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1.
Osteoarthritis Cartilage ; 30(3): 381-394, 2022 03.
Article in English | MEDLINE | ID: mdl-34757028

ABSTRACT

OBJECTIVE: To evaluate if gait biomechanics are associated with increased risk of structurally diagnosed disease onset or progression of lower limb osteoarthritis (OA). METHOD: A systematic review of Medline and Embase was conducted from inception to July 2021. Two reviewers independently screened records, extracted data and assessed risk of bias. Included studies reported gait biomechanics at baseline, and either structural imaging or joint replacement occurrence in the lower limb at follow-up. The primary outcome was the Odds Ratio (OR) (95% confidence interval (CI)) of the association between biomechanics and structural OA outcomes with data pooled for meta-analysis. RESULTS: Twenty-three studies reporting 25 different biomechanical metrics and 11 OA imaging outcomes were included (quality scores ranged 12-20/21). Twenty studies investigated knee OA progression; three studies investigated knee OA onset. Two studies investigated hip OA progression. 91% of studies reported a significant association between at least one biomechanical variable and OA onset or progression. There was an association between frontal plane biomechanics with medial tibiofemoral and hip OA progression and sagittal plane biomechanics with patellofemoral OA progression. Meta-analyses demonstrated increased odds of medial tibiofemoral OA progression with greater baseline peak knee adduction moment (KAM) (OR: 1.88 [95%CI: 1.08, 3.29]) and varus thrust presence (OR: 1.97 [95%CI: 1.32, 2.96]). CONCLUSION: Evidence suggests that certain gait biomechanics are associated with an increased odds of OA onset and progression in the knee, and progression in the hip. REGISTRATION NUMBER: PROSPERO CRD42019133920.


Subject(s)
Gait/physiology , Osteoarthritis, Hip/physiopathology , Osteoarthritis, Knee/physiopathology , Biomechanical Phenomena , Disease Progression , Humans , Risk Factors
2.
Obes Rev ; 19(1): 1-13, 2018 Jan.
Article in English | MEDLINE | ID: mdl-28975722

ABSTRACT

This systematic review synthesized the available evidence on the effect of short-term periods of intermittent energy restriction (weekly intermittent energy restriction; ≥7-d energy restriction) in comparison with usual care (daily continuous energy restriction), in the treatment of overweight and obesity in adults. Six electronic databases were searched from inception to October 2016. Only randomized controlled trials of interventions (≥12 weeks) in adults with overweight and obesity were included. Five studies were included in this review. Weekly intermittent energy restriction periods ranged from an energy intake between 1757 and 6276 kJ/d-1 . The mean duration of the interventions was 26 (range 14 to 48) weeks. Meta-analysis demonstrated no significant difference in weight loss between weekly intermittent energy restriction and continuous energy restriction post-intervention (weighted mean difference: -1.36 [-3.23, 0.51], p = 0.15) and at follow-up (weighted mean difference: -0.82 [-3.76, 2.11], p = 0.58). Both interventions achieved comparable weight loss of >5 kg and therefore were associated with clinical benefits to health. The findings support the use of weekly intermittent energy restriction as an alternative option for the treatment of obesity. Currently, there is insufficient evidence to support the long-term sustainable effects of weekly intermittent energy restriction on weight management.


Subject(s)
Caloric Restriction , Obesity/diet therapy , Overweight/diet therapy , Weight Loss , Diet, Reducing , Humans , Life Style , Patient Compliance , Randomized Controlled Trials as Topic
3.
J Neonatal Perinatal Med ; 10(1): 119-123, 2017.
Article in English | MEDLINE | ID: mdl-28304319

ABSTRACT

Infant delirium is an under-recognized clinical entity in neonatal intensive care, and earlier identification and treatment could minimize morbidities associated with this condition. We describe a case of a 6-month-old former 32 weeks gestation infant undergoing a prolonged mechanical ventilation course diagnosed with delirium related to the combination of his underlying illness and the use of multiple sedative and analgesic medications. Initiation of the atypical antipsychotic risperidone allowed for weaning from continuous infusions of benzodiazepines and opiods, and lower dosages of bolus-dosed sedation and analgesics. The patient experienced no adverse side effects from use of this neuroleptic.


Subject(s)
Analgesics, Opioid/adverse effects , Cardiac Catheterization , Delirium/therapy , Deprescriptions , Hypnotics and Sedatives/adverse effects , Postoperative Complications/therapy , Respiratory Distress Syndrome, Newborn/psychology , Amines/therapeutic use , Anti-Anxiety Agents/therapeutic use , Cyclohexanecarboxylic Acids/therapeutic use , Delirium/etiology , Dexmedetomidine/adverse effects , Diazepam/adverse effects , Female , Fentanyl/adverse effects , Gabapentin , Humans , Infant , Infant, Newborn , Infant, Premature , Intensive Care Units, Neonatal , Methadone/adverse effects , Midazolam/adverse effects , Phenobarbital/adverse effects , Postoperative Complications/etiology , Pregnancy , Respiration, Artificial , Respiratory Distress Syndrome, Newborn/complications , Risperidone/therapeutic use , gamma-Aminobutyric Acid/therapeutic use
5.
Toxicol Lett ; 168(1): 1-6, 2007 Jan 10.
Article in English | MEDLINE | ID: mdl-17129690

ABSTRACT

Reactive oxygen species (ROS) have been implicated in various pulmonary diseases by causing direct injury to lung epithelial cells. Signalling activity of cells through transcription factors such as nuclear factor kappa B (NF-kappaB) and AP-1 have been shown to be regulated by ROS, and the release of pro-inflammatory cytokines demonstrated in the study of inflammatory disease. In this study, we examined the effect of the oxidant tert-butylhydroperoxide (tBHP) on mouse J774 macrophages and its ability to cause the release of the pro-inflammatory cytokine tumour necrosis factor alpha (TNF-alpha). The role of calcium as a signalling molecule was studied using various calcium antagonists. The role of the signalling molecule cAMP was also investigated using phosphodiesterase inhibitors PDE1 and PDE4 families. Oxidative stress was investigated in lung epithelial (A549) cells with and without calcium antagonists and PDE inhibitors with regard to their ability to modulate release of the neutrophil chemoattractant interleukin 8 (IL-8). The oxidant tBHP significantly increased the cytosolic calcium concentration in J774 macrophages, which was prevented by the PDE1 inhibitor. The production of TNF-alpha protein by J774 macrophages was mediated by a pathway involving calcium as addition of calcium antagonists inhibited the tBHP stimulated increase in the cytokine. Inhibitors of both PDE1 and PDE4 completely prevented the tBHP stimulated TNF-alpha release suggesting that the cAMP pathway may be important in the oxidant induced signalling pathway leading to gene expression of pro-inflammatory cytokines. In the presence of oxidant alone, A549 epithelial cells released significant amounts of IL-8, which was inhibited by both calcium antagonist treatment and PDE inhibition treatment. These data suggest that ROS-mediated lung inflammation could be mediated at least in part by calcium and elevated PDE activity associated with decreased cAMP in both macrophages and epithelial cells. Inhibition of these pathways may provide a route for treatment of inflammatory lung diseases.


Subject(s)
Epithelial Cells/drug effects , Macrophages/drug effects , Oxidants/pharmacology , Oxidative Stress , Phosphodiesterase Inhibitors/pharmacology , tert-Butylhydroperoxide/pharmacology , 3',5'-Cyclic-AMP Phosphodiesterases/antagonists & inhibitors , 4-(3-Butoxy-4-methoxybenzyl)-2-imidazolidinone/pharmacology , Animals , Calcium/metabolism , Calcium Channel Blockers/pharmacology , Calcium-Calmodulin-Dependent Protein Kinases/antagonists & inhibitors , Cell Line , Chelating Agents/pharmacology , Cyclic Nucleotide Phosphodiesterases, Type 1 , Cyclic Nucleotide Phosphodiesterases, Type 4 , Egtazic Acid/analogs & derivatives , Egtazic Acid/pharmacology , Epithelial Cells/metabolism , Interleukin-8/metabolism , Lung/cytology , Macrophages/metabolism , Mice , Sulfonamides/pharmacology , Tumor Necrosis Factor-alpha/metabolism , Verapamil/pharmacology
7.
Am J Hosp Pharm ; 49(6): 1422-4, 1992 Jun.
Article in English | MEDLINE | ID: mdl-1529982

ABSTRACT

A clinical privileges program for pharmacists is described. In 1985 and 1989 the Department of Veterans Affairs (VA) issued circulars defining policy on clinical privileges for pharmacists at its medical centers. Pharmacists at one large VA medical center responded by developing a clinical privileges program. Bylaws under which medical staff members are granted clinical privileges were used as a model for the pharmacist program. A pharmacist seeking privileges prepares an application detailing his or her background and the practice areas involved in the request; the applicant also drafts a quality assurance protocol. The application is reviewed by a pharmacist clinical privileges review board (PCPRB). The PCPRB uses the quality assurance plan to verify that adequate measures are in place to meet standards of care. If a question of patient safety arises, the board meets to review the pharmacist's activities. Each pharmacist who is granted privileges must have a physician sponsor. Since the first meeting of the PCPRB in 1990, clinical privileges have been requested by all 24 clinical pharmacy specialists at the center. No pharmacist has been denied privileges, although the board has required additional training or improved quality assurance protocols for many. Acceptance of the program by the medical staff has been good. A clinical privileges program at a VA medical center offers pharmacists the opportunity to practice pharmaceutical care.


Subject(s)
Medical Staff Privileges/trends , Pharmacists , Pharmacy Service, Hospital/organization & administration , Physicians , Professional Review Organizations , Quality Assurance, Health Care , United States
8.
Can Fam Physician ; 36: 1749-53, 1990 Oct.
Article in English | MEDLINE | ID: mdl-21233997

ABSTRACT

Most clinical drug trials relating to acute otitis media have evaluated medications in terms of treatment. In this randomized double-blind, cross-over study, the effectiveness of an antihistamine decongestant in the prevention of AOM was investigated, rather than the treatment. The medication/placebo was started at the onset of a cold and continued throughout its duration. No treatment effect was evident in the results obtained with 308 children who completed the eight-month study. However, the results indicated a strong relationship between colds and AOM, and a trend toward higher occurrence of AOM in children under four years of age.

9.
Can Fam Physician ; 34: 2389-93, 1988 Nov.
Article in English | MEDLINE | ID: mdl-21253110

ABSTRACT

Most clinical drug trials relating to acute otitis media have evaluated medications in terms of treatment. In this randomized double-blind, cross-over study, the effectiveness of an antihistamine decongestant in the prevention of AOM was investigated, rather than the treatment. The medication/placebo was started at the onset of a cold and continued throughout its duration. No treatment effect was evident in the results obtained with 308 children who completed the eight-month study. However, the results indicated a strong relationship between colds and AOM, and a trend toward higher occurrence of AOM in children under four years of age.

10.
Can Fam Physician ; 32: 1225-35, 1986 Jun.
Article in English | MEDLINE | ID: mdl-21267165

ABSTRACT

Recent government studies have reported an oversupply of family physicians and recommended reductions in their numbers. Believing these recommendations to be based on overestimates, as the unfounded assumption is made that all non-specialists are family physicians in active practice, we attempted to determine how many physicians were actually in general practice in Edmonton, Alberta, in 1984. Using screening procedures followed by a mailed questionnaire to confirm our results and obtain further information about family practice, we identified only 309 general practitioners of 662 non-specialists. Only 45% of the total number of physicians who are not practising a specialty other than family medicine, and who are registered with the College of Physicians and Surgeons of Alberta, could be positively identified as family physicians. We therefore recommend that information on actual numbers of family physicians, rather than non-specialists as a whole, be made available to policy makers determining personnel requirements. Questionnaire results indicated certain problem areas in family practice, particularly long work weeks, inadequate coverage for practices, and lack of hospital privileges and obstetrical care. We suggest that professionals in family medicine address these problems.

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