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1.
Dig Dis Sci ; 60(12): 3764-70, 2015 Dec.
Article in English | MEDLINE | ID: mdl-26204973

ABSTRACT

BACKGROUND: Vaginal delivery is an identified risk factor for anal sphincter injury. Therefore, to identify postpartum injury, an antepartum value or a normal range is required. However, at present, the normal values of 3D manometry are not available for primigravida or pregnant mothers. AIMS: Our study aims at describing normal values of 3D manometry in primigravida. METHODS: We analyzed 3DARM data of 101 consecutive primigravid mothers in the third trimester. 3DARM was performed using the Given Imaging(®) ManoScan system. RESULTS: The mean age was 24.7 (SD 5.1) years. All patients had a normal Cleveland Clinic Incontinence Score. The mean resting pressure (RP) was 87.02 (SD 18.43) mmHg and the maximum squeeze pressure (SP) was 179.21 (SD 52.96) mmHg. The mean length of the high-pressure zone (HPZ) was 3.67 (SD 0.52) cm. Mean volumes for initial rectal sensation, urge, and discomfort were 50.36 (± 25.57), 76.70 (± 35.17), and 143.40 (± 66.26) ml, respectively. The pressure asymmetry was highest in the lower anal sphincter and lowest in the mid-sphincter. There was a statistically significant relationship between the HPZ and RP (Pearson ρ -0.23, p = 0.01), height (Pearson ρ 0.22, p = 0.028), and weight (Pearson ρ 0.25, p = 0.012). There were no statistically significant correlations between age, height, or weight with RP, SP, or balloon fill volumes. The characteristic appearance of the normal RP and SP was clearly visualized in all patients. CONCLUSIONS: Normal 3DARM values for Sri Lankan primigravid mothers have been established. These may be used as reference values by other investigators.


Subject(s)
Anal Canal/physiology , Gravidity/physiology , Manometry , Adult , Female , Humans , Pregnancy , Pressure , Reference Values , Young Adult
2.
Opt Express ; 23(8): 10188-97, 2015 Apr 20.
Article in English | MEDLINE | ID: mdl-25969061

ABSTRACT

In this paper we excite bound long range stripe plasmon modes with a highly focused laser beam. We demonstrate highly confined plasmons propagating along a 50 µm long silver stripe 750 nm wide and 30 nm thick. Two excitation techniques were studied: focusing the laser spot onto the waveguide end and focusing the laser spot onto a silver grating. By comparing the intensity of the out-coupling photons at the end of the stripe for both grating and end excitation we are able to show that gratings provide an increase of a factor of two in the output intensity and thus out-coupling of plasmons excited by this technique are easier to detect. Authors expect that the outcome of this paper will prove beneficial for the development of passive nano-optical devices based on stripe waveguides, by providing insight into the different excitation techniques available and the advantages of each technique.

3.
Ann Trop Paediatr ; 30(1): 73-5, 2010.
Article in English | MEDLINE | ID: mdl-20196939

ABSTRACT

Persistent umbilical drainage may be due to vestigial remnants of the omphalomesenteric duct. Rarely, it may be owing to the presence of ectopic pancreatic tissue within these remnants. An 18-month-old boy underwent surgical exploration for umbilical discharge. An umbilical nodule containing both ectopic gastric and pancreatic tissue was found. This is the first instance where both tissue types have been implicated as a cause.


Subject(s)
Bodily Secretions , Choristoma/diagnosis , Pancreas , Stomach , Umbilicus/pathology , Choristoma/surgery , Histocytochemistry , Humans , Infant , Male , Microscopy , Umbilicus/surgery
5.
Trans R Soc Trop Med Hyg ; 90(6): 684-8, 1996.
Article in English | MEDLINE | ID: mdl-9015519

ABSTRACT

In a double-blind trial on 37 asymptomatic microfilaraemic subjects (minimum 400 microfilariae [mf] per mL) with Wuchereria bancrofti infection, the safety, tolerability and macrofilaricidal efficacy of 12 fortnightly doses of ivermectin, 400 micrograms/kg (ivermectin group), was compared with 12 fortnightly doses of diethylcarbamazine (DEC), 10 mg/kg (DEC group), over a period of 129 weeks after treatment. A control group (LDIC group) was treated with low dose ivermectin to clear microfilaraemia, for ethical reasons. Both ivermectin and DEC in high multiple doses were well tolerated and clinically safe. Macrofilaricidal efficacy was assessed by prolonged clearance of microfilaraemia, appearance of local lesions, and reduction of circulating W. bancrofti adult antigen detected by an antigen capture enzyme-linked immunoassay based on the monoclonal antibody AD12. Mf counts fell more rapidly after ivermectin than after DEC, but low residual mf levels were equivalent in these groups after week 4. Conversely, filarial antigen levels fell more rapidly after DEC than after ivermectin, but low residual antigen levels in these groups were statistically equivalent at all times beyond 12 weeks. Mild, self-limited systemic reactions to therapy were observed in all 3 treatment groups. Local reactions, such as development of scrotal nodules, were observed in several subjects in the DEC and ivermectin groups. These results suggested that high dose ivermectin and DEC both had significant macrofilaricidal activity against W. bancrofti, but neither of these intensive therapeutic regimens consistently produced complete cures. Thus, new drugs or dosing schedules are needed to achieve the goal of killing all filarial parasites in the majority of patients.


Subject(s)
Diethylcarbamazine/therapeutic use , Filariasis/drug therapy , Filaricides/therapeutic use , Ivermectin/therapeutic use , Parasitemia/drug therapy , Wuchereria bancrofti/immunology , Animals , Antigens, Protozoan/blood , Diethylcarbamazine/administration & dosage , Diethylcarbamazine/adverse effects , Double-Blind Method , Filaricides/administration & dosage , Filaricides/adverse effects , Genital Diseases, Male/drug therapy , Genital Diseases, Male/parasitology , Humans , Ivermectin/administration & dosage , Ivermectin/adverse effects , Male , Random Allocation
6.
Arch Biochem Biophys ; 323(2): 471-6, 1995 Nov 10.
Article in English | MEDLINE | ID: mdl-7487113

ABSTRACT

Increasing evidence implicates free radical processes in the pathogenesis of ethanol-induced liver injury. One of the antioxidant defense systems in mammalian cells is the mitochondrial enzyme manganese superoxide dismutase (MnSOD). MnSOD activity is increased by agents that cause oxidative stress. One such agent is the cytokine tumor necrosis factor-alpha (TNF). Increased serum/tissue TNF levels have been observed in alcoholic liver disease, and TNF has been postulated to play a role in ethanol-induced liver injury. Substantial evidence suggests that ethanol itself can cause oxidative stress. In order to investigate the mechanism of the cellular adaptive response to ethanol-induced oxidative stress, the effects of short-term ethanol exposure on MnSOD RNA, protein, and activity were determined in a human hepatoma cell line (HepG2). We found that exposure to ethanol (25 mM concentration) for 72 h increased the protein level and enzyme activity of MnSOD. However, examination of the mRNA levels of the enzyme showed no corresponding increase. Long-term administration of ethanol (10 weeks) did not significantly increase MnSOD protein and MnSOD activity. MnSOD activity was significantly increased by TNF. Thus it appears that both TNF and ethanol are capable of increasing MnSOD activity presumably via enhanced oxidative stress. However, unlike TNF, acute ethanol administration increases the activity of MnSOD without increasing MnSOD mRNA. The increase in MnSOD after a short-term dose of ethanol is diminished with repeated ethanol administrations. These findings are compatible with the view that chronic exposure to ethanol suppresses the cellular adaptive response to oxidative stress. If this adaptive response of MnSOD is lessened, it may have implications in the increased toxicity due to prolonged ethanol exposure.


Subject(s)
Carcinoma, Hepatocellular/enzymology , Ethanol/pharmacology , Liver Neoplasms/enzymology , Superoxide Dismutase/metabolism , Tumor Necrosis Factor-alpha/pharmacology , Gene Expression/drug effects , Humans , RNA, Messenger/genetics , Tumor Cells, Cultured
8.
Ceylon Med J ; 31(2): 79-82, 1986 Jun.
Article in English | MEDLINE | ID: mdl-3568202
10.
Ceylon Med J ; 21(3): 206-7, 1976 Sep.
Article in English | MEDLINE | ID: mdl-1027534
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