ライフサイエンスコーパス: swab

1 ts detection in GW and the preceding genital swab.

2 fied HCV from rectal fluid obtained by blind swab.

3 .65 (95% CI 0.59-0.72) for stool relative to swab.

4 ty to detect intact bacterial species from a swab.

5 r toxigenic C. difficile by culturing rectal swabs.

6 r rayon swabs and 11.6% (98/846) for flocked swabs.

7 ted by polymerase chain reaction in the same swabs.

8 xtracellular 200 kDa carbohydrate, in saline swabs.

9 identification from remnant nares and wound swabs.

10 community had a median Ct of 21.5 for throat swabs.

11 t skin tissue, breast skin swabs, and buccal swabs.

12 in reaction performed on nasal/oropharyngeal swabs.

13 ase chain reaction of flocked nasopharyngeal swabs.

14 rts of M. tuberculosis DNA detection in oral swabs.

15 e subjects (90%) yielded at least 2 positive swabs.

16 for the direct detection of MRSA from nasal swabs.

17 rence among results from urethral and meatal swabs.

18 athogens can be identified relative to NP/OP swabs.

19 tal skin swabs, oral rinse samples, and anal swabs.

20 ols (0.3%) and for the first time in a nasal swab (0.1%).

21 Children were swabbed 10 times between 2 and 30 months of age.

22 or 6.3% of their oral-pharyngeal or cloacal swabs (233/3,678) were positive for IAV, and 56.8% of IA

23 In addition to the clinical rectal swabs, 250 contrived specimens (108 well-characterized C

24 ), rectal swabs (35 of 37 [95%]), and throat swabs (33 of 39 [85%]) rather than in cerebrospinal flui

25 identified in feces (42 of 44 [95%]), rectal swabs (35 of 37 [95%]), and throat swabs (33 of 39 [85%]

26 reatment, the participants collected genital swabs 4 times daily for testing by HSV polymerase chain

27 compare WB sampling methods (pipette versus swab); 43/71 BS specimens had been previously frozen.

28 significantly higher than that for urethral swabs (45% versus 3%, respectively; P < 0.0001).

29 ivity was 96.1% (91.7% to 98.2%) for vaginal swabs, 93.4% (88.3% to 96.4%) for endocervical swabs, an

30 ple, using the Aptima Unisex collection blue swab, a specimen was collected from the conical apex of

31 eal swabs, compared with collection of nasal swabs alone, for detection of common respiratory viruses

32 se results highlight the potential of direct swab analysis by DESI-MS for a wide range of clinical ap

33 nting the information obtained from clinical swab analysis with mucosal metabolome profiling using de

34 sing a traditional wound fiber liquid Stuart swab and an ESwab device, a flocked swab with a modified

35 ificant differences were observed between NP swab and blood specimens.

36 patterns did not differ significantly in NP swab and blood specimens.

37 Self-collected anal swab and oral rinse specimens were tested for HPV DNA (3

38 Swab and tissue specimens were cultured and analyzed by

39 men who underwent either urethral or meatal swabbing and compared the cellular content and Gram stai

40 h then allows the peptide to be recovered by swabbing and extracted for electrospray ionization-mass

41 We performed nasopharyngeal or nasal swabbing and/or serum sampling (n = 148) in Lancaster, U

42 n evaluated were 11.1% (122/1,103) for rayon swabs and 11.6% (98/846) for flocked swabs.

43 e cultured from 3.2% of pre-procedure rectal swabs and 2.5% of duodenal aspirates.

44 C. trachomatis was detected from 59 rectal swabs and 8 pharyngeal samples, with 97.7% and 99.5% agr

45 Nasopharyngeal swabs and blood samples were taken among 120 preschool c

46 lebsiella pneumoniae isolated from screening swabs and clinical diagnostic samples were characterized

47 negative predictive values (NPVs) for rayon swabs and ESwab specimens were 98.9% and 99.1%, respecti

48 erefore used chemical fingerprinting of skin swabs and genetic analysis to explore the chemical cues

49 nd provided nasopharyngeal and oropharyngeal swabs and induced sputum (cases only) for Bordetella per

50 ted with a reduction in viral titer in nasal swabs and lungs, following challenge with H1N1 pandemic

51 Throat swabs and oral fluid samples were tested by quantitative

52 In men, load was highest for rectal swabs and similar for urethral swabs and urine specimens

53 mergent care, we attempted to collect rectal swabs and stool from all participants.

54 compare the enteropathogen yields of rectal swabs and stool specimens in children with diarrhoea or

55 nts included the quantity of HSV in positive swabs and the frequency of genital lesions and shedding

56 mplex specimen types, including urine, wound swabs and tissue, and several types of respiratory and f

57 st for rectal swabs and similar for urethral swabs and urine specimens.

58 e expression profiles in nasopharyngeal (NP) swabs and whole blood samples during natural RSV and rhi

59 IM) Study participants who had HPV-6 genital swabs and/or GWs preceded by a viable normal genital swa

60 fewer consumables (2.4 versus 3.3 sticks and swabs) and rapid biochemical tests (1.0 versus 1.9) were

61 Oral rinse, penile swab, and vaginal swab specimens were evaluated by polym

62 mined by culturing ear, umbilicus, and nasal swabs, and (iii) the distribution of GBS serotypes.

63 abs, 93.4% (88.3% to 96.4%) for endocervical swabs, and 92.9% (87.8% to 96.0%) for female urine sampl

64 icrobiota of breast skin tissue, breast skin swabs, and buccal swabs.

65 Subsequently, serum samples, tonsil swabs, and feces were collected from sows (n = 22) and t

66 blood, probang samples, and saliva and nasal swabs, and herd-level samples, such as air samples, were

67 blood, nasopharyngeal/oropharyngeal (NP/OP) swabs, and induced sputum by culture and PCR.

68 CR of cerebrospinal fluid, blood, and rectal swabs, and tests for other causes, were negative.

69 Medical swabs are routinely used worldwide to sample human mucos

70 Urethral swabs are the samples of choice for point-of-care Gram s

71 the recommendation against the use of rectal swabs as diagnostic specimens be reconsidered.

72 f 21 (TRIM21) messenger RNA indexes in nasal swabs as potential biomarkers of viral respiratory infec

73 nce for women using endocervical and vaginal swabs as well as urine specimens.

74 th virus detectable by PCR in nasopharyngeal swab at day 3, and was assessed in participants who were

75 ese two studies support the potential use of swabs at temperatures above 36 degrees C and storage bey

76 t nasopharyngeal specimens were collected by swabbing between ages 2 and 24 months.

77 cal venipuncture whole blood (WB) and buccal swab (BS) specimens submitted to a field biocontainment

78 We measured the difference in swab cellular content using the Cepheid Xpert CT/NG samp

79 n of ZIKAV RNA was performed on conjunctival swabs collected from both eyes of these patients at the

80 d the taxonomic composition of 2,179 vaginal swabs collected prospectively and weekly during gestatio

81 en the ESwab and the FDA-cleared wound fiber swab collection device.

82 e of collecting both nasal and oropharyngeal swabs, compared with collection of nasal swabs alone, fo

83 Rectal swabs contained all of the diversity present in faecal s

84 For this study, throat swabs (Copan ESwabs) were collected from schoolchildren

85 However, as meatal swabs could be sampling a reduced surface area and resul

86 ase-producing Enterobacteriaceae from rectal swab culture.

87 duals) provided concurrent symptom and nasal swab data for 4166 person-weeks.

88 pecificity of the combined flocked and rayon swab data were 91.8% (95% CI, 87.4 to 94.8%) and 97.2% (

89 ation of carriage episodes from longitudinal swab data, and combined these results with whole genome

90 Testing of rectal swabs directly using the Xpert Carba-R assay is effectiv

91 dding was detected in 2.4% (173 of 7276 ) of swabs during pritelivir treatment compared with 5.3% (39

92 h qualitative (roll-plate) and quantitative (swab elution) methods.

93 .1%), and 96.1% (92.2% to 98.1%) for vaginal swabs, endocervical swabs, female urine samples, and mal

94 ed rayon nasal swabs (n = 1,103) and flocked swab (ESwab) nasal specimens (n = 846).

95 ted via polyester/polyethylene terephthalate swabs every other month and tested for bacteria, using q

96 Oral and genital swab exfoliated cells were collected simultaneously from

97 2% to 98.1%) for vaginal swabs, endocervical swabs, female urine samples, and male urine samples, res

98 for this study and had collected a lesional swab for polymerase chain reaction (PCR).

99 ance of a novel, easy-to-use, gentle flocked swab for sampling of OM was evaluated.

100 ractitioners with influenza-like illness are swabbed for laboratory testing; those testing positive f

101 healthcare professionals collected anorectal swabs for cytologic examination and human papillomavirus

102 ealth care worker (HCW)-collected pharyngeal swabs for detection of GAS by PCR.

103 medical records, and tested nasal and throat swabs for EV-D68 using real-time reverse- transcription

104 use nasopharyngeal or oropharyngeal (NP/OP) swabs for pathogen detection for patients hospitalized w

105 Midnasal swabs for respiratory virus PCR testing were collected d

106 We examined the children and obtained nasal swabs for the detection of RSV during each respiratory i

107 Nasal lavage for flow cytometry and nasal swabs for viral PCR were performed at enrollment and dur

108 ples were collected with cytobrush and rayon swabs from 30 women with high-grade cervical precancer.

109 Nasopharyngeal/oropharyngeal (NP/OP) swabs from 70 children <5 years with CAP of unknown etio

110 ions (by 5%-7%) in detection by PCR in NP/OP swabs from both cases and controls, with the exception o

111 country sites, nasopharyngeal/oropharyngeal swabs from children with and without pneumonia were test

112 come countries, nasopharyngeal/oropharyngeal swabs from children with severe pneumonia and age-freque

113 Swabs from clinically detected ulcers were tested for HS

114 collecting weekly symptom diaries and nasal swabs from families for 1 year, (2) analyzed data by rep

115 colonisation study, we screened 2923 rectal swabs from healthy volunteers, of which 19 were MCRPEC,

116 Rectal swabs from high-risk patients were screened for carbapen

117 isk factors for carriage of MCRPEC in rectal swabs from inpatients with MCRPEC and mcr-1 negative at

118 Using penile swabs from males aged 14-59 years, we estimated the HPV

119 Using over 150 genital swabs from North and South America and Africa, we detect

120 rs, of which 19 were MCRPEC, and 1200 rectal swabs from patients, of which 35 were MCRPEC.

121 a year and collected 4,190 individual nasal swabs from three distinct pig subpopulations.

122 We collected weekly oral swabs from young children and mothers in 32 Ugandan hous

123 ) study provided eyebrow hairs, forearm skin swabs, genital skin swabs, oral rinse samples, and anal

124 Twenty-four of the paired swabs had discordant results, with 10 and 14 positives d

125 Each day since 2009, nasopharyngeal swabs have been obtained from the first 4 Bedouin childr

126 As an alternative to urethral swabs, meatal swabs have been recommended for the collection of urethr

127 phyromonas (5.2 x 10(7) 16S rRNA gene copies/swab in the PrePex group and 1.1 x 10(6) 16S rRNA gene c

128 x group and 1.1 x 10(6) 16S rRNA gene copies/swab in uncircumcised men; P = .002), Peptoniphilus (1.0

129 I MS using an optimized protocol considering swab-inlet geometry, tip-sample angles and distances, ro

130 a CMOS-compatible process, and an efficient swabbing lift-off technique is introduced for the deposi

131 OSCC biopsies (cases) and 20 deep-epithelium swabs (matched control subjects) was sequenced for the V

132 le and -nonsusceptible strains into a rectal swab matrix and inoculating them onto swabs prior to tes

133 As an alternative to urethral swabs, meatal swabs have been recommended for the collec

134 males (iv), and whether cloacal and tracheal swabs might be used to detect herpesvirus.

135 iomass occurs directly from a standard rayon swab mounted on a rotating device and analyzed by DESI M

136 say with prospectively collected rayon nasal swabs (n = 1,103) and flocked swab (ESwab) nasal specime

137 veloped and evaluated using dry ectocervical swabs (n=392) from symptomatic females with vaginal disc

138 Flocked nasopharyngeal swabs, nasopharyngeal aspirates, and induced sputum perf

139 tion (RT) PCR were applied to nasopharyngeal swab (NPS) samples from all acutely HBoV1-infected child

140 ry specimens, such as flocked nasopharyngeal swabs (NPSs), nasopharyngeal aspirates (NPAs), and induc

141 as established through screening in perineum swabs obtained at admission and twice weekly and inocula

142 f RT-PCR assay and culture of nasopharyngeal swabs obtained from participants with symptoms of an inf

143 prevalence was increased in GWs and genital swabs of cases compared to controls.

144 Salmonella was isolated from rectal swabs of free-ranging and stranded grey seal pups (21.1%

145 in domestic birds in China, oral and cloacal swabs of healthy chickens, ducks, geese and pigeons were

146 ectively sampled in 2014 from vaginal/rectal swabs of healthy pregnant women in metropolitan Toronto,

147 red with mcr-1-negative isolates from rectal swabs of inpatients (colonisation study).

148 Swabs of labial, vulvar, perineal, perianal, endocervica

149 f weekly random sampling (i.e., using saliva swabs) of at least 10 animals per farm or daily air samp

150 testing by PCR; and (iii) compression of the swab on filter paper and, after DNA concentration, testi

151 brow hairs, forearm skin swabs, genital skin swabs, oral rinse samples, and anal swabs.

152 t infections based on parent-collected nasal swabs over the winter months.

153 ectious reference viruses and nasopharyngeal swab patient specimens were successfully tested using mu

154 rectal swab matrix and inoculating them onto swabs prior to testing.

155 our unique setting of a school-based throat swabbing program, the illumigene assay did not perform q

156 Self-collected pharyngeal swabs provide a reliable alternative to HCW collection f

157 al RNA copy numbers detected in conjunctival swabs ranged from 5.2 to 9.3 copies respectively.

158 ntamination on test surfaces, whereas sponge swabs recovered 76 to 94% of the total contamination, an

159 x 10(7) and 1.1 x 10(6) 16S rRNA gene copies/swab, respectively; P < .001), and Campylobacter ureolyt

160 x 10(5) and 1.6 x 10(7)16S rRNA gene copies/swab, respectively; P < .001).

161 x 10(7) and 1.8 x 10(6) 16S rRNA gene copies/swab, respectively; P < .05), Anaerococcus (1.0 x 10(7)

162 tected only with the HCW- and self-collected swabs, respectively (P = 0.41).

163 articipants provided a self-collected penile swab sample for HPV genotyping (Roche Linear Array) and

164 Oral swab samples are non-invasive, non-viscous, and easy to

165 H3N2 IAVs directly from nasal wash or nasal swab samples collected from laboratory-challenged animal

166 The antigen was detectable in 52% of swab samples collected from sinks across a University ca

167 s, the use of plate cultures inoculated from swab samples continues to be the standard practice in cl

168 levels measured in the nasal and pharyngeal swab samples derived from the same patients were also di

169 n's Hospital; clinical staff collected nasal swab samples from 25 patients and then operated test dev

170 ore, we analysed by BuV qPCR stool and nasal swab samples from 955 children with gastroenteritis, res

171 Efficiency of viral isolation from swab samples was confirmed by the limit of detection (as

172 Swab samples were collected and tested for the presence

173 Penile swab samples were collected from men aged 18-59 years.

174 Anal swab samples were obtained from sexually active men who

175 seline) and at discharge (follow-up), rectal swab samples were obtained, and compared with samples fr

176 s were as follows: 49% (51 of 104) for nasal swab samples, 53.8% (56 of 104) for nasal biopsy samples

177 ng patients were 66.4% (75 of 113) for nasal swab samples, 71.7% (81 of 113) for nasal turbinate biop

178 From pharyngeal swab samples, Xpert was 98% sensitive (95% CI, 87 to 99.

179 corded symptoms and provided blood and nasal swab samples.

180 rug Administration for use with extragenital swab samples.

181 Cytobrush and swab sampling provide a comparable VM composition.

182 rsity community structure, not realized with swab sampling.

183 , or 36 degrees C for up to 84 days and (ii) swabs seeded with C. trachomatis and N. gonorrhoeae and

184 A double rectal swab set was collected from 383 patients admitted at fou

185 gonorrhoeae infection or NGU in men, meatal swabs should be avoided in the absence of a visible disc

186 INTERPRETATION: Rectal swabs should be done when enteropathogen identification

187 HSV shedding was detected from 1480 of 9113 swab specimens (16%) collected on days without lesions.

188 the highest prevalence (65.1% of normal skin swab specimens and 30.6% of eyebrow hair specimens), inc

189 mens), and persistence (85.8% of normal skin swab specimens and 58.9% of eyebrow hair specimens) amon

190 ended for vaccination provided oropharyngeal swab specimens and completed questionnaires during 4 car

191 HSV-2 was detected from 2484 of 11 283 swab specimens collected (22%), with a median quantity o

192 V RT FRET-PCR to oral-pharyngeal and cloacal swab specimens collected from healthy poultry in 34 live

193 om sampling to identify 3,000 nasopharyngeal swab specimens collected from January 2009 through July

194 positive Ugandan adults collected anogenital swab specimens for HSV DNA quantification by polymerase

195 A total of 4225 oropharyngeal swab specimens from 3802 unique participants were analyz

196 Twelve rectal-swab specimens from dogs displaying clinical signs consi

197 Nasopharyngeal (NP) swab specimens from patients in a recent outbreak of res

198 e analyzed HSV-2 strains detected in genital swab specimens from trial participants who were randomly

199 Of the 2,479 eligible nasopharyngeal swab specimens included in the prospective study, 2,371

200 ants/placentae (n = 535) were recruited, and swab specimens of chorioamnion tissue, chorioamnion tiss

201 Among 76 clinical urine and swab specimens positive for N. gonorrhoeae by the Cobas

202 ed to urethral swabs, the adequacy of meatal swab specimens to collect sufficient cellular material f

203 Participants obtained genital swab specimens twice daily for HSV-2 detection and monit

204 ased detection of influenza virus from nasal swab specimens was developed and evaluated in a clinical

205 The flocked swab specimens were 92.9% sensitive (95% CI, 86.0 to 96.

206 Eye swab specimens were collected and molecular detection of

207 A total of 1,153 clinical swab specimens were collected and tested at 7 different

208 Anal swab specimens were collected for cytology and human pap

209 Paired nasal swab specimens were collected from patients who were und

210 Oropharyngeal swab specimens were collected weekly from Ugandan newbor

211 Throat and nasal swab specimens were collected, combined, and tested for

212 Oral rinse, penile swab, and vaginal swab specimens were evaluated by polymerase chain reacti

213 Nasopharyngeal swab specimens were obtained from infants who met a stan

214 Seven hundred fifty-seven throat swab specimens were tested by both methods.

215 Swab specimens were tested for Streptococcus pneumoniae,

216 ses per 1000 person-months among normal skin swab specimens, and 24.1 cases per 1000 person-months am

217 DNA was extracted from self-collected penile swab specimens, and HPV genotyping was performed by poly

218 yV infection in eyebrow hair and normal skin swab specimens, respectively.

219 ntly detected pathogen in either nasopharynx swab specimens, stool specimens, serum samples (15 of 45

220 mplification (HDA) method using 1,082 throat swab specimens.

221 blaOXA-48, and blaVIM) directly from rectal swab specimens.

222 V-1 and HSV-2 in cutaneous and mucocutaneous swab specimens.

223 M, blaOXA-48, and blaIMP-1 genes from rectal swab specimens.

224 the routine detection of HSV in superficial swab specimens.

225 iptase PCR (RT-PCR) using 411 nasopharyngeal swab specimens.

226 t amplification assay using 1,192 pharyngeal swab specimens.

227 information beyond that obtained with NP/OP swab specimens.

228 ded stool specimens and 1514 (>99%) provided swab specimens.

229 for the direct detection of MRSA from nasal swab specimens.

230 Using dual swabs, specimens from 755 patients were collected and te

231 A total of 57,690 swabs submitted for MRSA screening were enrolled in the

232 lood and plasma samples and post mortem oral swabs submitted to the Liberian Institute for Biomedical

233 without human DNA supplementation) and from swabs taken from the skin of four healthy volunteers.

234 15 participants had a total of 74 swabs taken less than 100 days from discharge.

235 Chicken swab tests showed that the impedance immunosensor had a

236 -6 B1 variants are more prevalent in genital swabs that precede GW development, and confer an increas

237 ly questionnaires and self-collected vaginal swabs that were scored by the Nugent method.

238 th a sampling kit and instructional video to swab the skin of their animals.

239 lected epithelial cells compared to urethral swabs, the adequacy of meatal swab specimens to collect

240 It is plausible that compared to rayon swabs; the most commonly used sampling devices, cytobrus

241 use selective culture of rectal surveillance swabs to identify isolates for molecular epidemiological

242 We used cheek swabs to obtain the genomic DNA of 200 ADHD male proband

243 norrhoeae was observed, although some mailed swabs took more than 5 weeks to reach the laboratory sit

244 I M40-A2 standard, we evaluated three liquid swab transport systems for the recovery of aerobic, anae

245 All tested liquid swab transport systems were fully compliant with the M40

246 wing revised information pertaining to newer swab types and testing protocols in the new CLSI M40-A2

247 Each patient was swabbed using a traditional wound fiber liquid Stuart sw

248 unselected (n= 67) pediatric nasopharyngeal swabs using an RNA sequencing (RNA-seq)-based metagenomi

249 om a total of 12,776), and evaluated vaginal swabs using polymerase chain reaction (PCR) (group III,

250 A nose/throat swab was tested for influenza virus by reverse transcrip

251 One swab was used for reference culture (MacConkey broth con

252 The other swab was used for the Xpert Carba-R assay.

253 Sponge swabbing was compared to contact plate sampling to asses

254 vity of Xpert for N. gonorrhoeae from rectal swabs was 100% (95% CI, 88 to 100%) versus 93% (95% CI,

255 he positive predictive value (PPV) for rayon swabs was 78.7%, versus 83.5% for ESwabs.

256 d/or GWs preceded by a viable normal genital swab were analyzed.

257 e/negative) for WB sampled by pipette versus swab were concordant for 78/79 (98.7%) WB samples, with

258 Sites to be swabbed were identified with input from field personnel.

259 ratios (ORs) for stool specimens relative to swabs were 1.24 (95% CI 1.11-1.38) in children with diar

260 all sensitivity and specificity of the rayon swabs were 91.0% (95% confidence interval [CI], 84.6 to

261 Nasopharyngeal swabs were collected >- 30 days after serum collection,

262 Nasal/throat swabs were collected and tested for rhinovirus and other

263 Rectal swabs were collected at time of acute diarrhea and 14 da

264 Nasopharyngeal and oropharyngeal swabs were collected during influenza-like illness (ILI)

265 Nasopharyngeal swabs were collected every 4-6 weeks in the first year o

266 Three pharyngeal swabs were collected from 999 pupils aged 10 to 18 years

267 Oral and skin swabs were collected from animals with frequent contact

268 Appendix swabs were collected from children undergoing appendecto

269 Nasal/pharyngeal and rectal swabs were collected from HRSC members at recruitment an

270 Naso- and oropharyngeal swabs were collected from persons with influenza-like il

271 Prospective studies in which swabs were collected from pregnant women according to US

272 Questionnaires and oropharyngeal swabs were collected from students.

273 Deep pharyngeal swabs were collected on days 3, 14, 28, and 35 of life,

274 viewed, and nasopharyngeal and oropharyngeal swabs were collected to detect respiratory pathogens.

275 he mailing study, 80%, 52% and 29% of seeded swabs were exposed to temperatures of >30 degrees C duri

276 Isolates from throat swabs were obtained and were emm typed.

277 At each visit, nasopharyngeal (NP) swabs were obtained from both, and symptoms were catalog

278 d spaces were sampled monthly, and screening swabs were obtained from patients at admission to the IC

279 1147 stool specimens and 1024 (68%) of 1514 swabs were positive for any pathogen (p<0.0001).

280 rough May 2012), only 13 (0.3%) nasal/throat swabs were positive for influenza C.

281 Nasopharyngeal swabs were taken before PCV13 immunization.

282 Nasal swabs were taken from health-care workers every 4 weeks,

283 ndard-of-care (SOC) triple-site testing, and swabs were taken to form a pooled sample (PS) (pharyngea

284 sting: TF and TT were assessed, conjunctival swabs were tested for chlamydial infection, and blood sp

285 Pooled nasal and throat swabs were tested using multiplex real-time PCR for 33 r

286 otypes from field buffaloes, palatine tonsil swabs were the sample of choice for recovering infectiou

287 Nasopharyngeal swabs were used to assess pneumococcal colonization in s

288 n two studies: (i) dry C. trachomatis-seeded swabs were used with ACT after storage at 4 degrees C, 2

289 egative controls spiked onto negative rectal swabs) were tested.

290 he study partner, sperm present on a vaginal swab wet mount, genital inflammation of either partner,

291 mpleted a questionnaire and provided a nasal swab which was analyzed for S. aureus, methicillin-resis

292 0 +/- 2 fM in 10-fold diluted nasopharyngeal swabs, which is comparable to currently available fast m

293 2% sensitive (95% CI, 81 to 97%) from rectal swabs, while both systems were 100% sensitive from phary

294 d Stuart swab and an ESwab device, a flocked swab with a modified liquid Amies microbiology transport

295 We compared the eSwab system to a swab with an anaerobic transport semisolid agar system f

296 equivalent to copy number of 4.9) in spiked swabs with different concentrations of ZIKAV (PFU/microL

297 lacyclovir resulted in a lower percentage of swabs with HSV detection over 28 days.

298 In swabs with HSV, the mean quantity of HSV was 3.2 log10 c

299 s and 67% (1024 of 1519 children) for rectal swabs, with an unadjusted OR of 0.65 (95% CI 0.59-0.72)

300 lation from vaginal, cervical, and/or rectal swabs; with separate subanalysis on GBS bacteriuria).