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1.
World J Urol ; 37(10): 2155-2164, 2019 Oct.
Article in English | MEDLINE | ID: mdl-30684035

ABSTRACT

PURPOSE: Confocal laser endomicroscopy (CLE) is a fluorescence-based fiber-optic imaging technique with the potential for intraoperative grading of upper tract urothelial carcinoma (UTUC). This study aims to (1) investigate the prevalence of the previously proposed CLE criteria for bladder cancer in papillary UTUC, (2) estimate the diagnostic value of CLE for UTUC grading and (3) propose a scoring system for a more quantifiable approach of CLE-based grading of UTUC. MATERIALS AND METHODS: Ureteroscopic CLE was performed in patients with UTUC. Following CLE imaging, co-localized biopsies were taken for histopathologic comparison. Postoperatively, two blinded raters assessed the CLE images. RESULTS: Fifty-three papillary UTUCs (34 low grade and 19 high grade) were imaged with CLE in 36 patients. All the previously described CLE criteria were identifiable in varying proportions. After excluding 10 non-diagnostic recordings (5 low grade and 5 high grade) due to insufficient image quality, the histopathologic grade was correctly identified with CLE in 26 low-grade UTUCs (90%) and in 12 high-grade UTUCs (86%). The most prevalent CLE criteria with the highest diagnostic potential were cellular organization, morphology and cohesiveness of cells. A scoring system was proposed with these criteria, which yielded similar diagnostic accuracies. CONCLUSIONS: Based on the previously proposed criteria, CLE enables accurate grading of papillary UTUC at a non-diagnostic rate of 19%. The most prevalent CLE criteria with the highest diagnostic potential for grading of papillary UTUC are cellular organization, morphology and cohesiveness of cells. The proposed scoring system may simplify the assessment of CLE images for UTUC grading but external validation is required.


Subject(s)
Carcinoma, Transitional Cell/pathology , Kidney Neoplasms/pathology , Microscopy, Confocal , Ureteral Neoplasms/pathology , Aged , Female , Humans , Male , Neoplasm Grading , Prospective Studies
2.
Int J Cardiol ; 276: 177-184, 2019 Feb 01.
Article in English | MEDLINE | ID: mdl-30497895

ABSTRACT

BACKGROUND: Peripartum cardiomyopathy (PPCM) is an important cause of pregnancy-associated heart failure, which appears in previously healthy women towards the end of pregnancy or within five months following delivery. Although the ECG is widely used in clinical practice, its prognostic value has not been established in PPCM. METHODS: We analysed 12-lead ECGs of patients with PPCM, taken at index presentation and follow-up visits at 6 and 12 months. Poor outcome was determined by the composite endpoint of death, readmission, NYHA functional class III/IV or left ventricular ejection fraction (LVEF) of ≤35% at follow-up. RESULTS: This cohort of 66 patients had a median age of 28.59 (IQR 25.43-32.19). The median LVEF at presentation (33%, IQR 25-40) improved significantly at follow-up (LVEF 49%, IQR 38-55, P < 0.001 at 6 months; 52% IQR 38-57, P = 0.001 at 12 months). Poor outcome occurred in 27.91% at 6 months and 41.18% at 1 year. Whereas sinus tachycardia at baseline was an independent predictor of poor outcome at 12 months (OR 6.56, 95% CI 1.17-20.41, P = 0.030), sinus arrhythmia was associated with event free survival (log rank P = 0.013). T wave inversion was associated with an LVEF ≤35% at presentation (P = 0.038), but did not predict poor outcome. A prolonged QTc interval at presentation (found in almost half of the cohort) was an independent predictor of poor outcome at 6 months (OR 6.34, 95% CI 1.06-37.80, P = 0.043). CONCLUSION(S): A prolonged QTc and sinus tachycardia at baseline were independent predictors of poor outcome in PPCM at 6 months and 1 year respectively.


Subject(s)
Cardiomyopathies/physiopathology , Electrocardiography/methods , Peripartum Period/physiology , Pregnancy Complications, Cardiovascular/physiopathology , Adult , Cardiomyopathies/diagnostic imaging , Cardiomyopathies/epidemiology , Cohort Studies , Female , Follow-Up Studies , Heart Failure/diagnostic imaging , Heart Failure/epidemiology , Heart Failure/physiopathology , Humans , Pregnancy , Pregnancy Complications, Cardiovascular/diagnostic imaging , Pregnancy Complications, Cardiovascular/epidemiology , Prognosis , Single-Blind Method , South Africa/epidemiology
3.
Cardiovasc J Afr ; 29(5): 289-295, 2018.
Article in English | MEDLINE | ID: mdl-30059130

ABSTRACT

OBJECTIVE: To document maternal and foetal morbidity and mortality in anticoagulated, pregnant patients with mechanical heart valves until 42 days postpartum. METHODS: In a tertiary single-centre, prospective cohort, 178 consecutive patients at the cardiac-obstetric clinic were screened for warfarin use between 1 July 2010 and 31 December 2015. Of 33 pregnancies identified, 29 were included. Patients received intravenous unfractionated heparin from six to 12 weeks' gestation and peripartum, and warfarin from 12 to 36 weeks. Maternal outcomes including death, major haemorrhage and thrombosis, and foetal outcomes were documented. RESULTS: There were two maternal deaths, five returns to theatre post-delivery, eight patients transfused, six major haemorrhages, one case of infective endocarditis and three ischaemic strokes. Ten pregnancies had poor foetal outcomes (six miscarriages, three terminations, one early neonatal death). Twenty patients required more than 30 days' hospitalisation, and 15 required three or more admissions. HIV positivity was associated with surgical delivery (p = 0.0017). CONCLUSION: Complication rates were high despite centralised care.


Subject(s)
Anticoagulants/adverse effects , Heart Valve Prosthesis Implantation , Heparin/adverse effects , Postpartum Hemorrhage/chemically induced , Pregnancy Complications, Cardiovascular/chemically induced , Warfarin/adverse effects , Abortion, Spontaneous/chemically induced , Adult , Anticoagulants/administration & dosage , Female , Fetal Mortality , Gestational Age , HIV Infections/drug therapy , HIV Infections/mortality , Heart Valve Prosthesis , Heart Valve Prosthesis Implantation/adverse effects , Heart Valve Prosthesis Implantation/instrumentation , Heparin/administration & dosage , Humans , Live Birth , Maternal Mortality , Postpartum Hemorrhage/diagnosis , Postpartum Hemorrhage/mortality , Postpartum Hemorrhage/therapy , Postpartum Period , Pregnancy , Pregnancy Complications, Cardiovascular/diagnosis , Pregnancy Complications, Cardiovascular/mortality , Pregnancy Complications, Cardiovascular/therapy , Pregnancy Complications, Infectious/drug therapy , Pregnancy Complications, Infectious/mortality , Prognosis , Prospective Studies , Risk Assessment , Risk Factors , South Africa , Time Factors , Warfarin/administration & dosage , Young Adult
4.
Lancet ; 344(8923): 661-4, 1994 Sep 03.
Article in English | MEDLINE | ID: mdl-7915353

ABSTRACT

The last confirmed case of poliomyelitis in Namibia had been reported in 1988. However, between Nov 8, 1993, and Jan 7, 1994, 27 cases of paralytic poliomyelitis were confirmed in the country. The outbreak was limited to the south health region; at least 80% of infants in this region have received four doses of oral poliovaccine (OPV) by the age of 1 year. Acute flaccid paralysis (AFP) was the predominant clinical presentation during the outbreak. The patients' ages ranged from 13 months to 12 years; 24 were younger than 5 years. Of the 26 patients whose vaccine status was known, 14 had received four doses of OPV, 6 had one or two doses, and 6 no vaccine. Genotypic analysis showed 86% homology of outbreak isolates with a 1982 Namibian isolate and west African isolates. Factors that may have had a role in the outbreak include establishment of a pool of susceptible people, rapid urbanisation, inadequate sanitation, poor water supply, and possible endemicity of poliovirus in neighbouring areas. Epidemics can occur in areas of high vaccine coverage. Our findings emphasise the need to improve AFP surveillance activities and the estimation of vaccine coverage to identify areas of potential susceptibility for outbreaks.


Subject(s)
Disease Outbreaks , Poliomyelitis/epidemiology , Antibodies, Viral/blood , Child , Child, Preschool , Humans , Infant , Namibia/epidemiology , Poliomyelitis/immunology , Poliomyelitis/microbiology , Poliovirus/isolation & purification , Poliovirus Vaccine, Oral/administration & dosage , Population Surveillance , Vaccination
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