| Literature DB >> 31315855 |
Yun Wang1, Michael B Nichol2, Bryan Py Yan3,4, Joanne Wu2, Brian Tomlinson3,4, Vivian Wy Lee5.
Abstract
OBJECTIVES: The objective was to explore the differences in medication use pattern of lipid-lowering drug (LLD) and antiplatelet agents among post-percutaneous coronary intervention patients with acute coronary syndrome aged <65 in Hong Kong (HK) and the USA.Entities:
Keywords: adherence; antiplatelet; compliance; continuity; drug utilisation; lipid-lowering
Year: 2019 PMID: 31315855 PMCID: PMC6661883 DOI: 10.1136/bmjopen-2018-024937
Source DB: PubMed Journal: BMJ Open ISSN: 2044-6055 Impact factor: 2.692
DDD defined by WHO
| ATC code | Name | DDD | Unit | Administrative route |
| B01AC06 | Acetylsalicylic acid | 1 | tablet | Oral |
| B01AC04 | Clopidogrel | 75 | mg | Oral |
| B01AC22 | Prasugrel | 10 | mg | Oral |
| B01AC24 | Ticagrelor | 0.18 | g | Oral |
| C10AA05 | Atorvastatin | 20 | mg | Oral |
| C10AA04 | Fluvastatin | 60 | mg | Oral |
| C10AA02 | Lovastatin | 45 | mg | Oral |
| C10AA03 | Pravastatin | 30 | mg | Oral |
| C10AA07 | Rosuvastatin | 10 | mg | Oral |
| C10AA01 | Simvastatin | 30 | mg | Oral |
| C10A×09 | Ezetimibe | 10 | mg | Oral |
| C10AC01 | Colestyramine | 14 | g | Oral |
| C10AD02 | Nicotinic acid | 2 | g | Oral |
| C10AB05 | Fenofibrate | 0.2 | g | Oral |
| C10AB04 | Gemfibrozil | 1.2 | g | Oral |
ATC, anatomical therapeutic chemical; DDD, daily defined dose.
Baseline characteristics of Hong Kong Chinese patients and American patients in Optum
| Hong Kong CDARS—Chinese | US Optum—American | P value | |
| Total | 270 | 1013 | |
| Gender, no. (%) | 0.001 | ||
| Male | 237 (87.78) | 797 (78.68) | |
| Female | 33 (12.22) | 216 (21.32) | |
| Age, years, mean±SD | 57.69 (5.61) | 57.12 (6.11) | 0.168 |
| Comorbidities, no. (%) | |||
| Diabetes | 36 (13.33) | 114 (11.25) | 0.345 |
| Hypertension | 33 (12.22) | 447 (44.13) | <0.001 |
| Prior cardiovascular disease | 33 (12.22) | 32 (3.16) | <0.001 |
CDARS, Clinical Data Analysis and Reporting System; SD, Standard Deviation.
Drug use pattern of statin and antiplatelet in Hong Kong Chinese patients and American patients in Optum
| Hong Kong CDARS—Chinese | US Optum—All | |||
| No. (%) patients | Mean±SD | No. (%) patients | Mean±SD | |
| Total | 270 | 1013 | ||
| DDD of all lipid-lowering drugs | 270 (100.00) | 352.53 (240.43) | 1013 (100.00) | 636.14 (472.03) |
| DDD of statin | 270 (100.00) | 350.86 (240.39) | 1013 (100.00) | 576.76 (416.70) |
| DDD of simvastatin | 270 (100.00) | 230.81 (180.59) | 1013 (100.00) | 117.31 (202.39) |
| DDD of atorvastatin | 270 (100.00) | 62.60 (222.05) | 1013 (100.00) | 342.48 (466.29) |
| DDD of rosuvastatin | 270 (100.00) | 57.18 (168.43) | 1013 (100.00) | 87.38 (259.56) |
| DDD of fluvastatin | 270 (100.00) | 0 (0) | 1013 (100.00) | 0 (0) |
| DDD of pitavastatin | 270 (100.00) | 0 (0) | 1013 (100.00) | 2.48 (47.38) |
| DDD of pravastatin | 270 (100.00) | 0 (0) | 1013 (100.00) | 28.22 (115.24) |
| DDD of lovustatin | 270 (100.00) | 0 (0) | 1013 (100.00) | 1.74 (19.24) |
| Average days per year on statins | 270 (100.00) | 338.06 (81.86) | 1013 (100.00) | 304.94 (109.60) |
| Good continuity (DDD/year ≥ 80%×365 days) with statins | 121 (44.81) | 711 (70.19) | ||
| Good adherence (MPR≥80%) with statins | 243 (90.00) | 792 (78.18) | ||
| Discontinuation rate of statin | 36 (13.33) | 347 (34.25) | ||
| Statin use pattern | ||||
| Constantly high-potency statin user | 12 (4.44) | 364 (35.93) | ||
| Constantly moderate-potency statin user | 132 (48.89) | 392 (38.70) | ||
| Constantly low-potency statin user | 42 (15.56) | 18 (1.78) | ||
| Switched statin potency | 77 (28.52) | 191 (18.85) | ||
| Never used statin | 7 (2.59) | 48 (4.74) | ||
| The intensity of first dose statin | ||||
| High | 15 (5.56) | 422 (41.66) | ||
| Moderate | 171 (63.33) | 508 (50.15) | ||
| Low | 77 (28.52) | 35 (3.46) | ||
| Not any | 7 (2.59) | 48 (4.74) | ||
| First statin chosen | ||||
| Atorvastatin | 12 (4.44) | 402 (39.68) | ||
| Fluvastatin | 0 (0) | 0 (0) | ||
| Rosuvsatin | 19 (7.04) | 116 (11.45) | ||
| Simvastatin | 232 (85.93) | 361 (35.64) | ||
| Lovastatin | 0 (0) | 12 (1.18) | ||
| Pravastatin | 0 (0) | 74 (7.31) | ||
| Pitavastatin | 0 (0) | 0 (0) | ||
| None | 7 (2.59) | 48 (4.74) | ||
| DDD of any antiplatelet agent (clopidogrel/ticagrelor/prasugrel) | 270 (100.00) | 326.62 (813.73) | 1013 (100.00) | 331.74 (105.04) |
| DDD of clopidogrel | 270 (100.00) | 288.65 (817.85) | 1013 (100.00) | 184.66 (163.07) |
| DDD of ticagrelor | 270 (100.00) | 13.30 (75.79) | 1013 (100.00) | 7.67 (48.29) |
| DDD of prasugrel | 270 (100.00) | 24.67 (89.39) | 1013 (100.00) | 108.00 (152.58) |
| Averages days per year on antiplatelet agents | 270 (100.00) | 262.69 (148.40) | 1013 (100.00) | 330.81 (73.89) |
| Good continuity (DDD/year≥80%×365 days) with antiplatelet agents | 172 (63.70) | 802 (79.17) | ||
| Good adherence (MPR≥80%) withantiplatelet agents | 182 (67.41) | 857 (84.60) | ||
| Discontinuation rate of antiplatelet agents | 125 (46.30) | 316 (31.19) | ||
| First antiplatelet agent chosen | ||||
| Clopidogrel | 246 (91.11) | 600 (59.23) | ||
| Ticagrelor | 19 (7.04) | 27 (2.67) | ||
| Prasugrel | 5 (1.85) | 335 (35.04) | ||
| Not any | 0 (0) | 31 (3.06) | ||
CDARS, Clinical Data Analysis and Reporting System; DDD, daily defined dose; MPR, medical possession ratio; SD, Standard Deviation.
OR for good adherence and continuity with statins and antiplatelet agents
| OR* | 95% CI | P value | |
| Good adherence (MPR≥80%) with statins | |||
| US Optum versus HK CDARS (adjusted†) | 0.37 | (0.23 to 0.58) | <0.001 |
| US Optum versus HK CDARS (PS weights for ATE‡) | 0.42 | (0.22 to 0.81) | 0.009 |
| US Optum versus HK CDARS (PS weights for ATT§) | 0.44 | (0.21 to 0.92) | 0.030 |
| Good continuity (DDD/year≥80%×365 days) with statins | |||
| US Optum versus HK CDARS (adjusted†) | 3.01 | (2.23 to 4.06) | <0.001 |
| US Optum versus HK CDARS (PS weights for ATE‡) | 4.28 | (2.94 to 6.22) | <0.001 |
| US Optum versus HK CDARS (PS weights for ATT§) | 4.90 | (3.25 to 7.38) | <0.001 |
| Good adherence (MPR≥80%) with antiplatelet agents | |||
| US Optum versus HK CDARS (adjusted†) | 2.23 | (1.60 to 3.12) | <0.001 |
| US Optum versus HK CDARS (PS weights for ATE‡) | 2.09 | (1.40 to 3.13) | <0.001 |
| US Optum versus HK CDARS (PS weights for ATT§) | 2.07 | (1.31 to 3.26) | 0.002 |
| Good continuity (DDD/year≥80%×365 days) with antiplatelet agents | |||
| US Optum versus HK CDARS (adjusted†) | 1.87 | (1.36 to 2.56) | <0.001 |
| US Optum versus HK CDARS (PS weights for ATE‡) | 1.70 | (1.16 to 2.49) | 0.007 |
| US Optum versus HK CDARS (PS weights for ATT§) | 1.64 | (1.06 to 2.54) | 0.026 |
*Relative to Chinese patients in HK CDARS.
†Adjusted for sex, age, comorbidities of diabetes and hypertension and prior cardiovascular disease.
‡PS weights for ATE.
§PS weights for the ATT.
ATE, average treatment effect; ATT, average treatment effect for the treated; CDARS, Clinical Data Analysis and Reporting System; CI, confidence interval; DDD, defined daily doses; MPR, medical possession ratio; OR, odds ratio; PS, propensity score.
HR for discontinuation with statins and antiplatelet agents
| HR* | 95% CI | P value | |
| Discontinuation with statins | |||
| US Optum versus HK CDARS (adjusted†) | 2.95 | (2.05 to 4.24) | <0.001 |
| US Optum versus HK CDARS (PS weights for ATE‡) | 3.51 | (2.12 to 5.81) | <0.001 |
| US Optum versus HK CDARS (PS weights for ATT§) | 3.76 | (2.06 to 6.88) | <0.001 |
| Discontinuation with antiplatelet agents | |||
| US Optum versus HK CDARS (adjusted†) | 0.55 | (0.43 to 0.69) | <0.001 |
| US Optum versus HK CDARS (PS weights for ATE‡) | 0.62 | (0.48 to 0.82) | 0.001 |
| US Optum versus HK CDARS (PS weights for ATT§) | 0.65 | (0.48 to 0.88) | 0.006 |
*Relative to Chinese patients in HK CDARS.
†Adjusted for sex, age, comorbidities of diabetes and hypertension and prior cardiovascular disease.
‡PS weights for ATE.
§PS weights for the ATT.
ATE, average treatment effect; ATT, average treatment effect for the treated; CDARS, Clinical Data Analysis and Reporting System; HR, hazard ratio; PS, propensity score.