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1.
BJS Open ; 7(3)2023 05 05.
Article in English | MEDLINE | ID: mdl-37161674

ABSTRACT

BACKGROUND: Electrolyte disturbances and dehydration are common after anterior resection for rectal cancer with a defunctioning loop ileostomy. High-quality population-based studies on the impact of a defunctioning loop ileostomy on renal failure are lacking. METHODS: This was a nationwide observational study, based on the Swedish Colorectal Cancer Registry of patients undergoing anterior resection for rectal cancer between 2008 and 2016, with follow-up until 2017. Patients with severe co-morbidity, with age greater than 80 years, and with pre-existing renal failure were excluded. Loop ileostomy at index surgery constituted exposure, while a diagnosis of renal failure was the outcome. Acute and chronic events were analysed separately. Inverse probability weighting with adjustment for confounding derived from a causal diagram was employed. Hazards ratios (HRs) with 95 per cent c.i. are reported. RESULTS: A total of 5355 patients were eligible for analysis. At 5-year follow-up, all renal failure events (acute and chronic) were 7.2 per cent and 3.3 per cent in the defunctioning stoma and no stoma groups respectively. In the weighted analysis, a HR of 11.59 (95 per cent c.i. 5.68 to 23.65) for renal failure in ostomates was detected at 1 year, with the largest effect from acute renal failure (HR 24.04 (95 per cent c.i. 8.38 to 68.93)). Later follow-up demonstrated a similar pattern, but with smaller effect sizes. CONCLUSION: Patients having a loop ileostomy in combination with anterior resection for rectal cancer are more likely to have renal failure, especially early after surgery. Strategies are needed, such as careful fluid management protocols, and further research into alternative stoma types or reduction in stoma formation.


Subject(s)
Rectal Neoplasms , Renal Insufficiency , Surgical Stomas , Humans , Aged, 80 and over , Ileostomy/adverse effects , Renal Insufficiency/epidemiology , Rectal Neoplasms/surgery , Registries
3.
Langenbecks Arch Surg ; 406(6): 1971-1977, 2021 Sep.
Article in English | MEDLINE | ID: mdl-34008097

ABSTRACT

PURPOSE: Anterior resection is the procedure of choice for tumours in the mid and upper rectum. Depending on tumour height, a total mesorectal excision (TME) or partial mesorectal excision (PME) can be performed. Low anastomoses in particular have a high risk of developing anastomotic leakage, which might be explained by blood perfusion compromise. A pilot study indicated a worse blood flow in TME patients in an open setting. The aim of this study was to further evaluate perianastomotic blood perfusion changes in relation to TME and PME in a predominantly laparoscopic context. METHOD: In this prospective cohort study, laser Doppler flowmetry was used to evaluate the perianastomotic colonic and rectal perfusion before and after surgery. The two surgical techniques were compared in terms of mean differences of perfusion units using a repeated measures ANOVA design, which also enabled interaction analyses between type of mesorectal excision and location of measurement. Anastomotic leakage until 90 days after surgery was reported for descriptive purposes. RESULTS: Some 28 patients were available for analysis: 17 TME and 11 PME patients. TME patients had a reduced blood perfusion postoperatively compared to PME patients in the aboral posterior area (mean difference: -57 vs 18 perfusion units; p = 0.010). An interaction between mesorectal excision type and anterior/posterior location was detected at the aboral level (p = 0.007). Two patients developed a minor leakage, diagnosed after discharge. CONCLUSION: Patients operated on using TME have a decreased blood flow in the aboral posterior quadrant of the rectum postoperatively compared to patients operated on using PME. This might explain differing rates of anastomotic leakage. TRIAL REGISTRATION: ClinicalTrials.gov Identifier: NCT02401100.


Subject(s)
Laparoscopy , Rectal Neoplasms , Anastomotic Leak , Humans , Pilot Projects , Prospective Studies , Rectal Neoplasms/surgery , Rectum/surgery
5.
Scand J Gastroenterol ; 45(7-8): 944-52, 2010 Aug.
Article in English | MEDLINE | ID: mdl-20384529

ABSTRACT

OBJECTIVE: The aim of this nationwide cohort study was to assess the risk for hepatocellular carcinoma (HCC) in patients with chronic hepatitis B virus (HBV) infection or HBV and hepatitis C virus (HCV) co-infection in Sweden, a low endemic country. MATERIAL AND METHODS: A total of 12,080 patients with HBV and 3238 patients with HBV-HCV co-infection were notified to the Swedish institute for Infectious Disease Control between 1990 and 2004. After excluding 1850 patients with acute HBV and 584 patients infected in adult life, we analyzed the cohort of 9646 subjects with chronic HBV infection. In the co-infection cohort, 1697 patients were analyzed after excluding 1541 cases with acute HBV. The Swedish national cancer registry was used for follow-up. The HCC incidence rate in the cohorts was compared with the HCC incidence rate in the general population and the standardized incidence ratio (SIR) was calculated for different strata according to estimated infection period. RESULTS: HCC was found in 45 patients in the HBV cohort. In the stratum of 40-49 years of infection we found a SIR of 47 and in stratum 50-59 years the SIR was 54. In the co-infected cohort 10 HCCs were found. The SIR in the stratum 20-29 years of infection was 34 and the SIR in the stratum 30 years and over was 91. CONCLUSIONS: This national cohort study of HBV infected and HBV-HCV co-infected subjects in a low endemic country confirms a highly increased risk of liver cancer compared to the general population.


Subject(s)
Carcinoma, Hepatocellular/epidemiology , Hepatitis B/epidemiology , Hepatitis C/epidemiology , Liver Neoplasms/epidemiology , Adult , Aged , Carcinoma, Hepatocellular/etiology , Carcinoma, Hepatocellular/virology , Female , Hepatitis B/complications , Hepatitis C/complications , Humans , Liver Neoplasms/etiology , Liver Neoplasms/virology , Male , Middle Aged , Sweden/epidemiology
6.
Emerg Infect Dis ; 15(12): 1937-47, 2009 Dec.
Article in English | MEDLINE | ID: mdl-19961673

ABSTRACT

Summer outbreaks of tularemia that occurred from 1995 through 2005 in 2 locations in Sweden affected 441 persons. We performed an epidemiologic investigation of these outbreaks using a novel strategy, involving high-resolution genotyping of Francisella tularensis isolates obtained from 136 patients (using 18 genetic markers developed from 6 F. tularensis genome sequences) and interviews with the patients. Strong spatial associations were found between F. tularensis subpopulations and the places of disease transmission; infection by some subpopulations occurred within areas as small as 2 km(2), indicating unidentified environmental point sources of tularemia. In both locations, disease clusters were associated with recreational areas beside water, and genetic subpopulations were present throughout the tularemia season and persisted over years. High-resolution genotyping in combination with patients' statements about geographic places of disease transmission provided valuable indications of likely sources of infection and the causal genotypes during these tularemia outbreaks.


Subject(s)
Disease Outbreaks , Tularemia/epidemiology , Adolescent , Adult , Child , Child, Preschool , Female , Francisella tularensis/classification , Francisella tularensis/genetics , Genotype , Humans , Infant , Male , Middle Aged , Phylogeny , Polymorphism, Single Nucleotide , Sweden/epidemiology , Time Factors , Tularemia/microbiology
7.
Clin Vaccine Immunol ; 15(8): 1238-43, 2008 Aug.
Article in English | MEDLINE | ID: mdl-18562568

ABSTRACT

We have developed and evaluated a novel and simplified whole-blood lymphocyte stimulation assay that focuses on the measurement of gamma interferon after 24 h of stimulation with whole-cell tularemia antigen and a tularemia enzyme-linked immunosorbent assay (ELISA) based on highly purified lipopolysaccharide antigen. Comparison of the kinetics of the two assays and those of the traditional tube agglutination test shows that the cellular immune response can be detected earlier by the lymphocyte stimulation assay. This test already shows a high proportion of positive results during the first week after the onset of the disease, may be applicable in everyday laboratory practice, and has the potential of changing routine diagnostics for tularemia. The new ELISA has a high sensitivity and becomes positive to a high degree during the second week of disease.


Subject(s)
Antibodies, Bacterial/blood , Antigens, Bacterial/immunology , Francisella tularensis/immunology , Lymphocyte Activation , Tularemia/immunology , Agglutination Tests , Enzyme-Linked Immunosorbent Assay , Humans , Immunoglobulin G/blood , Immunoglobulin M/blood , Interferon-gamma/biosynthesis , Kinetics , Tularemia/microbiology
8.
J Viral Hepat ; 15(7): 538-50, 2008 Jul.
Article in English | MEDLINE | ID: mdl-18397223

ABSTRACT

Studies on chronic viral hepatitis and mortality have often been made on selected populations or in high-endemic countries. The aim of this study was to investigate the causes of death and the mortality rates in the nationwide cohorts of people chronically infected with hepatitis B virus (HBV) and/or hepatitis C virus (HCV) in Sweden, a low-endemic country. All notifications on chronic HBV infection and HCV infection 1990-2003 were linked to the Cause of Death Register. A total of 9517 people with chronic HBV infection, 34 235 people with HCV infection and 1601 with chronic HBV-HCV co-infection were included, and the mean observation times were 6.4, 6.3 and 7.9 years, respectively. The mortality in the cohorts was compared with age- and gender-specific mortality in the general population and standardized mortality ratios (SMR) were calculated. All-cause mortality was significantly increased, SMR 2.3 (HBV), 5.8 (HCV) and 8.5 (HBV-HCV), with a great excess liver-related mortality in all cohorts, SMR 21.7, 35.5 and 46.2, respectively. In HCV and HBV-HCV infected there was an increased mortality due to drug-related psychiatric diagnoses (SMR: 20.7 and 27.6) and external causes (SMR: 12.4 and 11.4), predominantly at younger age. To conclude, this study demonstrated an increased all-cause mortality, with a great excess mortality from liver disease, in all cohorts. In people with HCV infection the highest excess mortality in younger ages was from drug-related and external reasons.


Subject(s)
Carcinoma, Hepatocellular/mortality , Hepatitis B, Chronic/mortality , Hepatitis C, Chronic/mortality , Liver Neoplasms/mortality , Cohort Studies , Female , Hepatitis B, Chronic/epidemiology , Hepatitis C, Chronic/epidemiology , Humans , Liver Neoplasms/etiology , Male , Medical Record Linkage , Population Surveillance/methods , Registries
9.
Scand J Infect Dis ; 39(10): 880-9, 2007.
Article in English | MEDLINE | ID: mdl-17886125

ABSTRACT

A retrospective study of clinical tularaemia in an emergent area in Sweden is presented. 234 patients seen during the y 2000-2004 were studied, using case files and a questionnaire. There was a predominance of ulceroglandular tularaemia (89%), occurring in late summer and early autumn, reflecting the dominance of mosquito-borne transmission. The incubation period varied from a few hours to 11 d, with a median of 3 d. Cutaneous manifestations of tularaemia, apart from primary lesions, were noted in 43% of the cases. Coughing was common, even in patients with ulceroglandular tularaemia, supporting the view that haematogenous spread to the respiratory system occurs. Regular laboratory tests, such as WBC, ESR and C-reactive protein, were in general only moderately elevated. In the earlier y studied, the Doctor's Delay was substantial as was the misdiagnosis and prescription of inadequate antibiotics. In the later y, however, the delay and misdiagnosis were significantly lower, reflecting the increased recognition of the disease by the physicians in the area. A few relapses occurred, all in patients treated with doxycycline. No lethality was seen, reflecting the benign course of tularaemia type B infection.


Subject(s)
Communicable Diseases, Emerging , Francisella tularensis , Tularemia , Adolescent , Adult , Aged , Aged, 80 and over , Communicable Diseases, Emerging/epidemiology , Communicable Diseases, Emerging/microbiology , Communicable Diseases, Emerging/physiopathology , Female , Francisella tularensis/classification , Francisella tularensis/genetics , Francisella tularensis/immunology , Francisella tularensis/isolation & purification , Humans , Lymphatic Diseases/epidemiology , Lymphatic Diseases/microbiology , Lymphatic Diseases/physiopathology , Male , Middle Aged , Skin Ulcer/epidemiology , Skin Ulcer/microbiology , Skin Ulcer/physiopathology , Sweden/epidemiology , Tularemia/diagnosis , Tularemia/epidemiology , Tularemia/microbiology , Tularemia/physiopathology
11.
Scand J Infect Dis ; 37(11-12): 833-7, 2005.
Article in English | MEDLINE | ID: mdl-16308216

ABSTRACT

A retrospective analysis to evaluate the clinical use of a diagnostic PCR for Francisella tularensis in patients with suspected ulceroglandular tularaemia was performed. 154 samples, 129 from patients with definitive tularaemia and 25 from patients where tularaemia could be ruled out, were analysed. The diagnostic PCR had a specificity of 96%, a sensitivity of 78.3%, and a Positive Predictive Value of 99%. Especially samples from encrusted lesions, even up to 4 weeks old, in patients with tularaemia, were PCR positive to a high degree when taken properly. The diagnostic PCR is useful in suspected ulceroglandular tularaemia, giving a fast and accurate diagnosis.


Subject(s)
Francisella tularensis/genetics , Francisella tularensis/isolation & purification , Polymerase Chain Reaction/methods , Tularemia/diagnosis , Adolescent , Adult , Aged , Aged, 80 and over , Child , Child, Preschool , Female , Humans , Lymphatic Diseases/microbiology , Lymphatic Diseases/pathology , Male , Middle Aged , Polymerase Chain Reaction/statistics & numerical data , Retrospective Studies , Sensitivity and Specificity , Skin Ulcer/microbiology , Skin Ulcer/pathology , Sweden , Tularemia/microbiology , Tularemia/pathology
12.
Hepatology ; 41(3): 652-9, 2005 Mar.
Article in English | MEDLINE | ID: mdl-15723449

ABSTRACT

The aim of this study was to evaluate the association between hepatitis C virus (HCV) infection and non-Hodgkin's lymphoma (NHL), multiple myeloma (MM), thyroid cancer (TC), chronic lymphatic leukemia (CLL), acute lymphatic leukemia (ALL), and Hodgkin's lymphoma (HL). A Swedish cohort of 27,150 HCV-infected persons notified during 1990-2000 was included in the study. The database was linked to other national registers to calculate the observation time, expressed as person-years, and to identify all incident malignancies in the cohort. The patients were stratified according to assumed time of previous HCV infection. The relative risk of malignancy was expressed as a standardized incidence ratio (SIR)-the observed number compared to the expected number. During 1990-2000 there were 50 NHL, 15 MM, 14 ALL, 8 TC, 6 CLL, and 4 HL diagnoses in the cohort. Altogether, 20 NHL, 7 MM, 5 TC, 4 CLL, 1 ALL, and 1 HL patient fulfilled the criteria to be included in the statistical analysis. The observation time was 122,272 person-years. The risk of NHL and MM was significantly increased in the stratum with more than 15 years of infection (SIR 1.89 [95% CI, 1.10-3.03] and 2.54 [95% CI, 1.11-5.69], respectively). The association was not significant in TC or CLL. In conclusion, we report the incidence of several malignancies in a nationwide cohort of HCV-infected persons. Although the delayed diagnosis of HCV probably has resulted in an underestimation of the risk, this study showed a significantly increased risk of NHL and MM.


Subject(s)
Hepatitis C/complications , Lymphoma, Non-Hodgkin/etiology , Adolescent , Adult , Aged , Aged, 80 and over , Child , Female , Humans , Leukemia, Lymphocytic, Chronic, B-Cell/etiology , Male , Middle Aged , Multiple Myeloma/etiology , Neoplasms , Precursor Cell Lymphoblastic Leukemia-Lymphoma/etiology , RNA, Viral/analysis , Risk Factors , Thyroid Neoplasms/etiology
13.
Scand J Infect Dis ; 35(8): 510-1, 2003.
Article in English | MEDLINE | ID: mdl-14514156

ABSTRACT

A case of tularaemia presenting with severe septicaemia and myositis is reported. The infection was presumed to be acquired by a bite from the horse fly Haematopota pluvialis, also known as the rain fly.


Subject(s)
Francisella tularensis/isolation & purification , Myositis/microbiology , Sepsis/microbiology , Tularemia/diagnosis , Aged , Anti-Bacterial Agents/therapeutic use , Female , Follow-Up Studies , Francisella tularensis/drug effects , Humans , Myositis/complications , Myositis/drug therapy , Risk Assessment , Sepsis/complications , Sepsis/drug therapy , Severity of Illness Index , Sweden , Treatment Outcome , Tularemia/complications , Tularemia/drug therapy
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