik AS, Alnafea M. Intrapulmonary administration of bone-marrow derived M1/M2 macrophages to enhance the resolution of LPS-induced lung inflammation: noninvasive monitoring using free-breathing MR and CT imaging protocols. BMC Med Imaging. 2015;15:16.

    Article  Google Scholar 

  19. He RT, Tu MG, Huang HL, Tsai MT, Wu J, Hsu JT. Improving the prediction of the trabecular bone microarchitectural parameters using dental cone-beam computed tomography. BMC Med Imaging. 2019;19(1):10.

    Article  Google Scholar 

  20. Shelmerdine SC, Simcock IC, Ciaran Hutchinson J, Guy A, Ashworth MT, Sebire NJ, et al. Post-mortem micro-CT for non-invasive autopsies: Experience in > 250 human fetuses. Am J Obst Gynecol. 2020.

  21. Hutchinson JC, Shelmerdine SC, Simcock IC, Sebire NJ, Arthurs OJ. Early clinical applications for imaging at microscopic detail: microfocus computed tomography (micro-CT). Br J Radiol. 2017;90(1075):20170113.

    Article  Google Scholar 

  22. Hutchinson JC, Arthurs OJ, Ashworth MT, Ramsey AT, Mifsud W, Lombardi CM, et al. Clinical utility of postmortem microcomputed tomography of the fetal heart: diagnostic imaging vs macroscopic dissection. Ultrasound Obstet Gynecol. 2016;47(1):58–64.

    Article  CAS  Google Scholar 

  23. Sandaite I, Lombardi C, Cook AC, Fabietti I, Deprest J, Boito S. Micro-computed tomography of isolated fetal hearts following termination of pregnancy: a feasibility study at 8–12 week's gestation. Prenat Diagn. 2020.

  24. Chen KC, Arad A, Song ZM, Croaker D. High-definition neural visualization of rodent brain using micro-CT scanning and non-local-means processing. BMC Med Imaging. 2018;18(1):38.

    Article  Google Scholar 

  25. Hutchinson JC, Kang X, Shelmerdine SC, Segers V, Lombardi CM, Cannie MM, et al. Postmortem microfocus computed tomography for early gestation fetuses: a validation study against conventional autopsy. Am J Obst Gynecol. 2018;218(4):445.

    Article  Google Scholar 

  26. Simcock IC, Shelmerdine SC, Hutchinson JC, Sebire NJ, Arthurs OJ. Human fetal whole-body postmortem microfocus computed tomographic imaging. Nat Protoc. 2021;16(5):2594–614.

    Article  CAS  Google Scholar 

  27. Simcock IC, Shelmerdine SC, Hutchinson JC, Sebire NJ, Arthurs OJ. Human fetal whole body post-mortem microfocus computed tomographic imaging. Nat Protoc. 2020. (accepted for publication).

  28. Genest DR, Williams MA, Greene MF. Estimating the time of death in stillborn fetuses: I. Histologic evaluation of fetal organs; an autopsy study of 150 stillborns. Obst Gynecol. 1992;80:575–84.

    CAS  Google Scholar 

  29. Shelmerdine SC, Hickson M, Sebire NJ, Arthurs OJ. Post-mortem magnetic resonance imaging appearances of feticide in perinatal deaths. Fetal Diagn Ther. 2019;45(4):221–9.

    Article  Google Scholar 

  30. Kang X, Sanchez TC, Arthurs OJ, Bevilacqua E, Cannie MM, Segers V, et al. Postmortem fetal imaging: prospective blinded comparison of two-dimensional ultrasound with magnetic resonance imaging. Ultrasound Obstet Gynecol. 2019;54(6):791–9.

    Article  CAS  Google Scholar 

  31. Shelmerdine SC, Arthurs OJ, Gilpin I, Norman W, Jones R, Taylor AM, et al. Is traditional perinatal autopsy needed after detailed fetal ultrasound and post-mortem MRI? Prenat Diagn. 2019;39(9):818–29.

    Article  Google Scholar 

  32. Simcock IC, Hutchinson JC, Shelmerdine SC, Matos JN, Sebire NJ, Fuentes VL, et al. Investigation of optimal sample preparation conditions with potassium triiodide and optimal imaging settings for microfocus computed tomography of excised cat hearts. Am J Vet Res. 2020;81:326–33.

    Article  Google Scholar 

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Acknowledgements

Not applicable.

Funding

ICS is funded by a National Institute for Health Research (NIHR) Clinical Doctoral Research Fellowship (ICA-CDRF-2017–03-53). OJA is funded by a NIHR Career Development Fellowship (NIHR-CDF-2017–10-037). SCS is supported by a RCUK/ UKRI Innovation Fellowship and Medical Research Council (MRC) Clinical Research Training Fellowship (Grant Ref: MR/R002118/1), jointly funded by the Royal College of Radiologists (RCR). This article presents independent research and the views expressed are those of the author(s) and not necessarily those of the funding bodies or the Department of Health & Social Care.

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Authors and Affiliations

  1. Department of Clinical Radiology, Great Ormond Street Hospital for Children, London, UK

    Ian Craig Simcock, Susan Cheng Shelmerdine, Guy Anna & Owen John Arthurs

  2. Great Ormond Street Hospital for Children, UCL Great Ormond Street Institute of Child Health, London, UK

    Ian Craig Simcock, Susan Cheng Shelmerdine, Dean Langan, Guy Anna, Neil James Sebire & Owen John Arthurs

  3. NIHR Great Ormond Street Hospital Biomedical Research Centre, London, UK

    Ian Craig Simcock, Susan Cheng Shelmerdine, Guy Anna, Neil James Sebire & Owen John Arthurs

  4. Department of Histopathology, Great Ormond Street Hospital for Children, London, UK

    Neil James Sebire

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  1. Ian Craig Simcock
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Contributions

All authors made substantial contributions to the conception and design of the work; ICS, SCS and AG acquired the data and ICS, SCS, DL, NJS and OJA analysed and interpreted the data; all authors drafted the work and substantively revised it.

Corresponding author

Correspondence to Ian Craig Simcock.

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Ethics approval and consent to participate

Ethical approval for this study was obtained as part of the evaluation and development of post-mortem imaging (REC 13/LO/1994). NRES Committee London – Camberwell St Giles approved all experimental protocols and these were used in accordance the Declaration of Helsinki and conformed to our Institutional guidelines. Written informed parental consent was obtained for post-mortem imaging.

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All data has been anonymised prior to analysis.

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The authors declare that they have no competing interests.

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Simcock, I.C., Shelmerdine, S.C., Langan, D. et al. Micro-CT yields high image quality in human fetal post-mortem imaging despite maceration. BMC Med Imaging 21, 128 (2021). https://doi.org/10.1186/s12880-021-00658-5

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  • DOI: https://doi.org/10.1186/s12880-021-00658-5

Keywords

  • Micro-CT
  • Human foetuses
  • Post-mortem imaging
  • Maceration
  • Image quality

BMC Medical Imaging

ISSN: 1471-2342

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