Measuring the intangible resources caregivers need to provide nurturing care during the complementary feeding period: a scoping review in low- and lower-middle-income countries.

OBJECTIVE: Caregivers require tangible (e.g. food and financial) and intangible resources to provide care to ensure child health, nutrition and development. Intangible resources include beliefs and knowledge, education, self-efficacy, perceived physical health, mental health, healthy stress levels, social support, empowerment, equitable gender attitudes, safety and security and time sufficiency. These intangible caregiver resources are included as intermediate outcomes in nutrition conceptual frameworks yet are rarely measured as part of maternal and child nutrition research or evaluations. To facilitate their measurement, this scoping review focused on understudied caregiver resources that have been measured during the complementary feeding period in low- and lower-middle-income countries. DESIGN: We screened 9,232 abstracts, reviewed 277 full-text articles and included 163 articles that measured caregiver resources related to complementary feeding or the nutritional status of children 6 months to 2 years of age. RESULTS: We identified measures of each caregiver resource, though the number of measures and quality of descriptions varied widely. Most articles (77 %) measured only one caregiver resource, mental health (n 83) and social support (n 54) most frequently. Psychometric properties were often reported for mental health measures, but less commonly for other constructs. Few studies reported adapting measures for specific contexts. Existing measures for mental health, equitable gender attitudes, safety and security and time sufficiency were commonly used; other constructs lacked standardised measures. CONCLUSIONS: Measurement of caregiver resources during the complementary feeding period is limited. Measuring caregiver resources is essential for prioritising caregivers and understanding how resources influence child care, feeding and nutrition.

External cephalic version: a retrospective chart review at a Canadian tertiary care centre.

OBJECTIVES: The primary objective is to identify our local external cephalic version (ECV) success rate, variables associated with increased likelihood of success, and complication rates. The secondary objective is to allow obstetrical care providers to accurately counsel patients undergoing trial of ECV. METHODS: We analyzed patient charts between January 2018 and December 2022 who underwent ECV. Variables included maternal age, parity, gestational age at time of ECV attempt, breech type, anesthetic, uterine relaxant, placental location, neonatal birthweight, and provider seniority. Outcomes were ECV success, mode of delivery, emergent cesarean delivery rate due to ECV, and NICU admission. Appropriate statistical analysis was performed. RESULTS: 258 patients were included. Overall success rate was 31%. Multiparity, transverse presentation, and neonatal birthweight > 3.3 kg were associated with significantly increased success rates. Uterine relaxant use was associated with a lower success rate than no relaxant use, which is potentially explained by significantly more frequent relaxant use in non-transverse presentations and non-significant trend in increased relaxant use in primiparous patients. Other factors including anesthetic use, maternal age, gestational age, placental location, and provider seniority did not significantly impact success. Emergency cesarean delivery rate was 10% and NICU admission rate was 8%, both of which were higher than anticipated. CONCLUSION: ECV remains an option for management of the term breech. Obstetrical providers at our centre and in others may use this study to more accurately counsel patients using local data and optimize likelihood of success based on patient and peri-procedural factors. OBJECTIFS: L'objectif principal est de déterminer le taux local de versions céphaliques externes (VCE) réussies, les variables associées à une grande probabilité de réussite et le taux de complications. L'objectif secondaire est d'outiller les prestataires de soins obstétricaux de sorte qu'ils puissent bien accompagner les patientes se soumettant à un essai de VCE. MÉTHODE: Nous avons analysé les dossiers des patientes s'étant soumises à une VCE dans la période de janvier 2018 à décembre 2022. Les variables analysées étaient l'âge maternel, la parité, l'âge gestationnel au moment de la tentative de VCE, le type de présentation du siège, l'anesthésie, le relaxant utérin, le positionnement du placenta, le poids à la naissance et les années d'expérience du prestataire. Les critères étaient la réussite de la VCE, le mode d'accouchement, le taux de césarienne d'urgence en raison de la VCE et l'admission aux soins intensifs néonataux. Une bonne analyse statistique a été réalisée. RÉSULTATS: Au total, 258 patientes ont été incluses. Le taux de réussite global a été de 31 %. La multiparité, la présentation transverse et le poids de naissance supérieur à 3,3 kg ont été associés à un taux de réussite significativement plus élevé. L'utilisation de relaxants utérins a été associée à un moins bon taux de réussite comparativement à l'absence de relaxant, ce qui peut s'expliquer par l'utilisation significativement plus fréquente de relaxants dans les présentations non transverses et une tendance non significative à l'augmentation du recours aux relaxants chez les primipares. D'autres facteurs, tels que l'utilisation d'anesthésiques, l'âge maternel, l'âge gestationnel, le positionnement du placenta et les années d'expérience du prestataire, n'ont pas eu d'effet significatif sur la réussite de l'intervention. Le taux de césarienne d'urgence était de 10 % et le taux d'admission aux soins intensifs néonataux était de 8 %, tous deux plus élevés que prévu. CONCLUSION: La VCE reste une option pour la prise en charge de la présentation du siège à terme. Les prestataires de soins obstétricaux de notre centre et d'autres centres peuvent utiliser cette étude pour bien accompagner les patientes en utilisant des données locales et optimiser les chances de réussite en fonction des facteurs liés à la patiente et à la période avant, pendant et après l'intervention.

Introduction of a Maternal-Fetal Medicine Tele-Ultrasound Program in Rural Alberta.

OBJECTIVES: We established a program of Maternal-Fetal Medicine (MFM) telemedicine that is safe and acceptable. Since December 2019, a multi-disciplinary team has been planning this quality improvement project. METHODS: We performed a pilot study to investigate the feasibility of using telemedicine and tele-ultrasound to enable prompt MFM consultations for patients in remote locations. We began with the training of sonographers followed by implementation in a small pilot. Interim analysis of the acceptability and feasibility of the program was done through patient surveys, images audit, and review of neonatal outcomes. RESULTS: Our background epidemiologic data showed that in Alberta, between 2017 and 2022, 460 patients travelled >6 hours, and 5038 travelled >2 hours from home to reach their site of birth. Patients were appropriately triaged to delivery/consultation at the tertiary level center based on diagnosis/suspicion of anomalies, such as abnormally invasive placenta, intrauterine growth restriction, hydrops, and partial agenesis of the corpus callosum, all of which were confirmed postdelivery. There was no neonatal mortality, and the single stillbirth was related to an unpreventable peri-viable co-twin demise. The patient survey demonstrated that for >85% of respondents the program reduced costs and stress. Ultrasound image audit found improvement and consistency in image quality after 3 months of training combined with supervision. CONCLUSION: MFM telemedicine is feasible and can be safe with adequate supervision. Additional support and resources are needed to scale and spread this quality improvement initiative.

#Cheers: An Examination of User-Generated Alcohol Advertising on Instagram.

Background: Alcohol marketing is a known risk factor for youth drinking. The growth in digital marketing has generated a new form of alcohol advertisement in which brands solicit and/or share consumer-generated or user-generated content. Objectives: The current study investigates the prevalence of UGC alcohol advertising on social media and examines the content of UGC advertising to determine potential violations of current regulatory guidelines. Results: The Instagram accounts of 20 Nova Scotia breweries were monitored for the month of July 2021. User-generated content made up a substantial portion (41%) of all Instagram stories (n = 1531), and there were 321 violations of the Canadian Radio-television and Telecommunications Commission code for broadcast advertising of alcoholic beverage. Ten percent of violations encouraged consumption, 59% depicted irresponsible use, 14% appealed to youth, 14% associated alcohol with activities requiring a degree of skill or care, 2.5% associated alcohol with social or personal success. Conclusions/Importance: These findings indicate that UGC is a commonly used marketing strategy among alcohol producers and the current self-regulatory system is insufficient in preventing advertising that appeals to youth and exacerbates a culture of immoderate consumption.

Level-loading a health system by transferring emergency department patients to a community hospital: Prospective cohort study.

BACKGROUND: Emergency department boarding and crowding lead to worse patient outcomes and patient satisfaction. OBJECTIVE: We describe the implementation of a program to transfer patients requiring medical admission from an academic emergency department to a community hospital's medical floor and analyze its effects on patient outcomes. METHODS: A prospective cohort study was performed. Data was collected on patient flow through the transfer program. Patient characteristics, boarding time in the emergency department, and hospital-based outcome measures were compared between patients in the transfer program who were successfully transferred to the community hospital and patients who were admitted to the academic medical center. RESULTS: 79 patients were successfully transferred to the community hospital between November 23, 2020 and August 5, 2021, resulting in 279 bed days in the community hospital. Successfully transferred patients experienced a statistically shorter ED boarding time (5.7 vs. 10.9 h, p < 0.0001), ED length of stay (10.5 vs 16.1 h, p < 0.0001), and hospital length of stay (3.5 vs 5.7 days, p < 0.0001) compared to patients initially referred to the transfer program who were admitted to the academic medical center. There were no reported adverse events during transfer, upgrades to the ICU within 24 h of admission, or inpatient deaths for patients who were transferred. CONCLUSION: We implemented an academic emergency department to partner community hospital transfer program that safely level-loads medical patients in a healthcare system.

Diabetes in Pregnancy.

OBJECTIVE: This guideline reviews the evidence relating to the diagnosis and obstetrical management of diabetes in pregnancy. OUTCOMES: The outcomes evaluated were short- and long-term maternal outcomes, including preeclampsia, Caesarean section, future diabetes, and other cardiovascular complications, and fetal outcomes, including congenital anomalies, stillbirth, macrosomia, birth trauma, hypoglycemia, and long-term effects. EVIDENCE: Published literature was retrieved through searches of PubMed and the Cochrane Library using appropriate controlled vocabulary (MeSH terms "diabetes" and "pregnancy"). Where appropriate, results were restricted to systematic reviews, randomized control trials/controlled clinical trials, and observational studies. There were no date limits, but results were limited to English or French language materials. VALUES: The quality of evidence was rated using the criteria described in the Report of the Canadian Task Force on Preventive Health Care (Table 1). SUMMARY STATEMENTS: Recommendations It is recognized that the use of different diagnostic thresholds for the "preferred" and "alternative" strategies could cause confusion in certain settings. Despite this, the committee has identified the importance of remaining aligned with the current Canadian Diabetes Association 2013 guidelines as being a priority. It is thus recommended that each care centre strategically align with 1 of the 2 strategies and implement protocols to ensure consistent and uniform reporting of test results.

Le diabète pendant la grossesse.

OBJECTIF: La présente Directive passe en revue les données probantes liées au diagnostic et à la prise en charge obstétricale du diabète durant la grossesse. ISSUES: Les issues évaluées étaient les issues maternelles à court et à long terme, dont la prééclampsie, la césarienne, le diabète éventuel et d'autres complications cardiovasculaires et les issues fœtales, dont les anomalies congénitales, la mortinaissance, la macrosomie, le traumatisme de la naissance, l'hypoglycémie et les effets à long terme. RéSULTATS: La littérature publiée a été récupérée par l'intermédiaire de recherches menées dans PubMed et The Cochrane Library au moyen d'un vocabulaire contrôlé (termes MeSH « diabète ¼ et « grossesse ¼) appropriés. Le cas échéant, les résultats ont été restreints aux analyses systématiques, aux essais comparatifs randomisés / essais cliniques comparatifs et aux études observationnelles. Aucune limite n'a été imposée en matière de date, mais les résultats ont été limités aux articles publiés en anglais ou en français. VALEURS: La qualité des résultats a été évaluée au moyen des critères décrits dans le rapport du Groupe d'étude canadien sur les soins de santé préventifs (Tableau 1). DéCLARATIONS SOMMAIRES: RECOMMANDATIONS.

Guidelines for the Management of a Pregnant Trauma Patient.

OBJECTIVE: Physical trauma affects 1 in 12 pregnant women and has a major impact on maternal mortality and morbidity and on pregnancy outcome. A multidisciplinary approach is warranted to optimize outcome for both the mother and her fetus. The aim of this document is to provide the obstetric care provider with an evidence-based systematic approach to the pregnant trauma patient. OUTCOMES: Significant health and economic outcomes considered in comparing alternative practices. EVIDENCE: Published literature was retrieved through searches of Medline, CINAHL, and The Cochrane Library from October 2007 to September 2013 using appropriate controlled vocabulary (e.g., pregnancy, Cesarean section, hypotension, domestic violence, shock) and key words (e.g., trauma, perimortem Cesarean, Kleihauer-Betke, supine hypotension, electrical shock). Results were restricted to systematic reviews, randomized control trials/controlled clinical trials, and observational studies published in English between January 1968 and September 2013. Searches were updated on a regular basis and incorporated in the guideline to February 2014. Grey (unpublished) literature was identified through searching the websites of health technology assessment and health technology-related agencies, clinical practice guideline collections, clinical trial registries, and national and international medical specialty societies. VALUES: The quality of evidence in this document was rated using the criteria described in the Report of the Canadian Task Force on Preventive Health Care (Table 1). BENEFITS, HARMS, AND COSTS: This guideline is expected to facilitate optimal and uniform care for pregnancies complicated by trauma. Summary Statement Specific traumatic injuries At this time, there is insufficient evidence to support the practice of disabling air bags for pregnant women. (III) Recommendations Primary survey 1. Every female of reproductive age with significant injuries should be considered pregnant until proven otherwise by a definitive pregnancy test or ultrasound scan. (III-C) 2. A nasogastric tube should be inserted in a semiconscious or unconscious injured pregnant woman to prevent aspiration of acidic gastric content. (III-C) 3. Oxygen supplementation should be given to maintain maternal oxygen saturation > 95% to ensure adequate fetal oxygenation. (II-1B) 4. If needed, a thoracostomy tube should be inserted in an injured pregnant woman 1 or 2 intercostal spaces higher than usual. (III-C) 5. Two large bore (14 to 16 gauge) intravenous lines should be placed in a seriously injured pregnant woman. (III-C) 6. Because of their adverse effect on uteroplacental perfusion, vasopressors in pregnant women should be used only for intractable hypotension that is unresponsive to fluid resuscitation. (II-3B) 7. After mid-pregnancy, the gravid uterus should be moved off the inferior vena cava to increase venous return and cardiac output in the acutely injured pregnant woman. This may be achieved by manual displacement of the uterus or left lateral tilt. Care should be taken to secure the spinal cord when using left lateral tilt. (II-1B) 8. To avoid rhesus D (Rh) alloimmunization in Rh-negative mothers, O-negative blood should be transfused when needed until cross-matched blood becomes available. (I-A) 9. The abdominal portion of military anti-shock trousers should not be inflated on a pregnant woman because this may reduce placental perfusion. (II-3B) Transfer to health care facility 10. Transfer or transport to a maternity facility (triage of a labour and delivery unit) is advocated when injuries are neither life- nor limb-threatening and the fetus is viable (≥ 23 weeks), and to the emergency room when the fetus is under 23 weeks' gestational age or considered to be non-viable. When the injury is major, the patient should be transferred or transported to the trauma unit or emergency room, regardless of gestational age. (III-B) 11. When the severity of injury is undetermined or when the gestational age is uncertain, the patient should be evaluated in the trauma unit or emergency room to rule out major injuries. (III-C) Evaluation of a pregnant trauma patient in the emergency room 12. In cases of major trauma, the assessment, stabilization, and care of the pregnant women is the first priority; then, if the fetus is viable (≥ 23 weeks), fetal heart rate auscultation and fetal monitoring can be initiated and an obstetrical consultation obtained as soon as feasible. (II-3B) 13. In pregnant women with a viable fetus (≥ 23 weeks) and suspected uterine contractions, placental abruption, or traumatic uterine rupture, urgent obstetrical consultation is recommended. (II-3B) 14. In cases of vaginal bleeding at or after 23 weeks, speculum or digital vaginal examination should be deferred until placenta previa is excluded by a prior or current ultrasound scan. (III-C) Adjunctive tests for maternal assessment 15. Radiographic studies indicated for maternal evaluation including abdominal computed tomography should not be deferred or delayed due to concerns regarding fetal exposure to radiation. (II-2B) 16. Use of gadolinium-based contrast agents can be considered when maternal benefit outweighs potential fetal risks. (III-C) 17. In addition to the routine blood tests, a pregnant trauma patient should have a coagulation panel including fibrinogen. (III-C) 18. Focused abdominal sonography for trauma should be considered for detection of intraperitoneal bleeding in pregnant trauma patients. (II-3B) 19. Abdominal computed tomography may be considered as an alternative to diagnostic peritoneal lavage or open lavage when intra-abdominal bleeding is suspected. (III-C) Fetal assessment 20. All pregnant trauma patients with a viable pregnancy (≥ 23 weeks) should undergo electronic fetal monitoring for at least 4 hours. (II-3B) 21. Pregnant trauma patients (≥ 23 weeks) with adverse factors including uterine tenderness, significant abdominal pain, vaginal bleeding, sustained contractions (> 1/10 min), rupture of the membranes, atypical or abnormal fetal heart rate pattern, high risk mechanism of injury, or serum fibrinogen < 200 mg/dL should be admitted for observation for 24 hours. (III-B) 22. Anti-D immunoglobulin should be given to all rhesus D-negative pregnant trauma patients. (III-B) 23. In Rh-negative pregnant trauma patients, quantification of maternal-fetal hemorrhage by tests such as Kleihauer-Betke should be done to determine the need for additional doses of anti-D immunoglobulin. (III-B) 24. An urgent obstetrical ultrasound scan should be undertaken when the gestational age is undetermined and need for delivery is anticipated. (III-C) 25. All pregnant trauma patients with a viable pregnancy who are admitted for fetal monitoring for greater than 4 hours should have an obstetrical ultrasound prior to discharge from hospital. (III-C) 26. Fetal well-being should be carefully documented in cases involving violence, especially for legal purposes. (III-C) Obstetrical complications of trauma 27. Management of suspected placental abruption should not be delayed pending confirmation by ultrasonography as ultrasound is not a sensitive tool for its diagnosis. (II-3D) Specific traumatic injuries 28. Tetanus vaccination is safe in pregnancy and should be given when indicated. (II-3B) 29. Every woman who sustains trauma should be questioned specifically about domestic or intimate partner violence. (II-3B) 30. During prenatal visits, the caregiver should emphasize the importance of wearing seatbelts properly at all times. (II-2B) Perimortem Caesarean section 31. A Caesarean section should be performed for viable pregnancies (≥ 23 weeks) no later than 4 minutes (when possible) following maternal cardiac arrest to aid with maternal resuscitation and fetal salvage. (III-B).

Objectif : Une femme enceinte sur 12 en vient à subir des traumatismes physiques et ceux-ci exercent des effets importants sur la mortalité et la morbidité maternelles, ainsi que sur l'issue de la grossesse. La mise en œuvre d'une approche multidisciplinaire s'avère justifiée pour assurer l'optimisation des issues, et ce, tant pour la mère que pour son fœtus. Le présent document a pour but d'offrir, aux fournisseurs de soins obstétricaux, une approche systématique factuelle qu'ils pourront utiliser pour assurer la prise en charge des patientes enceintes ayant subi un traumatisme. Issues : Issues sanitaires et économiques considérables, par comparaison avec les pratiques de rechange. Résultats : La littérature publiée a été récupérée par l'intermédiaire de recherches menées dans Medline, CINAHL et The Cochrane Library entre octobre 2007 et septembre 2013 au moyen d'un vocabulaire contrôlé (« pregnancy ¼, « Cesarean section ¼, « hypotension ¼, « domestic violence ¼, « shock ¼) et de mots clés (« trauma ¼, « perimortem Cesarean ¼, « Kleihauer-Betke ¼, « supine hypotension ¼, « electrical shock ¼) appropriés. Les résultats ont été restreints aux analyses systématiques, aux études observationnelles et aux essais comparatifs randomisés / essais cliniques comparatifs publiés en anglais entre janvier 1968 et septembre 2013. Les recherches ont été mises à jour de façon régulière et intégrées à la directive clinique jusqu'en février 2014. La littérature grise (non publiée) a été identifiée par l'intermédiaire de recherches menées dans les sites Web d'organismes s'intéressant à l'évaluation des technologies dans le domaine de la santé et d'organismes connexes, dans des collections de directives cliniques, dans des registres d'essais cliniques et auprès de sociétés de spécialité médicale nationales et internationales. Valeurs : La qualité des résultats a été évaluée au moyen des critères décrits dans le rapport du Groupe d'étude canadien sur les soins de santé préventifs (Tableau). Avantages, désavantages et coûts : Nous nous attendons à ce que la présente directive clinique facilite l'offre de soins optimaux et uniformes dans les cas de grossesse compliquée par un traumatisme. Déclaration sommaireLésions traumatiques particulières Pour l'instant, nous ne disposons pas de données probantes suffisantes pour soutenir la désactivation des coussins gonflables dans le cas des femmes enceintes. (III) RecommandationsExamen primaire 1. La présence d'une grossesse devrait être présumée chez toutes les femmes en âge de procréer ayant subi des blessures considérables, jusqu'à ce que le contraire ait été prouvé au moyen d'une échographie ou d'un test de grossesse définitif. (III-C) 2. Chez les femmes enceintes blessées inconscientes ou à demi conscientes, une sonde nasogastrique devrait être insérée afin de prévenir l'aspiration de contenu gastrique acide. (III-C) 3. Une oxygénothérapie devrait être mise en œuvre pour garantir le maintien d'une saturation maternelle en oxygène > 95 %, de façon à assurer une oxygénation fœtale adéquate. (II-1B) 4. Chez les femmes enceintes blessées, l'insertion d'une sonde de thoracostomie (à un endroit se situant à un ou deux espaces intercostaux de plus que d'habitude) pourrait être envisagée, au besoin. (III-C) 5. Chez les femmes enceintes gravement blessées, deux lignes intraveineuses de gros calibre (14-16) devraient être mises en place. (III-C) 6. En raison des effets indésirables qu'ils exercent sur la perfusion utéroplacentaire chez les femmes enceintes, les vasopresseurs ne devraient être utilisés qu'en présence d'une hypotension réfractaire qui ne réagit pas à la réanimation liquidienne. (II-3B) 7. Chez les femmes enceintes gravement blessées qui ont passé le cap de la mi-grossesse, l'utérus gravide devrait être repositionné de façon à ce qu'il ne comprime plus la veine cave inférieure, et ce, dans le but d'accroître le retour veineux et le débit cardiaque. Ce repositionnement peut être obtenu en déplaçant l'utérus manuellement ou en plaçant la patiente en position latérale gauche (en s'assurant alors d'immobiliser la moelle épinière de la patiente au préalable). (II-1B) 8. Pour prévenir l'allo-immunisation rhésus D chez les femmes Rh négatives, du sang O négatif devrait être transfusé, au besoin, jusqu'à ce que du sang provenant d'un donneur compatible soit obtenu. (I-A) 9. La partie abdominale du pantalon pneumatique hypotenseur ne devrait pas être gonflée en présence d'une grossesse, car cela pourrait atténuer la perfusion placentaire. (II-3B) Transfert vers un établissement de santé 10. Le transfert vers un service de maternité (service de triage d'une unité de travail et d'accouchement) est recommandé lorsque la patiente en question ne présente pas de blessures potentiellement mortelles ou pouvant mener à la perte d'un membre et lorsque le fœtus est viable (≥ 23 semaines); le transfert vers une salle des urgences est recommandé lorsque le fœtus n'a pas encore atteint l'âge gestationnel de 23 semaines ou lorsqu'il n'est pas considéré comme étant viable. En présence d'un traumatisme majeur, la patiente devrait être transférée ou transportée vers une unité de traumatologie ou une salle des urgences, sans égard à l'âge gestationnel. (III-B) 11. Lorsque la gravité du traumatisme est indéterminée ou lorsque l'âge gestationnel est incertain, la patiente devrait faire l'objet d'une évaluation menée dans une unité de traumatologie ou une salle des urgences en vue d'écarter la présence de blessures majeures. (III-C) Évaluation, au sein d'une salle des urgences, d'une patiente enceinte ayant subi un traumatisme 12. En présence d'un traumatisme majeur, la priorité doit être accordée à l'évaluation, à la stabilisation et à la prise en charge de la femme enceinte; par la suite, lorsque le fœtus est viable (≥ 23 semaines), l'auscultation de la fréquence cardiaque fœtale et un monitorage fœtal peuvent être mis en œuvre. De plus, une consultation en obstétrique devrait être obtenue dès que possible. (II-3B) 13. La tenue d'une consultation d'urgence en obstétrique est recommandée en ce qui concerne les femmes enceintes dont le fœtus est viable (≥ 23 semaines) et chez qui l'on soupçonne la présence de contractions utérines, d'un décollement placentaire ou d'une rupture utérine traumatique. (II-3B) 14. En présence de saignements vaginaux à 23 semaines ou par la suite, la tenue d'un examen vaginal au moyen d'un spéculum ou des doigts devrait être reportée jusqu'à ce que la présence d'un placenta praevia ait été écartée par échographie (préalable ou actuelle). (III-C) Tests d'appoint dans le cadre de l'évaluation maternelle 15. Les études de radiographie nécessaires aux fins de l'évaluation maternelle (dont la tomodensitométrie abdominale) ne devraient pas être retardées ni reportées en raison de préoccupations à l'égard de l'exposition du fœtus à des rayonnements. (II-2B) 16. L'utilisation de produits de contraste à base de gadolinium peut être envisagée lorsque les avantages maternels l'emportent sur les risques fœtaux potentiels. (III-C) 17. En plus des tests sanguins qui sont régulièrement menés dans le cadre de l'évaluation des patientes enceintes ayant subi un traumatisme, un profil de coagulation (comprenant la mesure du taux de fibrinogène) devrait être obtenu. (III-C) 18. Chez les patientes enceintes ayant subi un traumatisme, la tenue d'une échographie abdominale ciblée pour l'identification de traumatismes devrait être envisagée aux fins de la détection des saignements intrapéritonéaux. (II-3B) 19. Lorsque la présence de saignements intra-abdominaux est soupçonnée, la tomodensitométrie abdominale pourrait constituer une solution de rechange au lavage péritonéal diagnostique ou au lavage ouvert. (III-C) Évaluation fœtale 20. Toutes les patientes enceintes ayant subi un traumatisme qui présentent une grossesse viable (≥ 23 semaines) devraient faire l'objet d'un monitorage fœtal électronique pendant au moins 4 heures. (II-3B) 21. Les patientes enceintes ayant subi un traumatisme (≥ 23 semaines) qui présentent des facteurs indésirables (dont la sensibilité utérine, des douleurs abdominales considérables, des saignements vaginaux, des contractions soutenues [> 1/10 min], la rupture des membranes, un profil de fréquence cardiaque fœtale atypique ou anormal, un mécanisme de blessure à risque élevé ou un taux sérique de fibrinogène < 200 mg/dl) devraient être hospitalisées pour une période d'observation de 24 heures. (III-B) 22. De l'immunoglobuline anti-D devrait être administrée à toutes les patientes enceintes Rh négatives ayant subi un traumatisme. (III-B) 23. Chez les patientes enceintes Rh négatives ayant subi un traumatisme, l'hémorragie fœtomaternelle devrait être quantifiée au moyen de mesures telles que le test de Kleihauer-Betke, et ce, dans le but de déterminer la nécessité de procéder à l'administration de doses additionnelles d'immunoglobuline anti-D. (III-B) 24. Une échographie obstétricale devrait être menée d'urgence lorsque l'âge gestationnel est indéterminé et que la nécessité de procéder à l'accouchement est anticipée. (III-C) 25. Toutes les patientes enceintes ayant subi un traumatisme qui présentent une grossesse viable et qui sont hospitalisées aux fins de la tenue d'un monitorage fœtal pendant plus de 4 heures devraient faire l'objet d'une échographie obstétricale avant d'obtenir leur congé de l'hôpital. (III-C) 26. Il est important de disposer, particulièrement à des fins juridiques, d'une documentation rigoureuse du bien-être fœtal dans les cas mettant en cause de la violence. (III-C) Complications obstétricales du traumatisme 27. La prise en charge de la présence soupçonnée d'un décollement placentaire ne devrait pas être différée jusqu'à l'obtention d'une confirmation par échographie; l'échographie ne dispose pas de la sensibilité requise pour l'établissement d'un diagnostic de décollement placentaire. (II-3D) Lésions traumatiques particulières 28. La vaccination antitétanique est sûre pendant la grossesse et devrait être administrée, au besoin. (II-3B) 29. Toutes les femmes qui subissent un traumatisme devraient faire l'objet de questions visant particulièrement la violence familiale ou conjugale. (II-3B) 30. Dans le cadre des consultations prénatales, le fournisseur de soins devrait souligner l'importance du port de la ceinture de sécurité de façon adéquate, en tout temps. (II-2B) Césarienne péri-mortem 31. En présence d'une grossesse viable (≥ 23 semaines), la tenue d'une césarienne est recommandée au plus tard 4 minutes (dans la mesure du possible) à la suite de l'arrêt cardiaque chez la mère, et ce, en vue de faciliter la réanimation maternelle et le sauvetage du fœtus. (III-B).

Quantifying the impact of initial RNA primer length on nucleotide addition by RNA polymerase I.

Transient state kinetic studies of eukaryotic DNA-dependent RNA polymerases (Pols) in vitro provide quantitative characterization of enzyme activity at the level of individual nucleotide addition events. Previous work revealed heterogeneity in the rate constants governing nucleotide addition by yeast RNA polymerase I (Pol I) for each position on a template DNA. In contrast, the rate constants that described nucleotide addition by yeast RNA polymerase II (Pol II) were more homogeneous. This observation led to the question, what drives the variability of rate constants governing RNA synthesis by Pol I? Are the kinetics of nucleotide addition dictated by the position of the nascent RNA within the polymerase or by the identity of the next encoded nucleotide? In this study, we examine the impact of nucleotide position (i.e. nascent RNA primer length) on the rate constants governing nine sequential nucleotide addition events catalyzed by Pol I. The results reveal a conserved trend in the observed rate constants at each position for all primer lengths used, and highlight that the 9-nucleotide, or 9-mer, RNA primer provides the fastest observed rate constants. These findings suggest that the observed heterogeneity of rate constants for RNA synthesis by Pol I in vitro is driven primarily by the template sequence.

Effects of a range of 6 prefabricated orthotic insole designs on plantar pressure in a healthy population: A randomized, open-label crossover investigation.

BACKGROUND: Prefabricated orthotic insoles are widely commercially available for self-selection to treat foot and lower-body musculoskeletal pain, without requiring advice from health care professionals. Although they are generally designed to mimic traditional design features of custom-made orthotics used in clinical practice, the effects of prefabricated insoles on plantar pressure distribution are poorly understood. OBJECTIVE: This investigation aimed to evaluate and directly compare the effects of a range of 6 different commercially available prefabricated orthotic insole designs on plantar pressure in healthy individuals. METHODS: This was a single-center, randomized, open-label, crossover investigation. In-shoe dynamic pressure (F-scan) was investigated in 24 healthy subjects with normal foot posture, wearing standard shoes alone and in combination with 6 different orthotic insoles, consecutively, measured on a single day. The biomechanical impact of each insole was determined by the statistical significance of changes from baseline measurements (standard shoe alone). RESULTS: Insoles with heel cups and medial arch geometries consistently increased contact area at medial arch and whole-foot regions and reduced both plantar peak pressure (PP) and pressure time integral at medial arch and heel regions. CONCLUSIONS: This investigation has aided in further understanding the mode of action of prefabricated insoles in a healthy population. The insoles in this study redistributed plantar pressure at key regions of the foot, based on design features common to prefabricated insoles. Prefabricated orthotic insoles represent an easily accessible means of reducing lower-body musculoskeletal stress for those who spend prolonged periods of time on their feet.

Assessing the implementation of evidence-based alcohol policies on Atlantic Canadian post-secondary campuses: A comparative analysis.

OBJECTIVE: This study assessed the quality of campus alcohol policies against best practice to assist campus decision-makers in strengthening their campus alcohol policies and reducing student alcohol use and harm. METHODS: Drawing on empirical literature and expert opinion, we developed an evidence-based scoring rubric to assess the quality of campus alcohol policies across 10 alcohol policy domains. Campus alcohol policy data were collected from 12 Atlantic Canadian universities. All extracted data were verified by the institutions and then scored. RESULTS: On average, post-secondary institutions are implementing only a third of the evidence-based alcohol policies captured by the 10 domains assessed. The average campus policy score was 33% (range 15‒49%). Of the 10 domains examined, only enforcement achieved an average score above 50%, followed closely by leadership and surveillance at 48%. The two heaviest-weighted domains-availability and access, and advertising and sponsorship-had average scores of 27% and 24%, respectively. However, if post-secondary campuses adopted the highest scoring policies from across all 12 campuses, they could achieve a score of 74%, indicating improvement is possible. CONCLUSION: Atlantic Canadian universities are collectively achieving less than half their potential to reduce student alcohol-related harm. However, this study identifies opportunities where policies can be enhanced or modified. The fact that most policies are present at one or more campuses highlights that policy recommendations are an achievable goal for campuses. Campuses are encouraged to look to each other as models for improving their own policies.

RéSUMé: OBJECTIF: L'étude a évalué la qualité des politiques relatives à l'alcool sur les campus par rapport aux pratiques exemplaires afin d'aider les décideurs des campus à renforcer leurs politiques relatives à l'alcool et à réduire la consommation d'alcool et les méfaits connexes dans la population étudiante. MéTHODE: En faisant appel à la littérature empirique et aux opinions d'experts, nous avons élaboré une grille de notation factuelle pour évaluer la qualité des politiques relatives à l'alcool sur les campus dans 10 domaines associés aux politiques sur l'alcool. Les données des politiques relatives à l'alcool sur les campus sont extraites des politiques de 12 universités du Canada atlantique. Toutes les données extraites ont été confirmées par les établissements, après quoi nous leur avons attribué une note. RéSULTATS: En moyenne, les établissements postsecondaires ne mettent en œuvre que le tiers des politiques factuelles relatives à l'alcool faisant partie des 10 domaines évalués. La note moyenne des politiques des campus a été de 33 % (intervalle de 15 à 49 %). Des 10 domaines pris en compte, seule la mise en application a obtenu une note moyenne de plus de 50 %, suivie de près par le leadership et la surveillance, à 48 %. Les notes moyennes dans les deux domaines les plus lourdement pondérés (disponibilité et accès, et publicité et commandites) ont été de 27 % et de 24 %, respectivement. Toutefois, si les campus postsecondaires adoptaient les politiques les mieux notées des 12 campus, ils obtiendraient une note de 74 %; une amélioration est donc possible. CONCLUSION: Les universités du Canada atlantique réalisent collectivement moins de la moitié de leur potentiel de réduction des méfaits liés à l'alcool dans la population étudiante. Notre étude indique cependant des possibilités d'améliorer ou de modifier les politiques. Le fait que la plupart des politiques recommandées sont présentes sur un ou plusieurs campus montre qu'elles constituent un objectif réalisable. Nous encourageons chaque campus à améliorer ses propres politiques en s'inspirant de celles des autres.

The effects of SLICE®- and ivermectin-contaminated sediment on avoidance behaviour and oxygen consumption in marine benthic invertebrates.

Pest management strategies to reduce sea lice infestations in the salmon aquaculture industry include in-feed treatments with ivermectin (IVM) and SLICE® (active ingredient [AI] emamectin benzoate [EMB]), which can result in local contamination of the environment. These compounds partition to sediments, have moderate persistence, and may pose a risk to non-target benthic organisms. The sub-lethal effects of EMB, IVM and a combination of both (EMB/IVM) on the benthic amphipod Eohaustorius estuarius and polychaete Nereis virens at environmentally relevant sediment concentrations were examined in subchronic exposures (28-30-d). E. estuarius avoided sediment containing >50 µg/kg IVM alone and in combination with EMB. N. virens avoided sediment with >50 µg/kg IVM and >0.5 µg/kg EMB/IVM and exhibited impaired burrowing and locomotory behaviour with both treatments. Oxygen consumption was significantly decreased in E. estuarius (up to 50% compared to controls) and increased in N. virens (by âˆ¼ 200%) when exposed to EMB, IVM and EMB/IVM at concentrations <5 µg/kg. IVM, SLICE® and combination exposures at environmentally relevant concentrations caused adverse effects in E. estuarius and N. virens which could significantly alter organism fitness near salmon aquaculture operations.

The humanistic and economic burden of work-related musculoskeletal pain: a cross-sectional survey of workers in the United Kingdom.

OBJECTIVE: The aim of this study was to evaluate the impact of work-related musculoskeletal (MSK) lower body pain on health-related quality of life (HRQoL) and work productivity in a large sample of workers in the United Kingdom, as well as evaluating the potential economic impact of MSK pain. METHODS: Participants with self-reported work-related MSK pain were recruited from an online panel maintained by a third party (Qualtrics LLC). Participants completed three validated instruments online: the Brief Pain Inventory (BPI), the Assessment of Quality of Life Instrument (AQoL-4D), and the 6-item Work Productivity and Activity Impairment Questionnaire (WPAI). Sociodemographic details, work patterns and healthcare resource utilisation were also reported. One-way analysis of variance (ANOVA) and t-tests were used to explore differences between variables. Linear regression was applied to determine the impact of work-related MSK pain on HRQoL. RESULTS: All 1035 recruited participants completed the survey (57.4% female; mean age 43.4 years). Participants reported spending all (25.2%) or most (53%) of their time at work on their feet. Mean pain severity was 4.63 (standard deviation: 2.07); mean pain interference was 4.37 (2.49). There was a linear relationship between length of shift, time on feet and pain. Mean AQoL-4D scores were 0.609 (0.254). A mean of 4.12 h was lost per week due to pain. Absenteeism (last 7 days) was 9.5% (20.7%), and presenteeism 33.3% (24.9%). An average 1.55 visits were made to family practitioners (total cost: £19,866) and 1 hospital visit (£37,320) due to work-related MSK pain. CONCLUSION: This study demonstrated that work-related lower body pain has a significant impact in terms of individual HRQoL and as an economic societal burden.

A novel immuno-molecular strategy for the detection of Streptococcus pneumoniae serotypes in human cerebrospinal and middle ear fluids.

Streptococcus pneumoniae is one of the most common microorganisms causing acute otitis media (AOM) in children. While bacterial culture of middle ear fluid (MEF) is the gold standard to detect the etiological organisms, several host and pathogen factors impact the survival of the organisms resulting in false negatives. To overcome this limitation, we have developed and validated an innovative multiplex immuno-molecular assay to screen and detect the S. pneumoniae 15-valent pneumococcal conjugate vaccine (PCV15; STs 1, 3, 4, 5, 6A, 6B, 7F, 9V, 14, 18C, 19A, 19F, 22F, 23F, and 33F) vaccine serotypes in MEF. This novel in vitro approach involves two-step testing. First, the MEF specimens were tested for highly conserved pneumococcal genes, autolysin, lytA, and pneumolysin, ply using direct PCR to identify pneumococcus positive specimens. The pneumococcus positive specimens were screened for the presence of vaccine serotype specific pneumococcal polysaccharides using a 15-plex Pneumococcal Antigen Detection (PAD) assay, with specific capture and detection monoclonal antibodies. Due to the lack of availability of MEF samples, cerebrospinal fluid (CSF) was used as the surrogate matrix for the development and validation of the PCR-PAD assays. The PCR and PAD assays were separately evaluated for sensitivity and specificity. Subsequently, the PCR-PAD assays were cross-validated with human MEF samples (n = 39) which were culture confirmed to contain relevant bacterial strains. The combined PCR-PAD assays demonstrated high rate of agreement 94.9% (95% CI; 82.7, 99.4%) with historical Quellung serotype data of these MEF samples. This novel PCR-PAD assay demonstrates the feasibility of combining molecular and immunological assays to screen and identify PCV15 pneumococcal vaccine serotypes in AOM clinical samples.

Correlation of residual amniotic fluid and perinatal outcomes in periviable preterm premature rupture of membranes.

OBJECTIVE: To correlate maternal and fetal outcomes of pregnancies affected by preterm premature rupture of membranes (PPROM) at < 24 weeks' gestational age with the amount of residual amniotic fluid as determined by sonographic evaluation. METHODS: We searched the local maternal-fetal medicine database for the records of all women with PPROM prior to 24 completed weeks of pregnancy. The quantity of residual amniotic fluid determined by ultrasound was recorded and women were separated into two groups: (A) deepest vertical pocket (DVP) ≥ 1 cm, or (B) DVP < 1 cm (severe oligohydramnios). Hospital chart review was undertaken to determine latency to delivery, perinatal death, and maternal complications. Data were analyzed using Fisher exact and Wilcoxon-Mann-Whitney U tests. RESULTS: We identified 31 subjects, of whom nine elected termination of pregnancy (6 in group A, 3 in group B). Six of 10 subjects in group A had a live delivery without neonatal death, whereas only one of 12 subjects in group B had a live delivery (P = 0.020). Additional complications included placental abruption in 63% in group A and 45% in group B, chorioamnionitis in 50% and 70%, respectively, and postpartum endometritis in 0% and 9%, respectively. None of these differences were statistically significant. There were no cases of maternal sepsis or maternal death in either group. Group A was associated with a later GA at delivery (27.5 weeks vs. 23 weeks, P = 0.07), with the GA at rupture of the membranes similar for both groups. CONCLUSION: These results indicate that a higher level of residual amniotic fluid after periviable PPROM is associated with fetal survival and increased latency to delivery without an increase in maternal complications. This information will be valuable in counselling pregnant women with PPROM < 24 weeks.

RNA Polymerase I Is Uniquely Vulnerable to the Small-Molecule Inhibitor BMH-21.

Cancer cells require robust ribosome biogenesis to maintain rapid cell growth during tumorigenesis. Because RNA polymerase I (Pol I) transcription of the ribosomal DNA (rDNA) is the first and rate-limiting step of ribosome biogenesis, it has emerged as a promising anti-cancer target. Over the last decade, novel cancer therapeutics targeting Pol I have progressed to clinical trials. BMH-21 is a first-in-class small molecule that inhibits Pol I transcription and represses cancer cell growth. Several recent studies have uncovered key mechanisms by which BMH-21 inhibits ribosome biosynthesis but the selectivity of BMH-21 for Pol I has not been directly measured. Here, we quantify the effects of BMH-21 on Pol I, RNA polymerase II (Pol II), and RNA polymerase III (Pol III) in vitro using purified components. We found that BMH-21 directly impairs nucleotide addition by Pol I, with no or modest effect on Pols II and III, respectively. Additionally, we found that BMH-21 does not affect the stability of any of the Pols' elongation complexes. These data demonstrate that BMH-21 directly exploits unique vulnerabilities of Pol I.