Review
Copyright ©The Author(s) 2023.
World J Crit Care Med. Jun 9, 2023; 12(3): 92-115
Published online Jun 9, 2023. doi: 10.5492/wjccm.v12.i3.92
Table 1 Simplified polysomnographic features of the American Academy of Sleep Medicine’s phases of sleep
Sleep stage
Electroencephalogram
Electrooculogram
Chin electromyogram
Wake Alpha activity (sinusoidal 8-13 Hz)Rapid eye movements; Reading eye movements; Slow eye movements; BlinksNormal or high tone
N1< 50% alpha activity; > 50% low amplitude mixed frequency activity (4-7 Hz)Slow eye movementsVariable, usually lower than wake
N2Sleep spindles; K-complexesNoneVariable tone
N3Slow (delta) wave (0.5-2 Hz) ≥ 20%; Sleep spindles may occurNoneVariable tone
REMLow amplitude mixed frequency activity; No sleep spindles or K-complexesRapid eye movementsLow tone
Table 2 Comparison of studies assessing the effects of ventilator mode on sleep quantity and quality
Ref.
Study Design
n
Treatment arms
Sedation
Outcomes

Studies comparing pressure support ventilation against assist control ventilation
Parthasarathy et al[79], 2002Single centre, randomised, cross over study112 h each of: PSV; PS to achieve Vt 8 ml/kgACV; Vt: 8 mL/kg; f: Set as patient RR minus 4/minYesSleep efficiency: Arousal index, mean (SD)Not reported; ACV 39 (6); PSV 35 (7); No statistically significant difference between ventilation modes
Toublanc et al[81], 2007Single centre, randomised, cross over study204 h each of: PSV; PS = 6 cmH2O; Trigger sens = 0.5 cmH2OACV; Vt: 10 ml/kg; f: 12/min; Increased until no spontaneous inspiratory effortFree from sedation for 48 hSleep efficiency: Arousal index, mean (SD) No difference, values not reported; ACV 7 (SD 5); PSV 7 (SD 5); No statistically significant difference between ventilation modes
Cabello et al[82], 2008Single centre, randomised, cross over study156 h each of: cPSV; PS to achieve Vt 6-8 ml/kg (PBW); RR < 35/min; aPSVACV; Vt: 8 mL/kg; f: 10/min (back up)Free from sedation for 24 hSleep efficiency, median [IQR]: Arousal index, median [IQR]ACV 58 [48-82], cPSV 44 [29-30], aPSV 63 [29-80]; ACV 30 [17-41], PSV 28 [17-53], aPSV 23 [21-45]; No statistically significant difference between ventilation modes
Studies comparing pressure support ventilation against pressure control ventilation
Andréjak et al[83], 2013Single centre, randomised,cross over study264 h each of: PSV; PS = 6 cmH2O; Trigger sens = 0.5 cmH2OPCV; PS = 20 cmH2O; f: Greater than patient RR I/E ratio: 1/1.2 to 1/1.5Not reportedSleep efficiency, median [IQR]: Arousal index PCV 63 [9-100]; PSV 37 [0-96] Not reported; Significantly improved sleep efficiency with PCV
Studies comparing pressure support ventilation against proportional assist ventilation
Bosma et al[84], 2007Single centre, randomised, cross over study131 night each of: PSV PAVPropofol, midazolam or lorazepamSleep efficiency, mean (SD): Arousal index, median [IQR]: Patient-ventilator asynchrony per hour, mean (SD)PSV 58% (25); PAV 60 (23); PSV 16 (2-74); PAV 9 (1-41); PSV 53 (59); PAV 24 (15); PAV associated with statistically significantly fewer arousals and episodes of asynchrony
Alexopoulou et al[85], 2007Single centre, randomised, cross over study171 night each of: PSVbase; PS as before study; PShigh; Pressure assist increased by 40%-50% from PSVbase or until Paw = 30 cmH2OPAV+base; Set to achieve mean inspiratory pressure similar to PSVbase; PAV+high; Percentage of unloading increased by 40%-50% from PSVbase or until it reached 85%Group A; n = 11; Propofol; Group B; n = 9; Non-sedatedGroup A; Sleep efficiency, mean (SD): Arousal index, mean (SD): Group B; Sleep efficiency, mean (SD): Arousal index, mean (SD)PAV+base 99 (2); PAVhigh 98 (5); PSVbase 93 (11); PSVhigh 88 (16) (P < 0.05); PAV+base 4.6 (4.9); PAVhigh 7.4 (11); PSVbase 5.4 (3.6); PSVhigh 6.5 (6.7); PAV+base 76 (11); PAVhigh 71 (21); PSVbase 68 (19); PSVhigh 72 (15); PAV+base 12 (8.0); PAVhigh 11 (7.6); PSVbase 8.4 (4.8); PSVhigh 10.5 (9.9); In sedated patients (Group A), PAV+ is associated with a modest, albeit statistically significant at the 0.05 level, improvement in sleep efficiency; No statistically significant differences found between ventilation modes in non-sedated group
Alexopoulou et al[86], 2013Single centre, randomised,cross over study14Alternating 4-h blocks over 24 h of:Free from sedation and opioids for 24 hSleep efficiency, median [IQR]: Arousal index, median [IQR]PAV+ 51 [13-66]; PSV 27 [6-22]; PAV+ 11 [4-25]; PSV 12 [3-16]; No statistically significant improvement found with PAV+
PSV; PS maintained at pre-study levelPAV+; % of unloading set to achieve a mean inspiratory pressure similar to PSV
Studies comparing pressure support ventilation against neurally adjusted ventilatory assist
Delisle et al[236], 2011Single centre, randomised, cross over study142 non-consecutive 4-h blocks (d/night) of:Free from sedation and opioids for 24 hSleep efficiency, median [IQR]: Fragmentation index, median [IQR] NAVA 74 [52-77]; PSV 44 [29-74]; NAVA 18 [8-22]; PSV 34 [25-54]; NAVA statistically significant improvement in the efficiency and reduced fragmentation of sleep
PSV; PS to achieve Vt 8 mL/kg; RR < 35/minNAVA
Table 3 Comparison of American Academy of Sleep Medicine’s and Rechtschaffen and Kales criteria sleep stage nomenclature

AASM
R&K
WakeStage WStage W
NREM sleepStage N1Stage 1
Stage N2Stage 2
Stage N3Stage 3
Stage 4
REM sleepStage RStage REM
Table 4 Summary of objective methods of sleep measurement in the critically ill
Method
Benefits
Limitations
Full polysomnography (PSG)Gold standard technique; Provides polygraphic data on EEG, eye movements and chin tone; Established guidelines for interpreting data for normal sleepComplex set up; Relatively expensive; Poorly tolerated in 25% of patients; Interferes with nursing care; May interfere with patient sleep; Interpretation requires sleep specialist; No validated criteria for atypical EEG found commonly in critically ill
Bispectral index (BIS) monitorSmall anatomic footprint; Simplified set up compared to PSG; Does not require sleep specialist for interpretation; Less affected by atypical EEG common in critically illInaccurate differentiation of REM from N1/N2 sleep; Correlates weakly with RCSQ; No validated criteria for interpretation of results; Primarily designed to monitor depth of sedation
Limited lead EEGSmall anatomic footprint; Simplified set up compared to PSG; May not require sleep specialist for interpretationAccuracy dependent on device and auto-staging software; Interpretation dependent on sleep specialist if not using auto-staging
ActigraphyMinimally invasive; Simple set up; Easy to perform serial measures; Established use in outpatient settingPoor accuracy compared to PSG and nurse observation, including over-estimation of total sleep time and sleep efficiency; Confounded by immobility, weakness, sedation, and neurological injury
Under mattress sensorNon-invasive modality; Simple set upModerate agreement, but poor specificity compared to PSG; No correlation with RCSQ
Table 5 Summary of randomised clinical trials assessing nocturnal melatonin as a pharmacological sleep aid
Ref.
Design
Patients
Intervention & control
Sedation
Outcome
Ibrahim et al[158], 2006Single centre, double-blind, randomised trial32 ptsI: Melatonin 4 mg; C: placebo; For ≥ 48 hInfusions ceased for ≥ 12 hNo significant difference in total sleep time by modified SOT
Bourne et al[136], 2008Single centre, double-blind, randomised trial24 ptsI: Melatonin 10 mg; C: Placebo; For 4 nightsCeased for ≥ 30 hNo significant difference in total RCSQ or sleep efficiency by BIS
Foreman et al[222], 2015Single centre, pilot, randomised trial12 ptsI: Melatonin 3 mg plus eye masks and headphonesC: Standard care; For 1-7 dPropofol allowed. Opiates ceased > 24 hPrimary outcome not determined in 65% due to uninterpretable PSG
Mistraletti et al[221], 2015Single centre, double-blind, randomised trial82 ptsI: Melatonin 3+3 mg; C: Placebo; From day 3 of ICU until ICU dischargeEnteral hydroxyzine and lorazepam allowedNo significant difference in total sleep time by nurse observation
Gandolfi et al[224], 2020Double centre, double-blind, randomised trial 203 ptsI: Melatonin 10 mg; C: Placebo For 7 d or until hospital dischargeAs per treating clinicianStatistically improved total RCSQ, mean (SD): I: 61 (26) C: 70 (21) (P = 0.03); No significant difference in total sleep time by nurse observation
Wibrow et al[225], 2021Multicentre (12), double blind, randomised, trial 841 ptsI: Melatonin 4 mg; C: Placebo; For 14 d or until ICU dischargeAs per treating clinicianNo significant difference in total RCSQ