Hassane Awada
Saint Joseph's University
Network
Latest external collaboration on country level. Dive into details by clicking on the dots.
Publication
Featured researches published by Hassane Awada.
Arthritis Care and Research | 2012
Florence Tubach; Philippe Ravaud; Emilio Martín-Mola; Hassane Awada; Nicholas Bellamy; Claire Bombardier; David T. Felson; Najia Hajjaj-Hassouni; M. Hochberg; Isabelle Logeart; Marco Matucci-Cerinic; M.A.F.J. van de Laar; D. van der Heijde; Maxime Dougados
To estimate the minimum clinically important improvement (MCII) and patient acceptable symptom state (PASS) values for 4 generic outcomes in 5 rheumatic diseases and 7 countries.
Bone | 2002
G. El-Hajj Fuleihan; Rafic Baddoura; Hassane Awada; N Salam; Mariana Salamoun; P Rizk
Osteoporosis is a major public health problem in Western countries and is projected to have a similar impact in the Middle East. It has been suggested that peak bone mineral density (BMD), a major determinant of osteoporotic fractures later in life, may be lower in this part of the world compared with the Western world. However, subjects have not been randomly selected or systematically screened to rule out secondary causes of bone loss. The purpose of this study was to determine peak bone mass and lifestyle risk factors for bone loss in a randomly chosen sample of healthy Lebanese subjects from the greater Beirut area. Subjects 25-35 years of age were randomly selected from greater Beirut, which comprises one third of the Lebanese at large, and studied during the Fall of 1999. BMD was measured at the lumbar spine, hip, forearm, and total body. A questionnaire on lifestyle factors was administered to all subjects. Results were compared with the database of subjects from the USA provided by the manufacturer, and to the NHANES database for the total hip. Two hundred thirteen subjects were studied; 45 subjects rotated at all three centers for cross-calibration purposes. Peak BMD in Lebanese subjects was 0.2-0.9 SD below that of peak BMD in American subjects, depending on skeletal site, gender, and densitometer. These differences persisted after attempting to adjust for body size. Osteoporosis and osteopenia were more prevalent than in healthy young Americans. Height, weight, and total body fat were the most significant correlates of BMD/bone mineral content (BMC), accounting for 0.3-0.7 of the variance in bone mass measurement. Lifestyle factors had a very modest but significant contribution to bone mass variance. This is the first population-based study from the Middle East demonstrating that peak BMD is slightly lower in Lebanese subjects compared as with an established database from the USA. Due to the selection of relatively healthier subjects in our study than in the NHANES study, the actual differences between the two populations may be even greater. The impact of our findings on the epidemiology of osteoporotic fractures in Lebanon remains to be determined.
Arthritis Care and Research | 2015
N. Bellamy; Marc C. Hochberg; Florence Tubach; Emilio Martín-Mola; Hassane Awada; Claire Bombardier; Najia Hajjaj-Hassouni; I. Logeart; Marco Matucci-Cerinic; Mart A F J van de Laar; Désirée van der Heijde; Maxime Dougados
The ability to interpret scores from patient‐reported outcome measures at the individual patient level depends on the availability of valid, clinically meaningful benchmarks of response and state attainment. The goal was to develop multinational estimates for minimal clinically important improvement (MCII) and patient acceptable symptomatic state (PASS).
Journal of Clinical Densitometry | 2008
Ghada El-Hajj Fuleihan; Rafic Baddoura; Hassane Awada; Asma Arabi; Jad Okais
With the demographic explosion, the human, social, and economic costs of osteoporosis in developing countries, including the Middle East, will continue to rise. In 2002, the Lebanese Guidelines for Osteoporosis Assessment and Treatment were developed to optimize quality of osteoporosis care in Lebanon and the region. They were endorsed by 5 Lebanese medical scientific societies, and by the Eastern Mediterranean Regional Office branch of the World Health Organization (WHO). In April 2006, the Lebanese Society for Osteoporosis and Metabolic Bone Disorders (OSTEOS) led an initiative to update several recommendations detailed in the original document, based on relevant new local and international data. Data from a population-based sample of elderly Lebanese validated the following recommendations: fracture risk assessment, expressed as relative risk per standard deviation (RR/SD) decrease, was comparable in Lebanese subjects to similarly derived estimates from Western studies; the use of the NHANES database (hip), and the densitometer American database (spine) was as good, if not superior to the use of a Lebanese database for identifying subjects with prevalent vertebral fractures. The original recommendation regarding the use of a gender-specific western database, densitometer for spine and NHANES for T-score derivation for men, remains unchanged. For skeletal site selection, the update recommends measuring the spine and hip for women < or =65 yr, hip only for subjects >65 yr, and adding the forearm in conditions associated with cortical bone loss or in the case of inability to measure axial sites. The original recommendations for conservative management in premenopausal women were reiterated. This First Update of the Lebanese Osteoporosis Guidelines validates previous recommendations using evidence from a population-based sample of elderly Lebanese, and lays the ground for transitioning the Lebanese Osteoporosis Guidelines to the WHO global fracture risk assessment model.
The Journal of Rheumatology | 2016
Milla Johanna Kviatkovsky; Sofia Ramiro; Robert Landewé; Florence Tubach; N. Bellamy; Marc C. Hochberg; Philippe Ravaud; Emilio Martín-Mola; Hassane Awada; Claire Bombardier; David T. Felson; Najia Hajjaj-Hassouni; I. Logeart; Marco Matucci-Cerinic; Mart van der Laar; Désirée van der Heijde
Objective. To establish cutoffs for the minimum clinically important improvement (MCII) and the patient-acceptable symptom state (PASS) for the Bath Ankylosing Spondylitis Disease Activity Index (BASDAI) and the Bath Ankylosing Spondylitis Functional Index (BASFI) in patients with ankylosing spondylitis (AS). Methods. Patients with AS who started nonsteroidal antiinflammatory drugs were included. After 4 weeks, the PASS and the MCII were defined using external anchor questions (for the PASS, patients considering their condition of AS over the prior 48 h as “acceptable” forever; and for the MCII, those reporting moderate or slightly important improvement). Consistency of the MCII and PASS were tested according to HLA-B27 status, presence/absence of SpA extraarticular manifestations, age, sex, disease duration, and baseline BASDAI/BASFI score. The 75th percentile of the cumulative distribution was used to determine the MCII and PASS. Results. In total, 283 patients from a multinational cohort were included. Overall cutoffs for the PASS were 4.1 in the BASDAI and 3.8 in the BASFI. Cutoffs for the MCII were 0.7 and 0.4 for the BASDAI and BASFI, respectively. Subgroup analyses revealed that disease duration and baseline BASDAI/BASFI were significantly associated with the PASS and MCII. In a subanalysis limited to patients with active disease (baseline BASDAI ≥ 4), the MCII was 1.1 for the BASDAI and 0.6 for the BASFI. Conclusion. The conceptual viability of the PASS for the BASDAI is questionable because levels approach those required for the start of biological therapy. Because the MCII is less variable than the PASS, we propose its exclusive use, with cutoffs of 1.1/0.6 for the BASDAI/BASFI in patients with active disease. Because these values are based on a subset of the study population, we recommend confirmation in larger studies focused on patients with baseline BASDAI ≥ 4.
Bone | 2006
Asma Arabi; Rafic Baddoura; Hassane Awada; Mariana Salamoun; Ghazi Ayoub; Ghada El-Hajj Fuleihan
Best Practice & Research: Clinical Rheumatology | 2003
Hassane Awada; Ghada Abi-Karam; Fouad Fayad
Bone | 2007
Rafic Baddoura; Asma Arabi; Souha Haddad-Zebouni; Nabil Khoury; Mariana Salamoun; Ghazi Ayoub; Jad Okais; Hassane Awada; Ghada El-Hajj Fuleihan
Bone | 2007
Asma Arabi; Rafic Baddoura; Hassane Awada; Nabil Khoury; Souha Haddad; Ghazi Ayoub; Ghada El-Hajj Fuleihan
The American Journal of the Medical Sciences | 1998
Marie-Helene Gannage; Ghada Abi-Karam; Fouad W. Nasr; Hassane Awada