28, 95% CI = 554–3681) We found higher risk of resistance amon

28, 95% CI = 5.54–36.81). We found higher risk of resistance among patients with metastasis (OR = 8.42, 95% CI = 2.44–29.07), large tumor size (>3 cm) (OR = 7.73, 95% CI = 1.93–30.91), high β-hCG (>100 000 IU/L) (OR = 5.86, 95% CI = 1.07–32.02) and/or a diagnosis more than 4 months after pregnancy (OR = 3.30, 95% CI = 1.08–10.02), compared with their reference Akt signaling pathway group. We found no priority for the different

chemotherapy regimens. Intermediate risk GTN patients had a higher risk of resistance to chemotherapy compared with low-risk patients. Clinical trials and cost-effectiveness studies are needed to suggest a better treatment program for the intermediate risk group. “
“Aim:  The aim of this study was to evaluate urine microscopy, dipstick analysis and urinary symptoms in screening for urinary tract infection (UTI) in hyperemesis gravidarum (HG). Materials and Methods:  A prospective cross-sectional study was performed on women at check details first hospitalization for HG. A clean-catch mid-stream urine sample from each recruit was sent for microscopy (for bacteria, leucocytes and erythrocytes), dipstick analysis (for leukocyte esterase, nitrites, protein and hemoglobin) and microbiological culture. The presence of current

urinary symptoms was elicited by questionnaire. UTI is defined as at least 105 colony-forming units/mL of a single uropathogen on culture.

Screening test parameters were analyzed Suplatast tosilate against UTI. Results:  UTI was diagnosed in 15/292 subjects (5.1%). Receiver–operator characteristic curve analysis of microscopic urine leucocytes revealed area under the curve = 0.64, 95% confidence interval (CI) 0.5–0.79, P = 0.063 and erythrocytes area under the curve = 0.53, 95%CI 0.39–0.67, P = 0.67 for UTI indicating the limited screening utility of these parameters. Microscopic bacteriuria (likelihood ratio [LR] 1.1, 95%CI 0.7–1.5) and urine dipstick leukocyte esterase (LR 1.4, 95%CI 1.1–1.8), nitrites (LR 2.3, 95%CI 0.3–17.2), protein (LR 1.0, 95%CI 0.7–1.6) and hemoglobin (LR 0.8, 95%CI 0.4–1.5) were not useful screening tests for UTI in HG. Elicited symptoms were also not predictive of UTI. Conclusion:  Urine microscopy, dipstick analysis and urinary symptoms were not useful in screening for UTI in HG. UTI should be established by urine culture in HG before starting antibiotic treatment. “
“Developments in immunohistochemistry, which are closely linked with the advances in the analyses of genetic abnormalities and their associated molecular disorders as early and late histogenetic events, have contributed greatly to the improvement of pathological diagnostic confirmation and validation. Immunohistochemistry has also generated great benefit to the innovation of therapeutic strategies for various kinds of cancers.

Nevertheless, the

finding of high levels of concordance i

Nevertheless, the

finding of high levels of concordance is consistent with those of Kremer et al. [27], where 75% of a group of 79 patients with HIV infection perceived collaborative/active involvement in decision-making, using the Control Preferences Scale to measure decisional role perceptions. Concordance was significantly related to positive health-related factors, including better quality of life, less severe and burdensome symptom experience, better psychological symptoms, higher levels of adherence and greater satisfaction. In addition, higher concordance was related to higher CD4 cell count (at questionnaire completion and 6–12 months later). Better adherence did not appear to explain this relationship, as the strength of the relationship between concordance and CD4 cell count changed very little when adherence was added to the regression model. Other possible mechanisms STA-9090 price by which concordance could

exert its positive effects on CD4 cell count are increased perceived control over the illness [28], which could in turn influence health behaviours, or reduced uncertainty, anxiety or depression as a result of greater sharing of information [29] or increased confidence in the decision. Higher concordance could also increase efficacy with respect to the capacity to cope with HIV infection and its treatment [29], which has been shown to be associated with better psychological state (e.g. less depression) [30], which is itself associated with better immunological Veliparib in vivo outcomes [31]. Indeed, trends were also observed for less anxiety/depression and fewer suicidal thoughts with higher concordance, but the relationship between concordance and CD4 cell count remained significant after controlling for quality of life-anxiety/depression scores. Concordance was not associated Meloxicam with risk behaviour or VL. The first finding is consistent with the study by Beach et al. [32], which did not find a significant relationship between patient perceptions of ‘being

known as a person’ and risk behaviour. The components of concordance ‘shared decision-making process’ and ‘medical decision’ were each individually related to positive health-related outcomes, including satisfaction with medical care and treatment, quality of life and adherence. ‘Shared decision-making process’ might have been related to positive outcomes because patients who perceived greater involvement in the decision-making process experienced a greater sense of control over their illness [28] or greater coping efficacy [29] or because their expectations for care were more likely to be met [33]. ‘Medical decision’ could have been related to positive outcomes because the patient perceived that the doctor played a part in the decision. Vertinsky et al.

Marie Callen Private practice, Cincinnati, USA Dr Carol

Marie Callen Private practice, Cincinnati, USA Dr. Carol

Mason Consultant in Paediatric Dentistry, Great Ormond Street Hospital for Children NHS Trust, London, UK Prof. Dr. Stephen Porter Institute Director and Professor of Oral Medicine, UCL Eastman Dental Institute, London, UK Dr. Nina Skogedal Specialist in Paediatric Dentistry, National Resource Centre for Oral Health in Rare Medical Conditions (TAKO-centre), Lovisenberg Diakonale Hospital, Oslo, Norway. Dr. Kari Storhaug Director dr.odont., National Resource Centre for Oral Health in Rare Medical Conditions (TAKO-centre), Lovisenberg Diakonale click here Hospital, Oslo, Norway. Dr. Reinhard Schilke Department of Conservative Dentistry, Periodontologie und Preventive Dentistry, Hannover Medical School, Germany. 6.5.2 Patient Group  Patients and representatives from the DEBRA association groups of Australia, Belgium, Canada, Germany, New Zealand, and the United Kingdom were invited to review the document in order to make sure that the degree to which the evidence addresses patients’ concerns is reflected in the guideline. Anne W Lucky, MD Acting Director, Division of Pediatric dermatology Cincinnati

Children’s Hospital. Cincinnati, Ohio, USA Professor of Dermatology and Pediatrics The University of Cincinnati College of Medicine Cincinnati, Ohio USA Lesley Haynes Formerly Principal Paediatric selleck screening library Dietitian for EB, Great Ormond Street Hospital for Children, London, UK Lynne Hubbard Specialist Dietitian, St. Thomas’ Hospital, London, UK Christian Fingerhuth Lay reviewer, Chile The guideline was piloted in three centres for a period of three months. At the end of the pilot period a feedback form was sent to the authors. Dr. Victoria Clark Consultant in Paediatric Dentistry, Birmingham Children s Hospital, UK Dr. Gabriela Scagnet Dentist, DEBRA Argentina & Universidad de Buenos Aires and Hospital de Odontología Infantil Quinquela Martin Gobierno, Buenos Aires, Argentina Dr. Mariana Armada Hospital de Odontologia Infantil Quinquela Martin Gobierno, Buenos Aires, Argentina Dr.

Adela Stepanska Dentist, DEBRA Czech Republic Dr. Renata Gaillyova Department of Genetics, University Hospital, Brno, Czech Linifanib (ABT-869) Republic Dr. Sylvia Stepanska Practical dentist, Brno, Czech Republic One patient, Scott O’Sullivan from England, participated during the consensus meeting held in Santiago, Chile in November 2010 expressing his opinion and experience regarding dental treatment. Patients and representatives from seven DEBRA association groups were invited to review the document in July and August 2011. According to the context of implementation of this guideline, some barriers to be considered are: Lack of knowledge and training of some health professionals to implement the recommendations. A more detailed study on the effect of sucralfate. The authors would like to thank Dr. Victoria Clark, Dr.

Design  The colour of enamel was recorded (normal, white, yellow

Design.  The colour of enamel was recorded (normal, white, yellow or brown) in specific areas for ten extracted first permanent molars with MIH defects and ten extracted sound teeth. Laser fluorescence (LF) and

mineral density (MD) were measured for the same areas. A mixed model, using sample/tooth as a random effect, was used to estimate the relationship between the MD and the colour-coding, and between the MD and LF readings. Results.  The between-samples correlation coefficient for the colour coding and the MD was 0.99 (P < 0.001), and 0.83 (P < 0.001) for the LF and MD. Conclusions.  The degree of staining of MIH enamel, cAMP inhibitor as assessed visually or by LF, may be used clinically to reflect the severity of the defect. “
“International Journal of Paediatric Dentistry GSK2118436 research buy 2011;

21: 422–431 Background.  The genotypic diversity of both Streptococcus mutans and Streptococcus sobrinus in children with different caries experience remains unclear. Aim.  To investigate the genotypic diversity of S. mutans and S. sobrinus in children with severe early childhood caries (SECC) and in caries-free (CF) children. Methods.  Stimulated saliva of 87 SECC and 91 CF children aged 3–4 years was collected and submitted to cultivation, and MS colonies were enumerated. The genomic fingerprint analysis of S. mutans and S. sobrinus was carried out using AP-PCR. Results.  One to five genotypes of S. mutans were colonized in an oral cavity of SECC and CF children; 85.5% Thalidomide SECC children and 57.9% CF children harboured more than one genotype of S. mutans. One to three genotypes of S. sobrinus were detected from each SECC child; 31.25% SECC children harboured more than one genotype of S. sobrinus. And one genotype was colonized in each CF child. S. mutans isolates from different individuals displayed distinctive DNA fingerprints. Conclusions.  DNA fingerprints of S. mutans and S. sobrinus isolates from 3- to 4-year-old children displayed genetic polymorphism, and S. mutans has greater genetic diversity than S. sobrinus. SECC children harboured more genotypes of S. mutans and S. sobrinus

than CF children. “
“International Journal of Paediatric Dentistry 2011; 21: 23–28 Aim.  To investigate the prevalence and distribution of developmental enamel defects in children with cerebral palsy (CP) in Beijing, China. Design.  A total of 135 children aged 1.5–6 years with moderate or severe congenital CP diagnosed in Beijing Boai Hospital from year 2005 to 2009 were recruited. The children underwent dental examination at the hospital dental clinic. Results.  Enamel defects (opacity and/or hypoplasia) were found in 44 (32.6%) out of 135 CP children. Enamel hypoplasia was found in 35 (25.9%) of the CP children, opacity alone was found in 5 (3.7%) of the CP children, and mixed defects (opacity and hypoplasia) was found in 4 (3.0%) of the CP children.

Design  The colour of enamel was recorded (normal, white, yellow

Design.  The colour of enamel was recorded (normal, white, yellow or brown) in specific areas for ten extracted first permanent molars with MIH defects and ten extracted sound teeth. Laser fluorescence (LF) and

mineral density (MD) were measured for the same areas. A mixed model, using sample/tooth as a random effect, was used to estimate the relationship between the MD and the colour-coding, and between the MD and LF readings. Results.  The between-samples correlation coefficient for the colour coding and the MD was 0.99 (P < 0.001), and 0.83 (P < 0.001) for the LF and MD. Conclusions.  The degree of staining of MIH enamel, Cyclopamine as assessed visually or by LF, may be used clinically to reflect the severity of the defect. “
“International Journal of Paediatric Dentistry R428 nmr 2011;

21: 422–431 Background.  The genotypic diversity of both Streptococcus mutans and Streptococcus sobrinus in children with different caries experience remains unclear. Aim.  To investigate the genotypic diversity of S. mutans and S. sobrinus in children with severe early childhood caries (SECC) and in caries-free (CF) children. Methods.  Stimulated saliva of 87 SECC and 91 CF children aged 3–4 years was collected and submitted to cultivation, and MS colonies were enumerated. The genomic fingerprint analysis of S. mutans and S. sobrinus was carried out using AP-PCR. Results.  One to five genotypes of S. mutans were colonized in an oral cavity of SECC and CF children; 85.5% Y-27632 2HCl SECC children and 57.9% CF children harboured more than one genotype of S. mutans. One to three genotypes of S. sobrinus were detected from each SECC child; 31.25% SECC children harboured more than one genotype of S. sobrinus. And one genotype was colonized in each CF child. S. mutans isolates from different individuals displayed distinctive DNA fingerprints. Conclusions.  DNA fingerprints of S. mutans and S. sobrinus isolates from 3- to 4-year-old children displayed genetic polymorphism, and S. mutans has greater genetic diversity than S. sobrinus. SECC children harboured more genotypes of S. mutans and S. sobrinus

than CF children. “
“International Journal of Paediatric Dentistry 2011; 21: 23–28 Aim.  To investigate the prevalence and distribution of developmental enamel defects in children with cerebral palsy (CP) in Beijing, China. Design.  A total of 135 children aged 1.5–6 years with moderate or severe congenital CP diagnosed in Beijing Boai Hospital from year 2005 to 2009 were recruited. The children underwent dental examination at the hospital dental clinic. Results.  Enamel defects (opacity and/or hypoplasia) were found in 44 (32.6%) out of 135 CP children. Enamel hypoplasia was found in 35 (25.9%) of the CP children, opacity alone was found in 5 (3.7%) of the CP children, and mixed defects (opacity and hypoplasia) was found in 4 (3.0%) of the CP children.

, 1999; Eddyani et al, 2004; Kotlowski et al, 2004; Johnson et

, 1999; Eddyani et al., 2004; Kotlowski et al., 2004; Johnson et al., 2007), indicating

that M. ulcerans is probably present in such samples. However, other closely related Mycobacterium species including Mycobacterium liflandii, Mycobacterium Pseudoshottsii, and mycolactone-producing Mycobacterium marinum strains (Stinear et al., 1999; Stragier et al., 2007) have been found to harbor IS2404. Thus, the conventional IS2404 PCR assay cannot be relied upon for the specific detection of M. ulcerans. In order to increase specificity, facilitate rapid analysis of specimens, and to interpret the results of both environmental and clinical specimens Navitoclax with certainty, Fyfe et al. (2007) developed two TaqMan Multiplex real-time PCR assays targeting three independent repeated sequences in the M. ulcerans genome, two multicopy insertion sequences (IS2404, IS2606), and a multicopy sequence encoding the ketoreductase

B domain (KR-B). These real-time PCR assays quantify the copy number of the targets, allowing Selleckchem ZVADFMK the differentiation of M. ulcerans from other IS2404-containing mycobacteria. Moreover, the assay allows for the control of PCR inhibitors such as humic and fulvic acids, commonly present in environmental samples. In spite of its advantages for the analysis of clinical and environmental samples (high throughput, high sensitivity and specificity, less prone to contamination, and Evodiamine inhibition control), facilities for real-time PCR are available only in a few research laboratories in West-African BU-endemic countries, including Ghana. However, swift analysis of environmental samples could be crucial

in the search for the M. ulcerans reservoir. Therefore, the current study describes the first application of real-time PCR for the detection of M. ulcerans in environmental samples at the Noguchi Memorial Institute for Medical Research (NMIMR) in Accra, Ghana. Both the acquisition of these technologies through international technology transfer and their diffusion will foster effective technological change as follow-on innovation and adaptation occurs. The real-time PCR assays were carried out as described by Fyfe et al. (2007). Briefly, IS2404/internal positive control (IPC) mixtures contained 1 μL of template DNA, 0.9 μM of each primer, 0.25 μM of the probe, 1 × TaqMan® Universal PCR Master Mix (Applied Biosystems, Foster City, CA), and TaqMan exogenous IPC reagents (Applied Biosystems) in a total volume of 25 μL. IS2606/KR assays were preformed on IS2404-positive samples in a similar multiplex way without IPC. Detection was performed on a 7300 real-time PCR System (Applied Biosystems) using the following thermal profile: one cycle of 50 °C for 2 min, one cycle of 95 °C for 10 min, and 40 cycles of 95 °C for 15 s and 60 °C for 1 min.

Although the literature provides some insight, more studies are n

Although the literature provides some insight, more studies are needed to assess the value and impact of the knowledge and skills possessed by certified pharmacy technicians with standardized training compared with technicians with site-specific or limited training. The pharmacy technician provides essential Enzalutamide datasheet support to the pharmacist in areas including prescription entry, third-party insurance management, staff/patient scheduling and inventory control.

Delegating these responsibilities to the technician frees the pharmacist to focus on prescription accuracy, interact more extensively with patients, provide medication therapy management services and fulfill administrative duties. However, the expanded responsibilities of pharmacy technicians Erismodegib cost has been accompanied by concerns about a corresponding increase in dispensing errors.[1,2] A potential catalyst for dispensing errors may be the lack of standardized training for pharmacy technicians. This could ultimately result in technicians with responsibilities they are not adequately trained to perform. That scenario is a contributing factor leading some to advocate more stringent requirements and

credentialing for pharmacy technicians. Although there is a certified pharmacy technician designation, it is not a universal requirement in all states or work environments. Many pharmacies still rely on unstructured, on-the-job training for technicians provided by a pharmacist or co-worker. Standardized, universal credentialing would be an important step in assuring a trained and competent support staff; however, it poses its own set of challenges. For example, the development of this specialized workforce heptaminol with enhanced education and training would

probably dictate an increase in wages and technician liability, along with a transient shortage of qualified technicians. Pharmacy technician training and roles in Europe differ significantly from those in the USA.[3] Other than the UK, the authors could find little information regarding pharmacy technician training in Europe. Therefore, in the first section of the review we compared training in the USA with that in the UK. The major scope of this paper was to examine the training and roles of pharmacy technicians in the USA. This review will compare the USA and the UK regarding pharmacy technicians’ roles, it will summarize the current roles and responsibilities of pharmacy technicians in the USA, public perception of pharmacy technicians, pharmacy organizations’ perspectives on pharmacy technician credentialing, academic programmes for pharmacy technicians, accreditation of pharmacy technician programmes, pharmacy technician certification exams and differing perspectives on the push for standardized technician training. It will conclude with observations regarding the importance of standardized pharmacy technician training.

N100 effects from CS onset processing overlap with differential P

N100 effects from CS onset processing overlap with differential P1 processing of the CS stimulus

after 50 ms, and so forth). Auditory MultiCS conditioning using ultrashort tones as CS that reveal their emotional meaning almost instantaneously, as in vision, address this methodological constraints of MEG/EEG research associated with the dynamic nature of acoustic stimuli (i.e. signal convolution of evoked neural responses). Bröckelmann et al. (2011) first applied auditory MultiCS conditioning involving intramodal learning of associations between multiple click-like tones and neutral, appetitive Cyclopamine supplier and aversive emotional acoustic scenes. Neural click-tone processing was affected at time-intervals of the P20–50m (20–50 ms) and the N1m (100–130 ms). The emotion effect was localised to sensory, frontal and parietal cortex regions. As dominant effect, both emotion-associated CS stimulus groups (pleasant and unpleasant) evoked stronger neural processing than did neutrally associated tones; however, there was also a hemispheric preference with a relative dominance of aversion-associated CS on the right and approach-associated CS on the left side. As this study was the first of its type in the auditory

modality, we here tested whether the findings could be replicated and would generalise to cross-modal aversive MultiCS conditioning of multiple click-like tones with an electric shock as single UCS. We ultimately aimed at delivering converging evidence selleck across studies to strengthen our conclusions that auditory processing is modulated (i) rapidly after stimulus onset, during the N1m and the even earlier P20–50m time-interval, (ii) in a highly resolving manner with the capacity to differentiate a large number of click-like tones as a function of their associated affective significance after brief Cyclin-dependent kinase 3 learning and (iii) within a distributed frontal–parietal–temporal network attributable to the engagement of attention by emotionally salient tones. To this end, we adopted the MultiCS conditioning design and tested according hypotheses in a new set of subjects for electric shock conditioning. In sum, the

present results showed considerable overlap with, but also substantial differences from, the first study of auditory MultiCS conditioning. In the next paragraphs, we will discuss five aspects in more detail: first, the corresponding affect-specific N1m modulation; second, the hemispheric asymmetries in shock conditioning associated with preferential CS+ and CS− processing in the right and left hemisphere, respectively; third, the suggested underlying neural mechanisms; fourth, the lack of a significant modulation of the P20–50m component in the electric shock, as opposed to the auditory affective scene conditioning study; and fifth, the role of prefrontal cortex in emotion processing as revealed by MultiCS conditioning.

While, specific parental behaviours such as Parents’ perceived ab

While, specific parental behaviours such as Parents’ perceived ability to

withhold frequent cariogenic snacks from their children even when they fussed for Ibrutinib cell line it was inversely associated with the presence of dental decay in their child. Not all beneficial practices, however, had beneficial effects on dental caries; in this study, the frequency of tooth-brushing and/or tooth-brushing with supervision did not have a positive influence on the child’s caries experience. Although this agrees with some studies[27, 28], others have reported lower caries levels associated with frequent tooth-brushing[20, 29]. The controversial results and conclusions may be due to acidogenicity of biofilm or poor tooth-brushing techniques of children and/or their caregivers.

Interestingly, none of the factors mentioned in this Osimertinib mw section were significantly associated with dt/ds, implying the role of other more important indicators when assessing caries severity. Nevertheless, the information derived from both Gao et al.’s (2010)[4] and this study provides practical guidelines to steer health promotion efforts to specifically target certain knowledge and practices, especially for children and parents with higher caries rate in Singapore. Because of the perceived discomfort of many individuals with the disclosure of their family income, the type of dwelling was chosen to measure the socio-economic status (SES) in this study. In this study, the caries experience was not consistently associated with the type of dwelling, a relationship that has been otherwise well documented in other published reports[4, 30]. The inconsistent association could have been a function of the sampling from the public health medical clinics, which itself may be selective for patients from the lower socio-economic group. The utilization ADAM7 of the type of housing may also be a crude measure for the measurement

of socio-economic status in Singapore as it does not account for the extremely high housing cost in Singapore (e.g., more than 50% of the population live in government housing developments) as well as other social and cultural factors that may be unique in this country (e.g., extended family units etc). The limitations of this study include intra-operator reliability, small sample size, convenience sampling, the potential underestimation of caries experience because only a visual-tactile examination, without radiographs, was employed, and the innate inaccuracies in the answers encountered in the interviewer-administered questionnaire (e.g., truthful answers). Improvements to the current questionnaire could be made in future studies by the inclusion of specific questions with regard to fluoride intake (e.g.

Amongst the Burkholderia spp, there is a need to

differe

Amongst the Burkholderia spp., there is a need to

differentiate Burkholderia pseudomallei from Burkholderia cepacia, as misidentification could lead to false treatment of patients. In this study, conventional PCR assay targeting three genes was developed. Primers were designed for the amplification of Burkholderia genus-specific groEL gene, B. pseudomallei-specific mprA gene and B. cepacia-specific zmpA gene. The specificity and sensitivity of the assay was tested with 15 negative control strains and 71 Burkholderia spp. isolates including positive controls B. pseudomallei K96243 and ATCC B. cepacia strain. All B. pseudomallei strains were positive for groEL (139 bp) and mprA (162 bp), indicating a sensitivity of 100%. All B. cepacia strains Selleck Daporinad produced amplicons for detection of groEL and zmpA (147 bp). Specificity using negative strains was 100%. In this study, a PCR assay specific for Navitoclax chemical structure the detection of Burkholderia spp. and differentiation of the genus B. pseudomallei and B. cepacia was developed. The conventional assay has to be performed separately for each species due to the similar size of the PCR products amplified. This format may therefore be recommended for use as a diagnostic tool in laboratories where real-time PCR machines are not available. However, the real-time PCR was able to detect and differentiate the genus and species in single

duplex assay. The genus Burkholderia consists of more than 30 species of Gram-negative bacilli, nonspore forming and oxidase-positive soil saprophytes. Burkholderia pseudomallei and Burkholderia cepacia complex are known human pathogens. Burkholderia mallei causes glanders in horses and Burkholderia thailandensis is a nonpathogenic

bacterium. All Burkholderia spp. are motile except for B. mallei (Bossi et al., 2004). Burkholderia pseudomallei causes melioidosis in humans, which resembles glanders and is predominant in South-East Asia and Northern Australia. Burkholderia cepacia has been recognized as a major opportunistic pathogen Cobimetinib cell line in cystic fibrosis, necrotizing pneumonia and chronic granulomatous diseases in humans (Isles et al., 1984). In addition, B. cepacia causes urinary tract infections, wound infections and endocarditis (Speller et al., 1971). To date, various diagnostic methods such as culture (Anuntagool et al., 1993), serology (Illeri, 1965; Walsh et al., 1994; Chentamarakshan et al., 2001) and molecular detection methods (Rattanatongkom et al., 1997; Sura et al., 1997; Woo et al., 2002) have been developed for identification of Burkholderia spp. either from environmental or clinical samples. Although culture is known as the ‘gold standard’ for the detection of Burkholderia spp., it is time-consuming, often taking up to 48 h. Early confirmative detection of B. pseudomallei is essential for septicemic cases in which fatality can occur within 24–48 h.