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1.
Int Urol Nephrol ; 52(2): 387-392, 2020 Feb.
Article in English | MEDLINE | ID: mdl-31894555

ABSTRACT

PURPOSE: Scientific data regarding intravenous iron supplementation in peritoneal dialysis (PD) patients are scarce. In attempting to administer the minimum monthly IV iron dose that could improve erythropoiesis, we wanted to assess the safety and efficacy of monthly maintenance intravenous administration of 100 mg iron sucrose in PD patients. METHODS: In a 9-month prospective study, all clinically stable PD patients received intravenously 200 mg of iron sucrose as a loading dose, followed by monthly doses of 100 mg for five consecutive months. Levels of hemoglobin (Hb), ferritin, transferrin saturation (TSAT), reticulocyte hemoglobin content (CHr) and C-reactive protein (CRP) were measured before each administration and 3 months after the last iron infusion. Also, doses of concurrent erythropoietin administration were recorded. RESULTS: Eighteen patients were eligible for the study. Mean levels of Hb and ferritin increased significantly (from 10.0 to 10.9 mg/dL, p = 0.01 and from 143 to 260 ng/mL, p = 0.005), as well as the increase in TSAT levels approached borderline significance (from 26.2 to 33.1%, p = 0.07). During the 6 months of iron administration, the erythropoietin dose was reduced in five patients and discontinued in one. During the 3 months following the last iron infusion, three of them again raised the erythropoietin dose to previous levels. None of the patients experienced any side effects related to IV iron administration. CONCLUSIONS: A monthly maintenance intravenous dose of 100 mg iron sucrose may be a practical, effective, and safe in the short term, treatment of anemia in PD patients resulting in improved hemoglobin levels, iron indices, and erythropoietin response.


Subject(s)
Anemia/drug therapy , Ferric Oxide, Saccharated/administration & dosage , Hematinics/administration & dosage , Administration, Intravenous , Aged , Aged, 80 and over , Anemia/blood , Anemia/etiology , C-Reactive Protein/metabolism , Erythropoiesis/drug effects , Erythropoietin/administration & dosage , Female , Ferric Oxide, Saccharated/adverse effects , Ferritins/blood , Hematinics/adverse effects , Hemoglobins/metabolism , Humans , Male , Middle Aged , Peritoneal Dialysis/adverse effects , Prospective Studies , Renal Insufficiency, Chronic/therapy , Reticulocytes/metabolism , Transferrin/metabolism
2.
Clin Cardiol ; 40(8): 528-533, 2017 Aug.
Article in English | MEDLINE | ID: mdl-28295435

ABSTRACT

The prognosis of acute coronary syndromes (ACS) is affected by many factors. Normal thyroid homeostasis is known to alter during various critical illnesses, a condition that has been shown to correlate with the severity of the disease and increased mortality. The purpose of this article is to review literature to emphasize the considerable association of thyroid function with the cardiovascular system and summarize all existing evidence with regard to the role of thyroid hormones alterations during ACS. The electronic databases of PubMed, Medline, Scopus, and Cochrane were searched for relevant literature and studies. Alterations in thyroid hormone plasma concentrations, especially low triiodothyronine (T3) levels, represent a hormonal imbalance that is not uncommon among patients suffering an acute coronary event. Many studies have identified this abnormal thyroid hormonal status to be related to worse prognosis. Although further large-scale clinical trials are needed, the low T3 syndrome manifesting in patients during ACS might be useful in prognostic stratification.


Subject(s)
Acute Coronary Syndrome/blood , Cardiovascular System/metabolism , Thyrotropin/blood , Thyroxine/blood , Triiodothyronine/blood , Acute Coronary Syndrome/diagnosis , Acute Coronary Syndrome/physiopathology , Acute Coronary Syndrome/therapy , Animals , Biomarkers/blood , Cardiovascular System/physiopathology , Humans , Hypothyroidism/blood , Hypothyroidism/physiopathology , Hypothyroidism/therapy , Predictive Value of Tests , Prognosis , Risk Factors
3.
Obes Surg ; 26(5): 1010-5, 2016 May.
Article in English | MEDLINE | ID: mdl-26323659

ABSTRACT

BACKGROUND: The feasibility of a side-to-side jejunoileal anastomosis (SJA) to control type 2 diabetes mellitus (T2DM) was studied in non-obese diabetic Goto-Kakizaki (GK) rats. METHODS: Seventeen 14-week-old male GK rats were divided into three groups: SJA bypassing 60% of the small bowel length, sham-operated jejunoileal bypass (Sham group), and control animals. Rats were observed for 10 weeks after surgery. Fasting blood glucose (FBG) levels and oral glucose tolerance test (OGTT) were measured before and after the procedure. RESULTS: Animals with SJA exhibited normalization of FBG levels from the 1st and up to the 10th postoperative week when the experiment terminated. OGTT compared with sham-operated and control groups was also significantly better at 3 and 8 weeks postoperatively. CONCLUSIONS: A simple SJA, diverting the food and biliopancreatic secretion to the distal small bowel, was able to normalize both FBG levels and OGTT in a non-obese diabetic rat model.


Subject(s)
Diabetes Mellitus, Experimental/surgery , Diabetes Mellitus, Type 2/surgery , Jejunoileal Bypass , Animals , Blood Glucose/metabolism , Diabetes Mellitus, Experimental/metabolism , Diabetes Mellitus, Experimental/pathology , Diabetes Mellitus, Type 2/metabolism , Diabetes Mellitus, Type 2/pathology , Feasibility Studies , Glucose Tolerance Test , Insulin/blood , Intestine, Small/surgery , Male , Rats , Treatment Outcome
4.
Surg Obes Relat Dis ; 11(1): 70-6, 2015.
Article in English | MEDLINE | ID: mdl-25443051

ABSTRACT

BACKGROUND: There is a lack of adequate prospective data on quality-of-life (QOL) and its predictors in patients undergoing laparoscopic sleeve gastrectomy (LSG). The aim of this study was to assess longitudinal changes in QOL after LSG with the use of the obesity-specific Moorehead-Ardelt II questionnaire (MAII) and to identify clinical parameters associated with QOL outcome. METHODS: Morbidly obese patients consecutively admitted for LSG, over a 30-month period, were prospectively studied. QOL was assessed using the validated Greek version of the MAII questionnaire and a visual analogueue scale (VAS), preoperatively and at 6, 12, and 24 months postoperatively. Anthropometric data and obesity-related co-morbidities were recorded. RESULTS: A total of 111 patients with a mean age 36.8±9.2 years were included. Mean preoperative body mass index (BMI) was 49.1±7.5 kg/m2. Percentage excess BMI loss (%EBL) was 51.1±14.9, 64.2±17.9 and 66.4±18.0 at 6, 12, and 24 months, respectively. Postoperatively, all obesity-related co-morbidities were significantly improved. MAII score increased from -.40±1.30 preoperatively to 1.75±.83, 2.18±.80, and 1.95±.71 at 6, 12, and 24 months postoperatively (trend P<.001). Preoperative median (interquartile range) VAS was 3 (1) increasing to 9 (2), 10 (1), and 9 (1) at 6, 12, and 24 months postoperatively (P<.001). %EBL and reduction in obesity-related co-morbidities, especially resolution of diabetes and sleep apnea, correlated significantly with higher QOL during the course of the study. CONCLUSION: LSG, a safe and effective bariatric operation, results in sustained weight loss and significant improvements in QOL. Both weight loss and amelioration of co-morbidities contribute to higher level of postsurgical QOL.


Subject(s)
Gastrectomy/psychology , Laparoscopy/psychology , Obesity, Morbid/surgery , Quality of Life , Activities of Daily Living , Adult , Analysis of Variance , Bariatric Surgery/methods , Bariatric Surgery/psychology , Female , Gastrectomy/methods , Humans , Interpersonal Relations , Laparoscopy/methods , Male , Middle Aged , Obesity, Morbid/psychology , Postoperative Care , Preoperative Care , Prospective Studies , Self Concept , Surveys and Questionnaires , Young Adult
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