64,989 research outputs found
Detecting intestinal ischemia using near infrared spectroscopy
Blood supply to the intestine can suddenly be interrupted. Acute mesenteric intestinal ischemia often requires invasive surgery to restore blood supply to the intestine. Early correction of vascular insufficiency is the most important factor in improving patient survival when confronted with acute mesenteric intestinal ischemia. A prolonged loss of blood flow results in irreversible damage to the intestine that can lead to death. It is also imperative that dead segments of the intestines be removed. Several subjective criteria are relied upon to differentiate viable from non-viable tissue, unfortunately, these criteria can lead to an inaccurate assessment. A porcine model of intestinal ischemia was used to determine the efficacy of using near infrared (NIR) spectroscopy to find ischemic segments of the intestine and detect the onset of reperfusion following resolution of vascular occlusion. Nine segments of intestine were identified and six were assigned to three treatment groups; (1) segments undergoing no vascular manipulations, (2) segments undergoing arterial/venous occlusion and (3) segments undergoing arterial/venous occlusion followed by reperfusion. The remaining segments were used as spacers and interposed between each of the ischemia segments. A classification model, using partial least square discriminant analysis, was built on the spectra collected from the segments with no vascular manipulations and the segments that were solely subjected to arterial/venous occlusion. The spectra collected from the intestinal segments that experienced both occlusion and reperfusion were used to test the classification model. The model was able to detect and distinguish ischemic intestinal tissue with a specificity and sensitivity exceeding 80% with an overall classification accuracy of 89%. The method appears to be well suited as an intra-operative assessment method when intestinal ischemia is a concern.Michael G. Sowa, Elicia Kohlenberg, Jeri R. Payette, Lorenzo Leonardi, Michelle A. Levasseur and Christopher B. Rile
Laimaphelenchus australis Zhao, Davies, Riley & Nobbs, 2006, sp. nov.
<i>Laimaphelenchus australis</i> sp. nov. <p>Figs. 1–16</p> <p> <i>Measurements</i></p> <p>See Table 1.</p> <p> <i>Material examined</i></p> <p> Holotype, ɗ, Dartmoor, Victoria, Australia (37°48’ S, 141°12’ E). Taken from a sample of bark from <i>P. r a d i a t a</i>. Coll. Zeng Qi Zhao, 3.iv.2005. It has been deposited in the Australian National Insect Collection (ANIC) (slide no. 113).</p> <p>Paratypes, Waite Insect and Nematode Collection (WINC), The University of Adelaide, slide numbers 004653–004669, 0 0 4670, 0 0 4673, 0 0 4674, 004676–004678. Thirteen males and 17 females were examined and measured. Taken from five locations including: Kuitpo and Mt Gambier, South Australia; Dartmoor and Ballarat, Victoria; and Tumut, NSW.</p> <p> <i>Description</i></p> <p> <i>Female</i>. Short, relatively stout (ratio a range 24.2–31.6) nematodes; habitus ventrally arcuate, with curvature more pronounced in posterior region (Fig. 2). Cuticular debris from a previous moult retained on posterior body in some specimens. Body annules about 0.8 µm wide at mid­body. Lateral fields (Fig. 14) with 4 incisures, occupying about 15% of body width, not areolate, extending to origin of tubercle.</p> <p>Cephalic region rounded, offset, slightly wider than body at base (Fig. 7). SEM shows labial area with hemispherical sphere, no labial disc, smooth, oral aperture flattened (Fig. 13). Cephalic region with six labial sectors of equal width, amalgamated, separated by double, well­developed ribs. Cephalids not seen. Stylet slender with distinct basal swellings, 9.2–12.3 µm long.</p> <p>Median bulb rounded to oval, 11.5–14.6 µm long, and 9.2–12.3 µm wide, with crescentic valves in the middle, located 41.5–51.5 µm from the anterior end; its length 3.1–4.6 µm, width 2.7–3.8 µm. The nerve ring is located about one body width from the excretory pore at the point where the lumen of the intestinal tract widens.</p> <p>Excretory pore conspicuous, about one and a half body widths posterior to median bulb, 70.8–84.6 µm from anterior end. Hemizonid not seen.</p> <p>Oesophageal glands overlap intestine on dorsal side, extending for 115.4–147.7 µm. Oesophago­intestinal junction 1–1.5 body widths posterior to base of bulb.</p> <p>Reproductive system with outstretched ovary with oocytes in a single row; spermatheca filled with sperm cells; vagina sloping slightly towards anterior, not distally sclerotised. Post vulval uterine sac 21.5–44.6 µm long, occupying 22–41% of distance from vulva to anus; containing few cells. Vulva without anterior flap; in some specimens appears slightly protruding (Figs. 5, 15).</p> <p>Tail conoid, ventrally curved, with a single offset terminus, bearing 3–4 pedunculate tubercles, ending with 4–6 finger­like protrusions (Figs. 8, 16).</p> <p> <i>Male</i>. Morphology similar to that of female (Figs. 1, 9). Testis outstretched, spermatocytes in one single column. Spicules paired, dorsal limb 21.5–26.9 µm long, ventral limb 13.1–16.9 µm long, from distal to proximal end 15.4–19.2 µm long and 16.9–20.8 µm measured along median line; rosethorn­shaped, with prominent capitulum and rostrum broad with bluntly rounded tip (Figs. 4, 10). No gubernaculum present. Caudal papillae located at three positions: first pair preanal subventral, second pair postanal subventral, at about 40–45% of distance between cloaca to tail tip, and third pair at about 75–80% of distance between cloaca to tail tip (Fig. 12).</p> <p>Tail conoid, ventrally curved, with a single offset terminus, bearing 3–4 pedunculate tubercles, ending with 4–6 finger­like protrusions (Fig. 11).</p> <p> <i>Diagnosis</i></p> <p> <i>Laimaphelenchus australis</i> <b>sp. nov.</b> is characterised by having a distinct tail shape with an offset terminus, with 3–4 clearly pedunculate tubercles ending in 4–6 finger­like protrusions which curve towards the nematode body in both sexes; lateral fields with four lines; off set head; three pairs of subventral caudal papillae, one pair preanal, one pair at about 40–45% of distance between cloaca to tail end, and one pair at about 75–80% of distance between cloaca to tail end. The cephalic region lacks a distinct labial disc, and has six labial sectors of equal width, amalgamated, separated by pairs of well­developed ribs.</p> <p> <i>Relationships</i></p> <p> The genus <i>Laimaphelenchus</i> contains two groups of species, one with a vulval flap and one without (Baujard 1981; Hunt 1993). <i>Lamaphelenchus australis</i> <b>sp. nov.</b> belongs to the second group, bringing its members to five. The other species in this group are <i>L. pannocaudus</i> Massey, <i>L. phloesini</i> Massey, <i>L. pini</i> Baujard, and <i>L. patulus</i> Swart. <i>Laimaphelenchus australis</i> <b>sp. nov.</b> is separated from <i>L. penardi</i> Steiner, <i>L. deconincki</i> Elmiligy and Geraert, <i>L. pensobrinus</i> Massey, <i>L. cocuccii</i> Doucet, <i>L. unituberculus</i> Bajaj and Walia, <i>L. helicosoma</i> Peneva and Chipev, and <i>L. preissii</i> Zhao, Davies, Riley and Nobbs by the absence of a vulval flap in the former.</p> <p> Females of <i>L. australis</i> <b>sp. nov.</b> (371.5–459.2 µm) are close to <i>L. pini</i> (350–470 µm) (Baujard 1981), <i>L. patulus</i> (460–530 µm) (Swart 1997) and <i>L. phloeosini</i> (430–510 µm) (Massey 1974) in body length. They are shorter than all other described species; <i>L. penardi</i> (573–800 µm) (Filipipjev and Schuurmans Stekhoven 1941), <i>L. deconincki</i> (690–770 µm) (Elmiligy and Geraert 1972), <i>L. pensobrinus</i> (610 µm) (Massey 1966); <i>L. pannocaudus</i> (960 µm) (Massey 1966); <i>L. cocuccii</i> (570–740 µm) (Doucet 1992); <i>L. unituberculus</i> (690–800 µm) (Bajaj and Walia 2000), <i>L. helicosoma</i> (619 µm) (Peneva and Chipev 1999), and <i>L. preissii</i> (1007–1385 µm) (Zhao <i>et al.</i> 2006).</p> <p> The length of the post­uterine sac of <i>L. australis</i> <b>sp. nov.</b> (20–52 µm) (Swart 1997) overlaps that of <i>L. phloeosini</i> (28–50 µm) (Elmiligy and Geraert 1972), <i>L. pini</i> (18–30 µm) (Baujard 1981), <i>L. patulus</i> (25–40 µm) (Swart 1997), <i>L. deconincki</i> (32–46 µm) (Elmiligy and Geraert 1972), <i>L. cocuccii</i> (40–63 µm) (Doucet 1992), <i>L. unituberculus</i> (45–60 µm) (Bajaj and Walia 2000), <i>L. pensobrinus</i> (37–44 µm) (Massey 1966) and <i>L. helicosoma</i> (21 µm) (Peneva and Chipev 1999); but is shorter than that of <i>L. pannocaudus</i> (82–103 µm) (Massey 1966), <i>L. penardi</i> (72–173 µm) (Filipipjev and Schuurmans Stekhoven 1941) and <i>L. preissii</i> (86–157 µm) (Zhao <i>et al.</i> 2006).</p> <p> The vagina is surrounded by a relatively thin cuticularised tube, which is similar to most species in the genus, but it differs from <i>L. deconincki</i> which has a thick cuticularised tube (Elmiligy and Geraert 1972).</p> <p> With respect to the lateral field, <i>L. australis</i> <b>sp. nov.</b> has 4 incisures as do <i>L. pannocaudus, L. unituberculus L. pini, L. preissiii</i> and <i>L. phloeosini</i>. It differs from <i>L. penardi</i> and <i>P. pensobrinus</i> that have 2 incisures and <i>L. patulus, L. helicosoma, L. cocuccii, L. deconincki</i> with 3.</p> <p> In general, the morphology of the tail tip of <i>L. australis</i> <b>sp. nov.</b> is similar to all described species of the genus, except <i>L. helicosoma</i> which has poorly developed tubercles (Peneva and Chipev 1999), <i>L. unituberculus</i> which has a single stalked suckerlike tubercle (Bajaj and Walia 2000), and <i>L. preissii</i> which has a broad tubercle with many tiny projections (Zhao <i>et al.</i> 2006).</p> <p> In <i>L. australis</i> <b>sp. nov.</b>, the labial disc is reduced and amalgamated with the head capsule, the anterior lip is smooth, and the oral aperture is flattened. Its cephalic region has six labial sectors of equal width, which are amalgamated but separated by pairs of welldeveloped ribs. In this, it differs from all species in the genus except that of <i>L. cocuccii</i> (Doucet 1992). However, <i>L. australis</i> <b>sp. nov.</b> can be differentiated from <i>L. cocuccii</i> by the absence of the vulval flap.</p> <p> In addition to the differences in the anterior lip between <i>L. australis</i> <b>sp. nov.</b> and <i>L. pini</i>, they also can be differentiated by the position of the oesophago­intestinal junction. In <i>L. pini,</i> the oesophago­intestinal junction is immediately posterior to the base of the bulb (Baujard 1981) but in <i>L. australis</i> <b>sp. nov.</b>, it is 1–1.5 body widths behind the bulb.</p> <p> Males of <i>L. australis</i> <b>sp. nov.</b> (300.8–411.5 µm) are shorter than the female in body length. The spicule shape is similar to that of <i>L. patulus</i>, but it differs in that no gubernaculum­like structure is present at the distal end of spicules (Swart 1997). Three pairs of subventral caudal papillae are present; one pair preanal, a second pair subventral at about 40–45% of the distance from the cloaca to the tail tip, and a third pair at about 75–80% of the distance from the cloaca to the tail terminal. This is similar to all species in the genus in terms of the number of the papillae except <i>L. pensobrinus</i> and <i>L. preissii</i> that have 2 pairs of caudal papillae (Massey 1966; Zhao <i>et al.</i> 2006) and <i>L. cocuccii</i> where males are unknown (Doucet 1992). The male of <i>L. preissii</i> also has a bursa, lacking in <i>L. australis</i> <b>sp. nov.</b> The labial plate and the tail shape are the same as in the female.</p> <p> <i>Etymology</i></p> <p>Named for Australia, the country where it was first isolated.</p>Published as part of <i>Zhao, Zeng Q., Davies, Kerrie A., Riley, Ian T. & Nobbs, Jackie M., 2006, Laimaphelenchus australis sp. nov. (Nematoda: Aphelenchina) from exotic pines, Pinus radiata and P. pinaster, in Australia, pp. 35-44 in Zootaxa 1248</i> on pages 37-43, DOI: <a href="http://zenodo.org/record/172959">10.5281/zenodo.172959</a>
Differential Acquisition of m-Sequences using Recursive Soft Sequential Estimation
In this contribution a novel sequential estimation method is proposed for the acquisition of -sequences. This sequential estimation method exploits the principle of iterative soft-in-soft-out (SISO) decoding for enhancing the acquisition performance, and that of differential pre-processing for the sake of achieving an enhanced acquisition performance, when communicating over various communication environments. Hence the advocated acquisition arrangement is referred to as the Differential Recursive Soft Sequential Estimation (DRSSE) acquisition scheme. The DRSSE acquisition scheme exhibits a low complexity, which is similar to that of an -sequence generator, while achieving an acquisition time that is linearly dependent on the number of stages in the -sequence generator. A low acquisition time is achieved with the advent of the property that the proposed DRSSE scheme is capable of determining the real-time reliabilities associated with the decision concerning a set of, say , consecutive chips. This set of consecutive chips constitutes the sufficient initial condition for enabling the local -sequence generator to produce a synchronized local despreading -sequence replica. Owing to these attractive characteristics, the DRSSE acquisition scheme constitutes a promising initial synchronization scheme for acquisition of long -sequences, when communicating over various propagation environments
J. M. Owens, Mrs. Collection
Photograph of the Directors of S. T. L. & O. C. Railroad. L to R: standing, H. Overholser, J. M. Owen, S. A. Steward, F. L. Dobbin, F. M. Riley, (Seated) C. G. Jones, H. Will, T.M. Richardson, Sidney Clarke
∑_(l+m=k,l,m≥0) ((α+l-1)¦l) ((β+m-1)¦m)=((α+β+k-1)¦k) and its application to negative binomial distribution
We prove here the following equation: ∑_(l+m=k,l,m≥0) ((α+l-1)¦l) ((β+m-1)¦m)=((α+β+k-1)¦k) and give its application to prove the reproductive property of the negative binomial distribution.
These finite sum equation involving binomial coefficients and proof of the reproductive property are not known as far as the author knows.論文(Article)departmental bulletin pape
De Maiestate / Praeside M. Jacobo Thomasio, Moralis Philosoph. P. P., publice disputabit Johannes Dunte, R. L. Author & Respon: ad diem 9. Septembr. H L. Q. C.
DE MAIESTATE / PRAESIDE M. JACOBO THOMASIO, MORALIS PHILOSOPH. P. P., PUBLICE DISPUTABIT JOHANNES DUNTE, R. L. AUTHOR & RESPON: AD DIEM 9. SEPTEMBR. H L. Q. C.
De Maiestate / Praeside M. Jacobo Thomasio, Moralis Philosoph. P. P., publice disputabit Johannes Dunte, R. L. Author & Respon: ad diem 9. Septembr. H L. Q. C. (1)
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Beiträge (21
Erratum to: Effect of moderate red wine intake on cardiac prognosis after recent acute myocardial infarction of subjects with Type 2 diabetes mellitus (Diabetic Medicine, (2006), 23, 9, (974-981), 10.1111/j.1464-5491.2006.01886.x)
In an article by Marfella et al, the author name C. Saron is incorrect and should be listed as C. Sardu. Therefore the correct author list is: R. Marfella, F. Cacciapuoti, M. Siniscalchi, F. C. Sasso, F. Marchese, F. Cinone, E. Musacchio, M. A. Marfella, L. Ruggiero, G. Chiorazzo, D. Liberti, G. Chiorazzo, G. F. Nicoletti, C. Sardu, F. D'Andrea, C. Ammendola, M. Verza and L. Coppola.In an article by Marfella et al, the author name C. Saron is incorrect and should be listed as C. Sardu. Therefore the correct author list is: R. Marfella, F. Cacciapuoti, M. Siniscalchi, F. C. Sasso, F. Marchese, F. Cinone, E. Musacchio, M. A. Marfella, L. Ruggiero, G. Chiorazzo, D. Liberti, G. Chiorazzo, G. F. Nicoletti, C. Sardu, F. D'Andrea, C. Ammendola, M. Verza and L. Coppola
Margaret Martin Roth Award Winners, 1985-2024
Margaret Martin-Roth was named Indiana Nurse of the Year in 1980 by the Central Indiana March of Dimes. She retired in 1985. An annual Margaret Martin-Roth Award was established at that time that honors the tradition of patient and family centered care practiced by Margaret during her tenure at Riley Hospital for Children. Note that no award was presented from 2013-2015
Margaret Martin Roth Award Winners, 1985-2024
Margaret Martin-Roth was named Indiana Nurse of the Year in 1980 by the Central Indiana March of Dimes. She retired in 1985. An annual Margaret Martin-Roth Award was established at that time that honors the tradition of patient and family centered care practiced by Margaret during her tenure at Riley Hospital for Children. Note that no award was presented from 2013-2015
Halsted M. Stone, M.D., oral history interview, December 18, 1992
Dr. Laurie L. Brown, M.D., and Dr. Allen Brown, M.D., conducted this oral history interview at the 145th Annual Meeting of the South Carolina Medical Association (SCMA) at the Omni Hotel in Charleston, South Carolina, on April 23, 1993. In this interview, Dr. Halsted M. Stone, M.D., discusses his family, educational background, career in medicine, and service in organized medicine. Stone also discusses his tenure as a councilor for SCMA and as President for the association from 1980 to 1981. Among the issues facing the association and the field of medicine during his tenure, Dr. Stone notes: healthcare access, rising healthcare costs, high insurance premiums, national health insurance, the establishment of health maintenance organizations for industry professions, and the creation of a committee to help physicians renegotiate salary contracts. Stone also discusses his work in beginning the professional review organization (PSRO) and with South Carolina Governor Richard Riley to place non-physicians on all boards
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