Infants With Idiopathic T Cell Lymphopenia Identified On New York State Newborn Screen: A Follow Up Report

2014 ◽  
Vol 133 (2) ◽  
pp. AB93 ◽  
Author(s):  
Stephanie Albin ◽  
Harshna Mehta ◽  
Charlotte Cunningham-Rundles
Blood ◽  
2018 ◽  
Vol 132 (Supplement 1) ◽  
pp. 1642-1642
Author(s):  
Urvi A Shah ◽  
Nishi Shah ◽  
Baozhen Qiao ◽  
Ana Acuna Villaorduna ◽  
Aditi Shastri ◽  
...  

Abstract Introduction Adult T-cell leukemia/lymphoma (ATLL) is a rare, aggressive T cell neoplasm associated with a retrovirus human T cell lymphotropic virus (HTLV-1) and carries a dismal prognosis. Within the United States, New York, and Florida see the majority of cases due to the concentration of Caribbean immigrants (Zell, Assal et al. 2016, Malpica, Pimentel et al. 2018). SEER data does not include states like New York and Florida where most cases are seen and therefore a true estimate of the disease burden in this country is not known (Chihara, Ito et al. 2012, Adams, Newcomb et al. 2016). Aim We aim to study the epidemiology and clinical outcomes of ATLL in the United States particularly in the state of New York. Methods Data for New York was obtained from the New York State Cancer Registry (NYSCR). Data were also retrieved from 18 Surveillance, Epidemiology, and End Results (SEER) registries in the United States. Patients with ATLL (HTLV-1 positive) (includes all variants) were categorized using the International Classification of Diseases for Oncology, Third Edition codes ICD-O-3 as 9827/3. Race/ethnicity was categorized as non-Hispanic white, non-Hispanic black, all Hispanic and other/unknown in the NYSCR whereas it was categorized as non-Hispanic white, non-Hispanic black, all Hispanic, non-Hispanic American Indian/Alaska Native, non-Hispanic Asian or Pacific Islander, and non-Hispanic unknown race in SEER. ATLL patients ≥ 15 years of age were identified from 1995 to 2014 in SEER and all ages were included in NYSCR. Survival was estimated from SEER follow-up data with Kaplan Meier survival analysis. For NYSCR mean and median survival time (month) for deceased patients - cases diagnosed through death certificate only were removed. NYSCR does not conduct active patient follow-up and assumes patients are still alive if we didn't find a deathmatch through vital record or National Death Index linkages. Results Five hundred and eleven patients with ATLL were identified in SEER. These patients had a median survival of 8 months (m) which was worse than all other subtypes of peripheral T cell lymphoma. (Figure 1) Four hundred and twenty-nine patients with ATLL were identified in NYSCR and these patients had a median survival of 4.5 m. (Figure 2) Over the years from 2000 until 2014 the number of cases diagnosed within SEER registry coverage areas has not changed. In New York state however there has been a doubling in the number of cases diagnosed from 1995 to 2014. (Figure 3A, B) The non-Hispanic black population was diagnosed at a median age of 52.5 in SEER and 54 in NYSCR while the non-Hispanic whites were diagnosed at a median age of 71 in SEER and 64.5 in NYSCR. The Hispanic patients were diagnosed at a median age of 58.5 in NYSCR and 52.5 in SEER. (Figure 4A, B) There was no gender predominance with 50% males in both registries. ATLL patients in SEER were 47.2% non-Hispanic white, 31.7% non-Hispanic black, 9.8% Hispanic and 11.4% other/unknown. There were 5.5% Japanese patients (n=28) diagnosed in SEER. NYSCR had 22.4% non-Hispanic white, 59.4% non-Hispanic black, 15.9% Hispanic and 2.3% other/unknown. (Figure 5A, B) Within SEER registries most cases occurred in New Jersey, California, Connecticut and Georgia. (Figure 6) New York state had a significantly higher number of cases than these states. Seventy four percent cases diagnosed within New York state are diagnosed in New York city and only 26% of cases are diagnosed in upstate New York. Based on reported country of birth within New York state, only 27% of the ATLL cases diagnosed are born in the US whereas 49% are born in the Caribbean (most likely to be from Jamaica, Dominican Republic and Haiti). (Figure 7A, B, C) For SEER and NYSCR the age-adjusted cancer incidence rate by race year and other factors will be presented at the meeting. Conclusions ATLL has a worse prognosis than all other PTCL subtypes. New York State has a high endemicity for ATLL with a rising number of cases. The higher percentage of non-Hispanic black patients in New York compared to the rest of the country is consistent with the diverse racial demographics in this state. Survival varied significantly by race/ethnicity and disparities were evident especially for non-Hispanic blacks who were diagnosed at a younger median age and had a shorter survival. Further research into this aggressive disease is needed to improve outcomes for these patients. Disclosures No relevant conflicts of interest to declare.


2017 ◽  
Vol 183 ◽  
pp. 36-40 ◽  
Author(s):  
Stephanie Albin-Leeds ◽  
Juliana Ochoa ◽  
Harshna Mehta ◽  
Beth H. Vogel ◽  
Michele Caggana ◽  
...  

PEDIATRICS ◽  
1956 ◽  
Vol 18 (3) ◽  
pp. 506-508

APPEARANCE of "new diseases" is a phenomenon well known to observing pediatricians. When a new disease is first reported, there is often some doubt as to whether it is a separate entity, then a certain amount of hesitation while the definition and characteristics of the disease are being investigated, and finally a rush of increased diagnoses as the disease becomes more "popular" or is better understood. Very often therapy awaits elucidation of etiology, and, of course, therapy is not always successful. The problem of retrolental fibroplasia has constituted an interesting case in point which, while it has not followed all of the characteristics noted above, has certainly approached them. A recently published analysis of "The Rise and Fall of Retrolental Fibroplasia in New York State—A Preliminary Report" by Yankauer, Jacobziner, and Schneider (New York State J. Med., 56:1474, May 1, 1956), reviews in striking fashion the progress of the disease. In contrast to many reports of disease incidence, the paper from New York State is a model of care and precision. The authors point out that diagnosis and follow-up of this condition in New York State are encouraged by state laws regarding the care of the blind, as well as by the special programs for premature infants, which have been promoted by both the city and the state health departments. Furthermore, the reports on the disease have been carefully investigated and the fact of "popularity" mitigated by studying both the time at which the disease is reported in relation to the age of the child, and the evidence for confirmation of the diagnosis.


2020 ◽  
Vol 35 (3) ◽  
pp. 684-693 ◽  
Author(s):  
S L Robinson ◽  
T Parikh ◽  
T Lin ◽  
E M Bell ◽  
E Heisler ◽  
...  

Abstract STUDY QUESTION Are toddlers conceived by fertility treatment at higher risk of failing a screening tool for autism spectrum disorders (ASD) than toddlers not conceived by treatment? SUMMARY ANSWER Compared with children not conceived by infertility treatment, children conceived by any infertility treatment, ovulation induction with or without intrauterine insemination (OI/IUI), or assisted reproductive technologies (ART) appeared to have had higher odds of failing an ASD screening; however, results were inconclusive and need replication. WHAT IS KNOWN ALREADY Although most of the studies which have examined risk of ASD after ART show no association, the results are mixed. Thus, further studies are needed to clarify this association. STUDY DESIGN SIZE, DURATION The Upstate KIDS Study is a population-based, prospective cohort study of children born in New York State between 2008 and 2010. Children were screened for ASD using the Modified Checklist for Autism in Toddlers (M-CHAT) at ages 18 and 24 months. PARTICIPANTS/MATERIALS, SETTING, AND METHODS The New York State live-birth registry was used to identify newborns conceived with and without fertility treatment with a 1:3 ratio, frequency matched on region of birth. At 18 and 24 months, 3183 and 3063 mothers, respectively, completed the M-CHAT questionnaire. The current analysis included 2586 singletons and 1296 twins with M-CHAT information at 18 and/or 24 months. Multivariable logistic regression with generalized estimating equations (GEE) was used to estimate odds ratios (aOR) and 95% confidence intervals (CI) after adjustment for covariates such as maternal age, education and plurality. MAIN RESULTS AND THE ROLE OF CHANCE We found that 200 (5.2%) and 115 (3.0%) children failed the M-CHAT at 18 and 24 months, respectively. The associations between use of infertility treatment and failing the M-CHAT at 18 and/or 24 months were positive but inconclusive as they failed to exclude no association (18 months aOR 1.71, 95% CI: 0.81–3.61; 24 months aOR 1.78, 95% CI: 0.66–4.81; and both 18 and 24 months aOR 1.53, 95% CI: 0.78–2.99). The relationships between OI/IUI and ART with M-CHAT failure at 18 and/or 24 months were similar to those of using any fertility treatment. In vitro fertilization with intracytoplasmic sperm injection was not consistently positively or inversely associated with M-CHAT failure at each time point (18 months aOR 1.20, 95% CI: 0.51–2.83; 24 months aOR 0.93, 95% CI: 0.37–2.31; and both 18 and 24 months aOR 1.09, 95% CI: 0.50–2.60). LIMITATIONS REASONS FOR CAUTION The M-CHAT is a screening tool used for ASD risk assessment, and therefore, M-CHAT failure does not indicate ASD diagnosis. In addition, we did not have power to detect associations of small magnitude. Finally, non-response to follow-up may bias the results. WIDER IMPLICATIONS OF THE FINDINGS Despite lack of precision, the positive associations between ART and M-CHAT failure suggest that larger population-based studies with longer follow-up are needed. STUDY FUNDING/COMPETING INTEREST(S) Supported by the Intramural Research Program of the Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD; contracts HHSN275201200005C, HHSN267200700019C). The sponsor played no role in the study design, data collection, data analysis or interpretation, writing of the manuscript or decision to submit the article for publication. There are no conflicts of interest to declare. TRIAL REGISTRATION NUMBER Not applicable.


2020 ◽  
Vol 6 (3) ◽  
pp. 52 ◽  
Author(s):  
Vijaya Knight ◽  
Jennifer R. Heimall ◽  
Nicola Wright ◽  
Cullen M. Dutmer ◽  
Thomas G. Boyce ◽  
...  

Severe combined immunodeficiency (SCID) includes a group of monogenic disorders presenting with severe T cell lymphopenia (TCL) and high mortality, if untreated. The newborn screen (NBS) for SCID, included in the recommended universal screening panel (RUSP), has been widely adopted across the US and in many other countries. However, there is a lack of consensus regarding follow-up testing to confirm an abnormal result. The Clinical Immunology Society (CIS) membership was surveyed for confirmatory testing practices for an abnormal NBS SCID result, which included consideration of gestational age and birth weight, as well as flow cytometry panels. Considerable variability was observed in follow-up practices for an abnormal NBS SCID with 49% confirming by flow cytometry, 39% repeating TREC analysis, and the remainder either taking prematurity into consideration for subsequent testing or proceeding directly to genetic analysis. More than 50% of respondents did not take prematurity into consideration when determining follow-up. Confirmation of abnormal NBS SCID in premature infants continues to be challenging and is handled variably across centers, with some choosing to repeat NBS SCID testing until normal or until the infant reaches an adjusted gestational age of 37 weeks. A substantial proportion of respondents included naïve and memory T cell analysis with T, B, and NK lymphocyte subset quantitation in the initial confirmatory panel. These results have the potential to influence the diagnosis and management of an infant with TCL as illustrated by the clinical cases presented herein. Our data indicate that there is clearly a strong need for harmonization of follow-up testing for an abnormal NBS SCID result.


Buildings ◽  
2021 ◽  
Vol 11 (12) ◽  
pp. 631
Author(s):  
Elizabeth L. Hewitt ◽  
Jean Léon Boucher

This research explores socio-spatial characteristics of home retrofit projects in New York State and their association with the state’s free home energy audit program. Prior work by the authors found that zip codes with more elder individuals and higher levels of education are more likely to undertake an energy audit; it was also found that higher incomes may be negatively correlated with audit decisions. Less understood is the follow-up decision after an audit to undertake a retrofit. From a policy and climate perspective, the actionable retrofit decision is far more impactful than the informational audit, making it an important area of further research. This work examines this understudied area using a combination of datasets, including census data, American Community Survey (ACS) data, and retrofits data provided by the New York State Energy Research and Development Authority (NYSERDA). Findings indicate that many of the same socioeconomic characteristics that predict audits are influential in retrofit projects as well (age, education, higher home values). A strong statistical relationship was found between audits per capita and subsequent retrofit projects, which is to be expected, as NYSERDA requires audits of residents desiring efficiency retrofits. However, this also indicates that the role of the audit in information transfers may be highly influential in encouraging home energy efficiency projects. This finding underscores the policy importance of offering low- or no-cost energy audit incentives to encourage greater participation in home retrofit programs.


2002 ◽  
Vol 42 (1) ◽  
pp. 41-47 ◽  
Author(s):  
Elisa V. Bandera ◽  
Jo L. Freudenheim ◽  
James R. Marshall ◽  
Roger L. Priore ◽  
John Brasure ◽  
...  

2015 ◽  
Vol 3 (7_suppl2) ◽  
pp. 2325967115S0012 ◽  
Author(s):  
Moira McCarthy ◽  
Emily Dodwell ◽  
Ting Pan ◽  
Daniel W. Green

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