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1.
World J Surg ; 45(11): 3306-3312, 2021 11.
Article in English | MEDLINE | ID: mdl-34351487

ABSTRACT

PURPOSE: To mitigate intraoperative adverse events, it is important to understand the context in which these errors occur. The purpose of this study is to characterize the IAEs and potential distractions that occur in minimally invasive urologic procedures. METHODS: We conducted a prospective cohort study in patients undergoing laparoscopic urologic surgery at an academic health center. The OR Black Box, a unique technology system which captures video and audio recordings of the operating room as well as the operative field, was used to collect data regarding procedure type, critical step, IAEs, and distractions. RESULTS: Of a total of 80 cases analyzed, the majority of these cases were partial nephrectomy (n = 36; 45%), radical nephrectomy (n = 20; 25%), and adrenalectomy (n = 4; 5%). Across all cases, there were a total of 138 clinically significant IAEs, 10 of which (14%) were of the highest severity (five on the SEVerity of intraoperative Events and Rectification Tool (SEVERE) matrix). Of these, 70 (51%) occurred during an a priori defined critical step of the operation. Distractions were common across all cases. The median rate of external communication per case was 16 events (IQR 11-22); and per critical step was 4 (IQR 2.75-8), while median room traffic per case was 65 entries/exits (IQR 42-76); and per critical step was 17 (IQR 10-65). CONCLUSION: Our data demonstrate that IAEs occur frequently during all phases of the operation at hand. Future study will be required to examine the role of distractions and IAE as well as IAE and their relationship to post-operative clinical outcomes.


Subject(s)
Laparoscopy , Operating Rooms , Humans , Intraoperative Complications , Patient Safety , Prospective Studies
2.
Eur J Intern Med ; 73: 67-71, 2020 03.
Article in English | MEDLINE | ID: mdl-31836177

ABSTRACT

Point-of-care ultrasound (POCUS) is increasingly used to assess medical patients. It has many uses in daily clinical practice, including improved diagnostic timeliness and accuracy, and providing information about a patient's prognosis and follow-up. It has been integrated into numerous specialities, but remains relatively undefined in internal medicine training programs. Ultrasonography is a useful tool in the standard clinical practice of internists in numerous clinical scenarios (Emergency Department, hospital ward, general and specific consultations, and home care). Although POCUS has been recently included in the European curriculum of internal medicine, there are differences between European internists in its use, ranging from not at all to well structured educational programs. The use of POCUS needs to be widespread in internal medicine departments, and to accomplish this we must encourage structured training. This document details the consensus-based recommendations by the European Federation of Internal Medicine (EFIM) Ultrasound working group. We establish POCUS core competencies and clinical settings for internists in a symptom-based approach. We also propose training requirements, providing a framework for training programs at a national level.


Subject(s)
Internal Medicine , Point-of-Care Systems , Curriculum , Humans , Internal Medicine/education , Point-of-Care Testing , Ultrasonography
3.
Dyslexia ; 21(3): 197-211, 2015 Aug.
Article in English | MEDLINE | ID: mdl-25428888

ABSTRACT

This longitudinal study compares developmental changes in psychosocial functioning during the transition into school of children with and without dyslexia. In addition, it examines the effects of gender and family risk for dyslexia in terms of the associations between dyslexia and psychosocial functioning. Children's psychosocial functioning (social skills, inattention and externalizing and internalizing problems) was evaluated by their parents at ages 4, 6 and 9, and diagnosis for dyslexia was made at age 8 (in grade 2). The findings indicated that children with dyslexia were already rated as having poorer social skills and being more inattentive than were typical readers before their entry into school. Significant interactions of gender and diagnosis of dyslexia emerged for social skills and inattention. The social skills of boys with dyslexia improved after school entry as compared to the level of girls without dyslexia, whereas the social skills of girls with dyslexia did not improve. Boys with dyslexia were rated as showing a high level of inattention both prior to and after school entry, whereas, for girls with dyslexia, inattention ratings increased after school entry, eventually matching the boys' levels.


Subject(s)
Attention/physiology , Child Behavior/psychology , Dyslexia/physiopathology , Social Skills , Child , Child, Preschool , Female , Finland , Follow-Up Studies , Humans , Longitudinal Studies , Male , Schools , Sex Factors
4.
Occup Environ Med ; 65(4): 242-8, 2008 Apr.
Article in English | MEDLINE | ID: mdl-17933885

ABSTRACT

OBJECTIVES: To determine whether, from a healthcare perspective, a specific occupational health intervention is cost effective in reducing sickness absence when compared with usual care in occupational health in workers with high risk of sickness absence. METHODS: Economic evaluation alongside a randomised controlled trial. 418 workers with high risk of sickness absence from one corporation were randomised to intervention (n = 209) or to usual care (n = 209). The subjects in the intervention group were invited to occupational health service for a consultation. The intervention included, if appropriate, a referral to specialist treatment. Register data of sickness absence were available for 384 subjects and questionnaire data on healthcare costs from 272 subjects. Missing direct total cost data were imputed using a two-part regression model. Primary outcome measures were sickness absence days and direct healthcare costs up to 12 months after randomisation. Cost effectiveness (CE) was expressed as an incremental CE ratio, CE plane and CE acceptability curve with both available direct total cost data and missing total cost data imputed. RESULTS: After one year, the mean of sickness absence was 30 days in the usual care group (n = 192) and 11 days less (95% CI 1 to 20 days) in the intervention group (n = 192). Among the employees with available cost data, the mean days of sickness absence were 22 and 24, and the mean total cost euro974 and euro1049 in the intervention group (n = 134) and in the usual care group (n = 138), respectively. The intervention turned out to be dominant-both cost saving and more effective than usual occupational health care. The saving was euro43 per sickness absence day avoided with available direct total cost data, and euro17 with missing total cost data imputed. CONCLUSIONS: One year follow-up data show that occupational health intervention for workers with high risk of sickness absence is a cost effective use of healthcare resources.


Subject(s)
Absenteeism , Occupational Health Services/economics , Occupational Health/statistics & numerical data , Sick Leave/economics , Adolescent , Adult , Cost-Benefit Analysis , Female , Finland , Health Care Costs/statistics & numerical data , Health Resources/statistics & numerical data , Humans , Male , Middle Aged , Occupational Health Services/methods , Outcome and Process Assessment, Health Care/methods , Risk Assessment , Sick Leave/statistics & numerical data
5.
Occup Environ Med ; 65(4): 236-41, 2008 Apr.
Article in English | MEDLINE | ID: mdl-17681994

ABSTRACT

OBJECTIVES: To evaluate the effectiveness of two occupational health intervention programmes, both compared with usual care. METHODS: Based on a health survey, 1341 employees (88% males) in construction, service and maintenance work were classified into three groups: "low risk" (n = 386), "intermediate risk" (n = 537) and "high risk" (n = 418) of sickness absence. Two separate randomised trials were performed in the groups "high risk" and "intermediate risk", respectively. Those high risk subjects that were allocated to the intervention group (n = 209) were invited to occupational health service for a consultation. The intervention included, if appropriate, a referral to specialist treatment. Among the intermediate risk employees those in the intervention group (n = 268) were invited to call a phone advice centre. In both trials the control group received usual occupational health care. The primary outcome was sickness absence during a 12-month follow-up (register data). RESULTS: The high risk group, representing 31% of the cohort, accounted for 62% of sickness absence days. In the trial for the high risk group the mean sickness absence was 30 days in the usual care group and 19 days in the intervention group; the mean difference was 11 days (95% CI 1 to 20 days). In the trial for the intermediate risk group the mean sickness absence was 7 days in both arms (95% CI of the mean difference -2.3 to 2.4 days). CONCLUSIONS: The identification of high risk of work disability was successful. The occupational health intervention was effective in controlling work loss to a degree that is likely to be economically advantageous within the high risk group. The phone advice intervention for the intermediate risk group was not effective in controlling work loss primarily due to poor adherence.


Subject(s)
Absenteeism , Occupational Health Services/methods , Occupational Health/statistics & numerical data , Sick Leave/statistics & numerical data , Adolescent , Adult , Counseling , Epidemiologic Methods , Female , Finland , Humans , Male , Middle Aged , Outcome and Process Assessment, Health Care/methods , Patient Compliance , Referral and Consultation
6.
Percept Mot Skills ; 92(2): 479-94, 2001 Apr.
Article in English | MEDLINE | ID: mdl-11361312

ABSTRACT

Practice effects on a visuomotor test (the Developmental Test of Visuo-Motor Integration), a timed visual discrimination test (the Underlining Test), and two problem-solving tests (the Porteus Mazes Test and the Tower of Hanoi Test) were analyzed. Children of two age groups (Ms: 7.7 and 11.6 yr.) were chosen to study the effect of age on practice effects. The tests were repeated nine times with test-retest intervals of 2 mo. The Developmental Test of Visuo-Motor Integration showed no practice effects, while the Porteus Mazes Test, the Underlining Test, and the Tower of Hanoi Test showed significant practice effects. Practice effects were larger for the older age group on all the tests, except the Developmental Test of Visuo-Motor Integration. The Developmental Test of Visuo-Motor Integration and the Underlining Test showed good reliability, but those of the problem-solving tasks were less satisfactory. The stability of all the tests, except the Tower of Hanoi Test, was good.


Subject(s)
Motor Skills/physiology , Problem Solving , Visual Perception/physiology , Child , Female , Humans , Male
7.
Child Neuropsychol ; 7(4): 241-50, 2001 Dec.
Article in English | MEDLINE | ID: mdl-16210213

ABSTRACT

The present study describes the incidence of test refusal at neuropsychological assessment, investigates its correlates, and its stability. The participants were 124 children aged 3.5 years whose development has been followed from birth in the Jyväskylä Longitudinal Study of Dyslexia (JLD). The frequency of test refusal on the Finnish version of the NEPSY was analyzed with respect to the children's concurrent and earlier cognitive and language skills, assessed using tests and parental ratings. Refusal during test-taking was found to be relatively common at this age, and high frequency of refusal at an earlier age was associated with similar tendency at a later age. High test refusal was associated with compromised neuropsychological and linguistic test scores. Missing data due to refusal were more common in neuropsychological tasks requiring verbal production. It is concluded that test refusals reflect a child's poor underlying skills and an attempt to avoid failure, rather than noncompliant or oppositional behavior.


Subject(s)
Dyslexia/diagnosis , Neuropsychological Tests/statistics & numerical data , Refusal to Participate/statistics & numerical data , Child, Preschool , Cross-Sectional Studies , Defense Mechanisms , Dyslexia/psychology , Female , Humans , Language Development Disorders/diagnosis , Longitudinal Studies , Male , Patient Acceptance of Health Care/psychology , Patient Acceptance of Health Care/statistics & numerical data , Refusal to Participate/psychology , Statistics as Topic
8.
Am J Psychiatry ; 157(11): 1869-72, 2000 Nov.
Article in English | MEDLINE | ID: mdl-11058489

ABSTRACT

OBJECTIVE: The authors' goal was to investigate the treatment received before receipt of a disability pension for major depression in a representative sample of depressed patients. METHOD: The medical statements for a random sample of 277 subjects drawn from the Disability Pension Register of the Social Insurance Institution were examined. The subjects selected represented individuals in Finland who were granted a disability pension because of DSM-III-R major depression during a 12-month period in 1993-1994. RESULTS: For 254 (92%) of the subjects, the statements regarding pension eligibility were written either by a psychiatrist or a psychiatric resident for patients who were currently being treated in psychiatric settings. There was an additional diagnosis of a comorbid mental disorder or a somatic disease contributing to disability in two-thirds of the statements. Overall, the statements indicated that 242 (87%) of the subjects were prescribed antidepressant medication, but only 24 (9%) received weekly psychotherapy, and only 11 (4%) received ECT. CONCLUSIONS: Most subjects granted a disability pension for major depression in Finland have comorbid mental or physical disorders contributing to their disability. Before receiving their pension, most received antidepressant treatment, but few received the established nonpharmacological treatments.


Subject(s)
Depressive Disorder/diagnosis , Depressive Disorder/therapy , Insurance, Disability/statistics & numerical data , Pensions/statistics & numerical data , Adolescent , Adult , Antidepressive Agents/therapeutic use , Attitude to Health , Comorbidity , Depressive Disorder/epidemiology , Disability Evaluation , Female , Finland/epidemiology , Humans , Male , Mental Disorders/epidemiology , Middle Aged , Psychiatric Status Rating Scales/statistics & numerical data , Psychotherapy , Sampling Studies , Severity of Illness Index
9.
Assessment ; 7(3): 297-310, 2000 Sep.
Article in English | MEDLINE | ID: mdl-11037395

ABSTRACT

The purpose of this research was to analyze the effects of repeating an executive function test. Three versions of the Tower of Hanoi (TOH) test were repeated three times each, with test-retest intervals of 2 months. Two groups of children participated in the research (7.7 and 11.6 years, n = 22 and n = 28). Repeating the assessment improved the performance and decreased the total performance time in both of the groups. The older participants improved their performance faster than the younger ones. The reliability of all the scores, besides the error scores, seemed to be satisfactory after the first few assessments. The stability of the scores was maintained through all the assessments. The planning time did not explain the variations of the achieved score. The reasons for the initially low reliabilities are discussed, and modifications for the test administration and scoring are suggested.


Subject(s)
Aging/physiology , Cognition/physiology , Neuropsychological Tests , Age Factors , Female , Humans , Male , Reproducibility of Results
10.
Assessment ; 7(3): 311-20, 2000 Sep.
Article in English | MEDLINE | ID: mdl-11037396

ABSTRACT

Detailed time and error analyses of the Tower of Hanoi (TOH) test was performed using four repeated assessments of eight children (ages 9-12 years), who had perceptual and problem solving deficits. The time before each move was measured. In addition to the traditionally counted time scores, new, relative time scores were computed in order to separate the planning time from the general reaction speed. New error scores were defined and sum scores of serious errors (perserative moves, illegal moves, and wrong results) and mild errors (self-corrected moves, almost performed moves, and interrupted trials) were computed. The relative planning time correlated positively with the achieved score, and negatively with the serious errors. The serious errors correlated negatively with the achieved score. The relative planning time seems to measure the quality of planning better than does the raw planning time, and it is a recommended score for TOH analysis. The value of new error scores requires additional research.


Subject(s)
Cognition/physiology , Neuropsychological Tests , Humans
11.
J Agric Food Chem ; 48(12): 6085-93, 2000 Dec.
Article in English | MEDLINE | ID: mdl-11141273

ABSTRACT

Fatty acid composition, oil content, free fatty acid content, and peroxide value of Baltic herring (Clupea harengus membras) and two processed products (fried fillets and fish burgers) were investigated. The highest oil content of the fillets was found in autumn (10%), at the time when the free fatty acids had their minimum (1.4%). The main fatty acids were oleic (18-23%), palmitic (17%), palmitoleic (8-12%), and docosahexaeneoic (8-10%) acids. The proportion of saturated fatty acids was a constant 23% all year around, whereas mono- and polyunsaturated acids varied from 34 to 39% and 33 to 37%, respectively. During processing the oil content doubled and the fatty acid composition changed to the pattern of the rapeseed oil used for frying. Oleic acid was a major fatty acid in the products comprising over 40% of the total fatty acids. The proportion of n-3 acids decreased during processing but the total amount of polyunsaturated acids remained fairly constant.


Subject(s)
Fatty Acids/analysis , Fish Oils/analysis , Fish Products/analysis , Food Handling/methods , Animals , Fishes , Seasons
12.
J Learn Disabil ; 32(5): 457-63, 478, 1999.
Article in English | MEDLINE | ID: mdl-15510435

ABSTRACT

The relation between phonological abilities and reading acquisition and the interindividual variation in the development of different phonological manipulation skills were assessed for six 7-year-old Finnish nonreaders. Intensive time series data were collected by following the children for 13 months. Assessments were conducted every 4 weeks with five phonological manipulation tests. The results indicated gradual progress at the group level. However, analysis of the individual profiles indicated large interindividual variation in the rate of improvement and in the relation between different manipulation skills and reading acquisition.


Subject(s)
Awareness , Learning , Phonetics , Reading , Child , Follow-Up Studies , Humans , Speech Perception
13.
Acta Obstet Gynecol Scand ; 74(4): 262-5, 1995 Apr.
Article in English | MEDLINE | ID: mdl-7732798

ABSTRACT

BACKGROUND: To determine whether the effect of live attenuated oral polio virus vaccine given to pregnant women increases pregnancy complications. METHODS: A study of women who had been vaccinated against poliovirus during a national vaccination campaign and who had delivered by cesarean section in three obstetrical hospitals in southern Finland. One thousand seven hundred and forty-seven vaccinated women (in three study cohorts), and their 2293 nonvaccinated controls (in two reference cohorts) were analyzed. Subjects are out of 22,000 deliveries evaluated earlier. RESULTS: Vaccinated sectioned women did not show an excess of pregnancy complications. The mean rate of cesarean sections was 18.4% in the study cohorts and 18.9% in the reference cohorts counted from the 22,000 deliveries. CONCLUSIONS: Oral live attenuated polio virus vaccine does not increase pregnancy complications and is considered a safe alternative for vaccinating pregnant women.


Subject(s)
Poliovirus Vaccine, Oral , Pregnancy Complications/epidemiology , Vaccination/statistics & numerical data , Adult , Case-Control Studies , Cesarean Section , Cohort Studies , Female , Finland , Humans , Infant, Newborn , Pregnancy , Pregnancy Complications/surgery , Reference Values , Retrospective Studies , Time Factors , Vaccines, Attenuated
14.
N Engl J Med ; 332(6): 351-5, 1995 Feb 09.
Article in English | MEDLINE | ID: mdl-7823996

ABSTRACT

BACKGROUND: Bed rest and back-extension exercises are often prescribed for patients with acute low back pain, but the effectiveness of these two competing treatments remains controversial. METHODS: We conducted a controlled trial among employees of the city of Helsinki, Finland, who presented to an occupational health care center with acute, nonspecific low back pain. The patients were randomly assigned to one of three treatments: bed rest for two days (67 patients), back-mobilizing exercises (52 patients), or the continuation of ordinary activities as tolerated (the control group; 67 patients). Outcomes and costs were assessed after 3 and 12 weeks. RESULTS: After 3 and 12 weeks, the patients in the control group had better recovery than those prescribed either bed rest or exercises. There were statistically significant differences favoring the control group in the duration of pain, pain intensity, lumbar flexion, ability to work as measured subjectively, the Oswestry back-disability index, and number of days absent from work. Recovery was slowest among the patients assigned to bed rest. The overall costs of care did not differ significantly among the three groups. CONCLUSIONS: Among patients with acute low back pain, continuing ordinary activities within the limits permitted by the pain leads to more rapid recovery than either bed rest or back-mobilizing exercises.


Subject(s)
Activities of Daily Living , Bed Rest , Exercise Therapy , Low Back Pain/therapy , Acute Disease , Adult , Bed Rest/economics , Exercise Therapy/economics , Female , Follow-Up Studies , Health Care Costs , Humans , Low Back Pain/economics , Male , Patient Compliance , Treatment Outcome
16.
Clin Infect Dis ; 18(3): 414-20, 1994 Mar.
Article in English | MEDLINE | ID: mdl-8011825

ABSTRACT

Prompted by a nascent epidemic of poliomyelitis in Finland, a mass vaccination program with live oral poliovirus vaccine (OPV) was implemented in February and March 1985. The final rate of coverage was approximately 94%. Pregnant women were included, and a cohort study was launched to evaluate any harmful effects of OPV on the developing embryo. All records of births to mothers who were pregnant during the period of vaccination and whose infants were delivered at the three major hospitals in the Helsinki area were reviewed. Within the study cohort, mothers were grouped into three categories according to their trimester of pregnancy during the program. In addition, two reference cohorts were evaluated; these cohorts consisted of infants delivered at the same hospitals during the second half of 1984 and of 1986, respectively. Each of the three categories in the study cohort included approximately 3,000 children, while each reference cohort included approximately 6,000 children. Data were analyzed on the rate of intrauterine growth and the prevalences of stillbirth, neonatal death, congenital malformation, premature birth, perinatal infection, and neurological aberration. No differences were documented among the study and reference cohorts or among the three categories within the study cohort. Thus, under the conditions described here, the inclusion of pregnant women in programs of mass vaccination with OPV appears to be safe.


Subject(s)
Disease Outbreaks/prevention & control , Poliomyelitis/prevention & control , Poliovirus Vaccine, Oral/adverse effects , Pregnancy , Cohort Studies , Congenital Abnormalities/epidemiology , Embryonic and Fetal Development , Female , Fetal Death/epidemiology , Finland/epidemiology , Humans , Infant Mortality , Infant, Newborn , Male , Poliomyelitis/epidemiology , Pregnancy Outcome
17.
Am J Epidemiol ; 138(6): 407-14, 1993 Sep 15.
Article in English | MEDLINE | ID: mdl-8213746

ABSTRACT

To examine the possible association between maternal vaccination with oral polio-virus and congenital malformations of the child, use was made of a nationwide mass vaccination in Finland. During a restricted period in 1985, a vaccination with trivalent oral poliovirus was implemented with coverage of 94% of the population. The study population was chosen from three major hospitals in the Greater Helsinki Region in Finland which deliver over 95% of the children of their catchment area. One study and two reference cohorts were delineated; the former consisted of pregnancies that were in their first trimester during the vaccination period. The two reference cohorts included mothers from the same hospitals whose pregnancies were likewise in the first trimester during the corresponding time period in 1984 and 1986, i.e., 12 months before and after the study period. Each cohort consisted of approximately 3,000 mothers/children whose delivery and hospital records were manually perused by trained nurses. All the structural malformations reflecting an impaired organogenesis during the sensitive first trimester were monitored. A total of 209 (2.3%) such malformations were recorded and characterized. There were no differences between the study and reference cohorts (risk ratio = 0.7, 95% confidence interval 0.5-1.0). According to the authors' power estimate, an additional prevalence greater than 0.5% would have been detected. The authors conclude that administration of oral poliovirus vaccine during early pregnancy was not associated with an elevated risk of congenital malformations.


Subject(s)
Congenital Abnormalities/microbiology , Poliovirus Vaccine, Oral/adverse effects , Pregnancy Trimester, First , Cohort Studies , Female , Finland , Humans , Infant, Newborn , Pregnancy , Pregnancy Outcome , Prevalence , Risk Factors
18.
Contact Dermatitis ; 28(5): 276-81, 1993 May.
Article in English | MEDLINE | ID: mdl-8365126

ABSTRACT

Allergic contact dermatitis caused by gold is rare, and only isolated cases have been reported. Patch testing with gold may cause a long-lasting reaction. The purpose of this study is to describe a well-studied case of gold allergy caused by dental gold crowns. A gold-sensitized patient and a non-sensitized control subject were examined using patch tests, immunohistochemistry, electron microscopy and blast transformation reactions. Sodium thiosulfate, auranofin and sodium thiomalate gave positive patch test reactions. Immunohistochemistry and electron microscopy were performed from biopsies taken from allergic patch test reactions caused by gold sodium thiosulfate 1 day and 17 days after applying the patches, from normal skin and from a 17-day-old allergic patch test reaction caused by ammonium persulfate. Down-regulation had taken place by 17 days in the allergic ammonium persulfate reaction, but not in the 17-day allergic gold test reaction. The patient reacted to all but one of the gold-induced blast transformation tests, sodium chloroaurate being non-inductive. The non-sensitized control subject did not exhibit any reactions. In conclusion, gold sodium thiosulfate, gold sodium thiomalate and auranofin can be used as patch test substances for gold allergy, though long-lasting allergic patch test reactions may develop. In vitro gold salt induced blast transformation is an alternative test for gold allergy. The slow down-regulation of the allergic patch test reactions needs to be studied further.


Subject(s)
Crowns/adverse effects , Dermatitis, Allergic Contact/etiology , Gingivitis/chemically induced , Gold/adverse effects , Dental Assistants , Dermatitis, Allergic Contact/diagnosis , Female , Gingivitis/diagnosis , Humans , Immunohistochemistry , Microscopy, Electron , Middle Aged , Patch Tests , Time Factors
20.
Mutat Res ; 275(2): 81-6, 1992 Mar.
Article in English | MEDLINE | ID: mdl-1379341

ABSTRACT

Our objective was to explore whether the radiation fallout in Finland after the accident at the Chernobyl nuclear power plant in April 1986 led to an increased incidence of trisomy 21. In this geographic and temporal cohort study, the country was divided into three zones according to the amounts of radioactive fallout and internal radiation caused by two cesium isotopes. The 518 cytologically verified cases of trisomy 21 were divided into a control group (conceived before the accident), and a study group of children whose expected dates of birth were in the post-accident years 1987-1988, i.e., pregnancies commenced after May 1986. The cases were also divided into three subgroups according to the zones of radiation. There were no significant differences in prevalence of trisomy 21 between the control and study groups nor between the three zones in spite of the significant differences in the levels of radiation and in the body burden that prevailed throughout the study period. Power estimates showed that in the two zones of lower radiation, an increase of 0.5% in the prevalence would have been detected with a power of 0.85, and in the somewhat smaller zone of the highest radiation, with a power of 0.70. The study lends no further support to the view that the low radiation fallout in western Europe would have been causally associated with trisomy 21.


Subject(s)
Accidents , Chromosomes, Human, Pair 21/radiation effects , Down Syndrome/epidemiology , Nuclear Reactors , Prenatal Exposure Delayed Effects , Cesium Radioisotopes/adverse effects , Cohort Studies , Down Syndrome/etiology , Female , Finland/epidemiology , Humans , Infant, Newborn , Matched-Pair Analysis , Maternal Age , Power Plants , Pregnancy , Pregnancy, High-Risk , Prevalence , Radioactive Fallout/adverse effects , Trisomy , Ukraine
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