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. 2020 Apr 2;9(4):989. doi: 10.3390/jcm9040989

Table 1.

Study and patient characteristics.

Reference/Country Study Design/CVD Dx OSA Dx Method/
Threshold
Timing of OSA Testing Subgroup, n (%) AHI
Gessner 2017 [18] Retrospective Cohort Type 2 ≤3 d post admission OSA, 91 (41) 23
Germany ACS AHI ≥ 5 non-OSA, 132 (59) NR
Leao 2016 [19] Prospective Cohort Type 1 55 (31–77) d post admission OSA, 46 (63) 30.6 ± 23.0
Portugal ACS AHI ≥ 5 non-OSA, 27 (37) 2.3 ± 3.2
Barbé 2015 [20] RCT (ancillary) Type 3 ≤48 h post admission OSA, 213 (49) 30.6 ± 14.4
Spain ACS AHI > 15 non-OSA, 218 (51) 6.4 ± 4.2
Nakashima 2015 [21] Prospective cohort Type 1 prior to discharge OSA, 124 (46) NR
Japan ACS AHI ≥ 15 non-OSA, 148 (54) NR
Nakashima 2006 Prospective cohort Type 1 14–21 d post admission OSA, 37 (43) 31.7 ± 13.6
Japan [22] ACS AHI ≥ 15 non-OSA, 49 (57) 5.8 ± 4.2
Van den Broecke 2014 [23] Prospective cohort Type 2 ≤48 h post admission OSA, 4 (15) 24.7 ± 19.5
France ACS AHI ≥ 15 non-OSA, 23 (85) 2.5 ± 1.9
Loo 2014 [24] Prospective cohort Type 3 30 d post discharge OSA, 24 (35) 24.0 (16.9–52.0)
France ACS AHI ≥ 15 non-OSA, 44 (65) 4.9 (0.3–14.9)
Szymanski 2013 [25] Prospective cohort Type 3 during hospitalization OSA, 48 (30) NR
Poland ACS AHI ≥ 5 non-OSA, 109 (70) NR
Lee 2009 [3] Prospective cohort Type 2 between day 2–5 post PCI OSA, 69 (66) 38.1
Singapore ACS AHI ≥ 15 non-OSA, 36 (34) 8.5
Jia 2018 [26] Prospective Cohort Type 2 48–72 h post admission OSA, 373 (70) 37.2 ± 16.9
China ACS AHI > 15 non-OSA, 159 (30) 9.4 ± 3.4
Flores 2018 [27] RCT (ancillary) Type 3 24–72 h post admission OSA, 731 (43) 34 (4.4–51.3)
Spain ACS AHI ≥ 5 non-OSA, 983 (57) NR
Sanchez-de-la-Torre 2018 [28] Prospective cohort (ancillary) Type 3 24–72 h post admission OSA, 89 (43) 32.0 (20.8–46.6)
Spain ACS AHI ≥ 15 non-OSA, 119 (57) 4.8 (1.6–9.6)
Morra 2017 [29] Prospective cohort study Type 3 24–72 h post admission OSA, 62 (61) NR
France ACS AHI ≥ 5 non-OSA, 39 (39) NR
Xie 2016 [30] Prospective cohort Type 2 median 7 day post MI OSA, 40 (41) 42.5 (33.1–52.6)
USA ACS AHI ≥ 15 non-OSA, 58 (59) 30.0 (20.5–41.6)
Yumino 2007 [31] Prospective cohort Type 3 7–14 d post PCI OSA, 51 (57) 20.2 ± 10.9
Japan ACS AHI ≥ 10 non-OSA, 38 (43) 5.0 ± 3.2
Ludka 2014 [32] Prospective cohort Type 3 ≥48 h post admission OSA, 399 (66) NR
Czech Republic ACS AHI≥5 non-OSA, 208 (34) NR
Kauta 2014 [33] Prospective cohort Type 3 during hospitalization OSA, 65 (63) 24.7 ± 19.5
USA CVD AHI ≥ 5 non-OSA, 39 (37) 2.5 ± 1.9
Khayat 2015 [34] Prospective cohort Type 2 during hospitalization OSA, 525 (47) 36 ± 16
USA HF AHI ≥ 15 non-OSA, 592 (53) 9.5 ± 4.3
Omran 2018 [35] Retrospective cohort Type 3 during hospitalization OSA, 62 (37) 31.6 ± 15.9
Germany HF AHI ≥ 15 non-OSA, 105 (63) 8.8 ± 3.4
Suda 2018 [36] Prospective cohort Type 3 3 d (median) after initial clinical improvement OSA, 28 (27) NR
Japan HF AHI ≥ 5 non-OSA, 77 (73) NR
Arikawa 2009 [37] Prospective cohort Type 4 during hospitalization OSA, 21 (43) NA
Japan HF ODI ≥ 5 non-OSA, 28 (57) NA
Ohmura 2014 [38] Prospective cohort Type 4 after clinical improvement OSA, 41 (41) NA
Japan HF ODI ≥ 5 non-OSA, 59 (59) NA
Mohananey 2017 [39] Retrospective cohort Chart review NA OSA, 24623 (1.3) NA
United States ACS ICD-9CM 327.23 non-OSA, 1826002 (98.7) NA
Andrechuk 2016 [40] Prospective cohort BQ ≤72 h post admission OSA, 68 (60) NA
Brazil ACS BQ+ ≥ 2 categories non-OSA, 45 (40) NA
Marin 1998 [41] Prospective cohort Clinical+oximetry within 24 h post admission OSA, 55 (22) NA
Spain ACS heavy snorers, reported EDS, ODI > 10 non-OSA, 196 (78) NA
Sommerfeld 2017 [42] Prospective cohort Chart review NA OSA, 99 (29) NA
USA HF non-OSA, 245 (61) NA

Abbreviations: AHI = apnea hypopnea index, ACS = acute coronary syndromes, BQ = Berlin Questionnaire, CVD = cardiovascular disease, HF = heart failure, Dx = diagnosis, ESS = Epworth Sleepiness Scale, EDS = excessive daytime sleepiness, ICD-9CM = International Classification of Diseases, ninth revision, Clinical Modification, NA = not applicable NR = not reported, ODI = oxygen desaturation index, RCT = randomized controlled trial. Data expressed as mean ± SD unless otherwise stated or median (interquartile range) unless otherwise stated.