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1.
Leuk Res ; 38(4): 484-9, 2014 Apr.
Article in English | MEDLINE | ID: mdl-24565568

ABSTRACT

Automated morphological assessment of peripheral blood slides has become an important modality facilitating characterization and quantification of cells in a uniform, fast and robust manner. In this study, we evaluated the morphological diversity in peripheral blood films of 94 chronic lymphocytic leukemia (CLL) patients using the DM1200 CellaVision automated microscopy system. Aberrant lymphocytes and smudge cells were enumerated and correlated with CLL immunophenotype, chromosomal aberrations and prognostic parameters. Herein, we show that the percentages of aberrant and smudge cells was highly variable between patients and did not correlate with each other. Increased aberrant lymphocytes and fewer smudge cells were associated with an atypical immunophenotype including low expression of CD23, higher levels of FMC7 and bright surface levels of CD20. High fraction of aberrant lymphocytes also was associated with trisomy 12. These cells were predominantly of small/medium size, sometimes with cleft nuclei. No correlation was noted between aberrant or smudge cells and clinical stage, CD38, ZA70 or time to first treatment. Taken together, automated morphological analysis of peripheral blood leukocytes emerged as a powerful and robust tool for the quantitative morphological stratification of CLL. Integration of the automated morphological features discriminates between different CLL phenotypes and distinct chromosomal aberrations.


Subject(s)
Chromosome Aberrations , Leukemia, Lymphocytic, Chronic, B-Cell/genetics , Leukemia, Lymphocytic, Chronic, B-Cell/pathology , Leukocytes, Mononuclear/pathology , Automation, Laboratory , Case-Control Studies , Cell Shape , Diagnosis, Differential , Flow Cytometry , Humans , Immunophenotyping , Leukemia, Lymphocytic, Chronic, B-Cell/classification , Lymphocytes/pathology , Prognosis
2.
Ann Transplant ; 18: 567-75, 2013 Oct 21.
Article in English | MEDLINE | ID: mdl-24141383

ABSTRACT

BACKGROUND: Telomeres are non-coding regions of DNA that cap the ends of chromosomes. Their length is considered a marker of human replicative senescence and premature aging. Given the high association of liver transplantation with the metabolic syndrome, we hypothesized that liver transplant recipients may exhibit premature and accelerated aging. MATERIAL AND METHODS: Telomere length in peripheral blood lymphocytes was measured by polymerase chain reaction in 62 consecutive liver-transplant recipients and 59 healthy control subjects aged 20-76 years. Clinical and laboratory parameters were collected from the medical files. RESULTS: The liver transplant recipients were significantly older than the control subjects (p=0.012), with significantly higher rates of obesity (BMI >30 kg/m(2)), dyslipidemia, hypertension, diabetes, and fatty liver. Mean telomere length was significantly shorter in the transplant group (0.59±0.6 vs. 1.91±1.78 in the controls, p<0.0001). Within the transplant group, there was no significant association between mean telomere length and underlying liver disease or presence of the metabolic syndrome or its constituents. On multivariate analysis, telomere length was negatively associated with patient age (p=0.0001), male sex (p=0.04), acute rejection (p=0.005), and fatty liver (p=0.009), and was positively associated with time from transplantation (p=0.006). CONCLUSIONS: Liver transplantation is associated with shortened telomere length in peripheral blood lymphocytes, suggesting accelerated senescence.


Subject(s)
Liver Transplantation , Telomere Shortening , Telomere , Adult , Aged , Aging , Female , Humans , Male , Middle Aged
3.
Am J Emerg Med ; 31(12): 1703-6, 2013 Dec.
Article in English | MEDLINE | ID: mdl-24055481

ABSTRACT

BACKGROUND: Urine alkalinization is indicated for various medical conditions. Alkalinization is usually achieved by intravenous administration of alkali substances titrated by repeated urinalyses. Some situations such as mass casualty events might require urine alkalinization by the oral route. We evaluated the efficacy of oral sodium bicarbonate administration for urine alkalinization. METHODS: In a prospective open-label trial, 4 g of sodium bicarbonate was administered orally 3 times daily to 9 healthy volunteers for 24 hours. Serial blood and urine samples were collected, and urine pH was evaluated. Plasma electrolytes and pH were also measured for safety purposes. RESULTS: All participants had a urine pH of at least 7 after 10 hours. At 20 hours, all participants had a urine pH of at least 8. No adverse effects or abnormal blood results were documented during the 24-hour follow-up. CONCLUSIONS: Oral administration of a standard dose of sodium bicarbonate tablets resulted in effective urine alkalinization. Further research is needed to investigate the natural course of urine pH after cessation of our protocol and the efficacy of longer periods of treatment.


Subject(s)
Sodium Bicarbonate/pharmacology , Urine/chemistry , Acute Kidney Injury/etiology , Acute Kidney Injury/prevention & control , Administration, Oral , Adult , Crush Syndrome/complications , Humans , Hydrogen-Ion Concentration/drug effects , Male , Middle Aged , Sodium Bicarbonate/administration & dosage , Young Adult
4.
Leuk Res ; 37(10): 1222-8, 2013 Oct.
Article in English | MEDLINE | ID: mdl-23937985

ABSTRACT

Peripheral absolute monocyte count (AMC) has been reported to correlate with clinical outcome in different types of cancers. This association may relate to alteration in circulating monocytic subpopulations and tumor infiltrating macrophages. In this study we evaluated the clinical significance of peripheral AMC in 80 treatment naive patients with CLL. Measurement of AMC was based on direct morphological enumeration, due to our findings that complete blood count data may yield incorrect monocytes enumeration values in CLL. The median AMC in patients with CLL was within normal limits, however the AMC range exceeded the values of healthy individuals. The AMC trichotomized patients into 3 distinct sub-groups with different characteristics and outcomes. High AMC patients were younger and had higher absolute lymphocytes count, while patients with low AMC had prominent immune dysregulation (lower serum IgA levels, susceptibility to infections and a tendency for positive direct anti-globulin test). The low and high AMC patients had a shorter time to treatment compared to the intermediates AMC subgroups, whereas low AMC was associated with increased mortality caused by infectious complications. In conclusion, AMC quantification during the disease course classifies CLL patients into subgroups with unique clinical features and outcomes.


Subject(s)
Leukemia, Lymphocytic, Chronic, B-Cell/diagnosis , Leukemia, Lymphocytic, Chronic, B-Cell/immunology , Monocytes/immunology , Adult , Aged , Aged, 80 and over , Disease Progression , Female , Humans , Immunoglobulin A/blood , Immunoglobulin A/immunology , Leukemia, Lymphocytic, Chronic, B-Cell/mortality , Leukocyte Count , Male , Middle Aged , Neoplasm Staging
5.
J Immunol ; 190(2): 784-93, 2013 Jan 15.
Article in English | MEDLINE | ID: mdl-23241880

ABSTRACT

Emerging data on intraclonal diversity imply that this phenomenon may play a role in the clinical outcome of patients with chronic lymphocytic leukemia (CLL), where subsets of the CLL clone responding more robustly to external stimuli may gain a growth and survival advantage. In this study, we report intraclonal diversity resolved by responses to CD19 engagement in CLL cells, which can be classified into CD19-responsive (CD19-R) and -nonresponive subpopulations. Engagement of CD19 by anti-CD19 Ab rapidly induced cellular aggregation in the CD19-R CLL cells. The CD19-R CLL cells expressed higher surface levels of CD19 and c-myc mRNA, exhibited distinct morphological features, and were preferentially abolished in rituximab-treated patients. Both subpopulations reacted to sIgM stimulation in a similar manner and exhibited similar levels of Akt and Erk phosphorylation, pointing to functional signaling divergence within the BCR. CD19 unresponsiveness was partially reversible, where nonresponding CD19 cells spontaneously recover their signaling capacity following incubation in vitro, pointing to possible in vivo CD19-signaling attenuating mechanisms. This concept was supported by the lower CD19-R occurrence in bone marrow-derived samples compared with cells derived from the peripheral blood of the same patients. CLL patients with >15.25% of the CD19-R cell fraction had a shorter median time to treatment compared with patients with <15.25% of CD19-R cell fraction. In conclusion, divergence in CD19-mediated signaling unfolds both interpatient and intraclonal diversity in CLL. This signaling diversity is associated with physiological implications, including the location of the cells, their responses to anti-CLL therapeutics, and disease progression.


Subject(s)
Antigens, CD19/metabolism , Leukemia, Lymphocytic, Chronic, B-Cell/metabolism , Signal Transduction , Antibodies, Monoclonal, Murine-Derived/pharmacology , Antineoplastic Agents/pharmacology , Cells, Cultured , Cholesterol/metabolism , Disease Progression , Humans , Leukemia, Lymphocytic, Chronic, B-Cell/genetics , Membrane Microdomains/chemistry , Membrane Microdomains/drug effects , Membrane Microdomains/metabolism , Rituximab , Signal Transduction/drug effects
6.
Pediatr Crit Care Med ; 14(2): 164-70, 2013 Feb.
Article in English | MEDLINE | ID: mdl-23254983

ABSTRACT

OBJECTIVES: To identify trends in early-onset sepsis and late-onset sepsis neonatal rates and to evaluate the appropriateness of the empirical antibiotic protocols. DESIGN: A 17-yr (1993-2009) analysis of positive blood and cerebrospinal fluid cultures. SETTING: The two neonatal ICUs at the Hadassah- Hebrew University Medical Center. RESULTS: During this period, 991 infants had at least one episode of either bacteremia or meningitis. The overall incidence of early-onset sepsis was 0.64 per 1,000 live births with a nonsignificant trend over the study period (p = 0.37). The overall incidence of late-onset sepsis was 7.5 per 100 admissions with a significant positive trend in the incidence rates (p = 0.021). The incidence of late-onset sepsis was 7.5 per 100 admissions with a significant positive trend in the prevalence rates (p = 0.021). The prevalence of early-onset group B Streptococcus bacteremia decreased significantly throughout the study period. Among late-onset sepsis, Gram-positive and fungi infection rates were stable over time, while Gram-negative infection rates showed a significant positive trend (p = 0.007). No significant change in the susceptibility rate of the isolated Gram-negative bacteria in late-onset sepsis for the common antibacterial drugs was found. About 85% and 90% of the isolated organisms were susceptible to our early-onset sepsis (ampicillin and gentamicin) and late-onset sepsis (vancomycin and cefotaxime) protocols, respectively, and these rates were stable over the study period (p = .1 and .55, respectively). Sepsis-related mortality was higher among Gram- negative sepsis cases resistant to our empiric antibiotic protocol. CONCLUSIONS: Our empiric antibiotic protocols are appropriate despite their continuous use over the last 17 yrs. This may have been achieved by the use of a controlled antibiotic program and infection control efforts.


Subject(s)
Anti-Bacterial Agents/therapeutic use , Bacteremia/epidemiology , Bacteremia/microbiology , Drug Resistance, Bacterial , Intensive Care Units, Neonatal/trends , Meningitis, Bacterial/epidemiology , Meningitis, Bacterial/microbiology , Bacteremia/mortality , Birth Weight , Escherichia coli Infections/epidemiology , Humans , Incidence , Israel/epidemiology , Klebsiella Infections/epidemiology , Klebsiella pneumoniae , Meningitis, Bacterial/mortality , Streptococcal Infections/epidemiology , Streptococcus agalactiae , Time Factors
7.
Pediatr Neurol ; 47(6): 427-30, 2012 Dec.
Article in English | MEDLINE | ID: mdl-23127263

ABSTRACT

The correlation between lamotrigine serum concentration, efficacy, and toxicity in children is controversial. The database of the Clinical Pharmacology Laboratory at Assaf Harofeh Medical Center was retrospectively searched to identify lamotrigine serum concentrations in children aged 2-19 years with refractory epilepsy who received lamotrigine as monotherapy or polytherapy from 2007-2010. Data collected included age at epilepsy onset, additional antiepileptic drugs, lamotrigine dose, monthly seizure frequency before and after lamotrigine treatment, and side effects. Sixty blood samples were collected from 42 children aged 10.1 ± 4.9 years (range, 2-20 years). Seizure types included complex partial (n = 28), simple partial (n = 7), absence (n = 2), and generalized tonic-clonic (n = 23). Decreased seizure frequency was observed in 38 (63.3%) patients. No correlation with lamotrigine serum concentration was evident, but seizure frequency was significantly influenced by age and lamotrigine dose. Side effects were reported in 21 (35%) patients. Only diplopia was significantly correlated with lamotrigine serum concentration. Lamotrigine was more effective at lower doses and in older children. Lamotrigine serum concentration correlated significantly with diplopia, but not with other side effects or with clinical efficacy. Overall, lamotrigine is effective and safe in children with refractory epilepsy.


Subject(s)
Anticonvulsants/blood , Epilepsy/blood , Epilepsy/drug therapy , Triazines/blood , Adolescent , Anticonvulsants/therapeutic use , Child , Child, Preschool , Female , Humans , Lamotrigine , Male , Retrospective Studies , Triazines/therapeutic use , Young Adult
8.
Harefuah ; 151(6): 342-5, 378, 2012 Jun.
Article in Hebrew | MEDLINE | ID: mdl-22991863

ABSTRACT

BACKGROUND: As of February 2010, the 2009 H1N1 influenza has caused more than 15,000 deaths worldwide. Seasonal influenza vaccination rates among health care workers (HCW) have been universally low; the 2009 H1N1 influenza vaccination of HCW has also been disappointing. In several studies, a correlation between HCW seasonal influenza vaccination status and vaccine recommendation to adult patients was found. OBJECTIVE: To examine the correlation between the declared influenza vaccination status of pediatric staff and vaccine recommendations to their patients. INSTRUMENT: Anonymous questionnaire concerning attitudes and practices regarding seasonal and 2009 H1N1 influenza vaccination. RESPONDENTS: 141 pediatric staff attending a conference. RESULTS: Seventy two percent of the respondents had been or intended to be vaccinated against seasonal influenza, 62% against the 2009 H1N1 influenza, and 56% against both diseases. Ambulatory setting employment was positively associated with the recommendation of seasonal influenza vaccination to all children. By multivariate Logistic regression analysis, the "vaccinated or intending to be vaccinated against seasonal influenza" was the only significant independent variable associated with recommending universal pediatric seasonal influenza vaccine (OR=15, 95% CI 6.1-41.4, p < 0.001). Similarly, "being or intending to be vaccinated against the 2009 H1N1 influenza" was the only significant independent variable associated with recommending universal pediatric vaccination against this disease (OR = 5.2, 95% CI 1.85-14.6, P = 0.002). CONCLUSION: A strong correlation between the influenza vaccination status of pediatric staff and the recommendation of the vaccines to children emphasizes that intense education of providers is a crucial step in assuring a positive recommendation to families.


Subject(s)
Influenza A Virus, H1N1 Subtype/immunology , Influenza Vaccines/therapeutic use , Influenza, Human , Medical Staff , Vaccination , Adult , Child , Child Health Services/methods , Child Health Services/standards , Directive Counseling , Female , Humans , Influenza, Human/epidemiology , Influenza, Human/prevention & control , Influenza, Human/transmission , Israel/epidemiology , Logistic Models , Male , Medical Staff/psychology , Medical Staff/standards , Needs Assessment , Professional-Patient Relations , Staff Development , Vaccination/psychology , Vaccination/statistics & numerical data
9.
J Pediatr ; 161(6): 1116-9, 2012 Dec.
Article in English | MEDLINE | ID: mdl-22727870

ABSTRACT

OBJECTIVE: To evaluate the association between recombinant human growth hormone (rhGH) treatment and intraocular pressure (IOP) in children. STUDY DESIGN: This is an observational cohort study including comparison between children treated with rhGH for at least 12 months (treatment group), matched children prior to treatment (control group), and population age-adjusted normograms of IOP. All children underwent an ocular slit lamp assessment and Goldmann applanation tonometry. Charts were reviewed for cause of therapy, peak stimulated growth hormone level prior to therapy, treatment duration, insulin-like growth factor 1, and rhGH dosage. RESULTS: The treatment group included 55 children and the control group included 24 children. Mean age at examination was comparable at 11.4 ± 3.3 years and 10.3 ± 2.6 years, respectively (P = .13). Mean treatment duration was 37.5 ± 22.8 months and mean rhGH dose was 0.04 ± 0.01 mg/kg/d. Mean IOP was significantly increased in the treatment group compared with the control group and compared with age-matched normograms (16.09 ± 2.2 mm Hg, 13.26 ± 1.83 mm Hg and 14.6 ± 1.97 mm Hg, respectively, P < .001). IOP was positively correlated with treatment duration (r = 0.559, P < .001) and rhGH dosage (r = 0.274, P = .043). CONCLUSION: IOP in children treated with rhGH is increased compared with a similar population without treatment and compared with healthy population normograms. IOP is associated with longer treatment duration and higher dosages.


Subject(s)
Human Growth Hormone/adverse effects , Intraocular Pressure/drug effects , Ocular Hypertension/chemically induced , Adolescent , Child , Cohort Studies , Dose-Response Relationship, Drug , Drug Administration Schedule , Female , Human Growth Hormone/administration & dosage , Humans , Male , Ocular Hypertension/diagnosis , Recombinant Proteins/administration & dosage , Recombinant Proteins/adverse effects , Reference Standards , Single-Blind Method , Time Factors , Tonometry, Ocular/standards
10.
Chemotherapy ; 58(2): 95-101, 2012.
Article in English | MEDLINE | ID: mdl-22377846

ABSTRACT

BACKGROUND: Despite the growing number of clinical trials assessing preoperative systemic chemotherapy (PST) for locally advanced breast cancer, the optimal regimen has still to be defined. PURPOSE: This was to evaluate the toxicity, operability rate, pathological response rate and disease-free and overall survival associated with a PST regimen consisting of the sequential administration of single agents according to the individual tumor response. METHODS: Medical files were reviewed of 102 consecutive patients with breast cancer treated in 2000-2007 with a neoadjuvant sequential regimen of doxorubicin followed by taxane. The number of cycles and the addition of taxane were based on tumor response. RESULTS: Seventy percent of the patients had inoperable disease at diagnosis and 29% were given preoperative therapy for breast conservation. All patients underwent surgery, 65% achieved breast conservation. An overall pathological complete response (breast and nodes) was achieved in 14% of the patients, and a complete nodal pathologic response in 34%. At a median follow-up of 54 months, the overall survival rate was 82% and the disease-free survival rate was 70%. There was no treatment-related mortality. Febrile neutropenia occurred in 19% of the patients. CONCLUSIONS: A neoadjuvant regimen of doxorubicin with or without a sequential taxane, in which the number of cycles and the sequential administration of taxane are determined according to clinical response, appears to be safe and effective for patients with locally advanced breast cancer and yields a high rate of breast conservation. Tailored PST can spare patients receiving unnecessary chemotherapy.


Subject(s)
Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Breast Neoplasms/pathology , Neoadjuvant Therapy , Adult , Aged , Breast Neoplasms/drug therapy , Breast Neoplasms/mortality , Bridged-Ring Compounds/administration & dosage , Doxorubicin/administration & dosage , Female , Follow-Up Studies , Humans , Kaplan-Meier Estimate , Middle Aged , Neoplasm Staging , Prospective Studies , Receptor, ErbB-2/metabolism , Taxoids/administration & dosage
11.
Mayo Clin Proc ; 87(2): 136-42, 2012 Feb.
Article in English | MEDLINE | ID: mdl-22226833

ABSTRACT

OBJECTIVE: To determine the role of bone marrow biopsy (BMBX), performed in association with comprehensive blood and imaging tests, in the evaluation of patients with fever of unknown origin (FUO). PATIENTS AND METHODS: We reviewed the medical records of 475 hospitalized patients who underwent BMBX in our medical center from January 1, 2005, to April 30, 2010. We identified 75 patients who fulfilled the accepted classic Petersdorf criteria for FUO. All patients underwent in-hospital investigation for fever, including chest and abdominal computed tomography. RESULTS: In 20 patients (26.7%), BMBX established the final diagnosis. Sixteen patients had hematologic disorders, including 8 patients with non-Hodgkin lymphoma, 2 with acute leukemia, 1 with multiple myeloma, 1 with myelodysplastic syndrome, and 4 with myeloproliferative disorders. The remaining patients with diagnostic BMBX specimens had solid tumors (2 patients), granulomatous disease (1 patient), and hemophagocytic syndrome (1 patient). Multivariate analysis revealed the following as the significant positive predictive parameters for a diagnostic BMBX specimen: male sex (odds ratio [OR], 7.35; 95% confidence interval [CI], 1.19-45.45), clinical lymphadenopathy (OR, 21.98; 95% CI, 1.97-245.66), anemia (OR, 2.21; 95% CI, 1.28-3.80), and increased lactate dehydrogenase levels (OR, 1.003; 95% CI, 1.001-1.006). CONCLUSION: Bone marrow biopsy is still a useful ancillary procedure for establishing the diagnosis of FUO, particularly if used in the appropriate clinical setting. Clinical and laboratory parameters associated with hematologic disease are predictive of a diagnostic BMBX specimen in patients with FUO.


Subject(s)
Bone Marrow/pathology , Fever of Unknown Origin/diagnosis , Hematologic Diseases/diagnosis , Lymphohistiocytosis, Hemophagocytic/diagnosis , Lymphoma, Non-Hodgkin/diagnosis , Multiple Myeloma/diagnosis , Neoplasms/diagnosis , Adult , Aged , Biopsy , Female , Fever of Unknown Origin/etiology , Hematologic Diseases/complications , Hematologic Diseases/pathology , Humans , Leukemia/complications , Leukemia/diagnosis , Leukemia/pathology , Lymphohistiocytosis, Hemophagocytic/complications , Lymphohistiocytosis, Hemophagocytic/pathology , Lymphoma, Non-Hodgkin/complications , Lymphoma, Non-Hodgkin/pathology , Male , Middle Aged , Multiple Myeloma/complications , Multiple Myeloma/pathology , Neoplasms/complications , Neoplasms/pathology , Predictive Value of Tests , Sensitivity and Specificity
12.
Emerg Med J ; 29(9): 709-14, 2012 Sep.
Article in English | MEDLINE | ID: mdl-21900297

ABSTRACT

OBJECTIVE: To determine whether variables in physicians' backgrounds influenced their decision to forego resuscitating a patient they did not previously know. METHODS: Questionnaire survey of a convenience sample of 204 physicians working in the departments of internal medicine, anaesthesiology and cardiology in 11 hospitals in Israel. RESULTS: Twenty per cent of the participants had elected to forego resuscitating a patient they did not previously know without additional consultation. Physicians who had more frequently elected to forego resuscitation had practised medicine for more than 5 years (p=0.013), estimated the number of resuscitations they had performed as being higher (p=0.009), and perceived their experience in resuscitation as sufficient (p=0.001). The variable that predicted the outcome of always performing resuscitation in the logistic regression model was less than 5 years of experience in medicine (OR 0.227, 95% CI 0.065 to 0.793; p=0.02). CONCLUSION: Physicians' level of experience may affect the probability of a patient's receiving resuscitation, whereas the physicians' personal beliefs and values did not seem to affect this outcome.


Subject(s)
Attitude of Health Personnel , Physicians/psychology , Resuscitation Orders/psychology , Adult , Clinical Competence , Decision Making , Female , Humans , Israel , Logistic Models , Male , Middle Aged , Physician-Patient Relations , Referral and Consultation , Self Report
13.
Am J Clin Oncol ; 34(6): 619-24, 2011 Dec.
Article in English | MEDLINE | ID: mdl-21217400

ABSTRACT

PURPOSE: This prospective, nonrandomized study evaluates 4 schedules of granulocyte colony-stimulating factor (G-CSF) for patients with breast cancer receiving adjuvant dose-dense chemotherapy regarding febrile neutropenia, treatment delays, and costs. PATIENTS AND METHODS: Two hundred and thirty-one patients were enrolled to receive adjuvant dose-dense chemotherapy with 4 G-CSF schedules: filgrastim (300 mcg) days 3 to 10 [n = 84 (36.4%) group A]; days 3 to 7 [n = 26 (11.3%) group B]; days 5, 7, 9, and 11 [n = 64 (27.7%) group C], or pegfilgrastim (6 mg) on day 2 [n=57 (24.6%) group D]. RESULTS: Thirteen patients were hospitalized due to 14 episodes of febrile neutropenia; 3 in group A, 3 in group B, 1 in group C, and 6 in group D. No statistically significant difference was observed among the 4 groups. Fewer febrile neutropenic events were observed in group C than in group D (P=0.041). No statistically significant differences were observed in treatment delays or other hematological toxicities. Average overall G-CSF cost per patient in groups A and D was $8500 versus $4400 in groups B and C. CONCLUSIONS: We found a trend in favor of the shorter G-CSF schedule. A larger, prospective randomized trial should be carried out to evaluate shorter versus standard filgrastim and pegfilgrastim schedules with regard to clinical outcomes, hematological and nonhematological toxicities, and impact in costs.


Subject(s)
Breast Neoplasms , Granulocyte Colony-Stimulating Factor/administration & dosage , Neutropenia/drug therapy , Adult , Aged , Antineoplastic Combined Chemotherapy Protocols/adverse effects , Breast Neoplasms/drug therapy , Chemotherapy, Adjuvant/adverse effects , Female , Filgrastim , Granulocyte Colony-Stimulating Factor/economics , Humans , Male , Middle Aged , Neutropenia/chemically induced , Neutropenia/economics , Polyethylene Glycols , Recombinant Proteins/administration & dosage , Recombinant Proteins/economics
14.
Cancer Epidemiol ; 35(1): 11-6, 2011 Feb.
Article in English | MEDLINE | ID: mdl-21163720

ABSTRACT

BACKGROUND: The publication of the Women's Health Initiative Study in 2002 spurred reductions in hormone replacement therapy (HRT) use worldwide. Subsequent drops in breast cancer incidence have since been reported. We used person-level data from a large Israeli health plan to study the relationship between HRT use and breast cancer incidence. METHODS: We accessed pharmacy, mammography and cancer registry data for women ages 50 and over. Using Chi-square analysis, we examined changes over time in HRT and mammography utilization and breast cancer incidence [invasive and ductal carcinoma in situ (DCIS)]. Using calendar year-specific Cox proportional hazards analyses, we estimated the hazard of recent HRT use on cancer incidence. We used locally weighted scatterplot smoothing (LOWESS) and autoregressive integrated moving average (ARIMA) modeling to further examine this association. RESULTS: The study population ranged from 118,724 in 2000 to 154,447 in 2007. Thirteen percent of study women purchased HRT in 2000, vs. 4.0% in 2007 (p<0.001). Breast cancer incidence rose from 3.8/1000 to 4.3/1000 in 2005; the proportion of women undergoing mammography rose from 8% in 2000 to a peak of 34.1% in 2005 (p<0.001). Hazard ratios for the association of HRT with breast cancer ranged from 1.2 to 2.4. ARIMA demonstrated the association of both mammography (in the same month) and HRT use (in the preceding month) with cancer incidence. CONCLUSION: This study demonstrates the competing impacts of HRT and mammography on cancer incidence. Our findings support the conclusion that changes in HRT utilization are linked to reductions in breast cancer incidence.


Subject(s)
Breast Neoplasms/epidemiology , Hormone Replacement Therapy/trends , Adult , Aged , Female , Humans , Incidence , Middle Aged , Prognosis
15.
Basic Clin Pharmacol Toxicol ; 107(3): 737-41, 2010 Sep.
Article in English | MEDLINE | ID: mdl-20374236

ABSTRACT

Acute iron intoxication is one of the leading causes of overdose morbidity and mortality in children. The toxicity of iron has been postulated to be related to free radical formation and subsequent lipid peroxidation. Hyperbaric oxygen treatment can result in a number of beneficial biochemical, cellular and physiological effects, and has recently been shown to induce cellular protection against ischaemia, and in some cases against free radical formation. In the current study, we aimed to investigate the effects of hyperbaric oxygen treatment on mortality in acute iron intoxication in rats. After iron administration, 57 animals were divided into two groups: a treatment group receiving hyperbaric oxygen treatment (n = 30) and a control group (n = 27), and followed for 48 hr for signs of severe intoxication. In the second part of the study, 21 animals were divided into a treatment group receiving hyperbaric oxygen treatment (n = 10) and a control group (n = 11), and markers of oxidative stress were evaluated. We showed a significant reduction in mortality in hyperbaric oxygen-treated animals from 17 of 27 (62.9%) among untreated rats to 6 of 30 (20%). Surprisingly, in the treatment group, levels of oxidative stress markers were higher. We postulate that hyperbaric oxygen has a potentially beneficial effect in acute iron intoxication.


Subject(s)
Hyperbaric Oxygenation , Iron/poisoning , Animals , Male , Poisoning/mortality , Poisoning/therapy , Rats , Rats, Wistar , Toxicity Tests, Acute
16.
Pediatrics ; 125(2): e318-23, 2010 Feb.
Article in English | MEDLINE | ID: mdl-20100745

ABSTRACT

OBJECTIVE: An apparent life-threatening event (ALTE) caused by ingestion of drugs or toxins has been reported rarely among infants. None of these agents was homeopathic medication. We report 11 infants who presented with an ALTE after ingestion of Gali-col Baby, a homeopathic agent indicated for "infantile colic." METHODS: A retrospective case-control study was conducted. Charts of all infants who were younger than 1 year and were admitted with an ALTE from January 2005 through August 2008 to the pediatric division at the Barzilai Medical Center were reviewed. Age-matched infants who were admitted on the same dates for a reason other than ALTE served as a control group. Information on medications administered before admission was recorded. RESULTS: During the study period, 36 635 children visited the pediatric emergency department of the Barzilai Medical Center. There were 11 057 admissions to the pediatric division during this period, 115 of which were because of an ALTE. Eleven of these infants received Gali-col Baby before the event as opposed to none in the control group (P < .005). Three infants received a significant overdose, compared with the manufacturer's recommended dosage. After a thorough investigation, no other presumptive causes for ALTE were found among the 11 infants. CONCLUSIONS: Gali-col Baby is associated with an ALTE in some infants. There are no published controlled trials on the efficacy or safety of its use; therefore, better control and supervision of Gali-col Baby and probably other homeopathic medications are needed to prevent possible serious adverse effects.


Subject(s)
Apnea/chemically induced , Colic/drug therapy , Materia Medica/adverse effects , Plant Preparations/adverse effects , Case-Control Studies , Emergency Service, Hospital , Female , Humans , Infant , Infant, Newborn , Male
17.
J Hum Lact ; 25(2): 194-8, 2009 May.
Article in English | MEDLINE | ID: mdl-19286839

ABSTRACT

In this preliminary prospective study, breast milk is sampled surrounding 4 religious fast days to determine the effect of a more than 24-hour fast on breast milk composition. The participants are 48 healthy women nursing healthy babies between 1 and 6 months of age. Samples are collected within 2 days before the fast (baseline), immediately after the fast, and 24 hours after fast completion. Samples are tested for sodium, calcium, phosphorus, triglycerides, total protein, and lactose. From baseline to immediately after fast, mean sodium, calcium, and protein levels increase (P = .013, P < .0001, and P < .0001, respectively) and mean phosphorus and lactose levels decrease (P < .0001 and P = .003, respectively). Mean triglycerides are unchanged. Twenty-four hours after fast, parameters are no longer significantly different from baseline except for elevated mean protein levels (P = .022) and lactose that is still reduced (P = .017). A fast of this nature is statistically associated with certain biochemical changes in breast milk.


Subject(s)
Fasting/metabolism , Lactose/analysis , Milk Proteins/analysis , Milk, Human/chemistry , Adult , Calcium/analysis , Female , Humans , Phosphorus/analysis , Prospective Studies , Religion , Sodium/analysis , Triglycerides/analysis , Young Adult
18.
Acta Paediatr ; 98(2): 266-9, 2009 Feb.
Article in English | MEDLINE | ID: mdl-19021590

ABSTRACT

AIM: To quantify the number of chest and abdominal radiograms performed in surviving singleton extremely low birth weight (ELBW) infants in order to examine whether changes in imaging application occurred during the last 21 years (1987-2007). METHODS: Clinical and radiological data of 225 out of 229 surviving infants were obtained and associations with time and clinical variables were evaluated. RESULTS: The number of chest X-Rays performed per infant was 10.3 +/- 11.1 (mean +/- SD), median = 7; range = 0-77 and the number of abdominal radiograms was 5.6 +/- 7.1, median = 3; range = 0-61. The number of chest and abdominal X-Rays performed per patient during 1987-1996 was very similar to that of 1997-2007, and no appreciable change of trend was observed along the years. There were negative and statistically significant correlations between the gestational age and the number of radiograms performed per patient (chest X-Rays: r =-0.402; p < 0.001, abdominal X-Rays: r =-0.182; p = 0.006). Controlling for gestational age, reduced numbers of radiograms per patient (abdominal: b =-1.20, p = 0.235; chest: b =-3.08, p = 0.035) were demonstrated in the second period. Patients with complicated clinical course were exposed to significantly more radiograms. CONCLUSION: Controlling for gestational age, a reduced number of exposures to chest radiograms was demonstrated during 1997-2007 compared with 1987-1996. Measures to reduce radiation, especially in complicated cases, are advocated.


Subject(s)
Infant, Extremely Low Birth Weight , Radiography, Abdominal/statistics & numerical data , Radiography, Thoracic/statistics & numerical data , Humans , Infant, Newborn , Longitudinal Studies
19.
Isr Med Assoc J ; 10(6): 457-61, 2008 Jun.
Article in English | MEDLINE | ID: mdl-18669147

ABSTRACT

BACKGROUND: A substantial number of premature deliveries occur in hospitals lacking neonatal intensive care facilities. We previously demonstrated a comparable outcome of very low birth weight infants delivered in a level II nursery to that of inborn infants delivered in our tertiary care center, but a similar comparison of extremely low birth weight infants has not been done. OBJECTIVES: To compare the neonatal outcome (mortality, severe intraventricular hemorrhage/periventricular leukomalacia, bronchopulmonary dysplasia and intact survival) of inborn and outborn ELBW infants, accounting for sociodemographic, obstetric and perinatal variables. METHODS: We compared 97 ELBW infants (birth weight < or = 1000 g) delivered between the years 2000 and 2004 in a hospital providing neonatal intensive care to 53 ELBW babies delivered in a referring hospital. A univariate model was first applied to examine the associations of the individual independent variables with the outcome variable, followed by a logistic stepwise regression analysis for each of the outcome variables. The odds ratios for each predictor were reported as well as their P values and 95% confidence intervals. RESULTS: In the stepwise logistic regression analysis, accounting for a possible confounding effect of the independent variables, 'hospital of birth' remained a statistically significant predictor in the final step only for mortality, with odds ratio (inborns relative to outborns) of 3.32 (95% CI 1.19-9.28, P = 0.022). No statistically significant associations with the other outcome variables were found (severe IVH/PVL odds ratio = 1.99, 95% CI = 0.77-5.14, P = 0.155; BPD odds ratio = 0.60, 95% CI = 0.19-1.91, P= 0.384; intact survival OR = 0.56, 95% CI = 0.23-1.35, P = 0.195). CONCLUSIONS: ELBW outborn infants may share an outcome comparable with that of inborn babies, if adequate perinatal care is provided.


Subject(s)
Infant Welfare , Infant, Extremely Low Birth Weight , Intensive Care, Neonatal , Perinatal Care , Adult , Bronchopulmonary Dysplasia/epidemiology , Cerebral Hemorrhage/epidemiology , Cerebral Ventricles , Female , Gestational Age , Humans , Infant Mortality , Infant, Newborn , Intensive Care Units, Neonatal/statistics & numerical data , Leukomalacia, Periventricular/epidemiology , Logistic Models , Male , Odds Ratio , Risk Factors , Treatment Outcome
20.
Clin Infect Dis ; 46(12): 1859-63, 2008 Jun 15.
Article in English | MEDLINE | ID: mdl-18462172

ABSTRACT

BACKGROUND: The mouth is the most common site for measuring temperature. Oral mucositis may affect up to 40% of patients who receive chemotherapy. Thus far, mucositis has not been studied with regard to accurate thermometry. METHODS: One hundred consecutive patients (25 per group) were self-referred on the basis of perception of mucositis, temperature measurement at home, or malaise or were referred by a nurse on the basis of an assessment of a potential infectious process and/or mucositis. Oral and tympanic temperature were assessed simultaneously in patients with no fever and no mucositis (group A), those with mucositis (group B), those with fever and no mucositis (group C), and those with neutropenia but not fever or mucositis (group D). RESULTS: The 4 groups of patients had higher oral temperatures than tympanic temperatures (group A, 36.9 degrees C vs. 36.8 degrees C [delta = 0.12 degrees C; P = .062]; group B, 38.0 degrees C vs. 37.1 degrees C [delta = 0.89 degrees C; P < .001]; group C, 38.7 degrees C vs. 38.4 degrees C [delta = 0.27 degrees C; P < .001]; and group D, 37.0 degrees C vs. 36.7 degrees C [delta = 0.27 degrees C; P < .001]). Scheffe a-posteriori test revealed that only the delta temperature in group B differed significantly (95% confidence limits, -2.471, -1.584; P < .001). A linear regression model that examined the effect of other variables on the delta temperature found that only mucositis was a significant factor (95% confidence limits, 0.582, 0.820; P < .001). CONCLUSIONS: Mucositis causes an increase in oral temperature but does not elevate systemic body temperature, thereby casting doubt on the diagnosis of infection. Conceivably, mucositis may provide an "inflammation bias" that could lead to the overuse of antibiotics and growth factors in 20%-40% of patients with cancer. When one considers issues of antimicrobial resistance and cost, this concern should be tested and clarified in a prospective study based on accurate temperature measurement.


Subject(s)
Body Temperature , Communicable Diseases/diagnosis , Mouth/physiopathology , Mucositis , Aged , Female , Humans , Male , Middle Aged , Prospective Studies
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