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Can prospective systematic reviews of animal studies improve clinical translation?


Systematic reviews are powerful tools with the potential to generate high quality evidence. Their application to animal studies has been instrumental in exposing the poor quality of these studies, as well as a catalyst for improvements in study design, conduct and reporting. It has been suggested that prospective systematic reviews of animal studies (i.e. systematic reviews conducted prior to clinical trials) would allow scrutiny of the preclinical evidence, providing valuable information on safety and efficacy, and helping to determine whether clinical trials should proceed. However, while prospective systematic reviews allow valuable scrutiny of the preclinical animal data, they are not necessarily able to reliably predict the safety and efficacy of an intervention when trialled in humans. Consequently, they may not reliably safeguard humans participating in clinical trials and might potentially result in lost opportunities for beneficial clinical treatments. Furthermore, animal and human studies are often conducted concurrently, which not only makes prospective systematic reviews of animal studies impossible, but suggests that animal studies do not inform human studies in the manner presumed. We suggest that this points to a confused attitude regarding animal studies, whereby tradition demands that they precede human studies but practice indicates that their findings are often ignored. We argue that it is time to assess the relative contributions of animal and human research in order to better understand how clinical knowledge is actually produced.


Systematic reviews (SRs) are powerful tools with the potential to generate high quality evidence. Their application to animal studies has exposed the poor quality of the majority of these studies, highlighting that many essential procedures such as randomisation and blinding are frequently not performed or reported [1, 2]. SRs have also been a catalyst for improvements in the design, quality and reporting of animal studies [3, 4]. As unreliable data cannot be used to draw any reliable conclusions, SRs can eventually lead (as a result of transparency encouraging methodological improvements) to more reliable and useful data, as has been the case with clinical trials. SRs use already available data (producing new scientific information without using more animals) and can prevent the unnecessary duplication of animal experiments by establishing the status of a body of evidence in a field. Since commencing SRs of animal studies, for example, Radboud University in the Netherlands has seen a 35% drop in animals used [5]. Consequently, SRs have value in terms of reducing research waste and promoting the ‘reduce’ component of the 3Rs [6]. SRs of high-quality animal studies may also provide new insights and enable scientific decisions to be evidence-based. For example, they have potential to complement ongoing work to select optimal animal models [7,8,9] by directing researchers towards those that are most predictive, or they may direct researchers away from animal models altogether.

Can SRs of animal studies also improve clinical translation? Certainly they have potential to do so, as they can make the evidence obtained from animal studies more transparent and accessible. They are able to synthesise and summarise large bodies of evidence, identify knowledge gaps and produce definitive answers based on all the available evidence, removing the need to try and make sense of the sometimes contradictory findings that emerge from individual studies within a body of research. They are also able to throw light on the validity of the data emerging from preclinical animal studies, which is of key importance to those considering clinical trials. Consequently, many (including ourselves) have advocated that SRs of animal studies should be routinely conducted on a prospective basis, i.e. prior to commencing clinical trials [3, 4, 10,11,12,13,14,15,16,17,18,19]. However, at present most SRs of animal studies are conducted retrospectively, after the corresponding clinical trials have taken place.

What can retrospective SRs of animal studies tell us about the potential of prospective SRs?

In cases where clinical trials have either found no treatment effects, or harmful effects, SRs of animal studies are sometimes conducted retrospectively in an attempt to understand why the clinical trials went ahead. For example, after Horn et al’s SR of clinical trials of nimodipine for acute stroke found no evidence of a clinically important effect [20], the authors systematically reviewed the relevant animal studies [21] and concluded that these had not provided convincing evidence of benefit to support the decision to proceed to clinical trials. This was also the case for low level laser therapy for wound healing; after a SR of human studies found that the treatment was ineffective in humans [22], the authors systematically reviewed the animal studies [23] and concluded that they had not provided unequivocal evidence to substantiate the decision to conduct clinical trials. Similar conclusions were drawn in the cases of fluid resuscitation for bleeding trauma patients [24,25,26], endothelin for chronic heart failure [27, 28] and more recently, a booster vaccine (MVA85A) intended to confer extra protection against tuberculosis [29, 30]. In all these cases, it would be reasonable to conclude that conducting prospective SRs of the animal studies might have prevented expensive and unnecessary or risky clinical trials from proceeding; indeed this is often called for following the failure of a clinical trial, or the halting of a clinical trial that turns out to be dangerous [31].

In all the above cases however, there was concordance between the SRs of the animal and human data in terms of evidence of efficacy. Unfortunately this is not always the case, and it is the possibility of discordance that raises doubts about the benefits of conducting SRs of animal studies prior to clinical trials. For example, a clinical trial of probiotic supplementation found that it increased mortality in humans [32], but a retrospective SR of the animal data found no indication of any risk of mortality; in fact the animal studies found evidence of benefit. The authors concluded that if the SR of the animal studies had been conducted prior to the clinical trial, it would not have predicted the harmful effects of probiotic supplementation on humans [33].

This issue can be further explored using Perel et al.’s data [10]. These authors identified six interventions for which there was unambiguous SR evidence of a treatment effect for humans and then conducted SRs of the corresponding animal studies for the same six interventions. The quality of the animal experiments was judged to be poor across all six interventions. Based on the SR evidence they found that there was concordance or partial concordance between the animal and human data for three of the interventions (antenatal corticosteroids, thrombolytics and bisphosphonates). However, for the other three interventions there was discordance between the animal and human data: antifibrinolytics reduce surgical bleeding and the need for transfusion in humans [34] but the animal studies of antifibrinolytics were inconclusive [10]; corticosteroids benefit animals with brain injury [10] but increase mortality in humans with brain injury [35]; tirilazad reduces infarct volume and improves neuro-behavioural scores in animals with experimental stroke [10] but increases the risk of death and dependency in humans with stroke [36]. What would have happened if the SRs of these animal studies had been conducted prior to clinical trials? Because the SR of animal studies of antifibrinolytics found the data to be inconclusive, the (ultimately beneficial) clinical trials of antifibrinolytics may not have gone ahead. In the case of corticosteroids and tirilazad, it is to be hoped that the SRs would have alerted clinical scientists to the poor quality of the primary animal studies, leading them to conclude that the animal data were not sufficiently robust to provide a basis for clinical trials; if not, the trials would have proceeded and patients would have died. The point is that a SR is only as good as the studies it includes. Since animal studies are unable to reliably predict safety and efficacy in humans [37,38,39,40,41] it follows that SRs of animal studies will not be able to reliably predict safety and efficacy in humans either.

Will translational rates increase once the quality of animal studies improves?

The poor quality of preclinical animal studies is widely acknowledged [1, 10, 42,43,44]. MR-H’s team, for example, attempted to use a robot reviewer to evaluate the quality of animal studies for a risk of bias assessment, but was unable to train the robot reviewer as high calibre animal studies do not exist [45]. This lack of scientific rigour complicates matters, making it difficult to draw conclusions about animal to human translation. For example, if an animal study reports positive results, but the quality of that animal study is poor (as in the case of corticosteroids and tirilazad, in Perel et al.’s study above [10]), it is unclear whether those positive findings are ‘true’, or simply an artefact of poor study design. Many are of the view that improvements in scientific rigour and reporting will ultimately reveal greater concordance between animal and human data, but at present there is no evidence to support this view. In the field of stroke, for example, there have been concerted attempts to improve the quality of animal studies (e.g. [46, 47]), but these have not resulted in greater clinical translation [48,49,50,51,52]. This may be because the quality of the animal studies is still not sufficiently high, and/or it may be a result of the unpredictability that animal–human species differences introduce. As the quality of the animal studies in Perel et al.’s study [10] was judged to be poor for all 6 interventions, something other than study quality appears to have influenced the observed variation in concordance between animal and human data. A recent scoping review of 90 papers assessing the concordance of animal to human studies revealed that concordance ranges from 0 to 100% [53]. Although the number of studies increased with time, the concordance rates remained in the same broad range. This could indicate that despite efforts to improve the quality of animal studies, the risk of bias is still too high to draw reliable conclusions, or that animal to human translation will always be unpredictable due to animal–human species differences [54,55,56,57,58,59]. Animal–human species differences should not be underestimated, yet their contribution to the poor predictivity of animal models is vastly under-explored in comparison with other aspects that impact on translation, such as risk of bias and inappropriate animal models [60].

Is it feasible to conduct prospective SRs of animal studies?

To return to the idea of conducting SRs of animal studies prior to clinical trials, there is an added difficulty in the context of disease research, because animal and human studies frequently run concurrently. Although it is a widely held view that studies are first conducted in animals and that the results from these inform clinical research, in fact the law only requires animal studies to be conducted prior to clinical studies for safety testing, i.e. there is no legal requirement for animals to be used in basic research into drugs and diseases. An examination of the publication dates of animal and human studies for the same interventions [16, 17, 21] indicates that animal and human studies often run alongside each other rather than consecutively and that in several cases the animal studies continue after human studies have stopped. Table 1, drawing on data from Perel et al.’s study [10], shows that there are no cases in which clinical studies commenced only after animal studies were completed.

Table 1 Dates of animal and human studies for the same intervention, from Perel et al. [10] and reanalysed by Pound et al. [17]

If animal and human studies run concurrently, it begs the question of how necessary animal studies are to clinical research and progress. Table 1 suggests that clinical researchers do not wait for animal study findings before proceeding to conduct human studies. Furthermore, clinicians tend to cite clinical (rather than animal) studies when drawing up clinical guidelines [61] and anecdotal evidence suggests that medical ethics committees rarely look at animal data once human data are available. All of this points to a rather confused attitude to animal studies: tradition demands that they precede human studies, but in practice clinical scientists may ignore their findings.

How is clinical knowledge actually produced?

Translational research appears to be less linear that traditionally assumed, and the boundaries between the bench and the bedside more fluid [62]. In the field of regenerative medicine for example, it has been observed that innovation is frequently clinically driven, with basic laboratory science often validating existing clinical knowledge, rather than informing clinical research as is usually imagined [63]. This has been the case in the field of stroke too; thrombolytics went straight to clinical trials following success with heart attack, so while animal studies were conducted to investigate dosage, they were not necessary to establish that thrombolytics could be helpful for human stroke [64,65,66,67] (indeed microdosing in humans now offers a potential alternative approach for establishing dosage [68]). We need to better understand what is going on here, i.e. how much of the preclinical research effort is spent on animal studies designed to inform or predict the human situation, and how much is focused on other activities such as drug repurposing or reverse translation [69]. It is important to gain a more accurate picture of how new knowledge is produced, as well as the relative contributions of clinical and preclinical research activities in contributing to this new knowledge. Martin et al. [63] argue that clinical experimentation is a crucial driver in producing new knowledge and translating it into routine practice. For the sake of patients, we need to understand which are the most effective research practices for clinical knowledge production, so that more resources can flow into such practices.


SRs of animal studies are clearly valuable for a number of reasons; they enable scrutiny of the validity of the preclinical evidence, they raise awareness of poor study design and ultimately encourage improvements in scientific rigour and reporting, they provide transparency, and help prevent the unnecessary duplication of animal studies. However, while SRs of animal studies conducted prior to clinical trials would provide valuable evidence about the validity of the animal data, they would not necessarily be able to reliably predict the safety or efficacy of interventions when trialled in humans, due to the poor predictivity of the primary studies. Therefore calls for SRs of animal studies to be conducted prior to clinical trials need to have a health warning; they are valuable for assessing the quality of the preclinical evidence, but do not necessarily have predictive validity, meaning that prospective SRs of animal studies will not reliably safeguard those taking part in clinical trials. We argue further, that it may well be impossible to conduct prospective SRs of animal studies, since this would require that animal studies are completed prior to clinical studies, which does not always appear to be the case. Finally, we suggest that it is time to assess the relative contributions of animal and human research in order to better understand how clinical knowledge is actually produced.

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systematic review

M R-H:

Merel Ritskes-Hoitinga


  1. 1.

    Hirst JA, Howick J, Aronson JK, Roberts N, Perera R, Koshiaris C, Heneghan C. The need for randomization in animal trials: an overview of systematic reviews. PLoS ONE. 2014;9(6):e98856.

  2. 2.

    Henderson VC, Demko N, Hakala A, MacKinnon N, Federico CA, Fergusson D, Kimmelman J. A meta-analysis of threats to valid clinical inference in preclinical research of sunitinib. Elife. 2015;4:e08351.

  3. 3.

    Hooijmans C, Ritskes-Hoitinga M. Progress in using SRs of animal studies to improve translational research. PLoS Med. 2013;10(7):e1001482.

  4. 4.

    de Vries RB, Wever KE, Avey MT, Stephens ML, Sena ES, Leenaars M. The usefulness of SRs of animal experiments for the design of preclinical and clinical studies. ILAR J. 2014;55(3):427–37.

  5. 5.

    Cochrane. Cochrane-REWARD prizes for reducing waste: 2017 winners. Accessed 28/8/2019.

  6. 6.

    Russell WM, Burch RL, Hume CW. The principles of humane experimental technique. London: Methuen; 1959.

  7. 7.

    Veening-Griffioen DH, Ferreira GS, van Meer PJ, Boon WP, Gispen-de Wied CC, Moors EH, et al. Are some animal models more equal than others? A case study on the translational value of animal models of efficacy for Alzheimer’s disease. Eur J Pharmacol. 2019;859:172524.

  8. 8.

    Ferreira GS, Veening-Griffioen DH, Boon WP, Moors EH, Gispen-de Wied CC, Schellekens H, van Meer PJ. A standardised framework to identify optimal animal models for efficacy assessment in drug development. PLoS ONE. 2019;14(6):e0218014.

  9. 9.

    de Vries RB, Buma P, Leenaars M, Ritskes-Hoitinga M, Gordijn B. Reducing the number of laboratory animals used in tissue engineering research by restricting the variety of animal models Articular cartilage tissue engineering as a case study. Tissue Eng Part B Rev. 2012;18(6):427–35.

  10. 10.

    Perel P, Roberts I, Sena E, Wheble P, Briscoe C, Sandercock P, Macleod M, Mignini LE, Jayaram P, Khan KS. Comparison of treatment effects between animal experiments and clinical trials: systematic review. BMJ. 2007;334(7586):197.

  11. 11.

    Sena E, van der Worp HB, Howells D, Macleod M. How can we improve the pre-clinical development of drugs for stroke? Trends Neurosci. 2007;30(9):433–9.

  12. 12.

    Dirnagl U, Macleod MR. Stroke research at a road block: the streets from adversity should be paved with meta-analysis and good laboratory practice. Br J Pharmacol. 2009;157(7):1154–6.

  13. 13.

    Howells DW, Sena ES, O’collins V, Macleod MR. Improving the efficiency of the development of drugs for stroke. Int J Stroke. 2012;7(5):371–7.

  14. 14.

    Neuhaus AA, Rabie T, Sutherland BA, Papadakis M, Hadley G, Cai R, Buchan AM. Importance of preclinical research in the development of neuroprotective strategies for ischemic stroke. JAMA Neurol. 2014;71(5):634–9.

  15. 15.

    Suzuki H, Nakano F. To improve translational research in subarachnoid hemorrhage. Transl Stroke Res. 2018;9:1–3.

  16. 16.

    Pound P, Ebrahim S, Sandercock P, Bracken M, Roberts I. Where is the evidence that animal research benefits humans? BMJ. 2004;328:514.

  17. 17.

    Pound P, Nicol C. Retrospective harm benefit analysis of pre-clinical animal research for six treatment interventions. PLoS ONE. 2018;13(3):e0193758.

  18. 18.

    Van Luijk J, Leenaars M, Hooijmans C, Wever K, de Vries R, Ritskes-Hoitinga M. Towards evidence-based translational research: the pros and cons of conducting SRs of animal studies. Altex. 2012;30(2/13):256–7.

  19. 19.

    Ritskes-Hoitinga M, Wever K. Improving the conduct, reporting, and appraisal of animal research. BMJ. 2018;360:j4935.

  20. 20.

    Horn J, Limburg M. Calcium antagonists for acute ischemic stroke. Cochrane Database Syst Rev. 2000.

  21. 21.

    Horn J, De Haan RJ, Vermeulen M, Luiten PG, Limburg M. Nimodipine in animal model experiments of focal cerebral ischemia: a SR. Stroke. 2001;32(10):2433–8.

  22. 22.

    Lucas C, Stanborough RW, Freeman CL, De Haan RJ. Efficacy of low level laser therapy on wound healing in human subjects: a SR. Lasers Med Sci. 2000;15:84–93.

  23. 23.

    Lucas C, Criens-Poublon LJ, Cockrell CT, de Haan RJ. Wound healing in cell studies and animal model experiments by low level laser therapy; were clinical studies justified? A SR. Lasers Med Sci. 2002;17(2):110–34.

  24. 24.

    Roberts I, Evans P, Bunn F, Kwan I, Crowhurst E. Is the normalisation of blood pressure in bleeding trauma patients harmful? Lancet. 2001;357(9253):385–7.

  25. 25.

    Roberts I, Kwan I, Evans P, Haig S. Does animal experimentation inform human healthcare? Observations from a SR of international animal experiments on fluid resuscitation. BMJ. 2002;324(7335):474–6.

  26. 26.

    Mapstone J, Roberts I, Evans P. Fluid resuscitation strategies: a SR of animal trials. J Trauma Acute Care Surg. 2003;55(3):571–89.

  27. 27.

    Kalra PR, Moon JC, Coats AJ. Do results of the ENABLE (Endothelin Antagonist Bosentan for Lowering Cardiac Events in Heart Failure) study spell the end for non-selective endothelin antagonism in heart failure? Int J Cardiol. 2002;85:195–7.

  28. 28.

    Lee DS, Nguyen QT, Lapointe N, Austin PC, Ohlsson A, Tu JV, Stewart DJ, Rouleau JL. Meta-analysis of the effects of endothelin receptor blockade on survival in experimental heart failure. J Cardiac Fail. 2003;9(5):368–74.

  29. 29.

    Tameris MD, Hatherill M, Landry BS, Scriba TJ, Snowden MA, Lockhart S, Shea JE, McClain JB, Hussey GD, Hanekom WA, Mahomed H. Safety and efficacy of MVA85A, a new tuberculosis vaccine, in infants previously vaccinated with BCG: a randomised, placebo-controlled phase 2b trial. Lancet. 2013;381(9871):1021–8.

  30. 30.

    Kashangura R, Sena ES, Young T, Garner P. Effects of MVA85A vaccine on tuberculosis challenge in animals: SR. Int J Epidemiol. 2015;44(6):1970–81.

  31. 31.

    Symonds ME, Budge H. Comprehensive literature search for animal studies may have saved STRIDER trial. BMJ. 2018;362:k4007.

  32. 32.

    Besselink MG, van Santvoort HC, Buskens E, Boermeester MA, van Goor H, Timmerman HM, et al. Probiotic prophylaxis in predicted severe acute pancreatitis: a randomised, double-blind, placebo-controlled trial. Lancet. 2008;371(9613):651–9.

  33. 33.

    Hooijmans CR, de Vries RB, Rovers MM, Gooszen HG, Ritskes-Hoitinga M. The effects of probiotic supplementation on experimental acute pancreatitis: a systematic review and meta-analysis. PLoS ONE. 2012;7(11):e48811.

  34. 34.

    Henry DA, Moxey AJ, Carless PA, O’Connell D, McClelland B, Henderson KM, et al. Anti-fibrinolytic use for minimising perioperative allogeneic blood transfusion. Cochrane Database Syst Rev. 1999;4:CD001886.

  35. 35.

    Alderson P, Roberts I. Corticosteroids for acute traumatic brain injury. Cochrane Database Syst Rev. 2005;1:CD000196.

  36. 36.

    Tirilazad International Steering Committee. Tirilazad for acute ischaemic stroke. Cochrane Database Syst Rev. 2001;4:2087.

  37. 37.

    Cook D, Brown D, Alexander R, March R, Morgan P, Satterthwaite G, Pangalos MN. Lessons learned from the fate of AstraZeneca’s drug pipeline: a five-dimensional framework. Nat Rev Drug Discov. 2014;13(6):419–31.

  38. 38.

    Harrison RK. Phase II and phase III failures: 2013–2015. Nat Rev Drug Discovery. 2016;15:817–8.

  39. 39.

    Thomas DW, Burns J, Audette J, Carroll A, Dow-Hygelund C, Hay M. Clinical development success rates 2006–2015. 2016.,%20Biomedtracker,%20Amplion%202016.pdf Accessed 17 Dec 2019.

  40. 40.

    Hwang TJ, Carpenter D, Lauffenburger JC, Wang B, Franklin JM, Kesselheim AS. Failure of investigational drugs in late-stage clinical development and publication of trial results. JAMA Int Med. 2016;176(12):1826–33.

  41. 41.

    BioIndustry Association and the Medicines Discovery Catapult. State of the discovery nation 2018 and the role of the Medicines Discovery Catapult. 2018. Available at: Accessed 17 Dec 2019.

  42. 42.

    Macleod MR, McLean AL, Kyriakopoulou A, Serghiou S, de Wilde A, Sherratt N, Hirst T, Hemblade R, Bahor Z, Nunes-Fonseca C, Potluru A. Risk of bias in reports of in vivo research: a focus for improvement. PLoS Biol. 2015;13(10):e1002273.

  43. 43.

    Tsilidis KK, Panagiotou OA, Sena ES, Aretouli E, Evangelou E, Howells DW, Salman RA, Macleod MR, Ioannidis JP. Evaluation of excess significance bias in animal studies of neurological diseases. PLoS Biol. 2013;11(7):e1001609.

  44. 44.

    Holman C, Piper SK, Grittner U, Diamantaras AA, Kimmelman J, Siegerink B, Dirnagl U. Where have all the rodents gone? The effects of attrition in experimental research on cancer and stroke. PLoS Biol. 2016;14(1):e1002331.

  45. 45.

    Jennifer Stone. Personal communication, 2019.

  46. 46.

    STAIR (Stroke Therapy Academic Industry Roundtable), Stroke TA. Recommendations for standards regarding preclinical neuroprotective and restorative drug development. Stroke. 1999;30(12):2752.

  47. 47.

    Fisher M, Feuerstein G, Howells DW, Hurn PD, Kent TA, Savitz SI, Lo EH. Update of the stroke therapy academic industry roundtable preclinical recommendations. Stroke. 2009;40(6):2244–50.

  48. 48.

    Ginsberg MD. Current status of neuroprotection for cerebral ischemia: synoptic overview. Stroke. 2009;40(3):S111–4.

  49. 49.

    Budincevic H, Bielen I, Csiba L. Translational challenges of neuroprotection strategy in ischemic stroke. Transl Neurosci. 2011;2(4):344–50.

  50. 50.

    Minnerup J, Sutherland BA, Buchan AM, Kleinschnitz C. Neuroprotection for stroke: current status and future perspectives. Int J Mol Sci. 2012;13(9):11753–72.

  51. 51.

    Sutherland BA, Minnerup J, Balami JS, Arba F, Buchan AM, Kleinschnitz C. Neuroprotection for ischaemic stroke: translation from the bench to the bedside. Int J Stroke. 2012;7(5):407–18.

  52. 52.

    Herson PS, Traystman RJ. Animal models of stroke: translational potential at present and in 2050. Future Neurol. 2014;9(5):541–51.

  53. 53.

    Leenaars CH, Kouwenaar C, Stafleu FR, Bleich A, Ritskes-Hoitinga M, De Vries RB, Meijboom FL. Animal to human translation: a systematic scoping review of reported concordance rates. J Transl Med. 2019;17(1):223.

  54. 54.

    Mestas J, Hughes CC. Of mice and not men: differences between mouse and human immunology. J Immunol. 2004;172(5):2731–8.

  55. 55.

    Preuss TM. Who’s afraid of Homo sapiens? J Biomed Discov Collab. 2006;1(1):17.

  56. 56.

    Lynch VJ. Use with caution: developmental systems divergence and potential pitfalls of animal models. Yale J Biol Med. 2009;82(2):53.

  57. 57.

    Perlman RL. Evolution and medicine. Oxford: Oxford University Press; 2013.

  58. 58.

    Perlman RL. Mouse models of human disease. An evolutionary perspective. Evol Med Public Health. 2016;1:170–6.

  59. 59.

    Pound P, Ritskes-Hoitinga M. Is it possible to overcome issues of external validity in preclinical animal research? Why most animal models are bound to fail. J Transl Med. 2018;16(1):304.

  60. 60.

    Hyman SE. Revolution stalled. Sci Transl Med. 2012;4(155):155cm11.

  61. 61.

    Grant J, Cottrell R, Cluzeau F, Fawcett G. Evaluating ‘payback’ on biomedical research from papers cited in clinical guidelines: applied bibliometric study. BMJ. 2000;320:1107–11.

  62. 62.

    Fudge N, Sadler E, Fisher HR, Maher J, Wolfe CD, McKevitt C. Optimising translational research opportunities: a SR and narrative synthesis of basic and clinician scientists’ perspectives of factors which enable or hinder translational research. PLoS ONE. 2016;11(8):e0160475.

  63. 63.

    Martin P, Brown N, Kraft A. From bedside to bench? Communities of promise, translational research and the making of blood stem cells. Sci Cult. 2008;17(1):29–41.

  64. 64.

    Dirnagl U. Thomas Willis lecture: is translational stroke research broken, and if so, how can we fix it? Stroke. 2016;47(8):2148–53.

  65. 65.

    Dirnagl U. Personal communication, 2019.

  66. 66.

    Zerna C, Hill MD, Boltze J. Towards improved translational stroke research: progress and perspectives of the Recent National Institute of Neurological Disorders and Stroke Consensus Group Meeting. Stroke. 2017;48(9):2341–2.

  67. 67.

    Hill M. Personal communication, 2019.

  68. 68.

    Rani PU, Naidu MU. Phase 0-Microdosing strategy in clinical trials. Indian J Pharmacol. 2008;40(6):240.

  69. 69.

    Shakhnovich V. It’s time to reverse our thinking: the reverse translation research paradigm. Clin Transl Sci. 2018;11(2):98.

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Thanks go to Kathy Archibald for discussions on some of the points we raise.


This paper was not supported by any specific funding.

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PP wrote the first draft and MR-H contributed to subsequent versions, with both agreeing the final version. PP is the guarantor of the article. Both authors read and approved the final manuscript.

Correspondence to Pandora Pound.

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Pound, P., Ritskes-Hoitinga, M. Can prospective systematic reviews of animal studies improve clinical translation?. J Transl Med 18, 15 (2020).

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  • Systematic review
  • Preclinical
  • Animal research
  • Translation