RESUMEN
Costs related to a search and destroy policy and treatment for Staphylococcus aureus bacteraemia in the University Hospital Maastricht were calculated for the period 2000 and 2004. The financial cost-benefit break-even point of the search and destroy policy was determined by modelling. On average 22,412 patients were admitted per year for an average of 8.7 days. Each year 246 patients were screened for meticillin-resistant Staphylococcus aureus (MRSA) and 74 patients were decolonised and nursed in preventive isolation. The prevalence of MRSA in the University Hospital Maastricht was 0.7%, as calculated from positive blood cultures, and mean length of stay for all patients with S. aureus bloodstream infections was 39.9 days. The annual cost of pro-active searching for MRSA in the University Hospital Maastricht was euro 1,383,200, and euro 2,736,762 for MRSA prevention and treatment of S. aureus bloodstream infections. Simulation of a variety MRSA/meticillin-susceptible S. aureus (MSSA) ratios showed that even if the MRSA prevalence reaches 8%, prevention costs are still lower than the cost of treating S. aureus infections. In conclusion, the total cost of a search and destroy policy is lower than the cost of treating S. aureus bloodstream infections in the University Hospital Maastricht. At an MRSA prevalence of Asunto(s)
Bacteriemia/economía
, Infección Hospitalaria/prevención & control
, Costos de la Atención en Salud
, Control de Infecciones/economía
, Resistencia a la Meticilina
, Infecciones Estafilocócicas/economía
, Antibacterianos/economía
, Antibacterianos/uso terapéutico
, Bacteriemia/diagnóstico
, Bacteriemia/tratamiento farmacológico
, Bacteriemia/epidemiología
, Análisis Costo-Beneficio
, Infección Hospitalaria/economía
, Pruebas Diagnósticas de Rutina/economía
, Floxacilina/economía
, Floxacilina/uso terapéutico
, Política de Salud/economía
, Hospitales Universitarios/economía
, Humanos
, Control de Infecciones/métodos
, Países Bajos/epidemiología
, Infecciones Estafilocócicas/diagnóstico
, Infecciones Estafilocócicas/tratamiento farmacológico
, Infecciones Estafilocócicas/epidemiología
, Staphylococcus aureus
, Vancomicina/economía
, Vancomicina/uso terapéutico
Asunto(s)
Bacterias/aislamiento & purificación , Infecciones Bacterianas/microbiología , Unión Europea/organización & administración , Internet , Laboratorios/organización & administración , Vigilancia de la Población/métodos , Análisis de Secuencia de ADN/métodos , Bacterias/genética , Infecciones Bacterianas/epidemiología , HumanosRESUMEN
The mentally normal mother of a 4-year-old boy with del(18)(q21.3) syndrome was tested cytogenetically to study the possibility of an inherited structural rearrangement of chromosome 18. She was found to carry an unusual mosaicism involving chromosomes 18 and 21. Two unbalanced cell lines were seen as derivatives of a reciprocal translocation t(18;21), resulting in mosaicism of two cell lines, one with partial monosomy 18q and one with partial trisomy 18q. A literature review revealed that mosaicism of two or more cell lines with different unbalanced structural aberrations is extremely rare; moreover, chromosome 18 appeared to be involved in the majority of cases. We discuss possible mechanisms for the origin of this distinctive chromosomal constitution.
Asunto(s)
Cromosomas Humanos Par 18 , Mosaicismo , Recombinación Genética , Anomalías Múltiples/genética , Preescolar , Cromosomas Humanos Par 21 , Análisis Citogenético , Humanos , Masculino , Eliminación de SecuenciaRESUMEN
OBJECTIVE: To review the accuracy of a prenatal diagnosis of a missed chromosomal mosaicism in amniotic fluid cell cultures and to see whether adapting the Dutch guidelines would have made any difference to the outcome in this case. METHOD: Metaphases, obtained from cultured amniocytes and peripheral blood lymphocytes, were analyzed with different results. The amniocyte cultures were then reanalyzed and the risk of missing this mosaicism in prenatal analysis was assessed. RESULTS: The prenatal tests performed according to the Dutch guidelines showed a normal female karyotype, but more extensive postnatal analysis revealed a ring chromosome in 50% of the child's lymphocytes. Reanalysis of the original amniocytes confirmed the normal diagnosis, but when more cells from the same and other colonies were analyzed, the ring chromosome was detected. CONCLUSION: The chance of missing such a supernumerary ring mosaicism is very low (about 2% in our case). Given its very rare occurrence and the low chance of it being missed if the existing Dutch guidelines are followed, adapting the number of cells or colonies to be examined for all prenatal diagnoses does not appear to be justified.
Asunto(s)
Amniocentesis , Líquido Amniótico/citología , Reacciones Falso Negativas , Mosaicismo/diagnóstico , Cromosomas en Anillo , Adulto , Células Cultivadas , Femenino , Humanos , Hibridación Fluorescente in Situ , Lactante , Cariotipificación , Linfocitos/citología , Edad Materna , Mosaicismo/genética , Países Bajos , Guías de Práctica Clínica como Asunto , Embarazo , Embarazo de Alto Riesgo , Reproducibilidad de los ResultadosRESUMEN
We present three patients with variegated aneuploidy and premature centromere division (PCD), a rare chromosomal abnormality in humans. Comparison of these three and eight other patients with variegated aneuploidy related to PCD demonstrates a phenotype comprising most frequently microcephaly, CNS anomalies (with cerebellar affection and migration defects), mental retardation, pre-and postnatal growth retardation, flat and broad nasal bridge, apparently low-set ears, eye and skin abnormalities, and ambiguous genitalia in male patients. The occurrence of Wilms tumor in three patients, rhabdomyosarcoma in two others and acute leukemia in a fifth characterizes this condition as a chromosome or genome instability disorder with a high risk of malignancy. FISH studies in uncultured blood and buccal smear cells demonstrate that the random aneuploidies are not limited to cultured cells, but also occur in vivo.
Asunto(s)
Aneuploidia , Centrómero/genética , Neoplasias/genética , Anomalías Múltiples/genética , Anomalías Múltiples/patología , Adulto , Niño , Análisis Citogenético , Femenino , Predisposición Genética a la Enfermedad , Humanos , Lactante , Discapacidad Intelectual/complicaciones , Discapacidad Intelectual/genética , Masculino , Microcefalia/complicaciones , Microcefalia/genética , Neoplasias/etiologíaRESUMEN
Precarious acrocentric short arm in prenatal diagnosis: no chromosome 14 polymorphism, but trisomy 17p: We report on a girl with multiple congenital abnormalities and a prenatally diagnosed 46,XX,14p+ de novo karyotype. Fluorescence in situ hybridization (FISH) demonstrated that the extra material on the short arm of chromosome 14 was not just a polymorphism, but that it originated from chromosome 17. The phenotypic findings of this patient with pure trisomy 17p are compared with those of ten previously published cases.
Asunto(s)
Anomalías Múltiples/genética , Aberraciones Cromosómicas/diagnóstico , Aberraciones Cromosómicas/genética , Cromosomas Humanos Par 14/genética , Cromosomas Humanos Par 17/genética , Enfermedades Fetales/diagnóstico , Enfermedades Fetales/genética , Polimorfismo Genético/genética , Diagnóstico Prenatal , Trisomía/genética , Trastornos de los Cromosomas , Resultado Fatal , Femenino , Humanos , Hibridación Fluorescente in SituRESUMEN
An isochromosome of the long arm of chromosome 1 leading to tetrasomy 1q was detected as the sole chromosomal aberration in two cases of fetal teratoma arising from the oral cavity. This type of teratoma is extremely rare and has seldom been investigated cytogenetically. Studies of DNA markers in the tumor, normal fetal skin, and parental cells demonstrated that in both cases the additional 1q material was of maternal origin. In one of the patients, the teratoma had maternal 1q marker alleles that were not found in the fetal body cells. This implies that the tumor was not derived in a direct way from the fetal body tissue; instead, the chromosomally-normal fetus might be the result of some trisomic or tetrasomic zygote rescue mechanism.
Asunto(s)
Cromosomas Humanos Par 1 , Enfermedades Fetales/genética , Isocromosomas , Neoplasias de la Boca/genética , Neoplasias Craneales/genética , Teratoma/genética , Alelos , Femenino , Enfermedades Fetales/patología , Edad Gestacional , Humanos , Hibridación Fluorescente in Situ , Mitosis , Modelos Genéticos , Neoplasias de la Boca/diagnóstico por imagen , Neoplasias de la Boca/patología , Polimorfismo Genético , Embarazo , Factores Sexuales , Neoplasias Craneales/diagnóstico por imagen , Neoplasias Craneales/patología , Teratoma/diagnóstico por imagen , Teratoma/patología , Ultrasonografía PrenatalRESUMEN
Sperm analysis was performed in a male with oligoasthenoteratozoospermia (OAT) and a reciprocal t(Y;16) (q11. 21;q24), using four-color FISH. Intracytoplasmic sperm injection (ICSI) treatment in this patient had resulted in the birth of one chromosomally balanced and two chromosomally normal children. To assess the risk of having a chromosomally unbalanced conception after ICSI, morphologically normal spermatozoa were studied with a set of probes allowing detection of all segregation variants. There were 51% normal or balanced sperm cells. The fraction of sperm products resulting from alternate and adjacent I segregation was 87%, 12% were products of 3:1 disjunction, and the other 1% had other types of aneuploidy. If morphologically abnormal cells were also included in the FISH analysis, nearly 90% of all the spermatozoa were unbalanced. We conclude that although the majority of males with a Y/autosome translocation are infertile due to azoospermia, our patient produces sufficient morphologically and chromosomally normal spermatozoa to have chromosomally normal or balanced offspring after ICSI. Assuming that ICSI with an unbalanced spermatozoon from this patient would result in a nonviable embryo in many cases, the combination of in vitro and subsequent in vivo selection probably results in a risk of unbalanced offspring of much less than 50%. Hence, FISH studies on the sperm of translocation carriers are useful for estimating the risk of having unbalanced offspring after ICSI and in understanding the mechanisms underlying infertility in such carriers.
Asunto(s)
Cromosomas Humanos Par 16/genética , Oligospermia/genética , Espermatozoides/ultraestructura , Translocación Genética , Cromosoma Y/genética , Adulto , Aneuploidia , Citogenética , Femenino , Fertilización In Vitro , Humanos , Hibridación Fluorescente in Situ/métodos , Recién Nacido , Linfocitos/ultraestructura , Masculino , Oligospermia/terapia , Embarazo , Factores de RiesgoRESUMEN
A follow-up study was performed to investigate the impact of the detection of a chromosome abnormality in infertile men who are candidates for intracytoplasmic sperm injection (ICSI) treatment. In this collaborative study between clinical genetics centres and fertility clinics in the Netherlands, 75 ICSI couples of which the male partners had a chromosome abnormality were included. All couples were extensively counselled on the risk of having a chromosomally unbalanced child. Forty-two out of 75 couples chose to proceed with the ICSI treatment. So far, treatment has resulted in a pregnancy in 11 cases. Four of them opted to have invasive prenatal diagnosis. Despite the genetic risks related to a chromosome abnormality in infertile men, a small majority (56%) of the couples did not refrain from the ICSI treatment.
Asunto(s)
Aberraciones Cromosómicas , Trastornos de los Cromosomas , Citoplasma/fisiología , Infertilidad Masculina/genética , Micromanipulación , Espermatozoides/fisiología , Adulto , Aberraciones Cromosómicas/diagnóstico , Aberraciones Cromosómicas/fisiopatología , Femenino , Estudios de Seguimiento , Humanos , Cariotipificación , Masculino , Embarazo , Índice de Embarazo , Diagnóstico Prenatal , Valores de ReferenciaRESUMEN
In many B-cell malignancies, 14q32.3 chromosomal rearrangements involving the immunoglobulin heavy chain (IgH) locus have been shown to be pathognomonic for the disease. Although in myeloma heterogeneous and complex karyotypes are found, 14q32.3 translocations are prominent. However, owing to the telomeric position of the IgH locus, 14q32.3 translocations may be easily missed. We established fluorescence in situ hybridization (FISH) assays on chromosomes and DNA fibers to determine both the occurrence of 14q32.3 rearrangements in myeloma cell lines and the precise localization of the breakpoints in the IgH locus. Our results show that 14q32.3 chromosomal rearrangements are present in almost every myeloma cell line analyzed (17 of 19, 89%). Breakpoint analysis of the lines harboring one or more 14q32.3 rearrangements with the use of fiber-FISH revealed the involvement of switch regions in the IgH locus in 11 of 17 cell lines. Remarkably, pseudogamma genes without switch regions were involved in 3 of 17 cell lines, all derived from IgA myelomas. Three of 17 cell lines contained breakpoints outside a switch or immunoglobulin heavy chain constant region. The almost ubiquitous presence of 14q32.3 rearrangements suggests an obligatory role in the development of myeloma. The high incidence of breakpoints involving switch regions indicates an oncogenic event in a late stage of B-cell differentiation.
Asunto(s)
Cromosomas Humanos Par 14 , Cambio de Clase de Inmunoglobulina/genética , Hibridación Fluorescente in Situ , Mieloma Múltiple/genética , Aberraciones Cromosómicas , Frecuencia de los Genes , Humanos , Cadenas Pesadas de Inmunoglobulina/biosíntesis , Cadenas Pesadas de Inmunoglobulina/genética , Metafase , Mieloma Múltiple/patología , Células Tumorales CultivadasRESUMEN
A balanced translocation t(Y;16)(q11.21;q24) is described in a male with severe oligoasthenoteratozoospermia (OAT). Before having a chromosome investigation, the patient and his partner had undergone intracytoplasmic sperm injection (ICSI) treatment resulting in the birth of a healthy 46,XX child. After detection of the t(Y;16) translocation, the couple opted for further ICSI treatment, although they were extensively counselled on the risk of having chromosomally unbalanced offspring. This treatment resulted in a twin pregnancy, one with a 46,XX karyotype and the other a 46,X,t(Y;16) (q11.21;q24) karyotype, the same as the father. After an uncomplicated pregnancy two healthy children were born. We conclude that patients with a Y/autosome translocation as a cause of OAT can have chromosomally normal children after ICSI treatment.
Asunto(s)
Cromosomas Humanos Par 16 , Fertilización In Vitro , Oligospermia/genética , Oligospermia/terapia , Translocación Genética , Cromosoma Y , Adulto , Bandeo Cromosómico , Femenino , Humanos , Recién Nacido , Masculino , Embarazo , Resultado del Embarazo , Gemelos DicigóticosAsunto(s)
Aberraciones Cromosómicas/diagnóstico , Cromosomas Humanos Par 18 , Enfermedades Fetales/diagnóstico , Holoprosencefalia/diagnóstico , Diagnóstico Prenatal/métodos , Adulto , Amniocentesis , Muestra de la Vellosidad Coriónica , Aberraciones Cromosómicas/genética , Trastornos de los Cromosomas , Femenino , Enfermedades Fetales/genética , Holoprosencefalia/genética , Humanos , Cariotipificación , EmbarazoRESUMEN
A 46,XY female patient with streak gonads and a large deletion of Yp is described. The deletion included the Y chromosomal genes SRY, ZFY, and RPS4Y. The patient did not display any Turner stigmata, such as webbing of the neck, cardiac or other abnormalities. The findings argue against an important role of RPS4Y in the prevention of Turner stigmata in males and are consistent with a role of SRY in testis differentiation in humans.
Asunto(s)
Eliminación de Gen , Proteínas Nucleares , Aberraciones Cromosómicas Sexuales/genética , Factores de Transcripción , Adulto , Secuencia de Bases , ADN de Cadena Simple , Proteínas de Unión al ADN/genética , Femenino , Disgenesia Gonadal/genética , Disgenesia Gonadal/patología , Humanos , Cariotipificación , Masculino , Datos de Secuencia Molecular , Reacción en Cadena de la Polimerasa , Diferenciación Sexual/genética , Proteína de la Región Y Determinante del Sexo , Síndrome de Turner/genéticaRESUMEN
In a retrospective study, peripheral blood mononuclear cells from 13 patients with known ataxia telangiectasia (AT) (Louis Bar syndrome, McKusick #20890) were irradiated with different doses of X-rays prior to stimulation with phytohaemagglutinin. Mitogen response and cell cycle progression were assessed by two-parameter 5-bromo-2'-deoxyuridine/Hoechst--ethidium bromide flow cytometry. Compared to age-matched controls, AT cells show a severely defective mitogen response in both unirradiated and irradiated cells. Following irradiation with 1.5 Gy, AT cells exhibit significantly greater accumulations of cells in the G2 phase of the first cell cycle than controls. The ratio between the number of cells accumulated in the first cycle G2 phase and the growth fraction provides a clear distinction between AT and control cultures. In addition, two patients with microcephaly, normal intelligence, immunodeficiency, chromosomal instability and risk for lymphoreticular malignancies (Seemanová syndrome) and two patients with the Nijmegen breakage syndrome (both syndromes are listed as McKusick #25126) also exhibit very poor mitogen response and moderately increased G2 phase accumulations after X-irradiation. The simultaneous assessment of radiosensitivity and mitogen response in a single cell kinetic assay provides a speedy and accurate classification of cells of AT and AT-related syndromes.
Asunto(s)
Ataxia Telangiectasia/sangre , Citometría de Flujo , Interfase/efectos de los fármacos , Interfase/efectos de la radiación , Leucocitos Mononucleares/efectos de los fármacos , Leucocitos Mononucleares/efectos de la radiación , Mitosis/efectos de los fármacos , Mitosis/efectos de la radiación , Fitohemaglutininas/farmacología , Tolerancia a Radiación , Adolescente , Adulto , Ataxia Telangiectasia/diagnóstico , Células Cultivadas , Niño , Preescolar , Humanos , Lactante , Leucocitos Mononucleares/citología , Dosis de Radiación , Estudios RetrospectivosRESUMEN
We report on a microcephalic, growth-retarded newborn girl without major anomalies who has chromosome instability in lymphocytes and fibroblasts. Frequent involvement of bands 7p13, 7q34, 14q11, and 14q32 suggested the diagnosis of ataxia telangiectasia (AT) or a related disorder. Supportive evidence was radioresistant DNA synthesis in fibroblasts and radiation hypersensitivity of short-term lymphocyte cultures. Follow-up for nearly 4 years showed largely normal development, and no signs of telangiectasia, ataxia, or immunodeficiency. Serum AFP levels turned from elevated at age 5 months to normal at age 2 years. We propose that our patient belongs to the expanding category of "AT-related" genetic disorders, probably to the Nijmegen breakage syndrome.
Asunto(s)
Aberraciones Cromosómicas , Cromosomas Humanos Par 14 , Cromosomas Humanos Par 7 , Retardo del Crecimiento Fetal/genética , Linfocitos/efectos de la radiación , Microcefalia/genética , Ciclo Celular/efectos de la radiación , Replicación del ADN/efectos de los fármacos , Femenino , Retardo del Crecimiento Fetal/inmunología , Fibroblastos/fisiología , Fibroblastos/efectos de la radiación , Humanos , Inmunoglobulinas/análisis , Recién Nacido , Activación de Linfocitos/efectos de la radiación , Linfocitos/inmunología , Microcefalia/inmunología , Mitosis/efectos de la radiación , Síndrome , Rayos XRESUMEN
We report on five independent families with a chromosome instability disorder that earlier had been called the Nijmegen breakage syndrome (NBS). These families, two from the Netherlands and three from Czechoslovakia, had a total of eight patients, five of whom are still alive. The main clinical manifestations were microcephaly, short stature, a "bird-like" face, immunological defects involving both the humoral and cellular system. In four of the five living patients it has been possible to study the chromosomes of cultured lymphocytes. The basic karyotype in these patients were normal, but in 17% to 35% of the metaphases rearrangements were found, preferentially involving chromosomes 7 and/or 14 at the sites 7p13, 7q34, and 14q11. The chromosomes of all five living patients were very sensitive to ionizing radiation. In addition, the DNA synthesis in their cultured lymphocytes and fibroblasts was more resistant to X-rays than in cells from controls. The NBS shares a number of important features with ataxia telangiectasia (AT). Both syndromes are characterized by the occurrence of typical rearrangements of chromosomes 7 and/or 14, cellular and chromosomal hypersensitivity to X-irradiation, radioresistance of DNA replication and immunodeficiency. However, there are also obvious differences: NBS patients have microcephaly but neither ataxia nor telangiectasia, and in contrast to the situation in AT the alpha-fetoprotein level in their serum is normal.
Asunto(s)
Anomalías Múltiples/diagnóstico , Aberraciones Cromosómicas/diagnóstico , Cromosomas Humanos Par 14 , Cromosomas Humanos Par 7 , Reordenamiento Génico , Adolescente , Adulto , Niño , Trastornos de los Cromosomas , Cromosomas/efectos de la radiación , Cromosomas Humanos Par 13 , Estudios de Cohortes , Replicación del ADN/efectos de la radiación , Salud de la Familia , Femenino , Genes Recesivos , Humanos , Síndromes de Inmunodeficiencia/diagnóstico , Cariotipificación , Masculino , SíndromeRESUMEN
An ovarian carcinoma cell line (OTN 11) was produced from the ascitic fluid of a patient with a moderately to well differentiated papilliferous cystadenocarcinoma of the ovary. The cell line was characterized using electron microscopy karyotyping, immunohistochemical techniques with monoclonal antibodies against keratins as epithelial markers, and the monoclonal antibodies OV-TL 3 and OC 125 as ovarian carcinoma markers. These techniques revealed the epithelial and adenocarcinomatous nature of the cell line and the presence of ovarian carcinoma-related surface markers. The adenocarcinomatous nature of the cell line also became apparent after heterotransplantation of cell suspensions into nude mice and nude rats, in which adenomatous tumor structures were formed. These xenografts had the same ultrastructural and immunohistochemical properties as the cell line. Despite the adenocarcinomatous character of the tumor the cultured cells release estradiol into the culture medium. We may conclude that OTN 11 is an ovarian carcinoma cell line which has retained highly differentiated functions, such as the production of an ovarian hormone.
Asunto(s)
Cistoadenoma/patología , Estradiol/biosíntesis , Neoplasias Ováricas/patología , Adulto , Animales , Aberraciones Cromosómicas , Cistoadenoma/genética , Cistoadenoma/ultraestructura , Femenino , Humanos , Inmunohistoquímica , Queratinas/análisis , Ratones , Ratones Endogámicos BALB C , Trasplante de Neoplasias , Neoplasias Ováricas/genética , Neoplasias Ováricas/ultraestructura , Trasplante Heterólogo , Células Tumorales CultivadasRESUMEN
In this paper, a survey is given of the immunological disturbances in some chromosome instability disorders (e.g. Bloom syndrome, ataxia teleangiectasia and Nijmegen Breakage syndrome). Further, the clinical symptoms and the diagnostic approach will be discussed.
Asunto(s)
Aberraciones Cromosómicas , Síndromes de Inmunodeficiencia/genética , Formación de Anticuerpos , Ataxia Telangiectasia/genética , Síndrome de Bloom/genética , Humanos , Inmunidad Celular , Síndromes de Inmunodeficiencia/inmunologíaRESUMEN
Chromosome analysis was performed in 17 children with IgA-deficiency. In two patients a constitutional structural chromosome abnormality was found. A ring chromosome 22 was seen in one, while in the other a mosaicism of ring chromosome 18/18p+ was observed. Both patients were mentally retarded and showed distinct congenital defects. From ten asymptomatic patients, spontaneous as well as X-ray-induced chromosome instability was investigated. There was no increased spontaneous instability, and also after irradiation the induced chromosome damage was within normal control levels. A relationship between IgA-deficiency and X-ray hypersensitivity, as might be suggested by the frequently occurring coincidence of radiosensitivity and IgA-deficiency in ataxia telangiectasia patients, is not established.