Introduction: The hemoglobinopathies are a heterogeneous group of congenital anemias from Africa, Asia and the Mediterranean. Due to the migration of this population have spread worldwide, especially in Latin America and the Caribbean region, which Cartagena de Indias is included, with a large proportion of people of African descent. The lack of routine programs that include an appropriate methodology for precise identification of those affected and carriers, impossible to know the real behavior of this disease in our country and an early and appropriate to the patients before the disease manifests itself and produce its serious consequences. Objective: To estimate the incidence and describe the epidemiological profile of hemoglobinopathies in newborns Rafael Calvo Maternity Clinic of Cartagena, in the period from January to June 2010. Methods: Prospective descriptive study of a population of 1729 newborns. Samples were collected cord blood on filter paper. Isoelectric focusing electrophoresis (IEF )was used to separate the haemoglobins. Results: 94.4% (1633samples) were normal (hemoglobinFA), 4.5% (78samples) were heterozygous for haemoglobin S (HbFAS), 1% (17samples) were heterozygous for haemoglobin C (hemoglobinFAC) and 0.1% (1 sample) was double heterozygous SC (hemoglobinFSC). Conclusion: Due to the high incidence of hemoglobinopathies found in this pilot study highlights the importance and necessity of establishing an obligatory neonatal screening in the city of Cartagena, in order to make a timely diagnosis and monitoring of affected and carrier.
BackgroundA rapid bone loss and an increase in fractures have been described after liver transplantation, warranting focused management.Bisphosphonates are effective antiresorptive agents, but with a limited in patients with significant kidney disease, as the drugs are excreted by urine, accumulating and increasing the risk of adverse events (including at the kidney level). The evaluation of renal function in the patient with cirrhosis can be challenging and may be underestimated by standard methods[1]. This issue may impact the choice of the anti-osteoporosis (OP) agent.ObjectivesTo compare the variations on bisphosphonate treatment indication across different glomerular filtration rate (GFR) equations in patients with advanced liver disease included in a pre-transplantation study.MethodsDescriptive cross-sectional study of patients from a tertiary center selected for a multidisciplinary assessment before liver transplantation from February 2019 to December 2022.Sex, age, ethnicity, and serum creatinine and cystatin C (a more sensitive marker than creatinine for the estimation of GFR in patients with cirrhosis[2]) levels are collected. The indication for anti-OP treatment is established in the presence of T< -1.0 by densitometry (DXA), vertebral radiographic wedging or history of a fragility fracture. GFR adjusted by creatinine, cystatin C and creatinine-cystatin C was calculated using the online calculation tool MediCalc®. Results are later categorized as below or above 30ml/min2(usual cut-off to contraindicate the use of bisphosphonates[3]), finally comparing the rate of patients with GFR <30 ml/min across three methods.A descriptive study is presented. Comparison of variables are performed by Fisher’s exact test. P-values of <0.05 are considered statistically significant.ResultsA total of 162 patients (75.9% men) were included, all Caucasian, with a mean age of 60 years (SD 7.6) and a mean BMI of 27.9 (SD 4.9).Seventy-six percent (n=120) were candidates to anti-OP therapy, and 68.5% (n=111) ultimately received it (88% bisphosphonates, 11% denosumab, and 1% teriparatide). Three percent (n=5) presented a fragility fracture, and 9.5% (n=17) showed a radiographic vertebral fracture. Fifty-one percent (n=80) had osteopenia and 22.9% (n=36) osteoporosis at DXA scans.Regarding renal function, mean serum levels of creatinine and cystatin C were 0.99 mg/dl (SD 1) and 1.7 mg/L (SD 1), respectively. The mean estimated GFR levels using creatinine, cystatin C and creatinine-cystatin were 87 ml/min (SD 24.8), 49.3 (SD 23.4) and 63.9 (SD 23.3), respectively. The percentage of patients with GFR <30ml/min was 1.9% measured by creatinine, 20.5% calculated by cystatin, and 5.6% calculated by creatinine-cystatin (Figure 1). Differences between rates were statistically significant.In this sense, anti-OP therapy was tailored accordingly in 12 patients (10.9%) with treatment indication, using denosumab instead of bisphosphonates.p 0,008p <0,001Figure 1.Patients with GFR <30 ml/min by different equations.ConclusionIn a setting of advanced liver disease candidate to transplantation, renal function estimates significantly varied depending on the GFR equation used, thus largely modifying the rates of patients with contraindication for using bisphosphonates, despite the high fracture risk.Further studies are necessary to establish the best method to assess the renal function in advanced liver disease patients, in order to tailor anti-OP strategies.References[1]Skluzacek PA, Szewc RG, Nolan CR, et al. Prediction of GFR in liver transplant candidates. AM J Kidney Dis. 2003;42:1169-76.[2]Ebert N, Bevc S, Bökenkamp A, et al. Assessment of kidney function: clinical indications for measured GFR. Clinical Kidney Journal. 2001;14(8):1861-1870.[3]Riancho JA, Peris P, González-Macías J, et al. Guías de práctica clínica en la osteoporosis postmenopáusica, glucocorticoidea y del varón (actualización 2022). Rev Osteoporos Metab Miner. 2022;14(1):13-33.Acknowledgements:NIL.Disclosure of InterestsNone Declared.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
customersupport@researchsolutions.com
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.
Copyright © 2025 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.