Advice
Search strategy and evidence selection
Search strategy
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Databases were searched from inception to August 2014. The following keywords were used for the searches: Model Predictive Control Algorithm; Space Glucose Control; Space GlucoseControl; enhanced Model Predictive Control; eMPC; intensive care; critical care; ICU. The number of citations found is in brackets after each database:
Medline (via OVID) (36); Embase (via OVID) (36); MEDLINE(R) In‑Process & Other Non‑Indexed Citations (via OVID) (12); Cochrane Library (total 222 including: 167 Cochrane reviews, 19 Trials, and 19 Economic evaluation); CAB Abstracts (8); Web of Science Science Citation Index (13).
These citations were sifted through to find any relevant material, using the inclusion criteria below. -
ClinicalTrials.gov, WHO ICTRP, and Current Controlled Trials were also searched for ongoing trials.
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Information provided by the manufacturer in supporting this briefing was checked to identify any further information.
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The manufacturer's website was thoroughly investigated.
Evidence selection
The inclusion criteria were as follows:
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Patients: critically ill patients in intensive care requiring tight glycaemic control
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Intervention: the Space GlucoseControl system, a computer‑assisted device for glycaemic control, combining infusion pumps with an indication of dose level and timing derived from a propriety computer‑based algorithm – the enhanced Model Predictive Control (eMPC) algorithm.
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Comparator: any other glycaemic control protocol. These include routine management, or any other computer‑based algorithms.
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Outcomes: any relevant efficacy and safety clinical outcomes, including but not limited to:
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blood glucose values
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time to target range
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proportion of time within target range
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time within target range
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number of hypoglycaemic and hyperglycaemic episodes
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proportion of time spent below or above the cut‑off levels for hypoglycaemia and hyperglycaemia
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proposed next measurement time
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insulin infusion rate
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carbohydrate administration rate
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hospital mortality and length of ICU stay
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any adverse event
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Study design: for effectiveness – any comparative study; for other aspects of the device – any, including case reports.
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Only studies available in English language will be included.