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Osteoporotic fracture is a common public-health problem in the whole world. Although postfracture usage of anti-osteoporosis medications, may reduce mortality, recent results have been inconsistent. The investigators aim to examine associations between osteoporosis medication and mortality in older adults and any type of fracture patients. The investigators also aim to discuss the pleiotropic effects of different types of anti-osteoporosis medications.
Osteoporotic fracture has become a serious health and economic burden as life expectancy increases. In a WHO report, the burden of osteoporotic fractures in 2002 was 2.8 million disability-adjusted life years, which is more than that for hypertension and slightly less than that for diabetes mellitus or chronic obstructive pulmonary diseases. Many patients who have had a diagnosed fracture have never been diagnosed with osteoporosis, therefore, closing the gap in osteoporosis treatment is important. This situation is primarily due to the fact that osteoporosis symptoms are often not recognized until a fracture occurs. Osteoporotic fractures, especially those of the hip and vertebral, are associated with an increased risk of death. Early detection of high risk for osteoporotic fractures is important; however, post-fracture management, especially interventions intended to lower mortality, is an emerging public health issue in rapidly aging societies. The burden of osteoporotic fracture is higher than that of hypertension, however, osteoporosis is always given less attention than other chronic diseases by health professionals and the general population.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Used osteoporosis medication | Patients who had used osteoporosis medication after osteoporotic fractures. |
| |
| Did not use osteoporosis medication | Patients who didn't use osteoporosis medication after osteoporotic fractures. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Anti-osteoporosis medications | Drug | Medication exposure was defined as the usage of osteoporosis medications approved by the Taiwan Food and Drug Administration (TFDA), including alendronate, risedronate, ibandronate, zoledronic acid, denosumab, raloxifene, bazedoxifene, calcitonin, and teriparatide, but excluded patients using the osteoporosis medication for cancer-related treatments (such as high dosing frequency of zoledronic acid or denosumab). |
| Measure | Description | Time Frame |
|---|---|---|
| Number of deaths with and without anti-osteoporotic therapy after hip fracture surgery | This is the number of participants who died during the time of observation from Taiwan's National Health Insurance Research Database. | 12 years |
| Number of deaths with or without anti-osteoporosis therapy after hip or vertebral fracture surgery among older adults | This is the number of participants who died during the time of observation from Taiwan's National Health Insurance Research Database. | 12 years |
| Number of deaths with and without bisphosphonates after hip or spine fracture surgery | This is the number of participants who died during the time of observation from Taiwan's National Health Insurance Research Database. | 12 years |
| Number of deaths with different types of anti-osteoporosis treatments after post-fracture | This is the number of participants who died during the time of observation from Taiwan's National Health Insurance Research Database. | 12 years |
| Number of deaths in five leading causes of death with and without anti-osteoporosis treatment after post-fracture | This is the number of participants who died during the time of observation from Taiwan's National Death Registry. The five leading causes are defined as the main five leading causes. | 12 years |
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Inclusion Criteria:
Exclusion Criteria:
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The final study participants included those who satisfied the inclusion criteria for both osteoporosis and hip fracture cohorts, and they were followed until 2018.
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| Name | Affiliation | Role |
|---|---|---|
| Chih-Hsing Wu, MD | National Cheng Kung University | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Department of Family Medicine, National Cheng Kung Univ Hosp | Tainan | Taiwan |
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| ID | Term |
|---|---|
| D010024 | Osteoporosis |
| D058866 | Osteoporotic Fractures |
| D055118 | Medication Adherence |
| ID | Term |
|---|---|
| D001851 | Bone Diseases, Metabolic |
| D001847 | Bone Diseases |
| D009140 | Musculoskeletal Diseases |
| D008659 | Metabolic Diseases |
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| ID | Term |
|---|---|
| D004164 | Diphosphonates |
| D000069448 | Denosumab |
| ID | Term |
|---|---|
| D063065 | Organophosphonates |
| D009943 | Organophosphorus Compounds |
| D009930 | Organic Chemicals |
| D061067 | Antibodies, Monoclonal, Humanized |
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|
|
| D009750 |
| Nutritional and Metabolic Diseases |
| D050723 | Fractures, Bone |
| D014947 | Wounds and Injuries |
| D010349 | Patient Compliance |
| D010342 | Patient Acceptance of Health Care |
| D000074822 | Treatment Adherence and Compliance |
| D015438 | Health Behavior |
| D001519 | Behavior |
| D000911 | Antibodies, Monoclonal |
| D000906 | Antibodies |
| D007136 | Immunoglobulins |
| D007162 | Immunoproteins |
| D001798 | Blood Proteins |
| D011506 | Proteins |
| D000602 | Amino Acids, Peptides, and Proteins |
| D012712 | Serum Globulins |
| D005916 | Globulins |