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1.
J Vasc Interv Radiol ; 19(8): 1202-7, 2008 Aug.
Article in English | MEDLINE | ID: mdl-18656014

ABSTRACT

PURPOSE: To compare complications in catheters placed by the fluoroscopically guided percutaneous method versus directly visualized surgery. MATERIALS AND METHODS: A retrospective cohort analysis was performed. Mechanical complication rate data, including catheter leakage, malfunction, malposition, and bleeding, were compared between the two groups over a 1-year follow-up period. Additionally, exit site infection rates, tunnel infection rates, and peritonitis episodes were evaluated based on the incidence within 30 days of insertion and 30 days to 1 year after insertion. RESULTS: A total of 101 patients were analyzed (52 in the fluoroscopic guidance group, 49 in the direct visualization group). Prevalence of diabetes was similar: 56% in the directly visualized surgery group and 47% in the fluoroscopically guided treatment group (P = .37). Although the difference was not significant, complication rates tended to be higher in the directly visualized surgery group compared with the percutaneous placement group. These included catheter leakage (13% vs 4%; P = .093), malfunction (11% vs 9%; P = .73), malposition (13% vs 6%; P = .20), and bleeding (8% vs 2%; P = .21). There were no differences in early and late exit site infections and tunnel infections. Late peritonitis rates were lower in the percutaneous placement group (20%) than in the direct visualization group (42%) (P = .018). Diabetic patients had approximately six times greater risk of catheter malfunction than nondiabetic patients regardless of method of catheter insertion. CONCLUSIONS: Placement of peritoneal dialysis catheters percutaneously with fluoroscopic guidance is as safe as placement with direct visualization techniques.


Subject(s)
Catheters, Indwelling , Fluoroscopy/methods , Peritoneal Dialysis/instrumentation , Peritoneal Dialysis/methods , Radiography, Interventional/methods , Surgery, Computer-Assisted/methods , Cohort Studies , Female , Humans , Male , Middle Aged , Retrospective Studies , Treatment Outcome
2.
Plant Cell Rep ; 26(12): 2055-62, 2007 Dec.
Article in English | MEDLINE | ID: mdl-17680245

ABSTRACT

Plantlets of Dendrobium Chao Praya Smile maintained in vitro were induced to flower, which produced viable seeds within about 11 months. A two-layer (Gelrite-solidified layer topped with a layer of liquid medium of the same volume and composition) culture system containing benzyladenine (BA) at 11.1 muM induced the highest percent of flowering (45%) in plantlets within 6 months from germination. The percentage of inflorescence induction was increased to 72% by pre-selecting morphologically normal seedlings prior to two-layer culture. Plantlets in culture produced both complete (developmentally normal but smaller than flowers of field grown plants) and incomplete flowers. Pollen and female reproductive organs of in vitro-developed complete flowers were morphologically and anatomically similar to flowers of field grown plants. In addition, 65% of the pollen grains derived from in vitro-developed flower were tetrad suggesting that regular meiosis occurred during microsporogenesis. The percentage of germination of pollen grains derived from in vitro-developed flowers and flowers of field grown plants, incubated on modified Knops' medium for 8 days, were 18.2 and 52.8%, respectively. Despite a lower percentage of germination of the pollen grains derived from in vitro-developed flowers, flowers induced in culture could be self-pollinated and developed seedpods with viable seeds. Nearly 90% of these seeds developed into protocorms on germination in vitro. These seedlings were grown in culture and induced to flower in vitro again using the same procedure.


Subject(s)
Flowers/growth & development , Orchidaceae/growth & development , Seeds/growth & development , Breeding , Cells, Cultured , Flowers/physiology , Germination/physiology , Orchidaceae/cytology , Orchidaceae/physiology , Pollen/growth & development , Pollen/physiology , Pollination/physiology , Seeds/physiology
3.
Ann Vasc Surg ; 20(1): 75-82, 2006 Jan.
Article in English | MEDLINE | ID: mdl-16378153

ABSTRACT

In 1996, as part of Kaiser Permanente Southern California's participation in the Medicare End-Stage Renal Disease Managed Care Demonstration Project, a multidisciplinary continuous quality improvement (CQI) committee was formed, which included nephrologists, vascular surgeons, interventional radiologists, care managers, a renal quality-improvement nursing director, and renal program administrators. The goal of this report was to analyze the impact of this CQI program on hemodialysis outcomes within the organization. Kaiser Permanente is a national, integrated, nonprofit, staff model health maintenance organization with 8 million members. The southern California region has 3.1 million members and currently manages the health care of 3,700 hemodialysis patients, 300 peritoneal dialysis patients, and 1,000 kidney transplant patients. Thirty-one vascular surgeons and 29 interventional radiologists provide for their hemodialysis access needs. The Kidney Disease Dialysis Outcomes Quality Initiative (K/DOQI) guidelines were adopted, as well as measures to perform more venous transpositions and less common arteriovenous fistulas (AVFs) before graft placement. The outcomes assessed included incidence and prevalence of AVFs, grafts, and catheters; replacement access with AVFs; and combined AVF and graft thrombosis episodes per patient per year. Primary AVF incidence rates increased from 27% in 1997 to 88% in 2003. AVF prevalence rates increased from 30% in 1997 to 62% in 2003. Replacement access which is an AVF increased from 26% in 1998 to 58% in 2003. Yearly thrombosis episodes/patient decreased from 0.62 in 1998 to 0.34 in 2003. Catheter usage as of 2003 comprised an incidence of 65% and prevalence (> or =90 days) of 13%, which was essentially unchanged from 1999, despite improvements in fistula usage and thrombosis rate. The rate of AVF prevalence can be increased dramatically, exceeding the 40% K/DOQI recommendation, by using the CQI process. Increased prevalence of AVF is associated with a lower yearly incidence of thrombosis episodes/patient. Reducing excessive catheter usage appears to be a more difficult problem.


Subject(s)
Arteriovenous Shunt, Surgical , Health Maintenance Organizations , Kidney Failure, Chronic/therapy , Outcome Assessment, Health Care , Patient Care Team , Renal Dialysis , Aged , Arteriovenous Shunt, Surgical/statistics & numerical data , California , Catheterization , Catheters, Indwelling , Education, Medical, Continuing , Female , Humans , Kidney Failure, Chronic/ethnology , Male , Middle Aged , Patient Education as Topic , Practice Guidelines as Topic , Renal Dialysis/adverse effects , Thrombosis/prevention & control
4.
Plant Cell Rep ; 23(1-2): 91-8, 2004 Aug.
Article in English | MEDLINE | ID: mdl-15118833

ABSTRACT

A cyclic somatic embryogenic system was used to induce mutations in cassava variety PRC 60a in vitro. Globular-stage somatic embryos were selected as suitable experimental materials, and 50 Gy of gamma-rays was determined to be the optimal dose for inducing mutations. During subsequent field trials, more than 50% of the regenerated mutant lines varied morphologically from wild-type plants. Consequently, we used this approach to induce genetic variability for obtaining novel cassava cultivars. Among the different mutant lines obtained, lines S14 and S15 showed large morphological variations. In 10-month-old S14 and S15 mutant lines, storage root yield was reduced 17-fold and 60-fold, respectively, compared to wild-type plants, while the storage roots of S15 mutant plants also exhibited an almost 50% decrease in starch content and a significant reduction (30%) in amylose content. These two features were observed throughout the different developmental stages of the storage roots in S15 plants.


Subject(s)
Adenine/analogs & derivatives , Gene Expression Regulation, Plant/genetics , Genetic Engineering/methods , Manihot/genetics , Manihot/metabolism , Mutation , Seeds/metabolism , Starch/genetics , 2,4-Dichlorophenoxyacetic Acid/pharmacology , Adenine/pharmacology , Benzyl Compounds , Down-Regulation/genetics , Ethyl Methanesulfonate/pharmacology , Gamma Rays , Gene Expression Regulation, Plant/drug effects , Gene Expression Regulation, Plant/radiation effects , Genetic Variation/drug effects , Genetic Variation/genetics , Genetic Variation/radiation effects , Indoles/pharmacology , Kinetin , Manihot/growth & development , Mutagenesis/drug effects , Mutagenesis/radiation effects , Plant Roots/growth & development , Plant Roots/metabolism , Plant Roots/radiation effects , Purines , Seeds/growth & development , Seeds/radiation effects , Starch/biosynthesis , Starch/chemistry
6.
Nephrol News Issues ; 17(9): 25-7, 30, 2003 Aug.
Article in English | MEDLINE | ID: mdl-12971222

ABSTRACT

In the Southern California Kaiser Permanente health plan, all patients having serum creatinine measured will automatically have their GFR reported. Those with reduced GFR are identified and classified into one of the five CKD stages. The PCPs are encouraged to be involved in the care of patients in CKD stages 1-3. Education, guidelines, and algorithms are provided to the PCPs, and nephrology consultation is encouraged. Patients in CKD stage 3 with significant risk factors for developing ESRD and those in CKD stages 4 and 5 are referred to nephrologists. Patients are encouraged to participate [table: see text] in their own care by attending the educational classes provided.


Subject(s)
Health Maintenance Organizations/organization & administration , Kidney Failure, Chronic/therapy , Patient Education as Topic/organization & administration , Renal Dialysis , Humans , Primary Health Care/organization & administration , Program Evaluation
7.
Hemodial Int ; 7(4): 338-41, 2003 Oct 01.
Article in English | MEDLINE | ID: mdl-19379385

ABSTRACT

INTRODUCTION: A structured predialysis multidisciplinary team program is beneficial in improving quality of life in patients with end-stage renal disease (ESRD). Educating pre-ESRD patients about their disease is vital in their care. Patients who can identify signs and symptoms of impending problems can seek help and avoid complications that may lead to hospital admissions. Our dialysis center offers two predialysis classes in a structured format. The first class is for those patients with mild to moderate renal disease, whereas the second class is for those with advanced renal disease who are expected to need dialysis in 3 to 6 months. The patients are followed by a multidisciplinary team once they are enrolled in our chronic kidney disease program. METHODS: We retrospectively reviewed all the charts of patients who started dialysis at our center between 1997 and 2000. We identified 68 patients who participated in the predialysis education program and 35 patients who did not because of late referral or refusal to participate. We compared these two groups over a 100-day period (10 days before initial dialysis and 90 days after), for hospitalizations, emergency room (ER) visits, and dialysis access placement. Patients' comorbid conditions, complications, and length of hospitalizations were extracted from the medical records. RESULTS: The 68 patients who completed the predialysis program had an average age of 60.3 years, a total of 96 hospital days, and 39 ER visits. Average length of hospital stay for these patients was 1.4 days. Three patients (4.4%) required placement of temporary catheters for the initial dialysis. Fifty-one percent of these patients had diabetes mellitus. The 35 patients of average age of 54.9 years who did not go through the program had 347 total hospital days and 39 ER visits. Average length of hospitalization was 9.9 days. Thirteen patients (37%) required temporary catheters for initial dialysis. This group included 16 patients (45.7%) with diabetes. CONCLUSION: Patients who participated in a multidisciplinary predialysis education program had fewer complications, ER visits, and hospitalizations. They also had fewer temporary catheter placements, shorter hospital stays, and reduced costs associated with initial dialysis.

8.
J Pharm Sci ; 91(6): 1396-404, 2002 Jun.
Article in English | MEDLINE | ID: mdl-12115839

ABSTRACT

Previous studies on chitosan-insulin nanoparticles have reported diverse encapsulation efficiency and insulin release profiles despite similar formulation and preparation procedures. This study examined the efficiency and mechanism of association of insulin with chitosan nanoparticles in the pH range of 2.3 to 6.3. Nanoparticles of 237 to 235 nm were prepared by ionotropic gelation of chitosan with tripolyphosphate counterions. Insulin was quantified by an RP-HPLC method. The insulin association efficiency (AE) spanned a broad range from 2 to 85%, and was highly sensitive to formulation pH. Highest AE was measured at insulin loading concentrations >/= 4.28 U/mL and pH 6.1, close to the pI of native insulin and the pK(a) of chitosan. This association, attributed to physical adsorption of insulin through hydrophobic interactions with chitosan, was labile, and the associated insulin rapidly and completely released by dilution of the nanoparticles in aqueous media of pH 2 to 7.4. AE obtained at pH 5.3 was less than half that measured at pH 6.1 at corresponding insulin concentration, but the association at pH 5.3 appeared to be based on stronger interactions, because the release of insulin was pH-dependent and recovery was less than 25% even upon disintegration of the chitosan matrix. Interaction of insulin with the chitosan nanoparticles rendered the protein more susceptible to acid and enzymatic hydrolyses, the effects being more predominant in nanoparticles prepared at pH 5.3 than at pH 6.1.


Subject(s)
Chitin/chemistry , Insulin/chemistry , Administration, Oral , Chemistry, Pharmaceutical , Chitin/analogs & derivatives , Chitosan , Drug Carriers , Drug Delivery Systems , Hydrogen-Ion Concentration , Insulin/administration & dosage , Nanotechnology , Particle Size
9.
J Exp Bot ; 53(368): 551-8, 2002 Mar.
Article in English | MEDLINE | ID: mdl-11847254

ABSTRACT

Dehydration tolerance of in vitro orchid protocorms was investigated under controlled drying conditions and after abscisic acid (ABA) pretreatment. Protocorms were obtained by germinating seeds on Murashige and Skoog (MS) medium containing 10% (v/v) coconut water, 2% (w/v) sucrose and 0.8% (w/v) agar, and were dehydrated in relative humidities (RH) ranging from 7% to 93% at 25 degrees C. The critical water content of dehydration tolerance was determined, using the electrolyte leakage method. Drying rate affected the critical water content. Slow drying under high RH conditions achieved the greatest tolerance to dehydration. ABA pretreatment decreased the drying rate of protocorms, and increased dehydration tolerance. Improved tolerance to dehydration after ABA treatment was correlated with the effect of ABA on drying rate of protocorms. When critical water content of protocorms dried under different RH was plotted as a function of actual drying rate, no significant difference in tolerance to dehydration was observed between ABA-treated and control protocorms. ABA pretreatment and dehydration of orchid protocorms induced the synthesis of dehydrin, especially under the slow drying conditions. ABA pretreatment also promoted dry matter accumulation such as carbohydrates and soluble proteins and increased the concentration of K(+) and Na(+) ions in protocorms. The ABA-induced decrease in drying rate was correlated with lower osmotic potential, the enhanced maturity of protocorms and the accumulation of dehydrin in protocorms during pretreatment.


Subject(s)
Abscisic Acid/pharmacology , Orchidaceae/metabolism , Plant Growth Regulators/pharmacology , Plant Proteins/biosynthesis , Plant Structures/metabolism , Water/metabolism , Acclimatization/drug effects , Acclimatization/physiology , Blotting, Western , Calcium/analysis , Carotenoids/analysis , Chlorophyll/analysis , Heat-Shock Proteins/biosynthesis , Heat-Shock Proteins/drug effects , Orchidaceae/drug effects , Orchidaceae/growth & development , Osmotic Pressure , Plant Proteins/drug effects , Plant Structures/drug effects , Plant Structures/growth & development , Potassium/analysis , Sodium/analysis
10.
N Engl J Med ; 346(7): 491-6, 2002 Feb 14.
Article in English | MEDLINE | ID: mdl-11844850

ABSTRACT

BACKGROUND: In patients with decreased resistance to infection, Staphylococcus aureus is a major cause of bacteremia and its complications. The capsular polysaccharides are essential for the pathogenesis of and immunity to S. aureus infection and are targets for vaccines. METHODS: In a double-blind trial involving patients with end-stage renal disease who were receiving hemodialysis, we evaluated the safety, immunogenicity, and efficacy of a vaccine with S. aureus type 5 and 8 capsular polysaccharides conjugated to nontoxic recombinant Pseudomonas aeruginosa exotoxin A. Between April 1998 and August 1999, 1804 adult patients at 73 hemodialysis centers were randomly assigned to receive a single intramuscular injection of either vaccine or saline. IgG antibodies to S. aureus type 5 and 8 capsular polysaccharides were measured for up to two years, and episodes of S. aureus bacteremia were recorded. Efficacy was estimated by comparing the incidence of S. aureus bacteremia in the patients who received the vaccine with the incidence in the control patients. RESULTS: Reactions to the vaccine were generally mild to moderate, and most resolved within two days. The capsular polysaccharides elicited an antibody response of at least 80 microg per milliliter (the estimated minimal level conferring protection) in 80 percent of patients for type 5 and in 75 percent of patients for type 8. The efficacy during weeks 3 to 54 was only 26 percent (P=0.23). However, between weeks 3 and 40 after vaccination, S. aureus bacteremia developed in 11 of 892 patients in the vaccine group who could be evaluated for bacteremia, as compared with 26 of 906 patients in the control group (estimate of efficacy, 57 percent; 95 percent confidence interval, 10 to 81 percent; nominal P=0.02). CONCLUSIONS: In patients receiving hemodialysis, a conjugate vaccine can confer partial immunity against S. aureus bacteremia for approximately 40 weeks, after which protection wanes as antibody levels decrease.


Subject(s)
Bacteremia/prevention & control , Bacterial Vaccines , Kidney Failure, Chronic/complications , Renal Dialysis , Staphylococcal Infections/prevention & control , Staphylococcal Vaccines , Adult , Antibodies, Bacterial/blood , Bacteremia/etiology , Bacterial Vaccines/adverse effects , Bacterial Vaccines/immunology , Double-Blind Method , Humans , Kidney Failure, Chronic/therapy , Staphylococcal Infections/etiology , Staphylococcal Infections/immunology , Staphylococcus aureus/classification , Staphylococcus aureus/immunology , Staphylococcus aureus/isolation & purification , Vaccines, Conjugate/adverse effects , Vaccines, Conjugate/immunology
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