Sara Bocchinfuso
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Sara Bocchinfuso has a total of 17 co-authors. Here are the top co-authors by number of shared publications:
- Aryan Gajjar
Department of Internal Medicine, Division of Cardiology, David Geffen School of Medicine at UCLA, Los Angeles, CA 90095, USA
1 shared publication Farhana Shariff
Department of Surgery, University of Manitoba, Winnipeg, Manitoba, Canada
1 shared publication- Gerardo Perrotta
Department of Surgery, Mayo Clinic, Rochester, MN 55905, USA
1 shared publication Gianna Yau
Clinical Evaluative Sciences, Sunnybrook Research Institute, Toronto, Ontario, Canada
1 shared publicationKa Yan Ip
Clinical Evaluative Sciences, Sunnybrook Research Institute, Toronto, Ontario, Canada
1 shared publicationLeonardo Brandão
Institute of Health Policy, Management and Evaluation, Dalla Lana School of Public Health, University of Toronto, Toronto, Ontario, Canada
1 shared publication
Latest Publications
- Open Access
- 2 July 2026
- Vol. 16 (7) , e119507
Prevalence of osteopenia and incidence of fragility fracture in adult patients with gastrointestinal cancer: protocol for a systematic review and meta-analysis.
Osteopenia, defined as a bone mineral density (BMD) T-score between -1.0 and -2.5, is a precursor to osteoporosis and fragility fracture which results in substantial morbidity. Patients with gastrointestinal (GI) cancer are particularly vulnerable due to disease-specific mechanisms of bone loss and treatment-related toxicities, which compound the risk of osteoporotic fractures and adverse oncological outcomes. Despite this, the global prevalence of osteopenia and incidence of osteoporotic fracture in GI cancer populations remains poorly quantified, limiting opportunities for targeted surveillance, preventive strategies and policy development. This systematic review and meta-analysis will estimate the global prevalence of osteopenia and global incidence of osteoporotic fracture in cohorts of adults with non-metastatic GI cancer and explore variation across treatment type, cancer site, geographical region and diagnostic modality. This protocol follows the Preferred Reporting Items for Systematic Reviews and Meta-Analysis Protocols (PRISMA-P) guidance. We will conduct a comprehensive search of MEDLINE, Embase, CINAHL, PubMed, Web of Science, Cochrane Central and ClinicalTrials.gov from 1994 to 2026. Eligible studies will include observational or interventional cohorts reporting prevalence of osteopenia, assessed using dual-energy X-ray absorptiometry (DXA) or CT scan, or incidence of fragility fracture, as determined by imaging findings, administrative codes or clinical history in cohorts of adult non-metastatic cancer populations. Five reviewers will independently and in pairs screen citations and full-text articles, extract data, and assess study quality using the Joanna Briggs Institute checklist for prevalence studies for each outcome. The primary outcome is the global pooled prevalence of osteopenia (diagnosed using DXA), calculated using a random-effect generalised linear mixed model. Secondary outcomes are the global pooled incidence rate of fragility fracture, and the pooled fragility fracture incidence rate ratio (IRR) comparing patients with GI cancer with the general population. All estimates will be presented with 95% confidence intervals. Heterogeneity will be assessed with I2, τ2 and prediction intervals for each outcome. Sources of heterogeneity in osteopenia prevalence will be explored through subgroup analyses by primary cancer location, treatment exposure, and geographical region. Sensitivity analyses, including an analysis of the pooled prevalence of osteopenia diagnosed using CT, and limited to studies deemed low risk of bias, will be performed. Publication bias will be evaluated using Doi plots supplemented with Luis Furuya-Kanamori indices. We will assess certainty in the evidence-base in duplicate by using the Grading of Recommendations Assessment, Development and Evaluation methodology for systematic reviews involving prognosis. This study is a secondary analysis of aggregate, de-identified data extracted from previously published studies. As such, no new data were collected from human participants, and formal ethics board approval is not required. All aggregated data and analytical code used to complete this study will be made available on request to the corresponding author. The findings from this study will be disseminated through publication in a peer-reviewed scientific journal and presentation at national and international conferences. CRD420261286673.
- 2 July 2026
- Vol. 16 (7) , e119507
Open AccessPrevalence of osteopenia and incidence of fragility fracture in adult patients with gastrointestinal cancer: protocol for a systematic review and meta-analysis.
Osteopenia, defined as a bone mineral density (BMD) T-score between -1.0 and -2.5, is a precursor to osteoporosis and fragility fracture which results in substantial morbidity. Patients with gastrointestinal (GI) cancer are particularly vulnerable due to disease-specific mechanisms of bone loss and treatment-related toxicities, which compound the risk of osteoporotic fractures and adverse oncological outcomes. Despite this, the global prevalence of osteopenia and incidence of osteoporotic fracture in GI cancer populations remains poorly quantified, limiting opportunities for targeted surveillance, preventive strategies and policy development. This systematic review and meta-analysis will estimate the global prevalence of osteopenia and global incidence of osteoporotic fracture in cohorts of adults with non-metastatic GI cancer and explore variation across treatment type, cancer site, geographical region and diagnostic modality. This protocol follows the Preferred Reporting Items for Systematic Reviews and Meta-Analysis Protocols (PRISMA-P) guidance. We will conduct a comprehensive search of MEDLINE, Embase, CINAHL, PubMed, Web of Science, Cochrane Central and ClinicalTrials.gov from 1994 to 2026. Eligible studies will include observational or interventional cohorts reporting prevalence of osteopenia, assessed using dual-energy X-ray absorptiometry (DXA) or CT scan, or incidence of fragility fracture, as determined by imaging findings, administrative codes or clinical history in cohorts of adult non-metastatic cancer populations. Five reviewers will independently and in pairs screen citations and full-text articles, extract data, and assess study quality using the Joanna Briggs Institute checklist for prevalence studies for each outcome. The primary outcome is the global pooled prevalence of osteopenia (diagnosed using DXA), calculated using a random-effect generalised linear mixed model. Secondary outcomes are the global pooled incidence rate of fragility fracture, and the pooled fragility fracture incidence rate ratio (IRR) comparing patients with GI cancer with the general population. All estimates will be presented with 95% confidence intervals. Heterogeneity will be assessed with I2, τ2 and prediction intervals for each outcome. Sources of heterogeneity in osteopenia prevalence will be explored through subgroup analyses by primary cancer location, treatment exposure, and geographical region. Sensitivity analyses, including an analysis of the pooled prevalence of osteopenia diagnosed using CT, and limited to studies deemed low risk of bias, will be performed. Publication bias will be evaluated using Doi plots supplemented with Luis Furuya-Kanamori indices. We will assess certainty in the evidence-base in duplicate by using the Grading of Recommendations Assessment, Development and Evaluation methodology for systematic reviews involving prognosis. This study is a secondary analysis of aggregate, de-identified data extracted from previously published studies. As such, no new data were collected from human participants, and formal ethics board approval is not required. All aggregated data and analytical code used to complete this study will be made available on request to the corresponding author. The findings from this study will be disseminated through publication in a peer-reviewed scientific journal and presentation at national and international conferences. CRD420261286673.
- Open Access
- 5 September 2024
- Published by MDPI AG in Journal of Clinical Medicine
- Vol. 13 (17) , 5279
Novel Surgical Interventions for the Treatment of Obesity
Metabolic and bariatric surgery is widely recognized as the most effective and durable treatment for the disease of obesity and its associated comorbidities. In recent years, the field has seen significant advancements, introducing numerous innovative surgical options. This review aims to comprehensively examine these emerging surgical techniques, which have recently received endorsement from the American Society for Metabolic and Bariatric Surgery (ASMBS). Additionally, we will explore new technologies and methodologies supported by the latest scientific evidence. Our analysis will include a critical evaluation of the efficacy, safety, and long-term outcomes of these novel approaches, providing a detailed update on the current state of metabolic and bariatric surgery, highlighting key developments and their potential implications for clinical practice.
- 5 September 2024
- Published by MDPI AG in Journal of Clinical Medicine
- Vol. 13 (17) , 5279
Open AccessNovel Surgical Interventions for the Treatment of Obesity
Metabolic and bariatric surgery is widely recognized as the most effective and durable treatment for the disease of obesity and its associated comorbidities. In recent years, the field has seen significant advancements, introducing numerous innovative surgical options. This review aims to comprehensively examine these emerging surgical techniques, which have recently received endorsement from the American Society for Metabolic and Bariatric Surgery (ASMBS). Additionally, we will explore new technologies and methodologies supported by the latest scientific evidence. Our analysis will include a critical evaluation of the efficacy, safety, and long-term outcomes of these novel approaches, providing a detailed update on the current state of metabolic and bariatric surgery, highlighting key developments and their potential implications for clinical practice.