Eyeglasses

眼镜
  • 文章类型: Journal Article
    背景:当代24小时运动行为(24-HMB)指南提供了有关体力活动(PA)所花费时间的建议,屏幕时间(ST),睡眠(SL)有证据表明,符合此类指南对生理和心理健康有益。然而,在青少年处方眼镜/隐形眼镜中,符合24-HMB指南的患病率并不清楚.本横断面分析的主要目的是检查美国青少年处方眼镜/隐形眼镜中部分或完全符合24-HMB指南的患病率,以及在满足人口统计准则方面的变化,健康状况,和环境属性。
    方法:来自2021年全国儿童健康调查(NSCH)的数据产生了8523名6-17岁青年(54.22%的女孩)处方眼镜/隐形眼镜的目标亚群。使用美国儿童和青少年的代表性样本来估计符合24-HMB指南的患病率,并进行了多项逻辑回归分析,以按人口统计检验满足24-HMB指南的几率,健康状况,和环境变量。
    结果:总体而言,只有6.57%符合所有三个24-HMB指南,23.74%的人不符合三项24-HMB指南中的任何一项,和3.57%,10.88%,29.98%的人符合体力活动的单一指导方针,屏幕时间,或睡眠持续时间,分别,而25.27%的人符合两项24-HMB指南中的任何一项。女性参与者不太可能符合PA+SL指南(OR=0.57,95%CI[0.38,0.56]),但更可能符合ST+SL指南(OR=1.52,95%CI[1.20,1.91])。西班牙裔参与者不太可能符合PA+ST(OR=0.28,95%CI[0.14,0.52])指南和所有三个指南(OR=0.41,95%CI[0.23,0.71]),而被确定为黑人(OR=0.33,95%CI[0.21,0.51])的参与者明显不太可能符合ST+SL指南。关于健康状况,超重状态,反复/慢性身体疼痛,早产,与满足两个或两个以上24-HMB指南有不利关系。生活在有公园或游乐场的社区和社区安全与符合准则有积极的联系,而生活在有人行道或步行道的社区与符合PAST准则有消极的联系。
    结论:在美国青少年规定的眼镜/隐形眼镜中,满足所有三个24-HMB指南的患病率很低,尤其是女性参与者的低患病率,西班牙裔和黑人参与者,超重状态的参与者,反复/慢性疼痛,早产,生活在有人行道的社区。政策制定者应主动在这一特殊年龄组中推广综合准则,以提高健康福利。
    BACKGROUND: Contemporary 24-h movement behavior (24-HMB) guidelines provide recommendations on time spent on physical activity (PA), screen time (ST), and sleep (SL). There is evidence of physiological and psychological health benefits associated with meeting such guidelines. However, the prevalence of meeting 24-HMB guidelines among youth prescribed eyeglasses/contact lenses is less clear. The primary purpose of this cross-sectional analysis was to examine the prevalence of partially or fully meeting 24-HMB guidelines in U.S. youth prescribed eyeglasses/contact lenses, and variations in meeting the guidelines by demographic, health status, and environmental attributes.
    METHODS: Data from the 2021 National Survey of Children\'s Health (NSCH) yielded a target subpopulation of 8523 youth aged 6-17 years (54.22 % girls) prescribed eyeglasses/contact lenses. The representative sample of US children and adolescents was used to estimate the prevalence of meeting 24-HMB guidelines, and a multinomial logistic regression analysis was conducted to examine the odds of meeting 24-HMB guidelines by demographic, health status, and environmental variables.
    RESULTS: Overall, only 6.57 % met all three 24-HMB guidelines, 23.74 % did not meet any of the three 24-HMB guidelines, and 3.57 %, 10.88 %, and 29.98 % met single guidelines for physical activity, screen time, or sleep duration, respectively, while 25.27 % met any of two 24-HMB guidelines. Female participants were less likely to meet PA + SL guidelines (OR = 0.57, 95 % CI [0.38, 0.56]) but more likely to meet ST + SL guidelines (OR = 1.52, 95 % CI [1.20, 1.91]). Hispanic participants were less likely to meet PA + ST (OR = 0.28, 95 % CI [0.14, 0.52]) guidelines and all three guidelines (OR = 0.41, 95 % CI [0.23, 0.71]) while participants identified as black (OR = 0.33, 95 % CI [0.21, 0.51]) were significantly less likely to meet ST + SL guidelines. With respect to health status, overweight status, repeated/chronic physical pain, and born premature, were detrimentally associated with meeting two or more 24-HMB guidelines. Living in neighborhoods with parks or playgrounds and neighborhood safety were positively linked to meeting the guidelines while living in neighborhoods with sidewalks or walking paths was negatively linked to meeting PA + ST guidelines.
    CONCLUSIONS: In U.S. youth prescribed eyeglasses/contact lenses the prevalence of meeting all three 24-HMB guidelines was low, especially the low prevalence observed in female participants, Hispanic and black participants, participants with overweight status, repeated/chronic pain, born premature, living in neighborhoods with sidewalks. Policy makers should take initiative to promote integrated guidelines among this special age group for health benefits.
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  • 文章类型: Journal Article
    目的:本研究旨在确定临床指南,为儿童矫正屈光不正提供建议,使用重新搜索和评估指南II(AGREEII)工具评估这些指南的总体质量,随后使用改良的Delphi技术就高质量指南的处方建议达成共识。
    方法:使用数据库和专业网站对处方指南进行了全面搜索。通过对六个AGREEII域进行评分来对合格指南进行质量评估。随后,10位专家使用了改良的Delphi技术(副专家验光师,眼科医生和骨科医师)就从被确定为高质量的指南中提取的处方推荐声明达成共识。进行了三轮比赛,其中使用9分Likert量表对这些陈述的一致性进行评分,并提供自由文本选项以进行任何其他评论。
    结果:确定了5个合格的指南。AGREEII工具表明,准则的质量差异很大,只有一个准则被确定为高质量的。在Delphi程序中总共审查了168份处方陈述。其中,95项声明达成专家共识,认为是适当的处方建议。
    结论:目前的儿童屈光不正指南仍有很大的改进余地。我们使用改良的Delphi技术来找到处方建议的共识点,以支持专业人员为儿童处方屈光不正矫正。我们建议需要进一步工作,以解决准则中的差距。
    OBJECTIVE: This study aimed to identify clinical guidelines that provide recommendations on prescribing refractive error correction in children, evaluate the overall quality of these guidelines using the Appraisal of Guidelines for REsearch and Evaluation II (AGREE II) tool and subsequently gain consensus on the prescribing recommendations from high-quality guidelines using the modified Delphi technique.
    METHODS: A comprehensive search for prescribing guidelines was conducted using databases and professional websites. The quality appraisal of eligible guidelines was undertaken by scoring the six AGREE II domains. Subsequently, the modified Delphi technique was used by 10 experts (sub-specialist optometrists, ophthalmologists and orthoptists) to gain consensus on the prescribing recommendation statements extracted from guidelines that had been identified as high quality. Three rounds were conducted in which agreement of these statements were scored using a 9-point Likert scale with a free-text option for any additional comments.
    RESULTS: Five eligible guidelines were identified. The AGREE II tool demonstrated that the guidelines varied substantially in quality, with only one guideline identified as being of high quality. A total of 168 prescribing statements were reviewed in the Delphi procedure. Of these, 95 statements reached expert consensus as being appropriate prescribing recommendations.
    CONCLUSIONS: There is significant scope for improving current guidelines for prescribing refractive error correction in children. We used the modified Delphi technique to find points of agreement on prescribing recommendations to support professionals prescribing refractive error correction in children. We recommend that further work is needed to address gaps in the guidelines.
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  • 文章类型: Journal Article
    背景:视力健康对于生活的许多方面至关重要,尤其是在儿童和青少年等发展中人群中。然而,患有视觉障碍的儿童和青少年比例很高。值得注意的是,越来越多的证据表明,符合24小时运动行为(24-HMB)指南与儿童和青少年积极的身心健康结果相关.然而,处方眼镜/隐形眼镜与符合24-HMB指南之间的关系尚待研究。因此,这项研究旨在通过使用2021年全国儿童健康调查(NSCH)数据集来解决现有文献中的这一差距。
    方法:在这项横断面研究中,数据是从2021年NSCH检索的。总共包括14,193名6至17岁的美国儿童和青少年进行数据分析。我们使用了关于24-HMB指南的NSCH项目(即,身体活动,屏幕时间,和睡眠时间)以及由儿童的法定监护人回答的眼镜/隐形眼镜的处方。进行二元逻辑回归以调查符合24-HMB指南是否与处方眼镜/隐形眼镜相关,以及佩戴眼镜/隐形眼镜是否可以预测儿童和青少年遵守24-HMB指南。
    结果:超过一半的参与者(59.53%)佩戴眼镜/隐形眼镜,只有8.40%的参与者符合所有三项24-HMB指南。与不符合24-HMB指南相比,满足1(OR=0.76,95%CI=0.62-0.93,p=0.008),两个(OR=0.54,95%CI=0.43-0.67,p<0.001),所有3项24-HMB指南(OR=0.47,95%CI=0.34~0.64,p<0.001)均与儿童和青少年使用处方眼镜/隐形眼镜的风险较低相关.
    结论:当前研究的结果提供了证据,表明6至17岁的美国儿童和青少年戴眼镜/隐形眼镜的患病率相对较高。此外,符合24-HMB指南与处方眼镜/隐形眼镜的风险较低相关.未来需要重点研究24-HMB干预措施对儿童和青少年视力健康的影响,以更好地为公共卫生行动提供信息。
    BACKGROUND: Vision health is crucial for many aspects of life especially in developing populations such as children and adolescents. However, there is a high proportion of children and adolescents who suffer from visual impairments. Notably, accumulating evidence indicates that meeting the 24-hour movement behaviors (24-HMB) guidelines is associated with positive physical and mental health outcomes in children and adolescents. However, the relationship between being prescribed eyeglasses/contact lenses and meeting the 24-HMB guidelines has yet to be investigated. Thus, this study aimed to address this gap in the existing literature by using the 2021 National Survey of Children\'s Health (NSCH) dataset.
    METHODS: In this cross-sectional study, data was retrieved from the 2021 NSCH. A total of 14,193 U.S. children and adolescents aged between 6 and 17 years were included for data analyses. We used items of the NSCH concerning the 24-HMB guidelines (i.e., physical activity, screen time, and sleep duration) and prescription of eyeglasses/contact lenses that were answered by the legal guardian of the children. Binary logistic regression was performed to investigate whether meeting the 24-HMB guidelines is associated with prescription eyeglasses/contact lenses and whether wearing eyeglasses/contact lenses predicts adherence to the 24-HMB guidelines among children and adolescents.
    RESULTS: More than half of the participants (59.53%) wore eyeglasses/contact lenses and only 8.40% of them met all three of the 24-HMB guidelines. Compared to meeting none of the 24-HMB guidelines, meeting one (OR = 0.76, 95% CI = 0.62-0.93, p = 0.008), two (OR = 0.54, 95% CI = 0.43-0.67, p < 0.001), and all three 24-HMB guidelines (OR = 0.47, 95% CI = 0.34-0.64, p < 0.001) were associated with a lower risk of being prescribed eyeglasses/contact lenses among children and adolescents.
    CONCLUSIONS: The findings of the current study provided evidence that the prevalence of U.S. children and adolescents aged between 6 and 17 years who wore eyeglasses/contact lenses was relatively high. Furthermore, meeting the 24-HMB guidelines was associated with a lower risk of being prescribed eyeglasses/contact lenses. Future studies focusing on the effects of 24-HMB interventions on vision health among children and adolescents are needed to better inform public health actions.
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  • 文章类型: Journal Article
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  • 文章类型: Journal Article
    The American Heart Association (AHA) guidelines for cardiopulmonary resuscitation (CPR) are nowadays recognized as the world\'s most authoritative resuscitation guidelines. Adherence to these guidelines optimizes the management of critically ill patients and increases their chances of survival after cardiac arrest. Despite their availability, suboptimal quality of CPR is still common. Currently, the median hospital survival rate after pediatric in-hospital cardiac arrest is 36%, whereas it falls below 10% for out-of-hospital cardiac arrest. Among emerging information technologies and devices able to support caregivers during resuscitation and increase adherence to AHA guidelines, augmented reality (AR) glasses have not yet been assessed. In order to assess their potential, we adapted AHA Pediatric Advanced Life Support (PALS) guidelines for AR glasses.
    The study aimed to determine whether adapting AHA guidelines for AR glasses increased adherence by reducing deviation and time to initiation of critical life-saving maneuvers during pediatric CPR when compared with the use of PALS pocket reference cards.
    We conducted a randomized controlled trial with two parallel groups of voluntary pediatric residents, comparing AR glasses to PALS pocket reference cards during a simulation-based pediatric cardiac arrest scenario-pulseless ventricular tachycardia (pVT). The primary outcome was the elapsed time in seconds in each allocation group, from onset of pVT to the first defibrillation attempt. Secondary outcomes were time elapsed to (1) initiation of chest compression, (2) subsequent defibrillation attempts, and (3) administration of drugs, as well as the time intervals between defibrillation attempts and drug doses, shock doses, and number of shocks. All these outcomes were assessed for deviation from AHA guidelines.
    Twenty residents were randomized into 2 groups. Time to first defibrillation attempt (mean: 146 s) and adherence to AHA guidelines in terms of time to other critical resuscitation endpoints and drug dose delivery were not improved using AR glasses. However, errors and deviations were significantly reduced in terms of defibrillation doses when compared with the use of the PALS pocket reference cards. In a total of 40 defibrillation attempts, residents not wearing AR glasses used wrong doses in 65% (26/40) of cases, including 21 shock overdoses >100 J, for a cumulative defibrillation dose of 18.7 Joules per kg. These errors were reduced by 53% (21/40, P<.001) and cumulative defibrillation dose by 37% (5.14/14, P=.001) with AR glasses.
    AR glasses did not decrease time to first defibrillation attempt and other critical resuscitation endpoints when compared with PALS pocket cards. However, they improved adherence and performance among residents in terms of administering the defibrillation doses set by AHA.
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  • 文章类型: Journal Article
    The mucopolysaccharidoses (MPS) are a group of rare lysosomal storage disorders characterized by the accumulation of glycosaminoglycans in several tissues and organs. This accumulation results in an array of clinical manifestations and premature death in severe cases. Ocular problems are very common in children with MPS and may involve the cornea, sclera, trabecular meshwork, retina, optic nerve and also the posterior visual pathways. The aims of this study are to give an overview of ocular problems in MPS and to provide clinical guidelines for paediatric ophthalmologists for early diagnosis and management of ocular manifestations in children with MPS. Diagnostic problems may arise in children with severe corneal clouding, hampering visualization of the fundus. Intraocular pressures may be falsely high, even leading to suspicion and unnecessary pressure-lowering treatment. Simple interventions such as the use of prescription glasses or photochromatic glasses can considerably improve quality of life in children with MPS.
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  • 文章类型: Journal Article
    This paper discusses the considerations for prescribing a refractive correction in infants and children up to and including school age, with reference to the current literature. The focus is on children who do not have other disorders, for example, binocular vision anomalies, such as strabismus, significant heterophoria or convergence excess. However, refractive amblyogenic factors are discussed, as is prescribing for refractive amblyopia. Based on this discussion, guidelines are proposed, which indicate when to prescribe spectacles and what amount of refractive error should be corrected. It may be argued that these are premature because there are many questions that remain unanswered and we do not have the quality of evidence that we would like; the clinician, however, must make decisions on whether and what to prescribe when examining a child. These guidelines are to aid clinicians in their current clinical decision making.
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    文章类型: Journal Article
    This document affirms the Department of Veterans Affairs (VA) medical regulations concerning when VA will furnish veterans with sensori-neural aids (e.g., eyeglasses, contact lenses, hearing aids), which implement a requirement imposed in the Veteran\'s Health Care Eligibility Reform Act of 1996, Public Law 104-262.
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