Ellen Holter - Academia.edu (original) (raw)

Papers by Ellen Holter

Research paper thumbnail of Fatal cytomegalovirus (CMV) colitis in a patient receiving low dose prednisolone therapy

Scandinavian Journal of Infectious Diseases, 1991

Cytomegalovirus (CMV) colitis is uncommon in patients who are not gravely immunodepressed. We rep... more Cytomegalovirus (CMV) colitis is uncommon in patients who are not gravely immunodepressed. We report a case of fatal CMV colitis in a 54-year-old woman on low dose steroid therapy. She was admitted to hospital after sudden onset of abdominal pain and hemorrhagic watery diarrhea. After 25 days in the hospital, treatment with high dosage of methylprednisolone was started for presumed ulcerative colitis. Her condition worsened and she died 52 days after admission. It is important to recognize CMV colitis as differential diagnosis to inflammatory bowel disease, particularly when the colitis is refractory to immunosuppressive treatment.

Research paper thumbnail of A Prospective Study of the Natural Course of Cytomegalovirus Infection and Disease in Renal Allograft RECIPIENTS1

Transplantation, 2000

Cytomegalovirus (CMV) infection is the single most frequent infectious complication in renal tran... more Cytomegalovirus (CMV) infection is the single most frequent infectious complication in renal transplant recipients. Because no CMV-prophylaxis is given and ganciclovir is used only as deferred therapy for CMV disease at our center, we have been able to study the natural course of CMV infections. The aim was to assess risk factors for CMV infection and disease and thus identify subgroups of patients likely to benefit from CMV prophylaxis or preemptive therapy. Between October 1994 and July 1997, 477 consecutive renal transplant recipients (397 first transplants and 80 retransplants) were included in the study. The patients were followed prospectively for 3 months with serial measurements of CMV pp65 antigen for monitoring activity of CMV infections. The incidence of CMV infections in first transplants was 68% in D+R- and D+/-R+ serostatus groups, whereas the incidence of CMV disease was higher in D+R- (56%) than in D+/-R+ (20%, P<0.001). No difference in severity of CMV disease in D+R- and D+/-R+ was seen except for an increased incidence of hepatitis in primary infections. One of 14 deaths could be associated with CMV disease in a seropositive recipient. Cox regression analysis showed that rejection (RR 2.5, P<0.01) and serostatus group D+R- (RR 3.9, P<0.001) were significant risk factors for development of CMV disease. The maximum CMV pp65 antigen count had significant correlation to disease only in CMV seropositive recipients, P<0.001. Conclusion. Renal transplant recipients can safely be given deferred ganciclovir therapy for CMV disease if they are intensively monitored for CMV infection. Patients with primary CMV infection (D+R-), CMV infected patients undergoing anti-rejection therapy and R+ patients with high CMV pp65 counts seem to have a particular potential for benefit from preemptive anti-CMV-therapy.

Research paper thumbnail of Fatal cytomegalovirus (CMV) colitis in a patient receiving low dose prednisolone therapy

Scandinavian Journal of Infectious Diseases, 1991

Cytomegalovirus (CMV) colitis is uncommon in patients who are not gravely immunodepressed. We rep... more Cytomegalovirus (CMV) colitis is uncommon in patients who are not gravely immunodepressed. We report a case of fatal CMV colitis in a 54-year-old woman on low dose steroid therapy. She was admitted to hospital after sudden onset of abdominal pain and hemorrhagic watery diarrhea. After 25 days in the hospital, treatment with high dosage of methylprednisolone was started for presumed ulcerative colitis. Her condition worsened and she died 52 days after admission. It is important to recognize CMV colitis as differential diagnosis to inflammatory bowel disease, particularly when the colitis is refractory to immunosuppressive treatment.

Research paper thumbnail of Serum Adiponectin Concentration Prior to Clinical Onset of Preeclampsia

Hypertension in Pregnancy, 2006

This study assesses whether the adipokine adiponectin is a useful marker in pregnant women who su... more This study assesses whether the adipokine adiponectin is a useful marker in pregnant women who subsequently develop preeclampsia (PE). A retrospective case-control study was conducted to measure the total serum levels of adiponectin, measured by radioimmunoassay kit, in serum samples stored in serological biobanks. Total serum adiponectin concentrations between the groups were not significantly different (p = 0.22). There were no obvious clinical signs of the preeclamptic inflammatory process at the time when samples were drawn. Using this design, total adiponectin appeared not be a useful pre-clinical marker of PE.

Research paper thumbnail of Reactivation of hepatitis B virus infectionin an anti-HBc and anti-HBs positivepatient after allogeneic bone marrow transplantation

European Journal of Haematology, 2000

Research paper thumbnail of Diagnosis of cytomegalovirus infection in kidney transplant recipients by a quantitative RNA-DNA hybrid capture assay for cytomegalovirus DNA in leukocytes

European Journal of Clinical Microbiology & Infectious Diseases, 1998

The clinical value of a new RNA-DNA hybridization assay for quantification of cytomegalovirus (CM... more The clinical value of a new RNA-DNA hybridization assay for quantification of cytomegalovirus (CMV) DNA in leukocytes [Hybrid Capture CMV DNA Assay (HCA); Murex Biotech, UK] was evaluated. The HCA was compared with an assay for CMV pp65 antigen in leukocytes and an in-house CMV polymerase chain reaction PCR (CMV-PCR) on parallel blood samples. The HCA and the CMV-PCR were less sensitive than the CMV pp65 assay, but the positive predictive value of all three methods for CMV disease was 50% or less. However, when quantitation of viral load by HCA and CMV pp65 assay was taken into consideration, both assays were superior to CMV-PCR in predicting CMV disease.

Research paper thumbnail of Cytomegalovirus DNA concentration in plasma predicts development of cytomegalovirus disease in kidney transplant recipients

Clinical Microbiology and Infection, 2002

The clinical significance of cytomegalovirus (CMV) DNA detection in post-kidney transplantation i... more The clinical significance of cytomegalovirus (CMV) DNA detection in post-kidney transplantation infection surveillance was examined by comparing the performance of three assays for detection of CMV in blood: the test for CMV-pp65-antigen in leukocytes, which is routinely employed in our laboratory, the quantitative plasma CMV-DNApolymerase chain reaction (PCR; Cobas Amplicor CMV Monitor test 1 ) and the qualitative plasma CMV-DNA-PCR (Amplicor CMV test 1 ). Thirteen kidney transplant recipients were monitored with serial samples taken over a period of 3 months following transplantation. The quantitative CMV-PCR was the test with highest sensitivity, 95.9%, vs. 88.9% and 76.9% for the CMV-pp65 antigen assay and qualitative CMV-PCR, respectively. The virus load in the first positive specimens, assessed as DNA-copies/ mL, was significantly associated with CMV disease because five of the six patients who developed disease, but only one of the seven who did not develop disease, had more than 3000 CMV-DNA-copies/mL. The number of CMV-pp65 antigen-positive cells in the first positive specimens did not have predictive value for development of CMV disease. Assessment of CMV in plasma by the quantitative CMV-PCR is especially useful since it has a high sensitivity and the amount of CMV DNA in plasma is a good predictor of CMV disease. Microbiol Infect 2002; 8: 431-434 Cytomegalovirus (CMV) is still a major pathogen in organ transplant recipients despite the implementation of new diagnostic tools and improved strategies for anti-CMV prophylaxis and treatment. In a recent study on CMV infections in 477 kidney transplant recipients, we showed that among patients at risk for primary CMV infection, 68% acquired CMV infection, and of these, 81% developed CMV disease . In patients at risk for CMV-reactivated infection, 69% had a reactivated CMV infection but only 26% developed CMV disease. This illustrates one of the major problems in the management of CMV infections in transplant recipients. Only a certain proportion of patients at risk will have an active CMV infection and even fewer will develop CMV disease.

Research paper thumbnail of Detection of human cytomegalovirus (HCMV) pp67-mRNA and pp65 antigenemia in relation to development of clinical HCMV disease in renal transplant recipients

Clinical Microbiology and Infection, 2001

Objective To evaluate the performance of the recently introduced method based on detection of hum... more Objective To evaluate the performance of the recently introduced method based on detection of human cytomegalovirus (HCMV) pp67 mRNA in blood by the nucleic acid sequence-based ampli®cation (NucliSens), in comparison to semiquantitative detection of pp65 HCMV antigen in white blood cells, in relation to development of clinical HCMV disease.

Research paper thumbnail of Sudden infant death syndrome (SIDS)—Standardised investigations and classification: Recommendations

Forensic Science International, 2007

Sudden infant death syndrome (SIDS) still accounts for considerable numbers of unexpected infant ... more Sudden infant death syndrome (SIDS) still accounts for considerable numbers of unexpected infant deaths in many countries. While numerous theories have been advanced to explain these events, it is increasingly clear that this group of infant deaths results from the complex interaction of a variety of heritable and idiosyncratic endogenous factors interacting with exogenous factors. This has been elegantly summarised in the ''three hit'' or ''triple risk'' model. Contradictions and lack of consistencies in the literature have arisen from diverse autopsy approaches, variable applications of diagnostic criteria and inconsistent use of definitions. An approach to sudden infant death is outlined with discussion of appropriate tissue sampling, ancillary investigations and the use of controls in research projects. Standardisation of infant death investigations

Research paper thumbnail of Fatal cytomegalovirus (CMV) colitis in a patient receiving low dose prednisolone therapy

Scandinavian Journal of Infectious Diseases, 1991

Cytomegalovirus (CMV) colitis is uncommon in patients who are not gravely immunodepressed. We rep... more Cytomegalovirus (CMV) colitis is uncommon in patients who are not gravely immunodepressed. We report a case of fatal CMV colitis in a 54-year-old woman on low dose steroid therapy. She was admitted to hospital after sudden onset of abdominal pain and hemorrhagic watery diarrhea. After 25 days in the hospital, treatment with high dosage of methylprednisolone was started for presumed ulcerative colitis. Her condition worsened and she died 52 days after admission. It is important to recognize CMV colitis as differential diagnosis to inflammatory bowel disease, particularly when the colitis is refractory to immunosuppressive treatment.

Research paper thumbnail of A Prospective Study of the Natural Course of Cytomegalovirus Infection and Disease in Renal Allograft RECIPIENTS1

Transplantation, 2000

Cytomegalovirus (CMV) infection is the single most frequent infectious complication in renal tran... more Cytomegalovirus (CMV) infection is the single most frequent infectious complication in renal transplant recipients. Because no CMV-prophylaxis is given and ganciclovir is used only as deferred therapy for CMV disease at our center, we have been able to study the natural course of CMV infections. The aim was to assess risk factors for CMV infection and disease and thus identify subgroups of patients likely to benefit from CMV prophylaxis or preemptive therapy. Between October 1994 and July 1997, 477 consecutive renal transplant recipients (397 first transplants and 80 retransplants) were included in the study. The patients were followed prospectively for 3 months with serial measurements of CMV pp65 antigen for monitoring activity of CMV infections. The incidence of CMV infections in first transplants was 68% in D+R- and D+/-R+ serostatus groups, whereas the incidence of CMV disease was higher in D+R- (56%) than in D+/-R+ (20%, P<0.001). No difference in severity of CMV disease in D+R- and D+/-R+ was seen except for an increased incidence of hepatitis in primary infections. One of 14 deaths could be associated with CMV disease in a seropositive recipient. Cox regression analysis showed that rejection (RR 2.5, P<0.01) and serostatus group D+R- (RR 3.9, P<0.001) were significant risk factors for development of CMV disease. The maximum CMV pp65 antigen count had significant correlation to disease only in CMV seropositive recipients, P<0.001. Conclusion. Renal transplant recipients can safely be given deferred ganciclovir therapy for CMV disease if they are intensively monitored for CMV infection. Patients with primary CMV infection (D+R-), CMV infected patients undergoing anti-rejection therapy and R+ patients with high CMV pp65 counts seem to have a particular potential for benefit from preemptive anti-CMV-therapy.

Research paper thumbnail of Fatal cytomegalovirus (CMV) colitis in a patient receiving low dose prednisolone therapy

Scandinavian Journal of Infectious Diseases, 1991

Cytomegalovirus (CMV) colitis is uncommon in patients who are not gravely immunodepressed. We rep... more Cytomegalovirus (CMV) colitis is uncommon in patients who are not gravely immunodepressed. We report a case of fatal CMV colitis in a 54-year-old woman on low dose steroid therapy. She was admitted to hospital after sudden onset of abdominal pain and hemorrhagic watery diarrhea. After 25 days in the hospital, treatment with high dosage of methylprednisolone was started for presumed ulcerative colitis. Her condition worsened and she died 52 days after admission. It is important to recognize CMV colitis as differential diagnosis to inflammatory bowel disease, particularly when the colitis is refractory to immunosuppressive treatment.

Research paper thumbnail of Serum Adiponectin Concentration Prior to Clinical Onset of Preeclampsia

Hypertension in Pregnancy, 2006

This study assesses whether the adipokine adiponectin is a useful marker in pregnant women who su... more This study assesses whether the adipokine adiponectin is a useful marker in pregnant women who subsequently develop preeclampsia (PE). A retrospective case-control study was conducted to measure the total serum levels of adiponectin, measured by radioimmunoassay kit, in serum samples stored in serological biobanks. Total serum adiponectin concentrations between the groups were not significantly different (p = 0.22). There were no obvious clinical signs of the preeclamptic inflammatory process at the time when samples were drawn. Using this design, total adiponectin appeared not be a useful pre-clinical marker of PE.

Research paper thumbnail of Reactivation of hepatitis B virus infectionin an anti-HBc and anti-HBs positivepatient after allogeneic bone marrow transplantation

European Journal of Haematology, 2000

Research paper thumbnail of Diagnosis of cytomegalovirus infection in kidney transplant recipients by a quantitative RNA-DNA hybrid capture assay for cytomegalovirus DNA in leukocytes

European Journal of Clinical Microbiology & Infectious Diseases, 1998

The clinical value of a new RNA-DNA hybridization assay for quantification of cytomegalovirus (CM... more The clinical value of a new RNA-DNA hybridization assay for quantification of cytomegalovirus (CMV) DNA in leukocytes [Hybrid Capture CMV DNA Assay (HCA); Murex Biotech, UK] was evaluated. The HCA was compared with an assay for CMV pp65 antigen in leukocytes and an in-house CMV polymerase chain reaction PCR (CMV-PCR) on parallel blood samples. The HCA and the CMV-PCR were less sensitive than the CMV pp65 assay, but the positive predictive value of all three methods for CMV disease was 50% or less. However, when quantitation of viral load by HCA and CMV pp65 assay was taken into consideration, both assays were superior to CMV-PCR in predicting CMV disease.

Research paper thumbnail of Cytomegalovirus DNA concentration in plasma predicts development of cytomegalovirus disease in kidney transplant recipients

Clinical Microbiology and Infection, 2002

The clinical significance of cytomegalovirus (CMV) DNA detection in post-kidney transplantation i... more The clinical significance of cytomegalovirus (CMV) DNA detection in post-kidney transplantation infection surveillance was examined by comparing the performance of three assays for detection of CMV in blood: the test for CMV-pp65-antigen in leukocytes, which is routinely employed in our laboratory, the quantitative plasma CMV-DNApolymerase chain reaction (PCR; Cobas Amplicor CMV Monitor test 1 ) and the qualitative plasma CMV-DNA-PCR (Amplicor CMV test 1 ). Thirteen kidney transplant recipients were monitored with serial samples taken over a period of 3 months following transplantation. The quantitative CMV-PCR was the test with highest sensitivity, 95.9%, vs. 88.9% and 76.9% for the CMV-pp65 antigen assay and qualitative CMV-PCR, respectively. The virus load in the first positive specimens, assessed as DNA-copies/ mL, was significantly associated with CMV disease because five of the six patients who developed disease, but only one of the seven who did not develop disease, had more than 3000 CMV-DNA-copies/mL. The number of CMV-pp65 antigen-positive cells in the first positive specimens did not have predictive value for development of CMV disease. Assessment of CMV in plasma by the quantitative CMV-PCR is especially useful since it has a high sensitivity and the amount of CMV DNA in plasma is a good predictor of CMV disease. Microbiol Infect 2002; 8: 431-434 Cytomegalovirus (CMV) is still a major pathogen in organ transplant recipients despite the implementation of new diagnostic tools and improved strategies for anti-CMV prophylaxis and treatment. In a recent study on CMV infections in 477 kidney transplant recipients, we showed that among patients at risk for primary CMV infection, 68% acquired CMV infection, and of these, 81% developed CMV disease . In patients at risk for CMV-reactivated infection, 69% had a reactivated CMV infection but only 26% developed CMV disease. This illustrates one of the major problems in the management of CMV infections in transplant recipients. Only a certain proportion of patients at risk will have an active CMV infection and even fewer will develop CMV disease.

Research paper thumbnail of Detection of human cytomegalovirus (HCMV) pp67-mRNA and pp65 antigenemia in relation to development of clinical HCMV disease in renal transplant recipients

Clinical Microbiology and Infection, 2001

Objective To evaluate the performance of the recently introduced method based on detection of hum... more Objective To evaluate the performance of the recently introduced method based on detection of human cytomegalovirus (HCMV) pp67 mRNA in blood by the nucleic acid sequence-based ampli®cation (NucliSens), in comparison to semiquantitative detection of pp65 HCMV antigen in white blood cells, in relation to development of clinical HCMV disease.

Research paper thumbnail of Sudden infant death syndrome (SIDS)—Standardised investigations and classification: Recommendations

Forensic Science International, 2007

Sudden infant death syndrome (SIDS) still accounts for considerable numbers of unexpected infant ... more Sudden infant death syndrome (SIDS) still accounts for considerable numbers of unexpected infant deaths in many countries. While numerous theories have been advanced to explain these events, it is increasingly clear that this group of infant deaths results from the complex interaction of a variety of heritable and idiosyncratic endogenous factors interacting with exogenous factors. This has been elegantly summarised in the ''three hit'' or ''triple risk'' model. Contradictions and lack of consistencies in the literature have arisen from diverse autopsy approaches, variable applications of diagnostic criteria and inconsistent use of definitions. An approach to sudden infant death is outlined with discussion of appropriate tissue sampling, ancillary investigations and the use of controls in research projects. Standardisation of infant death investigations