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1.
Pancreatology ; 13(1): 8-17, 2013.
Article in English | MEDLINE | ID: mdl-23395564

ABSTRACT

Chronic pancreatitis (CP) is a relatively uncommon, complex and heterogeneous disease. The absence of a gold standard applicable to the initial phases of CP makes its early diagnosis difficult. Some of its complications, particularly chronic pain, can be difficult to manage. There is much variability in the diagnosis and treatment of CP and its complications amongst centers and professionals. The Spanish Pancreatic Club has developed a consensus on the management of CP. Two coordinators chose a multidisciplinary panel of 24 experts on this disease. A list of questions was drafted, and two experts reviewed each question. Then, a draft was produced and shared with the entire panel of experts and discussed in a face-to-face meeting. This first part of the consensus addresses the diagnosis of CP and its complications.


Subject(s)
Pancreatitis, Chronic/diagnosis , Alcoholism/complications , Autoimmune Diseases , Blood Glucose/metabolism , Diabetes Mellitus/etiology , Glycated Hemoglobin/metabolism , Humans , Pancreas/diagnostic imaging , Pancreatitis, Chronic/complications , Pancreatitis, Chronic/diagnostic imaging , Smoking/adverse effects , Ultrasonography
2.
Pancreatology ; 13(1): 18-28, 2013.
Article in English | MEDLINE | ID: mdl-23395565

ABSTRACT

Chronic pancreatitis (CP) is a complex disease with a wide range of clinical manifestations. This range comprises from asymptomatic patients to patients with disabling symptoms or complications. The management of CP is frequently different between geographic areas and even medical centers. This is due to the paucity of high quality studies and clinical practice guidelines regarding its diagnosis and treatment. The aim of the Spanish Pancreatic Club was to give current evidence-based recommendations for the management of CP. Two coordinators chose a multidisciplinary panel of 24 experts on this disease. These experts were selected according to clinical and research experience in CP. A list of questions was made and two experts reviewed each question. A draft was later produced and discussed with the entire panel of experts in a face-to-face meeting. The level of evidence was based on the ratings given by the Oxford Centre for Evidence-Based Medicine. In the second part of the consensus, recommendations were given regarding the management of pain, pseudocysts, duodenal and biliary stenosis, pancreatic fistula and ascites, left portal hypertension, diabetes mellitus, exocrine pancreatic insufficiency, and nutritional support in CP.


Subject(s)
Pancreatitis, Chronic/therapy , Acetaminophen/therapeutic use , Anti-Inflammatory Agents, Non-Steroidal/therapeutic use , Cholangiopancreatography, Endoscopic Retrograde , Constriction, Pathologic/therapy , Drainage , Evidence-Based Medicine , Exocrine Pancreatic Insufficiency/therapy , Nutritional Status , Pain Management , Pancreatic Pseudocyst/therapy , Pancreatitis, Chronic/diet therapy , Pancreatitis, Chronic/surgery
3.
Nutr. hosp ; 27(6): 1782-1802, nov.-dic. 2012. ilus, tab
Article in Spanish | IBECS | ID: ibc-112161

ABSTRACT

Revisamos las recomendaciones internacionales de ingesta oral de ácidos grasos n-3.y su contenido en las fórmulas de nutrición enteral. Sus acciones metabólicas dependen de su metabolización a EPA y DHA. La actividad de las 5D y 6D desaturasas, que catalizan este proceso, aumenta con el ejercicio, insulina, estrógenos de mujer fértil y proliferadores peroxisómicos, mientras que disminuye con el ayuno, déficit de proteínas y oligoelementos, edad > 30 años, sedentarismo, tabaco, alcohol, colesterol, ácidos grasos trans y saturados, insulinopenia y hormonas de estrés (adrenalina y glucocorticoides). La mayoría de las guías recomiendan 20-35% de la energía total en forma de grasas, repartidas en saturadas 7-10%, poliinsaturadas 6-10% y monoinsutaradas en España 20%. El de AG n-3 es de 0,5-2 g/día o bien 0,5-2% de la ingesta calórica total, con un límite superior de 3 g/día. El de AG n-6 es del 2,5-10% del aporte calórico total y el cociente recomendado n-6/n-3 no está bien definido pero la mayoría recomienan 5/1. El contenido en EPA y DHA, debe ser de al menos los 500 mg diarios. Por último, la ratio EPA/DHA en la mayoría es de 2/1. Las fórmulas de nutrición estándar presentan un contenido en grasas adecuado, pero la mayoría de los productos que contienen EPA y DHA exceden el límite de los 3 g/día. De los productos hiperproteicos y/o concentrados por vía oral sólo un producto de este grupo contiene EPA y DHA. Las del anciano frágil no todas aportan EPA y DHA y las que los contienen, su concentración puede ser incluso excesiva y en una relación poco parecida a la del aceite de pescado (AU)


We review the international recommendations on oral intake of n-3 fatty acids and their content in the enteral nutrition formulas. Their metabolic actions depend on their metabolization to EPA and DHA. The activity of desaturases catalyzing this process increases with exercise, insulin, estrogens in the fertile women, and peroxisomal proliferators, whereas it decreases with fasting, protein and oligoelements deficiencies, age < 30 years, sedentary lifestyle, cigarette smoking, alcohol, cholesterol, trans and saturated fatty acids, insulin deficiency, and stress hormones (adrenalin and glucocorticoids). Most of the guidelines recommend that 20-35% of the total energy comes from fat, being 7-10% saturated fats, 6-10% polyunsaturated, and 20% monounsaturated, in Spain. The recommendation for n-3 FA is 0.5-2 g/day or 0.5-2% of total caloric intake, with an upper limit of 3 g/day. For n-6 FA, 2.5-10% of total caloric intake, the n-6/n-3 ratio not being well established although most of the guidelines recommend 5:1. The EPA and DHA content should be at least 500 mg per day. Finally, the EPA/DHA ratio is 2:1 in most of them. Standard nutrition formulas present an appropriate fat content, although most of the products containing EPA and DHA exceed the limit of 3 g/day. Among the products with hyperprotein and/or concentrated, only of them contains EPA y DHA. Not all the formulas used for the frail elderly contain EPA or DHA, and in those containing them their concentration may be excessive and with a proportion very dissimilar to that of fish oil (AU)


Subject(s)
Humans , Enteral Nutrition/methods , Nutritional Support/methods , Fatty Acids, Omega-3/administration & dosage , Docosahexaenoic Acids/administration & dosage , Eicosapentaenoic Acid/administration & dosage , Practice Patterns, Physicians'
4.
Nutr Hosp ; 27(6): 1782-802, 2012.
Article in Spanish | MEDLINE | ID: mdl-23588426

ABSTRACT

We review the international recommendations on oral intake of n-3 fatty acids and their content in the enteral nutrition formulas. Their metabolic actions depend on their metabolization to EPA and DHA. The activity of desaturases catalyzing this process increases with exercise, insulin, estrogens in the fertile women, and peroxisomal proliferators, whereas it decreases with fasting, protein and oligoelements deficiencies, age < 30 years, sedentary lifestyle, cigarette smoking, alcohol, cholesterol, trans and saturated fatty acids, insulin deficiency, and stress hormones (adrenalin and glucocorticoids). Most of the guidelines recommend that 20-35% of the total energy comes from fat, being 7-10% saturated fats, 6-10% polyunsaturated, and 20% monounsaturated, in Spain. The recommendation for n-3 FA is 0.5-2 g/day or 0.5-2% of total caloric intake, with an upper limit of 3 g/day. For n-6 FA, 2.5-10% of total caloric intake, the n-6/n-3 ratio not being well established although most of the guidelines recommend 5:1. The EPA and DHA content should be at least 500 mg per day. Finally, the EPA/DHA ratio is 2:1 in most of them. Standard nutrition formulas present an appropriate fat content, although most of the products containing EPA and DHA exceed the limit of 3 g/day. Among the products with hyperprotein and/or concentrated, only of them contains EPA y DHA. Not all the formulas used for the frail elderly contain EPA or DHA, and in those containing them their concentration may be excessive and with a proportion very dissimilar to that of fish oil.


Subject(s)
Enteral Nutrition/methods , Fatty Acids, Omega-3/administration & dosage , Recommended Dietary Allowances , Docosahexaenoic Acids/administration & dosage , Eicosapentaenoic Acid/administration & dosage , Energy Intake , Enteral Nutrition/standards , Enzymes/metabolism , Fatty Acids, Essential/administration & dosage , Fatty Acids, Omega-6/analysis , Food, Formulated , Humans , Immune System/physiology , Terminology as Topic
5.
Endocrinol. nutr. (Ed. impr.) ; 55(supl.2): 53-57, ene. 2008. tab
Article in Spanish | IBECS | ID: ibc-61986

ABSTRACT

En la evolución natural de la diabetes mellitus tipo 2, la capacidad secretora de insulina por el páncreas se agota de forma progresiva, empeorando el control glucémico. Por ello, en la historia natural del paciente diabético tipo 2, el tratamiento suele pasar de dieta y ejercicio físico a antidiabéticos orales y, finalmente, suele ser necesario el tratamiento con insulina para lograr un buen control metabólico. Cuando aún existe reserva pancreática, la asociación de insulina a antidiabéticos orales es la mejor opción, y puede optarse por utilizar una dosis de análogo de acción lenta, de insulina premezclada o de insulina NPH. Cuando la reserva pancreática está agotada o cuando no se logra un buen control del paciente con una única dosis de insulina, se debe plantear el tratamiento con varias dosis de insulina premezclada, o bien el régimen basal-bolo. La decisión entre ambos tipos de tratamiento debe realizarse de forma individual, en función de las características individuales del paciente (AU)


In the natural history of type 2 diabetes, pancreatic insulin secretion is progressively depleted and metabolic control worsens. Treatment of these patients usually starts with diet and exercise, with subsequent use of oral glucose-lowering drugs, finally ending with insulin therapy to achieve good metabolic control. When there is still endogenous insulin secretion, the combination of insulin and oral glucose-lowering drugs is usually preferred, using a once-daily long-acting insulin analog, premixed insulin, or NPH insulin. When the patient no longer has any endogenous insulin secretion, or when good metabolic control cannot be achieved with a once-daily regimen, treatment with several insulin doses is required. This treatment consists of a basal-bolus regimen or several doses of premixed insulin. The choice between the 2 types of treatment should be based on the patient’s individual characteristics (AU)


Subject(s)
Humans , Male , Female , Diabetes Mellitus, Type 2/epidemiology , Diabetes Mellitus, Type 2/therapy , Insulin/therapeutic use , Hypoglycemic Agents/therapeutic use , Insulin/biosynthesis , Insulin/classification
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