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  1. Article ; Online: Cochrane in CORR® : Reducing Medication Errors for Adults in Hospital Settings.

    Mesgarpour, Bita / Sadeghirad, Behnam

    Clinical orthopaedics and related research

    2022  Volume 481, Issue 1, Page(s) 17–24

    MeSH term(s) Adult ; Humans ; Medication Errors ; Hospitals
    Language English
    Publishing date 2022-12-05
    Publishing country United States
    Document type Journal Article ; Comment
    ZDB-ID 80301-7
    ISSN 1528-1132 ; 0009-921X
    ISSN (online) 1528-1132
    ISSN 0009-921X
    DOI 10.1097/CORR.0000000000002497
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Comment on Duarte et al. Systematic Review and Network Meta-analysis of Neurostimulation for Painful Diabetic Neuropathy. Diabetes Care 2022;45:2466-2475.

    Sadeghirad, Behnam / Wang, Xiaoqin / Busse, Jason W

    Diabetes care

    2023  Volume 46, Issue 5, Page(s) e112

    MeSH term(s) Humans ; Diabetes Mellitus, Type 1 ; Diabetes Mellitus, Type 2 ; Diabetic Neuropathies/therapy ; Network Meta-Analysis
    Language English
    Publishing date 2023-05-09
    Publishing country United States
    Document type Letter ; Comment
    ZDB-ID 441231-x
    ISSN 1935-5548 ; 0149-5992
    ISSN (online) 1935-5548
    ISSN 0149-5992
    DOI 10.2337/dc22-2449
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: The GRADE Working Group and CINeMA approaches provided inconsistent certainty of evidence ratings for a network meta-analysis of opioids for chronic noncancer pain.

    Noori, Atefeh / Sadeghirad, Behnam / Thabane, Lehana / Bhandari, Mohit / Guyatt, Gordon H / Busse, Jason W

    Journal of clinical epidemiology

    2024  Volume 169, Page(s) 111276

    Abstract: Objectives: Assessment of the certainty of evidence (CoE) from network meta-analysis is critical to convey the strength of inferences for clinical decision-making. Both the GRADE (Grading of Recommendations Assessment, Development and Evaluation) ... ...

    Abstract Objectives: Assessment of the certainty of evidence (CoE) from network meta-analysis is critical to convey the strength of inferences for clinical decision-making. Both the GRADE (Grading of Recommendations Assessment, Development and Evaluation) Working Group (GWG) and the Confidence in Network Meta-Analysis (CINeMA) framework have been designed to assess the CoE of treatment effects informed by network meta-analysis; however, the concordance of results is uncertain.
    Study design and setting: We assessed the CoE for treatment effects of individual opioids on pain relief and physical functioning from a network meta-analysis for chronic noncancer pain using the GWG approach and the CINeMA framework. Both approaches evaluate the CoE as high, moderate, low or very low. We quantified the number of discrepant CoE ratings between approaches and the magnitude of the difference (ie, one level, two levels, or three levels).
    Results: Across 105 comparisons among individual opioids for pain relief, the GWG and CINeMA approaches provided different CoE ratings in 34% of cases (36 of 105). Across 66 comparisons for physical functioning, there was discordance in 17% of cases (11 of 66). All discrepancies were separated by one level. The CINeMA framework typically provided lower CoE ratings compared to the GWG approach, predominantly because of differences in the assessment of transitivity and heterogeneity.
    Conclusion: Our findings suggest there are differences between the CoE ratings provided by the GWG and CINeMA approaches when applied to network meta-analyses. Further research is needed to replicate or refute our findings in other network meta-analyses and assess the implications for clinical decision-making.
    Language English
    Publishing date 2024-02-08
    Publishing country United States
    Document type Journal Article
    ZDB-ID 639306-8
    ISSN 1878-5921 ; 0895-4356
    ISSN (online) 1878-5921
    ISSN 0895-4356
    DOI 10.1016/j.jclinepi.2024.111276
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  4. Article ; Online: Factors Associated with Initiating Cannabis Use After Legalization in Canada: A Cross-Sectional Study.

    Ashoorion, Vahid / Sadeghirad, Behnam / Sandhu, Harman S / Busse, Jason W

    Cannabis and cannabinoid research

    2022  Volume 8, Issue 6, Page(s) 1126–1132

    Abstract: Background: ...

    Abstract Background:
    MeSH term(s) Humans ; Canada/epidemiology ; Cannabis ; Cross-Sectional Studies ; Marijuana Use/epidemiology ; Marijuana Use/legislation & jurisprudence
    Language English
    Publishing date 2022-07-04
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2867624-5
    ISSN 2378-8763 ; 2578-5125
    ISSN (online) 2378-8763
    ISSN 2578-5125
    DOI 10.1089/can.2022.0095
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  5. Article ; Online: Pharmacotherapy in paediatric type 2 diabetes mellitus: a protocol for a systematic review and network meta-analysis of randomised trials.

    Zhou, Fangwen / Deng, Jiawen / Banfield, Laura / Thabane, Lehana / Sadeghirad, Behnam / Samaan, M Constantine

    BMJ open

    2022  Volume 12, Issue 9, Page(s) e065287

    Abstract: Introduction: The rates of type 2 diabetes mellitus (T2DM) in children and adolescents have risen globally over the past few years. While a few diabetes pharmacotherapies have been used in this population, their comparative benefits and harms are ... ...

    Abstract Introduction: The rates of type 2 diabetes mellitus (T2DM) in children and adolescents have risen globally over the past few years. While a few diabetes pharmacotherapies have been used in this population, their comparative benefits and harms are unclear. Thus, we will conduct a systematic review and network meta-analysis (NMA) of randomised controlled trials (RCTs) to compare the efficacy and safety of pharmacotherapies for managing paediatric T2DM.
    Methods and analysis: We will include RCTs that enrolled T2DM patients ≤18 years of age and who were randomised to monotherapy or combination pharmacotherapies with or without lifestyle interventions. Comparator groups will include placebo or non-pharmacological treatments including lifestyle interventions.Treatment outcomes will include change from baseline in glycated haemoglobin A1c, body mass index z-score, weight, systolic/diastolic blood pressure, fasting plasma glucose, fasting insulin and lipid profiles, T2DM-related complications, as well as the incidence of treatment-related adverse events.Literature searches will be conducted in Medline, Embase, CINAHL, CENTRAL and Web of Science. We will also search the grey literature and the reference list of included trials and relevant reviews. Two reviewers will assess the eligibility of articles identified through our searches and will extract data from eligible studies independently. We will use a modified Cochrane instrument to evaluate the risk of bias. Disagreements will be resolved through consensus or arbitration by a third reviewer.A frequentist random-effects model will be used for conducting NMA. The quality of evidence will be assessed using the Confidence in Network Meta-Analysis platform. We will assess the effect modification through network meta-regression and subgroup analyses for sex, age at study inclusion, duration of T2DM, follow-up duration and risk of bias ratings.
    Ethics and dissemination: This study will not require ethics approval. We will disseminate our findings through publication in a peer-reviewed journal and conference presentations.
    Prospero registration number: CRD42022310100.
    MeSH term(s) Adolescent ; Blood Glucose ; Child ; Diabetes Mellitus, Type 2/drug therapy ; Glycated Hemoglobin A ; Humans ; Insulin/therapeutic use ; Lipids ; Meta-Analysis as Topic ; Network Meta-Analysis ; Randomized Controlled Trials as Topic ; Systematic Reviews as Topic
    Chemical Substances Blood Glucose ; Glycated Hemoglobin A ; Insulin ; Lipids
    Language English
    Publishing date 2022-09-26
    Publishing country England
    Document type Journal Article
    ZDB-ID 2599832-8
    ISSN 2044-6055 ; 2044-6055
    ISSN (online) 2044-6055
    ISSN 2044-6055
    DOI 10.1136/bmjopen-2022-065287
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Development and validation of an international preoperative risk assessment model for postoperative delirium.

    Dodsworth, Benjamin T / Reeve, Kelly / Falco, Lisa / Hueting, Tom / Sadeghirad, Behnam / Mbuagbaw, Lawrence / Goettel, Nicolai / Schmutz Gelsomino, Nayeli

    Age and ageing

    2023  Volume 52, Issue 6

    Abstract: Background: Postoperative delirium (POD) is a frequent complication in older adults, characterised by disturbances in attention, awareness and cognition, and associated with prolonged hospitalisation, poor functional recovery, cognitive decline, long- ... ...

    Abstract Background: Postoperative delirium (POD) is a frequent complication in older adults, characterised by disturbances in attention, awareness and cognition, and associated with prolonged hospitalisation, poor functional recovery, cognitive decline, long-term dementia and increased mortality. Early identification of patients at risk of POD can considerably aid prevention.
    Methods: We have developed a preoperative POD risk prediction algorithm using data from eight studies identified during a systematic review and providing individual-level data. Ten-fold cross-validation was used for predictor selection and internal validation of the final penalised logistic regression model. The external validation used data from university hospitals in Switzerland and Germany.
    Results: Development included 2,250 surgical (excluding cardiac and intracranial) patients 60 years of age or older, 444 of whom developed POD. The final model included age, body mass index, American Society of Anaesthesiologists (ASA) score, history of delirium, cognitive impairment, medications, optional C-reactive protein (CRP), surgical risk and whether the operation is a laparotomy/thoracotomy. At internal validation, the algorithm had an AUC of 0.80 (95% CI: 0.77-0.82) with CRP and 0.79 (95% CI: 0.77-0.82) without CRP. The external validation consisted of 359 patients, 87 of whom developed POD. The external validation yielded an AUC of 0.74 (95% CI: 0.68-0.80).
    Conclusions: The algorithm is named PIPRA (Pre-Interventional Preventive Risk Assessment), has European conformity (ce) certification, is available at http://pipra.ch/ and is accepted for clinical use. It can be used to optimise patient care and prioritise interventions for vulnerable patients and presents an effective way to implement POD prevention strategies in clinical practice.
    MeSH term(s) Humans ; Aged ; Emergence Delirium/complications ; Delirium/diagnosis ; Delirium/etiology ; Delirium/prevention & control ; Risk Factors ; Postoperative Complications/diagnosis ; Postoperative Complications/etiology ; Postoperative Complications/prevention & control ; Risk Assessment ; C-Reactive Protein
    Chemical Substances C-Reactive Protein (9007-41-4)
    Language English
    Publishing date 2023-06-03
    Publishing country England
    Document type Systematic Review ; Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 186788-x
    ISSN 1468-2834 ; 0002-0729
    ISSN (online) 1468-2834
    ISSN 0002-0729
    DOI 10.1093/ageing/afad086
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  7. Article ; Online: The Scientific Basis of Guideline Recommendations on Sugar Intake.

    Sadeghirad, Behnam / Johnston, Bradley C

    Annals of internal medicine

    2017  Volume 167, Issue 3, Page(s) 219

    Language English
    Publishing date 2017-08-01
    Publishing country United States
    Document type Journal Article
    ZDB-ID 336-0
    ISSN 1539-3704 ; 0003-4819
    ISSN (online) 1539-3704
    ISSN 0003-4819
    DOI 10.7326/L17-0255
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  8. Article ; Online: Cannabis for medical use versus opioids for chronic non-cancer pain: a systematic review and network meta-analysis of randomised clinical trials.

    Jeddi, Haron M / Busse, Jason W / Sadeghirad, Behnam / Levine, Mitchell / Zoratti, Michael J / Wang, Li / Noori, Atefeh / Couban, Rachel J / Tarride, Jean-Eric

    BMJ open

    2024  Volume 14, Issue 1, Page(s) e068182

    Abstract: Objective: The objective of this study is to evaluate the comparative benefits and harms of opioids and cannabis for medical use for chronic non-cancer pain.: Design: Systematic review and network meta-analysis.: Data sources: EMBASE, MEDLINE, ... ...

    Abstract Objective: The objective of this study is to evaluate the comparative benefits and harms of opioids and cannabis for medical use for chronic non-cancer pain.
    Design: Systematic review and network meta-analysis.
    Data sources: EMBASE, MEDLINE, CINAHL, AMED, PsycINFO, PubMed, Web of Science, Cannabis-Med, Epistemonikos and the Cochrane Library (CENTRAL) from inception to March 2021.
    Study selection: Randomised trials comparing any type of cannabis for medical use or opioids, against each other or placebo, with patient follow-up ≥4 weeks.
    Data extraction and synthesis: Paired reviewers independently extracted data. We used Bayesian random-effects network meta-analyses to summarise the evidence and the Grading of Recommendations, Assessment, Development and Evaluations (GRADE) approach to evaluate the certainty of evidence and communicate our findings.
    Results: Ninety trials involving 22 028 patients were eligible for review, among which the length of follow-up ranged from 28 to 180 days. Moderate certainty evidence showed that opioids provide small improvements in pain, physical functioning and sleep quality versus placebo; low to moderate certainty evidence supported similar effects for cannabis versus placebo. Neither was more effective than placebo for role, social or emotional functioning (all high to moderate certainty evidence). Moderate certainty evidence showed there is probably little to no difference between cannabis for medical use and opioids for physical functioning (weighted mean difference (WMD) 0.47 on the 100-point 36-item Short Form Survey physical component summary score, 95% credible interval (CrI) -1.97 to 2.99), and cannabis resulted in fewer discontinuations due to adverse events versus opioids (OR 0.55, 95% CrI 0.36 to 0.83). Low certainty evidence suggested little to no difference between cannabis and opioids for pain relief (WMD 0.23 cm on a 10 cm Visual Analogue Scale (VAS), 95% CrI -0.06 to 0.53) or sleep quality (WMD 0.49 mm on a 100 mm VAS, 95% CrI -4.72 to 5.59).
    Conclusions: Cannabis for medical use may be similarly effective and result in fewer discontinuations than opioids for chronic non-cancer pain.
    Prospero registration number: CRD42020185184.
    MeSH term(s) Humans ; Analgesics, Opioid/therapeutic use ; Bayes Theorem ; Cannabinoid Receptor Agonists/therapeutic use ; Cannabis ; Chronic Pain/drug therapy ; Network Meta-Analysis ; Randomized Controlled Trials as Topic
    Chemical Substances Analgesics, Opioid ; Cannabinoid Receptor Agonists
    Language English
    Publishing date 2024-01-03
    Publishing country England
    Document type Comparative Study ; Journal Article ; Meta-Analysis ; Research Support, Non-U.S. Gov't ; Systematic Review
    ZDB-ID 2599832-8
    ISSN 2044-6055 ; 2044-6055
    ISSN (online) 2044-6055
    ISSN 2044-6055
    DOI 10.1136/bmjopen-2022-068182
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  9. Article ; Online: Therapist-guided remote versus in-person cognitive behavioural therapy: a systematic review and meta-analysis of randomized controlled trials.

    Zandieh, Sara / Abdollahzadeh, Seyedeh Maryam / Sadeghirad, Behnam / Wang, Li / McCabe, Randi E / Yao, Liam / Inness, Briar E / Pathak, Ananya / Couban, Rachel J / Crandon, Holly / Torabiardakani, Kian / Bieling, Peter / Busse, Jason W

    CMAJ : Canadian Medical Association journal = journal de l'Association medicale canadienne

    2024  Volume 196, Issue 10, Page(s) E327–E340

    Abstract: Background: Cognitive behavioural therapy (CBT) has been shown to be effective for several psychiatric and somatic conditions; however, most randomized controlled trials (RCTs) have administered treatment in person and whether remote delivery is ... ...

    Abstract Background: Cognitive behavioural therapy (CBT) has been shown to be effective for several psychiatric and somatic conditions; however, most randomized controlled trials (RCTs) have administered treatment in person and whether remote delivery is similarly effective remains uncertain. We sought to compare the effectiveness of therapist-guided remote CBT and in-person CBT.
    Methods: We systematically searched MEDLINE, Embase, PsycINFO, CINAHL, and the Cochrane Central Register of Controlled Trials from inception to July 4, 2023, for RCTs that enrolled adults (aged ≥ 18 yr) presenting with any clinical condition and that randomized participants to either therapist-guided remote CBT (e.g., teleconference, videoconference) or in-person CBT. Paired reviewers assessed risk of bias and extracted data independently and in duplicate. We performed random-effects model meta-analyses to pool patient-important primary outcomes across eligible RCTs as standardized mean differences (SMDs). We used Grading of Recommendations Assessment, Development and Evaluation (GRADE) guidance to assess the certainty of evidence and used the Instrument to Assess the Credibility of Effect Modification Analyses (ICEMAN) to rate the credibility of subgroup effects.
    Results: We included 54 RCTs that enrolled a total of 5463 patients. Seventeen studies focused on treatment of anxiety and related disorders, 14 on depressive symptoms, 7 on insomnia, 6 on chronic pain or fatigue syndromes, 5 on body image or eating disorders, 3 on tinnitus, 1 on alcohol use disorder, and 1 on mood and anxiety disorders. Moderate-certainty evidence showed little to no difference in the effectiveness of therapist-guided remote and in-person CBT on primary outcomes (SMD -0.02, 95% confidence interval -0.12 to 0.07).
    Interpretation: Moderate-certainty evidence showed little to no difference in the effectiveness of in-person and therapist-guided remote CBT across a range of mental health and somatic disorders, suggesting potential for the use of therapist-guided remote CBT to facilitate greater access to evidence-based care.
    MeSH term(s) Adult ; Humans ; Alcoholism/therapy ; Anxiety Disorders/therapy ; Cognitive Behavioral Therapy/methods ; Randomized Controlled Trials as Topic
    Language English
    Publishing date 2024-03-17
    Publishing country Canada
    Document type Meta-Analysis ; Systematic Review ; Journal Article
    ZDB-ID 215506-0
    ISSN 1488-2329 ; 0008-4409 ; 0820-3946
    ISSN (online) 1488-2329
    ISSN 0008-4409 ; 0820-3946
    DOI 10.1503/cmaj.230274
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  10. Article ; Online: Comparison of safety and effectiveness of antiretroviral therapy regimens among pregnant women living with HIV at preconception or during pregnancy: a systematic review and network meta-analysis of randomized trials.

    Mehrabi, Fatemeh / Karamouzian, Mohammad / Farhoudi, Behnam / Moradi Falah Langeroodi, Shahryar / Mehmandoost, Soheil / Abbaszadeh, Samaneh / Motaghi, Shahrzad / Mirzazadeh, Ali / Sadeghirad, Behnam / Sharifi, Hamid

    BMC infectious diseases

    2024  Volume 24, Issue 1, Page(s) 417

    Abstract: Background: Mother-to-child transmission is the primary cause of HIV cases among children. Antiretroviral therapy (ART) plays a critical role in preventing mother-to-child transmission and reducing HIV progression, morbidity, and mortality among mothers. ...

    Abstract Background: Mother-to-child transmission is the primary cause of HIV cases among children. Antiretroviral therapy (ART) plays a critical role in preventing mother-to-child transmission and reducing HIV progression, morbidity, and mortality among mothers. However, after more than two decades of ART during pregnancy, the comparative effectiveness and safety of ART medications during pregnancy are unclear, and existing evidence is contradictory. This study aimed to assess the effectiveness and safety of different ART regimens among pregnant women living with HIV at preconception or during pregnancy.
    Methods: We searched MEDLINE, Embase, Cochrane Central Register of Controlled Trials, and Web of Science. We included randomized trials that enrolled pregnant women living with HIV and randomized them to receive ART for at least four weeks. Pairs of reviewers independently completed screening for eligible studies, extracted data, and assessed the risk of bias using the Cochrane risk of bias tool. Our outcomes of interest included low birth weight, stillbirth, preterm birth, mother-to-child transmission of HIV, neonatal death, and congenital anomalies. Network meta-analysis was performed using a random-effects frequentist model, and the certainty of evidence was evaluated using the GRADE approach.
    Results: We found 14 eligible randomized trials enrolling 9,561 pregnant women. The median duration of ART uptake ranged from 6.0 to 17.4 weeks. No treatment was statistically better than a placebo in reducing the rate of neonatal mortality, stillbirth, congenital defects, preterm birth, or low birth weight deliveries. Compared to placebo, zidovudine (ZDV)/lamivudine (3TC) and ZDV monotherapy likely reduce mother-to-child transmission (odds ratio (OR): 0.13; 95% CI: 0.05 to 0.31, high-certainty; and OR: 0.50; 95% CI: 0.33 to 0.74, moderate-certainty). Moderate-certainty evidence suggested that ZDV/3TC was associated with decreased odds of stillbirth (OR: 0.47; 95% CI: 0.09 to 2.60).
    Conclusions: Our analysis provides high- to moderate-certainty evidence that ZDV/3TC and ZDV are more effective in reducing the odds of mother-to-child transmission, with ZDV/3TC also demonstrating decreased odds of stillbirth. Notably, our findings suggest an elevated odds of stillbirth and preterm birth associated with all other ART regimens.
    MeSH term(s) Female ; Pregnancy ; Infant, Newborn ; Humans ; Pregnancy Complications, Infectious/drug therapy ; Pregnant Women ; Stillbirth ; Network Meta-Analysis ; Premature Birth/epidemiology ; Infectious Disease Transmission, Vertical/prevention & control ; Randomized Controlled Trials as Topic ; HIV Infections/prevention & control
    Language English
    Publishing date 2024-04-19
    Publishing country England
    Document type Meta-Analysis ; Systematic Review
    ZDB-ID 2041550-3
    ISSN 1471-2334 ; 1471-2334
    ISSN (online) 1471-2334
    ISSN 1471-2334
    DOI 10.1186/s12879-024-09303-2
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