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1.
J Fish Dis ; 40(6): 797-809, 2017 Jun.
Article in English | MEDLINE | ID: mdl-27723105

ABSTRACT

Spontaneous mortality of seemingly healthy, farmed Atlantic salmon (Salmo salar L) is an increasing problem in Norwegian aquaculture. In this study, we present a morphological study of the previously undescribed syndrome of arteriosclerosis of the ventral aorta and epicarditis of the adjacent bulbus arteriosus found in farmed Atlantic salmon, with wild-captured fish as a control group. Both the ventral aorta and epicardium are vital for correct arterial compliance and vascular resistance in the respiratory capillaries of the gills. We discuss the possible implications of ventral aorta arteriosclerosis and epicarditis for blood vascular health and in particular for the increasing frequency of spontaneous gill bleeding in farmed salmon. As both these conditions primarily occur in farmed salmon, we suggest that they should be considered pathological.


Subject(s)
Arteriosclerosis/veterinary , Fish Diseases/pathology , Pericarditis/veterinary , Salmo salar , Animals , Aorta/pathology , Aorta/ultrastructure , Aquaculture , Arteriosclerosis/pathology , Gills/pathology , Hemorrhage/veterinary , Microscopy, Electron, Scanning , Norway , Pericarditis/pathology , Syndrome
2.
Water Sci Technol ; 63(3): 508-15, 2011.
Article in English | MEDLINE | ID: mdl-21278474

ABSTRACT

Stormwater-quality models can be useful tools for predicting pollutant loads and identifying sources of contamination. Most models in current use handle pollutants such as metals, nutrients and suspended solids, whereas models including emerging organic contaminants are rare. This study aims at developing and evaluating a model for simulating stormwater flows of two groups of organic pollutants; nonylphenols and phthalates. Sources, emission patterns and environmental fate were examined to create a model framework for the organic contaminants. The model was calibrated using field data from three urban catchments. The results show that the simulated pollutant concentrations are overestimated compared to the measured concentrations, which are often close to or below the analytical detection limit. The high uncertainty and the low predictive power of the model may be explained by factors such as incorrect catchment data, lack of knowledge on buildup, washoff and other processes involved in substance fate, and an underreporting of pollutant concentrations in stormwater. More data on release patterns and sewer fate are needed to adequately simulate stormwater concentrations of nonylphenols and phthalates. A conventional substance flow analysis based on bookkeeping, evaluated in parallel to the computer model, has proven to be useful for calculating fluxes of nonylphenols and phthalates in urban catchments.


Subject(s)
Cities , Computer Simulation , Models, Theoretical , Phenols/analysis , Phthalic Acids/analysis , Rain/chemistry , Water Pollutants, Chemical/analysis , Water/standards
3.
Water Sci Technol ; 62(5): 1154-60, 2010.
Article in English | MEDLINE | ID: mdl-20818059

ABSTRACT

The occurrence of nonylphenol and several phthalates in water environments is highly undesired because of their negative effects on aquatic organisms. The objectives of this study were to identify emission sources of phthalates, nonylphenol and its ethoxylates (NP/EOs) in urban stormwater, and to quantify the substance fluxes from the source to the stormwater system, using the methodology of substance flow analysis (SFA). The SFA, applied on an urban motorway area, showed that phthalates are mainly emitted from vehicles and coated roofing material, whereas the major NP/EOs sources are vehicles and concrete. It was estimated that approximately 4.1 kg of four selected phthalates and more than 400 g of NP/EOs are emitted annually to stormwater in the studied area. The SFA approach presented in this study, using factors that express the emission rate of a specific substance from a specific source, could be applied in urban catchments of various character to estimate fluxes of water contaminants.


Subject(s)
Phenols/chemistry , Phthalic Acids/chemistry , Water Movements , Water Pollutants, Chemical/chemistry , Cities , Environmental Monitoring
5.
Ups J Med Sci ; 105(2): 135-50, 2000.
Article in English | MEDLINE | ID: mdl-11095110

ABSTRACT

In Uppsala, extensive epidemiological and clinical studies on insulin resistance and diabetes have been ongoing for the past 30 years. A prospective cohort study of men born 1920-24, living in Uppsala County, was initiated during 1969-74 (the Uppsala Longitudinal Study of Adult Men, ULSAM). Risk factors for cardiovascular disease were examined in 2,322 men, and re-examinations have been performed every 10 years. At the first follow-up, when the men were 60 years old, insulin resistance was found to be a risk factor for development of hypertension and diabetes. In addition, treatment with antihypertensive medication was an independent risk factor for development of diabetes. These findings resulted in a series of clinical studies on metabolic effects of antihypertensive agents. At the second follow-up, when the men were 70 years old, the development of hypertension and diabetes was once again in focus, but at this time, cross-sectional and prospective studies of other cardiovascular determinants, such as circadian blood pressure pattern, left ventricular geometry and function, muscle morphology, ion status, fibrinolysis and cognitive function, were also performed. The cohort has furthermore been linked to the Swedish census and hospital discharge and cause of death registries, it has been used for studies on relationships between birth weight and cardiovascular disease, and genetic analyses have been performed, taking advantage of the long observation time obtained in this cohort. The cohort is currently being re-examined for the third time, and will hopefully continue to provide valuable information on the epidemiology of diabetes and cardiovascular disease in the future.


Subject(s)
Diabetes Mellitus/etiology , Insulin Resistance , Aged , Birth Weight , Cognition , Heart Failure/etiology , Humans , Hypertension/etiology , Hypertrophy, Left Ventricular/etiology , Insulin Resistance/genetics , Iron/metabolism , Male , Middle Aged , Muscle, Skeletal/pathology , Plasminogen Activator Inhibitor 1/analysis
6.
Acta Obstet Gynecol Scand ; 79(11): 979-83, 2000 Nov.
Article in English | MEDLINE | ID: mdl-11081684

ABSTRACT

OBJECTIVES: To elucidate whether the duration of previous use of combined oral contraceptives (COC) is associated with disabling back or pelvic pain during pregnancy and pain persisting eight months after delivery. METHODS: Questionnaires were distributed to a group of women at 36 weeks of pregnancy and eight months after their delivery. There were no exclusion criteria. Disabling pain was defined as moderate or severe pain restricting physical activity. Multiple logistic regression analysis of disabling pain during pregnancy and persistent pain after delivery comprised the duration of COC use adjusted for age, pain in a previous pregnancy and a history of back pain when not pregnant. RESULTS: The study comprised 161 women. Pain during pregnancy was classified as disabling in 57 of the women (35%), pain in a previous pregnancy being a risk factor, odds ratio (OR) 5.0 (95% CI 2.1; 12.1), whereas no association was found with the duration of COC use. Persistent pain eight months after delivery was reported by 41 women (26%), risk factors being a history of back pain when not pregnant; OR 7.5 (2.8; 19.5), disabling pain in the recent pregnancy; OR 5.0 (1.9; 13.4), and short use of COC; 0-<1 year; OR 4.2 (1.3; 12.9), 1-<5 years; OR 4.6 (1.5; 14.4) (reference=>10 years). CONCLUSION: The results indicate that non- or short term users of COC have an increased risk of persistent pain after delivery compared to long term users. No association was found between the duration of COC use and back or pelvic pain during pregnancy.


Subject(s)
Back Pain/chemically induced , Contraceptives, Oral, Combined/adverse effects , Pelvic Pain/chemically induced , Pregnancy Complications/chemically induced , Adult , Back Pain/etiology , Female , Humans , Pelvic Pain/etiology , Pregnancy , Pregnancy Complications/etiology , Retrospective Studies , Risk Factors , Severity of Illness Index
7.
Acta Obstet Gynecol Scand ; 79(4): 269-75, 2000 Apr.
Article in English | MEDLINE | ID: mdl-10746841

ABSTRACT

OBJECTIVE: To elucidate whether there is an association between symphyseal distention, circulating relaxin levels and pelvic pain in pregnancy. METHODS: Serum relaxin and symphyseal width were assessed in 19 consecutive referral cases with severe pelvic pain at 35 weeks of pregnancy and in a cohort of 49 women at 12 and 35 weeks of pregnancy. The referral cases were received over a period of two years and four months and the cohort was recruited over a period of two months. Relaxin was measured with an ELISA test and symphyseal width assessed using ultrasonography. All women with pelvic pain were clinically assessed. The women were divided into three groups; Group A (n= 38), cohort cases with no or mild pain; Group B (n= 11), cohort cases with disabling pain; and Group C (n= 19), referral cases. RESULTS: At 35 weeks of pregnancy, mean symphyseal width was 4.5 mm (s.d. 1.0 mm) in Group A, 5.7 mm (s.d. 2.6 mm) in Group B, and 7.4 mm (s.d. 3.5 mm) in Group C. The difference between Groups A and B is statistically significant (p=0.044) as is that between Groups A and C (p<0.0001). Serum relaxin levels were not associated with symphyseal distention or disabling pain. CONCLUSION: Severe pelvic pain during pregnancy was strongly associated with an increased symphyseal distention. However, the severity of pain did not predict the degree of symphyseal distention in the individual case, indicating that other mechanisms are also involved. Serum relaxin levels were not associated with the degree of symphyseal distention or with pelvic pain in pregnancy.


Subject(s)
Pelvic Pain/physiopathology , Pregnancy Complications/physiopathology , Relaxin/blood , Adult , Case-Control Studies , Cross-Sectional Studies , Female , Humans , Pelvic Pain/blood , Pelvis/abnormalities , Pelvis/diagnostic imaging , Pregnancy , Pregnancy Complications/blood , Relaxin/pharmacology , Ultrasonography
8.
BJOG ; 107(2): 209-16, 2000 Feb.
Article in English | MEDLINE | ID: mdl-10688504

ABSTRACT

OBJECTIVE: To determine whether the Misgav Ladach caesarean section technique can offer benefits compared with conventional caesarean section technique in the prevailing conditions of a busy African tertiary centre. DESIGN: A randomised controlled trial. SETTING: A tertiary African obstetric unit with 18,000 deliveries annually. PARTICIPANTS: Three hundred and thirty-nine women undergoing caesarean section. METHODS: Eight residents and registrars were instructed in the Misgav Ladach technique for caesarean section during one week, after which the study commenced. The course participants instructed their colleagues; in total, 16 doctors participated. Women requiring caesarean section were randomised to Misgav Ladach or to the conventional lower midline incision procedure, excluding those with a previous scar. RESULTS: During 11 weeks 339 randomised procedures (328 of which were emergency procedures) were carried out. Mean operating time was 25 x 3 minutes for Misgav Ladach and 32 x 6 minutes for the lower midline incision procedure (95% CI -8 x 3; -6 x 3). Mean blood loss was 354 mL and 447 mL (-133; -53), and the number of sutures 3 x 1 and 6 x 1 (-3 x 1; -2 x 9), respectively. No significant difference was found in Apgar scores. Mobilisation was earlier with the Misgav Ladach procedure. No difference was found in overall post-operative infection rates i.e. wound infection or febrile illness, but the combination of wound infection and fever was more common in the Misgav Ladach group. CONCLUSION: The Misgav Ladach caesarean section confers benefits such as reduced blood loss, conservation of time and suture material, and rapid mobilisation, but more studies are needed to explore modifications aimed at reducing post-operative infections in settings with limited resources.


Subject(s)
Cesarean Section/methods , Adolescent , Adult , Anti-Bacterial Agents/therapeutic use , Blood Loss, Surgical/prevention & control , Female , Humans , Pregnancy , Pregnancy Complications/etiology , Surgical Wound Infection/etiology , Surgical Wound Infection/prevention & control , Tanzania , Time Factors , Urban Health Services
9.
Acta Obstet Gynecol Scand ; 79(1): 24-30, 2000 Jan.
Article in English | MEDLINE | ID: mdl-10646812

ABSTRACT

BACKGROUND: Pelvic pain in pregnancy has been suggested to be more common in Scandinavia than in the rest of the world, to be culturally specific for the region and to reflect a change in attitude among pregnant women. Little is known of the prevalence of pelvic pain in pregnancy in low-income countries. OBJECTIVE: To explore whether perceived pelvic pain among pregnant women differs between affluent and poor societies. SUBJECTS AND METHODS: Four observational studies, comprising a total of 752 women, were carried out in circumstances ranging from wealth to poverty, focusing on the reported prevalence, location and degree of pelvic pain in pregnancy. In Uppsala, Sweden, and in Rufiji, Tanzania, the women were interviewed in late pregnancy. In Jakobstad, Finland, and in Zanzibar Town, Zanzibar, the women were approached after delivery before discharge. RESULTS: The reported prevalence of pelvic pain in pregnancy was 49% in Uppsala and 66% in Rufiji, 77% in Jakobstad and 81% in Zanzibar, with an overall similarity of location and degree of pain. CONCLUSION: No geographical differences were found in perceived pelvic pain among pregnant women, irrespective of the socio-economy of the countries.


Subject(s)
Developing Countries , Pelvic Pain/epidemiology , Pregnancy Complications/epidemiology , State Medicine , Adult , Back Pain/epidemiology , Culture , Female , Humans , Poverty , Pregnancy , Scandinavian and Nordic Countries/epidemiology , Socioeconomic Factors , Tanzania/epidemiology
10.
J Intern Med ; 248(6): 501-10, 2000 Dec.
Article in English | MEDLINE | ID: mdl-11155143

ABSTRACT

OBJECTIVES: The principal aim was to study ambulatory and office blood pressure in a population of elderly men. We also wanted to describe the prevalence of hypertension and investigate the blood pressure control in treated elderly hypertensives. DESIGN: A cross-sectional study of a population of elderly men, conducted between 1991 and 1995. SUBJECTS: Seventy-year-old men (n = 1060), participants of a cohort study that began in 1970. MAIN OUTCOME MEASURES: Office and 24 h ambulatory blood pressure. RESULTS: Average 24 h blood pressure in the population was 133 +/- 16/75 +/- 8 mmHg, and daytime blood pressure 140 +/- 16/80 +/- 9 mmHg. Corresponding values in untreated subjects (n = 685) were 131 +/- 16/74 +/- 7 and 139 +/- 16/79 +/- 8, respectively. An office recording of 140/90 mmHg corresponded to an ambulatory pressure of 130/78 (24 h) and 137/83 mmHg (daytime) in untreated subjects. In subjects identified as normotensives according to office blood pressure (n = 270), the 95th percentiles of average 24 h and daytime blood pressures were 142/80 and 153/85 mmHg, respectively. The prevalence of hypertension, defined as office blood pressure greater than or = 140/90 mmHg, was 66%. Despite treatment, treated hypertensives (n = 285) showed higher office (157/89 vs. 127/76 mmHg) and 24 h ambulatory (138/78 vs. 122/71 mmHg) pressures than normotensives (P < 0.05). Fourteen per cent of the treated hypertensives had an office blood pressure < 140/90 mmHg. CONCLUSIONS: Our results provide a basis for 24 h ambulatory blood pressure reference values in elderly men. The study confirms previous findings of a high prevalence of hypertension at older age. It also indicates that blood pressure is inadequately controlled in elderly treated hypertensives.


Subject(s)
Aging/physiology , Blood Pressure/physiology , Circadian Rhythm/physiology , Aged , Aging/drug effects , Analysis of Variance , Blood Pressure/drug effects , Blood Pressure Monitoring, Ambulatory/methods , Blood Pressure Monitoring, Ambulatory/statistics & numerical data , Circadian Rhythm/drug effects , Cross-Sectional Studies , Humans , Hypertension/diagnosis , Hypertension/drug therapy , Hypertension/epidemiology , Linear Models , Longitudinal Studies , Male , Middle Aged , Prevalence , Risk Factors , Surveys and Questionnaires , Sweden/epidemiology
11.
Acta Obstet Gynecol Scand ; 78(8): 681-5, 1999 Sep.
Article in English | MEDLINE | ID: mdl-10468059

ABSTRACT

OBJECTIVE: To elucidate whether there is an association between pregnancy-related back and pelvic pain and changes in bone density. METHODS: In this prospective cohort study, bone density was measured in the distal and ultra-distal forearm at 12 and 35 weeks of pregnancy and at 5 months post partum. The location and degree of any back or pelvic pain was registered. The patients were classified into four subgroups on the basis of presence or absence of disabling pain in late pregnancy and presence or absence of pain at 5 months' follow-up. Forty-nine women participated. RESULTS: Bone density decreases during pregnancy and lactation. Trabecular bone is mainly lost during pregnancy and cortical bone during lactation. No association between back or pelvic pain during pregnancy and bone loss was found. Between 35 weeks of pregnancy and 5 months post partum, bone loss in all the women was estimated as 1.1% of cortical bone (p < 0.001) and 0.6% of trabecular bone (n.s.). During the same period five women with mild pain during pregnancy and pain at follow-up lost 3.9% of cortical bone (p=0.043) and 5.3% of trabecular bone (p=0.043). Although this bone loss was significant compared to the other subgroups, the small study size does not permit general conclusions to be drawn from this finding. CONCLUSION: The results indicate that bone density decreases during pregnancy and lactation. The decrease in bone density was not associated with back or pelvic pain during pregnancy. It remains unclear whether bone loss is associated with back and pelvic pain during lactation.


Subject(s)
Back Pain/pathology , Bone Density , Bone Resorption/pathology , Pelvic Pain/pathology , Pregnancy Complications/pathology , Absorptiometry, Photon , Back Pain/classification , Back Pain/diagnostic imaging , Bone Resorption/classification , Bone Resorption/diagnostic imaging , Disabled Persons , Female , Humans , Lactation , Pain Measurement , Pelvic Pain/classification , Pelvic Pain/diagnostic imaging , Postpartum Period , Pregnancy , Pregnancy Complications/classification , Pregnancy Complications/diagnostic imaging , Pregnancy Trimester, First , Pregnancy Trimester, Third , Prospective Studies , Radionuclide Imaging , Radius/diagnostic imaging , Radius/pathology , Ulna/diagnostic imaging , Ulna/pathology
12.
Acta Obstet Gynecol Scand ; 78(2): 125-30, 1999 Feb.
Article in English | MEDLINE | ID: mdl-10023875

ABSTRACT

OBJECTIVE: To elucidate whether there is a relationship between pregnancy-related pelvic pain and degree of symphyseal laxity. METHODS: Forty-nine women were interviewed and examined and ultrasonographic measurement of symphyseal width and vertical shift was conducted at 12 and 35 weeks of pregnancy and at 5 months post partum. The patients were retrospectively classified into four groups on the basis of presence and degree of pain in late pregnancy and presence or absence of pain at follow up. RESULTS: The prevalence of pelvic pain of any degree during pregnancy was 49%, of pronounced pain 16.3% and of severe pain 6.1%. Nineteen percent had any remaining pain at 5 months post partum. The median symphyseal width at 12 and 35 weeks of pregnancy and at 5 months post partum was 3.5 mm, 4.6 mm and 2.8 mm, the median vertical shift 0.0 mm, 0.8 and 0.9 mm respectively. Those with disabling pain during pregnancy and no pain at follow up had greater symphyseal width (6.3 mm) and vertical shift (1.8 mm) at 35 weeks of pregnancy than controls; 4.5 mm (p<0.01) and 0.5 mm (p<0.01) respectively. Those with disabling pain during pregnancy and persistent pain at follow up did not differ significantly from controls in symphyseal width or shift. The most severe cases were in this group. CONCLUSION: There is a minor pregnancy-induced physiological increase in laxity of the symphyseal soft tissue. There is no evidence that the degree of symphyseal distention determines the severity of pelvic pain in pregnancy or after childbirth.


Subject(s)
Pelvic Pain/diagnostic imaging , Pregnancy Complications/diagnostic imaging , Pubic Symphysis/diagnostic imaging , Ultrasonography, Prenatal , Adult , Dilatation, Pathologic/diagnostic imaging , Female , Humans , Joint Instability/diagnostic imaging , Joint Instability/pathology , Pregnancy , Prevalence , Pubic Symphysis/pathology , Puerperal Disorders/diagnostic imaging , Retrospective Studies
13.
Biochem Biophys Res Commun ; 239(1): 265-8, 1997 Oct 09.
Article in English | MEDLINE | ID: mdl-9345307

ABSTRACT

Six healthy volunteers showed significantly higher plasma islet amyloid polypeptide levels following an oral glucose tolerance test compared to fasting levels. The urine IAPP concentration before and after the OGTT was comparable to that in plasma. Reverse phase HPLC and radioimmunoassay analysis of urine samples revealed a single IAPP-immunoreactive peak. Before hemodialysis, the plasma levels of IAPP and C-peptide, but not of insulin, were significantly elevated in eight fasting patients with chronic renal failure, compared to eight healthy matched control subjects. After hemodialysis, there was a tendency for decreased IAPP levels compared to before dialysis. In summary, elevated levels of plasma IAPP were found in patients with chronic renal failure and the peptide is eliminated by hemodialysis. Furthermore, immunoreactive IAPP is normally present in the urine. These results suggest that IAPP is, at least in part, renally eliminated from the plasma by excretion (glomerular filtration and/or tubular secretion.


Subject(s)
Amyloid/metabolism , Kidney/metabolism , Adult , Aged , Aged, 80 and over , Amyloid/blood , Amyloid/urine , Blood Glucose/metabolism , C-Peptide/blood , Chromatography, High Pressure Liquid , Creatinine/blood , Female , Humans , Insulin/blood , Islet Amyloid Polypeptide , Male , Middle Aged , Radioimmunoassay , Renal Dialysis , Urea/blood
14.
Acta Obstet Gynecol Scand ; 76(3): 227-32, 1997 Mar.
Article in English | MEDLINE | ID: mdl-9093136

ABSTRACT

OBJECTIVE: To elucidate whether there is a distention of the symphysis pubis intra partum and whether a history of pelvic pain during pregnancy is associated with increased distention during delivery. METHODS: Using ultrasonography, the width of the symphysis pubis was measured on two occasions during delivery; firstly, upon engagement of the fetal head in the pelvic inlet, secondly, when the largest diameter of the fetal head was at the level of the ischiadic spines. The first measurement was conducted in 24 patients, the second measurement was obtained in 16 of these patients. RESULTS: The average width of the symphysis pubis at onset of labor was 5.8 mm. The average distention of the symphysis during labor was 1.1 mm for those without pelvic pain and 0.2 mm for those with a history of pelvic pain during pregnancy (p = 0.02). Parity and ensuing birth weight had no statistically significant influence on degree of distention. CONCLUSION: The symphyseal distention during labor is minimal regardless of parity and size of the child. No added symphyseal distensibility was found in patients with a history of pelvic pain.


Subject(s)
Pelvic Pain/etiology , Pregnancy Complications/etiology , Pubic Symphysis/diagnostic imaging , Pubic Symphysis/pathology , Adult , Female , Humans , Labor, Obstetric/physiology , Pelvic Pain/pathology , Pelvic Pain/physiopathology , Pregnancy , Pregnancy Complications/pathology , Pregnancy Complications/physiopathology , Ultrasonography
16.
Gynecol Obstet Invest ; 42(3): 151-3, 1996.
Article in English | MEDLINE | ID: mdl-8938463

ABSTRACT

The width of the symphysis pubis was measured in a skeleton model using slide rule, ultrasonography and x-ray. Ultrasonography gave a 0.5-mm and x-ray a 1.0-mm narrower gap than the slide rule. Further, 15 nonpregnant females undergoing urography volunteered for an extra ultrasonography of the symphysis pubis. The widths of the symphysis as measured from the x-ray exposures and the ultrasonography were compared. Regression analysis gave a regression coefficient of 0.979 and a correlation coefficient of 0.850. Ultrasonography offers at least the same precision as x-ray for assessing the width of the symphyseal gap.


Subject(s)
Pubic Symphysis/diagnostic imaging , Adult , Female , Humans , Pregnancy , Pubic Symphysis/anatomy & histology , Radiography , Regression Analysis , Ultrasonography
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