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1.
Adv Nutr ; 15(3): 100183, 2024 03.
Article in English | MEDLINE | ID: mdl-38309530

ABSTRACT

Supporting optimal newborn nutrition and the positive maternal-infant relationship while encouraging safe sleep practices are essential components of maternal and newborn care in the hospital setting following birth. Breastfeeding is widely recognized as the best practice to support the nutritional needs and well-being of the infant, and recommendations have been developed by the WHO, the American Academy of Pediatrics (AAP), and the United States Centers for Disease Control to encourage and successfully support breastfeeding efforts before hospital discharge. The 10 Steps to Successful Breastfeeding, developed and promoted by the WHO, form the basis of the Baby-Friendly Hospital Initiative (BFHI) and have become the international framework for public health initiatives to promote breastfeeding. An evaluation of hospital performance implementing the 10 steps through the process of "Baby-Friendly Designation" (BFD) has been suggested by many breastfeeding advocates as the optimal pathway to attain the goals of the BFHI. However, the WHO has recognized that BFD may not be an appropriate goal in all settings, and indicated, as part of their updated 2018 guidance, that "facilities may make changes in their policies and procedures to obtain the designation, but these changes are not always sustainable, especially when there are no regular monitoring systems in place." In addition, unintended associated issues regarding newborn safety and maternal dissatisfaction with some of the 10 steps have emerged. This perspective discusses the challenges faced by hospitals attempting to implement the BFHI 10 steps and suggests potential solutions to make progress in those efforts with or without BFD and also the efforts needed to support formula feedings when appropriate.


Subject(s)
Breast Feeding , Health Promotion , Infant , Infant, Newborn , Female , Humans , Child , United States , Health Promotion/methods , Hospitals , Postpartum Period , Public Health
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5.
J Pediatr ; 219: 281-283.e1, 2020 04.
Article in English | MEDLINE | ID: mdl-32008766
6.
J Pediatr ; 218: 16-21.e1, 2020 03.
Article in English | MEDLINE | ID: mdl-31623856

ABSTRACT

OBJECTIVES: To compare the impact of Baby-Friendly designation vs rates of in-hospital breastfeeding initiation on breastfeeding outcomes at 3, 6, and 12 months postdischarge. STUDY DESIGN: Breastfeeding outcome data from the 2018 Centers for Disease Control (CDC) Breastfeeding Report Card were used as a basis for determining outcomes from the corresponding 2015 birth cohort. Linear regression models were used to determine the strength of association of breastfeeding initiation and Baby-Friendly hospital penetrance and attainment of postdischarge breastfeeding rates. All hospital births from all 50 states, 3 territories, and the District of Columbia were included in the study. RESULTS: Statewide breastfeeding initiation rates were positively associated with targeted breastfeeding outcomes. Similar associations were not found for Baby-Friendly hospital designation penetrance. CONCLUSIONS: To attain the Healthy People 2020 breastfeeding objectives, future public policy initiatives should consider the interaction of population demographics, individual hospital programs, and public health strategies used to support breastfeeding in states reporting high breastfeeding initiation rates.


Subject(s)
Breast Feeding/statistics & numerical data , Centers for Disease Control and Prevention, U.S./statistics & numerical data , Health Promotion , Hospital Records/statistics & numerical data , Public Policy , Humans , Infant , Retrospective Studies , United States
7.
JAMA Pediatr ; 173(5): 496-497, 2019 05 01.
Article in English | MEDLINE | ID: mdl-30855660
9.
J Pediatr ; 200: 297-298, 2018 09.
Article in English | MEDLINE | ID: mdl-29961645

Subject(s)
Asphyxia , Humans , Skin Care
10.
J Pediatr ; 200: 299, 2018 09.
Article in English | MEDLINE | ID: mdl-29887388
11.
J Pediatr ; 196: 104-108, 2018 05.
Article in English | MEDLINE | ID: mdl-29452740

ABSTRACT

OBJECTIVE: To evaluate the epidemiology of sudden unexpected infant death (SUID) over a 20-year period in the US, to assess the potential frequency of sudden unexpected postnatal collapse in the early days of life, and to determine if SUID rates in the neonatal period (0-27 days) have changed in parallel with rates in the postneonatal periods, including the percentages attributed to codes that include accidental suffocation. STUDY DESIGN: Data from the US Centers for Disease Control and Prevention Linked Birth/Infant Death Records for 1995-2014 were analyzed for the first hour, day, week, and month of life. A comparison of neonatal and postneonatal data related to SUID, including accidental suffocation, was carried out. RESULTS: Death records for 1995-2014 indicate that, although SUID rates in the postneonatal period have declined subsequent to the 1992 American Academy of Pediatrics sleep position policy change, newborn SUIDs have failed to decrease, and the percentage of SUIDs attributed to unsafe sleep conditions has increased significantly in both periods; 29.2% of the neonatal cases occurred within the first 6 days of life. CONCLUSIONS: The frequency of SUIDs during the neonatal period warrants ongoing attention to all circumstances contributing to this category of deaths. The development of a standardized definition of sudden unexpected postnatal collapse and a national registry of these events is recommended. Ongoing research on the effects of early neonatal practices on postneonatal SUID should also be encouraged.


Subject(s)
Asphyxia/complications , Infant Mortality/trends , Sudden Infant Death/etiology , Cause of Death , Death Certificates , Female , Humans , Incidence , Infant , Infant, Newborn , Male , Parents , Patient Education as Topic , Registries , Regression Analysis , Risk Factors , Sleep , Time Factors , United States
17.
Eur Urol ; 67(2): 334-41, 2015 Feb.
Article in English | MEDLINE | ID: mdl-24968970

ABSTRACT

BACKGROUND: A need remains for new therapeutic approaches for men with advanced prostate cancer, particularly earlier in the disease course. OBJECTIVE: To assess the ability of an oral selective estrogen receptor α agonist (GTx-758) to lower testosterone concentrations compared with leuprolide while minimizing estrogen deficiency-related side effects of androgen-deprivation therapy. DESIGN, SETTING, AND PARTICIPANTS: Hormone-naive advanced prostate cancer patients were randomized to oral GTx-758 1000 mg/d, 2000 mg/d, or leuprolide depot. INTERVENTION: GTx-758 and leuprolide. OUTCOME MEASUREMENTS AND STATISTICAL ANALYSIS: The primary end point was the proportion of patients achieving total testosterone ≤ 50 ng/dl by day 60. Secondary end points included serum free testosterone, prostate-specific antigen (PSA), sex hormone-binding globulin, hot flashes, bone turnover markers, and insulin-like growth factor (IGF)-1 levels. RESULTS AND LIMITATIONS: Of 159 randomized patients, leuprolide reduced total testosterone to ≤ 50 ng/dl in a greater proportion of patients than GTx-758 by day 60 (43.4%, 63.6%, and 88.2% of subjects receiving GTx-758 1000 mg [p<0.001], GTx-758 2000 mg [p=0.004], and leuprolide, respectively). GTx-758 reduced free testosterone and PSA earlier and to a greater degree than leuprolide. GTx-758 led to fewer hot flashes, decreases in bone turnover markers, and alterations in IGF-1 compared with leuprolide. A higher incidence of venous thromboembolic events (VTEs) was seen with GTx-758 (4.1%) compared with leuprolide (0.0%). CONCLUSIONS: Although leuprolide reduced total testosterone to ≤ 50 ng/dl in a greater proportion of patients compared with GTx-758, GTx-758 was superior in lowering free testosterone and PSA. GTx-758 reduced estrogen deficiency side effects of hot flashes, bone loss, and insulin resistance but with a higher incidence of VTEs. PATIENT SUMMARY: This paper reports findings that leuprolide lowered total testosterone more than GTx-758 but that GTx-758 lowered free testosterone and prostate-specific antigen more than leuprolide. GTx-758 also reduced estrogen deficiency side effects, albeit at a higher rate of vascular events. TRIAL REGISTRATION: Clinicaltrials.gov identifier NCT01615120.


Subject(s)
Antineoplastic Agents, Hormonal/therapeutic use , Benzamides/therapeutic use , Biomarkers, Tumor/blood , Leuprolide/therapeutic use , Neoplasms, Hormone-Dependent/drug therapy , Prostatic Neoplasms/drug therapy , Selective Estrogen Receptor Modulators/therapeutic use , Testosterone/blood , Administration, Oral , Aged , Aged, 80 and over , Antineoplastic Agents, Hormonal/administration & dosage , Antineoplastic Agents, Hormonal/adverse effects , Benzamides/administration & dosage , Benzamides/adverse effects , Delayed-Action Preparations , Down-Regulation , Humans , Leuprolide/administration & dosage , Leuprolide/adverse effects , Male , Middle Aged , Neoplasms, Hormone-Dependent/blood , Neoplasms, Hormone-Dependent/pathology , Prospective Studies , Prostatic Neoplasms/blood , Prostatic Neoplasms/pathology , Selective Estrogen Receptor Modulators/administration & dosage , Selective Estrogen Receptor Modulators/adverse effects , Treatment Outcome , United States
18.
Am J Perinatol ; 31(8): 677-82, 2014 Sep.
Article in English | MEDLINE | ID: mdl-24057424

ABSTRACT

OBJECTIVE: This study was designed to describe our experience in implementing the American Academy of Pediatrics (AAP) recommendation to test infants in a car bed if they fail a car seat challenge test. STUDY DESIGN: Car seat challenge testing was performed for 90 minutes or the anticipated duration of the trip home, whichever was longer. Based on the pulse oximetry saturation values (90-92% or < 90%) two categories of test failure were used. Infants who failed in the car seat were tested in the car bed. Testing took place in both the normal newborn nursery (NBN) and special care nursery (SCN). NBN babies who failed in the car bed were transferred to our SCN for additional assessment and management. RESULTS: A total of 197 infants were tested in car seats out of which 177 (89.8%) passed the test. Of the 20 infants who failed, 16 passed the car bed challenge test on the first attempt and were discharged in those devices. All infants who failed the car bed challenge were NBN patients. CONCLUSIONS: Using 93% as the acceptable lower limit of oxygenation we successfully implemented the AAP recommendations for car bed challenge testing in our nursery.


Subject(s)
Apnea/prevention & control , Bradycardia/prevention & control , Child Restraint Systems , Hospitals, Community , Practice Guidelines as Topic , Respiratory Insufficiency/prevention & control , Beds , Humans , Infant, Newborn , Infant, Premature , Oximetry , Patient Discharge , Patient Positioning , Pediatrics , Societies, Medical
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