PMID- 26346805 OWN - NLM STAT- MEDLINE DCOM- 20160609 LR - 20220318 IS - 2046-4924 (Electronic) IS - 1366-5278 (Print) IS - 1366-5278 (Linking) VI - 19 IP - 70 DP - 2015 Sep TI - Surgical Trial In Traumatic intraCerebral Haemorrhage (STITCH): a randomised controlled trial of Early Surgery compared with Initial Conservative Treatment. PG - 1-138 LID - 10.3310/hta19700 [doi] AB - BACKGROUND: While it is accepted practice to remove extradural (EDH) and subdural haematomas (SDH) following traumatic brain injury, the role of surgery in parenchymal traumatic intracerebral haemorrhage (TICH) is controversial. There is no evidence to support Early Surgery in this condition. OBJECTIVES: There have been a number of trials investigating surgery for spontaneous intracerebral haemorrhage but none for TICH. This study aimed to establish whether or not a policy of Early Surgery for TICH improves outcome compared with a policy of Initial Conservative Treatment. DESIGN: This was an international multicentre pragmatic parallel group trial. Patients were randomised via an independent telephone/web-based randomisation service. SETTING: Neurosurgical units in 59 hospitals in 20 countries registered to take part in the study. PARTICIPANTS: The study planned to recruit 840 adult patients. Patients had to be within 48 hours of head injury with no more than two intracerebral haematomas greater than 10 ml. They did not have a SDH or EDH that required evacuation or any severe comorbidity that would mean they could not achieve a favourable outcome if they made a complete recovery from their head injury. INTERVENTIONS: Patients were randomised to Early Surgery within 12 hours or to Initial Conservative Treatment with delayed evacuation if it became clinically appropriate. MAIN OUTCOME MEASURES: The Extended Glasgow Outcome Scale (GOSE) was measured at 6 months via a postal questionnaire. The primary outcome was the traditional dichotomised split into favourable outcome (good recovery or moderate disability) and unfavourable outcome (severe disability, vegetative, dead). Secondary outcomes included mortality and an ordinal assessment of Glasgow Outcome Scale and Rankin Scale. RESULTS: Patient recruitment began in December 2009 but was halted by the funding body because of low UK recruitment in September 2012. In total, 170 patients were randomised from 31 centres in 13 countries: 83 to Early Surgery and 87 to Initial Conservative Treatment. Six-month outcomes were obtained for 99% of 168 eligible patients (82 Early Surgery and 85 Initial Conservative Treatment patients). Patients in the Early Surgery group were 10.5% more likely to have a favourable outcome (absolute benefit), but this difference did not quite reach statistical significance because of the reduced sample size. Fifty-two (63%) had a favourable outcome with Early Surgery, compared with 45 (53%) with Initial Conservative Treatment [odds ratio 0.65; 95% confidence interval (CI) 0.35 to 1.21; p = 0.17]. Mortality was significantly higher in the Initial Conservative Treatment group (33% vs. 15%; absolute difference 18.3%; 95% CI 5.7% to 30.9%; p = 0.006). The Rankin Scale and GOSE were significantly improved with Early Surgery using a trend analysis (p = 0.047 and p = 0.043 respectively). CONCLUSIONS: This is the first ever trial of surgery for TICH and indicates that Early Surgery may be a valuable tool in the treatment of TICH, especially if the Glasgow Coma Score is between 9 and 12, as was also found in Surgical Trial In spontaneous intraCerebral Haemorrhage (STICH) and Surgical Trial In spontaneous lobar intraCerebral Haemorrhage (STICH II). Further research is clearly warranted. TRIAL REGISTRATION: Current Controlled Trials ISRCTN 19321911. FUNDING: This project was funded by the National Institute for Health Research (NIHR) Health Technology Assessment programme and will be published in full in Health Technology Assessment; Vol. 19, No. 70. See the NIHR Journals Library website for further project information. FAU - Gregson, Barbara A AU - Gregson BA AD - Neurosurgical Trials Group, Institute of Neuroscience, Newcastle University, Newcastle upon Tyne, UK. FAU - Rowan, Elise N AU - Rowan EN AD - Neurosurgical Trials Group, Institute of Neuroscience, Newcastle University, Newcastle upon Tyne, UK. FAU - Francis, Richard AU - Francis R AD - Neurosurgical Trials Group, Institute of Neuroscience, Newcastle University, Newcastle upon Tyne, UK. FAU - McNamee, Paul AU - McNamee P AD - Health Economics Research Unit, University of Aberdeen, Aberdeen, UK. FAU - Boyers, Dwayne AU - Boyers D AD - Health Economics Research Unit, University of Aberdeen, Aberdeen, UK. FAU - Mitchell, Patrick AU - Mitchell P AD - Neurosurgical Trials Group, Institute of Neuroscience, Newcastle University, Newcastle upon Tyne, UK. FAU - McColl, Elaine AU - McColl E AD - Newcastle Clinical Trials Unit, Newcastle University, Newcastle upon Tyne, UK. FAU - Chambers, Iain R AU - Chambers IR AD - South Tees Hospitals Foundation Trust, James Cook University Hospital, Middlesbrough, UK. FAU - Unterberg, Andreas AU - Unterberg A AD - Department of Neurosurgery, University of Heidelberg, D-69120 Heidelberg, Germany. FAU - Mendelow, A David AU - Mendelow AD AD - Neurosurgical Trials Group, Institute of Neuroscience, Newcastle University, Newcastle upon Tyne, UK. CN - STITCH(TRAUMA) investigators LA - eng SI - ISRCTN/ISRCTN19321911 GR - HERU1/CSO_/Chief Scientist Office/United Kingdom GR - HSRU1/CSO_/Chief Scientist Office/United Kingdom PT - Comparative Study PT - Journal Article PT - Multicenter Study PT - Randomized Controlled Trial PT - Research Support, Non-U.S. Gov't PL - England TA - Health Technol Assess JT - Health technology assessment (Winchester, England) JID - 9706284 SB - IM MH - Acute Disease MH - Adolescent MH - Adult MH - Aged MH - Aged, 80 and over MH - Cerebral Hemorrhage, Traumatic/mortality/surgery/*therapy MH - Female MH - Hematoma/mortality/surgery/*therapy MH - Humans MH - Male MH - Middle Aged MH - Patient Selection MH - Sample Size MH - Time-to-Treatment MH - Treatment Outcome MH - Young Adult PMC - PMC4780887 EDAT- 2015/09/09 06:00 MHDA- 2016/06/10 06:00 PMCR- 2016/03/07 CRDT- 2015/09/09 06:00 PHST- 2015/09/09 06:00 [entrez] PHST- 2015/09/09 06:00 [pubmed] PHST- 2016/06/10 06:00 [medline] PHST- 2016/03/07 00:00 [pmc-release] AID - 10.3310/hta19700 [doi] PST - ppublish SO - Health Technol Assess. 2015 Sep;19(70):1-138. doi: 10.3310/hta19700.