The Use of Platelet Antibody Testing at a Tertiary Medical Center.

Blood ◽  
2004 ◽  
Vol 104 (11) ◽  
pp. 3631-3631
Author(s):  
Beth H. Shaz ◽  
Margot S. Kruskall

Abstract Detection of platelet antibodies is often helpful in the diagnosis of platelet transfusion refractoriness (PR), neonatal alloimmune thrombocytopenia (NAIT), and post-transfusion purpura (PTP), but is controversial in idopathic thrombocytopenia purpura (ITP). We performed a retrospective chart review to determine the utilization and value of a solid-phase ELISA assay consisting of 6 wells coated with platelet glycoproteins (GP), and one well with HLA class I antigens (GTI PakPlus, Brookfield WI) at our medical center. For a 3 year period between June 2001 and June 2004, 183 tests for 163 patients were ordered for the following diagnostic questions: 151 tests for ITP, 19 for PR, 6 for NAIT, 2 for transfusion-related acute lung injury (TRALI), 5 for unclear reasons, and none for PTP. The mean patient age was 55 (range 12 – 94), 55% were male, 50% were inpatients, and the mean platelet count (excluding mothers with NAIT and a patient with TRALI) was 60x109/l (range 5–215 x 109/l). There were 48 patients who had 51 positive tests (28%), of which 61% were inpatients. The mean platelet count was 47 x 109/l (range 5–115 x 109/l). Only one or more GP wells were positive in 57% of positive tests, only the HLA class I well was positive in 27%, and ≥one GP well plus the HLA well were positive in 16%. To determine how results were used, we reviewed the medical records associated with each positive test. Out of 51 positive tests, no mention was made of the test order or result in 21 (41%). For 6 tests (12%), the order was noted, but no results were mentioned. In the other 24 tests, the result was used to make a diagnosis in 12 cases (3 NAIT, 3 PR, 6 ITP), and in 12 the result was used to confirm an already known diagnosis (1 NAIT, 4 PR, 7 ITP). Therapy was started before the test was completed on 17 occasions (4 PR, 13 ITP). Eighteen patients had repeat testing (38 tests). The interval of time between tests was 112 days on average (range 8–365), including 5 sets within 28 days. The results were unchanged in 11 patients (61%); in 5 patients GP wells changed from positive to negative; and in 2 patients the HLA well changed, including a patient with pre- and post-transfusion samples for evaluation of TRALI, and another in whom the test went from positive to negative. In 3 mothers evaluated for NAIT with positive results (1 HPA-1a, 2 HPA-5b), confirmation was obtained at a reference laboratory (Blood Center for Southeastern Wisconsin). A total of fifteen patients were evaluated for PR with 19 samples. Seventeen samples underwent parallel testing (HLA lymphocytotoxic antibody screen alone, or with platelet antibody detection at the reference laboratory); 13 results (76%) were confirmed. All four mismatches were between the HLA ELISA well and the HLA antibody screen: in 2 samples the PakPlus was positive but the HLA antibody screen was negative; in the other 2 a negative HLA well was accompanied by a high PRA (63%, 80%). These results demonstrated that 1) the ELISA assay was routinely negative in patients with platelet counts >115 x 109/l; 2) 53% of positive results were ignored in the medical records; 3) the test had a moderate reproducibility (61%), but could have been related to clinical changes in the patients; and 4) the yield of clinically useful information for patients with ITP (151 tests, 13 positive results utilized for clinical management) was low. For PR, the PakPlus is reliable but only qualitative, compared to the quantitative HLA antibody screen. The test appears most useful for rapid antibody identification in NAIT and is of limited clinical utility for ITP.

Diagnostics ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 244
Author(s):  
Kei Yoneda ◽  
Naoto Kamiya ◽  
Takanobu Utsumi ◽  
Ken Wakai ◽  
Ryo Oka ◽  
...  

(1) Background: This study aimed to evaluate the associations of lymphovascular invasion (LVI) at first transurethral resection of bladder (TURBT) and radical cystectomy (RC) with survival outcomes, and to evaluate the concordance between LVI at first TURBT and RC. (2) Methods: We analyzed 216 patients who underwent first TURBT and 64 patients who underwent RC at Toho University Sakura Medical Center. (3) Results: LVI was identified in 22.7% of patients who underwent first TURBT, and in 32.8% of patients who underwent RC. Univariate analysis identified ≥cT3, metastasis and LVI at first TURBT as factors significantly associated with overall survival (OS) and cancer-specific survival (CSS). Multivariate analysis identified metastasis (hazard ratio (HR) 6.560, p = 0.009) and LVI at first TURBT (HR 9.205, p = 0.003) as significant predictors of CSS. On the other hand, in patients who underwent RC, ≥pT3, presence of G3 and LVI was significantly associated with OS and CSS in univariate analysis. Multivariate analysis identified inclusion of G3 as a significant predictor of OS and CSS. The concordance rate between LVI at first TURBT and RC was 48.0%. Patients with positive results for LVI at first TURBT and RC displayed poorer prognosis than other patients (p < 0.05). (4) Conclusions: We found that the combination of LVI at first TURBT and RC was likely to provide a more significant prognostic factor.


2020 ◽  
Vol 58 (12) ◽  
Author(s):  
Kyle G. Rodino ◽  
Michel Toledano ◽  
Andrew P. Norgan ◽  
Bobbi S. Pritt ◽  
Matthew J. Binnicker ◽  
...  

ABSTRACT Shotgun metagenomic sequencing can detect nucleic acids from bacteria, fungi, viruses, and/or parasites in clinical specimens; however, little data exist to guide its optimal application to clinical practice. We retrospectively reviewed results of shotgun metagenomic sequencing testing requested on cerebrospinal fluid samples submitted to an outside reference laboratory from December 2017 through December 2019. Of the 53 samples from Mayo Clinic patients, 47 were requested by neurologists, with infectious diseases consultation in 23 cases. The majority of patients presented with difficult-to-diagnose subacute or chronic conditions. Positive results were reported for 9 (17%) Mayo Clinic patient samples, with 6 interpreted as likely contamination. Potential pathogens reported included bunyavirus, human herpesvirus 7, and enterovirus D-68, ultimately impacting care in two cases. Twenty-seven additional samples were submitted from Mayo Clinic Laboratories reference clients, with positive results reported for three (11%): two with potential pathogens (West Nile virus and Toxoplasma gondii) and one with Streptococcus species with other bacteria below the reporting threshold (considered to represent contamination). Of 68 negative results, 10 included comments on decreased sensitivity due to high DNA background (n = 5), high RNA background (n = 1), insufficient RNA read depth (n = 3), or quality control (QC) failure with an external RNA control (n = 1). The overall positive-result rate was 15% (12/80), with 58% (7/12) of these interpreted as being inconsistent with the patient’s clinical presentation. Overall, potential pathogens were found in a low percentage of cases, and positive results were often of unclear clinical significance. Testing was commonly employed in cases of diagnostic uncertainty and when immunotherapy was being considered.


Respiration ◽  
2020 ◽  
Vol 99 (9) ◽  
pp. 739-747
Author(s):  
Yupeng Li ◽  
Yu Shang ◽  
Yi Yang ◽  
Menghan Wang ◽  
Dongping Yu ◽  
...  

<b><i>Background:</i></b> Coronavirus disease 2019 (COVID-19) has become a global emerging infectious disease. <b><i>Objectives:</i></b> To analyze the initial clinical characteristics of COVID-19 suspected and confirmed patients on admission in order to find out which kinds may be more likely to get positive nucleic acid testing results, and to explore the risk factors associated with all-cause death. <b><i>Methods:</i></b> Medical records from 309 highly suspected cases with pneumonia were collected from February 13, 2020, to March 14, 2020, in a COVID-19-designated hospital of Wuhan. The majority of the clinical data were collected on the first day of hospital admission. <b><i>Results:</i></b> Of 309 patients with median age 64 years (interquartile ranges [IQR], 53–72 years), 111 patients (35.9%) were confirmed by nucleic acid testing (median age 64 years, IQR: 56–71 years; 48 males). Of those 111 patients, 13 (11.7%) patients died. In multivariate analysis, factors associated with positive testing included fatigue (odds ratios [OR] = 3.14; 95% confidence interval [CI]: 1.88–5.24, <i>p</i> &#x3c; 0.001), cough (OR = 0.55; 95% CI: 0.32–0.95, <i>p</i> = 0.032), no less than 1 comorbidity (OR = 1.77; 95% CI: 1.06–2.98, <i>p</i> = 0.030), and severe pneumonia (OR = 2.67; 95% CI: 1.20–5.97, <i>p</i> = 0.016). Furthermore, age, dyspnea, noneffective antibiotic treatment, white blood cell, lymphocyte, platelets, and organ dysfunction (e.g., higher lactate dehydrogenase) were significantly associated with all-cause in-hospital death in patients with COVID-19. <b><i>Conclusion:</i></b> Patients with severe forms of this disease were more likely to get positive results. Age and organ dysfunction were associated with a greater risk of death.


Blood ◽  
2005 ◽  
Vol 106 (11) ◽  
pp. 3739-3739
Author(s):  
A. Majid Shojania ◽  
Kenneth von Kuster

Abstract Since 1999, due to mandatory fortification of grain products with folic acid, folate deficiency has become very rare. We elected to find out whether there is still any justification in ordering folate assays in medical practice. Methods: All the Red cell folates (RFA) at St. Boniface General Hospital (SBGH) for the period of January 1, 1996–Dec 31, 2001 and all of serum folates (SFA) and RFAs at Health Sciences Centre (HSC) for the period of January 1-December 31, 2001 were reviewed. The medical records of all patients who had low SFA or RFA were reviewed to find the cause of low folate results. At SBGH L. Casei microbiological assay and at HSC, a competitive binding assay of folates was used. Results: Among 2153 SFAs performed at HSC 10 (0.46%) were below normal. All 10 were anemic but their SFAs were not as low as those seen in folate deficiency anemia. Only one case had a high mean corpuscular volume (MCV). This patient had ethanol induced pancreatitis and his macrocytosis was considered to be due to ethanol abuse. Two patients had celiac disease. In the other seven patients there was no evidence of folate deficiency anemia and no explanation could be found from the review of their medical records as to why their SFAs were low. Among 560 RFAs performed at HSC, 4 patients (0.7%) had low RFAs. In one case, the low RFA was due to B12 deficiency. The second case was the same patient with ethanol induced pancreatitis who also had low SFA. The other two had celiac disease. AT SBGH, there was a progressive increase in mean RFA and a decrease in percentage of those with low RFA during each year in the period between 1996 and 2001. In 1996 the mean RFA was 509 nmol/L and 95 out of 511 (18.5%) had low RFA. During the 3 year period of 1999–2001, the mean RFA was 947 nmol/L and 19 out of 991(1.6%) RFAs were low. Of these 19 patients, 9 were ethanol abusers with alcoholic liver disease, 7 had celiac disease, two had low RFA due to severe B12 deficiency and one was an AIDS patient who was admitted because of extreme malnutrition and had a low RFA, a low serum B12 (SB12) and a low serum ferritin. Of 7 patients with celiac disease, only one had had a high MCV. Discussion: There are generally three reasons why physicians order folate assays. The most common reason is to detect folate deficiency as the cause of anemia. Our study shows that folate deficiency is now very rare. In none of the patients with low SFA or RFA could we attribute the anemia to folate deficiency. The second reason is for investigation of hyperhomocysteinemia. Since folate deficiency is now very rare and management of hyperhomocysteinemia is the same whether SFA or RFA are low or normal, having SFA or RFA result would not change the patient’s management. The third reason for ordering RFA is for screening for malabsorption syndrome. During 30 months period of July 1, 1999–December 31, 2001, the search of the Laboratory Information System at SBGH, revealed 29 patients with serological evidence of celiac disease, who also had SFA or RFA results. Of these 29, five had low SFAs and two had low RFAs. Conclusion: We find very little support for the need to order serum or red cell folate in medical practice. In those rare occasions, when folate deficiency is suspected by the patient’s history or laboratory findings, it is simpler and more economical to treat the patient with folic acid (as long as one makes sure the SB12 is normal) than ordering folate assays and waiting for the results that most likely going to be normal.


2009 ◽  
Vol 161 (2) ◽  
pp. 231-235 ◽  
Author(s):  
Peter Kamenicky ◽  
Christine Dos Santos ◽  
Consuelo Espinosa ◽  
Sylvie Salenave ◽  
Françoise Galland ◽  
...  

ContextA discrepancy between serum GH and IGF1 concentrations is frequent in patients with acromegaly. Here, we examined whether the exon 3-deleted (d3) GH receptor (GHR) variant, which has been linked to increased responsiveness to GH treatment in short children, influences the GH/IGF1 relationship in patients with acromegaly.ObjectiveTo study the possible influence of the GHR genotype on the GH/IGF1 relationship in untreated acromegalic patients.DesignGHR genotype analysis with retrospective clinical and biochemical data collection performed in a single third-reference medical center.Patients and methodsClinical data were obtained from the medical records of 105 acromegalic patients who had GH and IGF1 assays in the same laboratory and who were genotyped for the full-length (fl) or d3-GHR alleles.ResultsThe distribution of GHR genotypes was 51% fl/fl, 30% fl/d3, and 19% d3/d3. Patients with d3/d3 genotype were younger than the patients in the other two groups (P<0.05). Baseline GH and IGF1 concentrations did not differ among the three groups. The linear correlation between GH and IGF1 concentrations was similar in the three genotypic groups.ConclusionsThe exon 3 GHR genotype does not affect the GH/IGF1 relationship in untreated acromegalic patients with high circulating GH and IGF1 levels.


1941 ◽  
Vol 41 (2) ◽  
pp. 180-196 ◽  
Author(s):  
H. Barkworth ◽  
J. O. Irwin

1. The primary aim of the experiment was to find out if certain combinations of container and gas tube give a greater proportion of positive results than others (with the same strength of inoculation) and if possible to elucidate the causes of any differences between combinations.The earlier results indicated that the best combination was a 7 × 1 ½ in. test-tube with a 4 × ¾ in. gas tube. Later experiments failed to maintain this preference but did show a definite disadvantage in using a very small gas tube. Whether this is due to the absolute sinallness of the gas tube or the smallness of its volume relative to the total amount of liquid used cannot be decided, for the latter was the same in all combinations. This was the only shape or sizefactor that was definitely influential on the evidence of these experiments. Yet if size of gas tube is intrinsically important the absence of reactions with acid but no gas is puzzling.Attempts to break down the points involved in changes in shape and size of gas tube and container into a number of simple factors showed that several considerations might be involved, too many to cover in one experimental lay-out; but by including extreme combinations it was hoped that some indication might be obtained of the more important factors. With the new and successful combination of 7 × 1½ in. test-tube with 4 × ¾ in. gas tube, the gas tube holds 22% of the total volume of medium plus inoculum, the same proportion as the standard 6 × ⅝ in. test-tifbe and in. gas tube. This seems to be in support of standard practice if it is relative volumes that are important.2. The analysis of plate counts shows that the opacity method, with the strain employed, gives complete control of the population and the three methods of assessing the plate count were in good agreement with one another.The χ2 values were as a rule subnormal. This result excludes the possibility of any lack of control of the population in any one set of plates, but the reason for the subnormality is of some interest. It may plausibly be attributed to the factor of competition among developing colonies for the nutrient medium available so that the chance of development of a colony is smaller when a large number of others are present than when there are only a few. A toxic emanation from a colony which excluded the formation of another colony within a certain distance of it would have the same effect.3. In the main experiment the percentage of positive tubes was about half (20% as against 45%) that to be expected from the plate counts on the usual Poisson hypothesis; or looking at the matter the other way the mean number of organisms per tube (0·22) deduced from the percentage of positives was about half the 0·5 expected from the plate counts. We have found no reason for this and in two subsequent experiments the agreement was satisfactory.4. No difference was found between 2 × ⅜ and If in. gas tubes with a 6 × ⅝ in. test-tube or between rimmed and rimless gas tubes.


2018 ◽  
Vol 2018 ◽  
pp. 1-5
Author(s):  
Yoav Y. Pikkel ◽  
Daniel Krebs ◽  
Vadim Igal ◽  
Adi Sharabi-Nov ◽  
Irena Epstein ◽  
...  

Purpose. To find if CHA2DS2-VASc scale can accurately predict the treatment, prognosis, and outcome for primary open-angle glaucoma (POAG). Patients and methods. A survey of 250,000 patient years was taken, using the records of the Ophthalmology Department at Ziv Medical Center. Data was collected regarding the retinal nerve fiber layer (RNFL), visual field (VF), line of treatment (LOT) of glaucoma, and all the data needed to accurately calculate CHA2DS2-VASc score for each patient. Results. Sixty-seven patients were included in the statistical analysis. The mean age was 72.5 years. The mean CHA2DS2-VASc score was 3.27 + −1.7. Positive Pearson’s correlation coefficients were found for LOT and CHA2DS2-VASc score, 0.35, and for RNFL grade and CHA2DS2-VASc score, 0.37. The correlation was negative for RNFL width and CHA2DS2-VASc score, −0.35. Conclusions. CHA2DS2-VASc score was shown to be correlated with glaucoma. This correlation was manifested positively by the LOT needed to stop glaucoma progression, with higher CHA2DS2-VASc scores correlated with more aggressive treatment. Since glaucoma is a disease with a progressing nature, it is important to treat patients aggressively on one hand, while offering the most benign treatment as possible on the other hand. Modification of the CHA2DS2-VASc score could achieve an even higher correlation.


2014 ◽  
Vol 58 (4) ◽  
pp. 553-558 ◽  
Author(s):  
Kinga Wieczorek ◽  
Jacek Osek

Abstract A total of 2668 swabs from poultry (n = 2166), pig (n = 311), and cattle (n = 191) carcasses were collected in slaughterhouses all over Poland and tested for the presence of Campylobacter. It was found that 1319 (49.4%) of them were contaminated with these bacteria. The percentages of the positive samples were different in each year of the study and the highest proportion of Campylobacter contaminated samples occurred in 2009, when 64.1% of investigated carcasses were positive. On the other hand, the lowest prevalence of Campylobacter was observed in 2013, in the last year of the survey. In all kind of carcass samples both C. jejuni and C. coli were identified, although the pork meat was more contaminated with C. coli (75.3% of positive samples) than with C. jejuni (24.7%), whereas poultry was nearly equally positive for C. jejuni and C. coli (50.6% and 49.4% respectively). The analysis of seasonal contamination of the carcasses revealed that more positive results were found during the second half of year than between January and June. The prevalence of Campylobacter showed that in all provinces, except one (Pomorskie), the mean percentage of the positive samples was above 40%. The most contaminated samples were identified in Lubelskie (69.3%) and Zachodniopomorskie (66.3%) regions. The obtained results showed that slaughtered animals in Poland, especially broilers, were often contaminated with Campylobacter, either C. jejuni or C. coli.


Kidney360 ◽  
2020 ◽  
Vol 1 (8) ◽  
pp. 797-800
Author(s):  
Alian Al-Balas ◽  
Ammar Almehmi ◽  
Michael Allon

BackgroundHemorrhage is the most serious potential complication of percutaneous kidney biopsy. Patients are typically observed for at least 6–8 hours after a kidney biopsy, with serial measurements of vital signs and hemoglobin to monitor for major hemorrhage. This study assessed whether an immediate postbiopsy ultrasound can reliably exclude delayed major hemorrhage.MethodsWe retrospectively evaluated the clinical outcomes in 147 patients undergoing an outpatient native kidney biopsy with an 18-gauge needle at a large medical center during a 2.5-year period (January 2017 to June 2019). All patients underwent a standardized postbiopsy ultrasound to assess for active extravasation of blood. We extracted from the medical records vital signs and hemoglobin values obtained before the biopsy and at 2, 4, and 6 hours after the procedure. We ascertained whether any patients with a negative postbiopsy ultrasound developed a delayed major hemorrhage.ResultsEach patient underwent two or three biopsy passes. The mean patient age was 48±17 years, 49% were female, 37% were black, 53% had hypertension, and 16% had diabetes. Of the 142 patients without evidence of active extravasation on ultrasound, the BP, heart rate, and hemoglobin remained stable during 6 hours of observation. All were discharged after 6 hours, and none had a late bleeding complication.ConclusionsIf the immediate postkidney biopsy ultrasound does not show active bleeding, the patient is extremely unlikely to develop a late major hemorrhagic complication (negative predictive value, 100%). Such patients can be discharged home safely after a 2-hour observation, thereby simplifying their management.


1814 ◽  
Vol 104 ◽  
pp. 102-106 ◽  

In a paper formerly communicated to this Society by Sir Everard Home, and since published in the Philosophical Transactions for the year 1809, some facts were stated which render it probable that the various animal secretions are dependent on the influence of the nervous system, and this opinion seemed to derive support from some physiological experiments which were afterwards instituted by myself, and in which it was observed, that after the functions of the brain had been destroyed, although the action of the heart continued, and the circulation of the blood was maintained as under ordinary circumstances, the secreting organs invariably ceased to perform their office. It has been attempted by former physiologists to determine how far the nerves are necessary to secretion, but there are considerable obstacles in the way of this inquiry, and no observations, that have been hitherto made, appear to throw a great deal of light on the subject. The only method, which can be devised, of ascertaining by direct experiment, whether the nerves are really necessary to secretion, is that of dividing the nervous branches by which the glands are supplied. But this, with respect to the greater number of the glands, is an experiment impossible to perform; and, with respect to others, can not be executed without so much disturbance and injury to the other parts, as must render it extremely difficult to arrive at any positive results. Perhaps in future investigations, some circumstances may arise, which will enable us to determine more satisfactorily this important physiological question. In the mean time, as the labours of physiologists have hitherto contributed so little to this purpose, any facts that tend to its elucidation may deserve to be recorded, and I am therefore induced to lay before the Society the following experiments, which afford one example of a secretion being dependent on the influence of the nerves.


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