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Cardiovascular (diabetic) Cardiovascular (general)
Endocrinology:
Diabetes:
NHS expenditure on diabetes is pounds 165 per
second.(2002) 6-16%of beds in the NHS is occupied by diabetic patients Waiting time for 1st appointments as bad as 14 weeks. One in 10 acute medical beds is occupied by diabetic patients.
1000 patients are on insulin pump in UK 30 patients on insulin pump in the Mersey region. There are 30 different insulin types, 10 pen devices, and 11 BGMs. IN the UKPDS, mean HBA1C fell from 9 to 7% and weight by 4.5% after 3 months of dietary modification. Every year of diabetes adds about 5% of increased CVS risk
The overall lifetime risk in white populations of developing type I diabetes is 0.4%. The lifetime risk for type I diabetes is 1-2% if mother is diabetic; 3-6% if father is diabetic, and 6% if siblings are diabetic. The lifetime risk of type 1 diabetes in a first degree relative is six percent, but this rises to 25-50 percent in identical twins. When a first degree relative as a high titre of islet cell antibody the risk increases to 8% per year with an accumulated risk of 70 percent in ten-years. The concordance rate for type I dm in dizygotic twins is 5-10% while that in monozygotic twins is 27-36% Presence of all three antibodies (islet cell antibodies, antiglutamic acid decarboxylase antibodies and anti tyrosine phosphatase antibodies) produces a 88% chance of developing type I diabetes in the next 10 years. The cumulative incidence of microalbuminuria in patients with type 1 diabetes at 30 years disease duration is approximately 40%. Approximately 20% of type 1 patients develop proteinuria after a disease duration of 25 years. 90% of type I diabetics in the UK have either HLA DR3, DR4 or both. 25% of type I dm will have evidence of thyroid disease, with about 5% being clinically hypothyroid. 7% of type I dm will have coeliac disease, but upto 40% can be asymptomatic for it. 20% of type I dm has pernicious anaemia. 2% of type I dm has antibodies to 21 hydroxylase, the marker for addisons disease. 40% of children with congenital rubella will develop islet antibodies, and 50% of these will develop type I dm. MODY: MODY 1: (HNF 4alpha) :Accounts for <0.0001% of all type 2 patients and about 5% of cases of MODY. 20% need insulin therapy. 40% need Oral hypoglycemic therapy. MODY 2: (Glucokinase) <0.2% of type 2 patients. This type accounts for 10% of cases of MODY. 90% are controlled with diet alone. MODY 3: ( HNF1alpha) : 1-2% of type 2 patients. This subgroup accounts for 70% of MODY patients. One third require insulin and one third require oral agents. The human pancreas has 1 million islet cells, weighing 1 gm, and containing 1 mg insulin. 6% of presumed type 2 dm have positive ICA antibodies, while 10% of presumed type 2dm have positive GAD antibodies (UKPDS), causing LADA. 94% of patients with ICA and 84% of patients with GAD antibodies required insulin at 6 year follow up.
Prevalence of type 2 dm
in the UK is 3%.
20% of microalbuminuric type 2 patients who survive for 10 years develop proteinuria. The prevalence of proteinuria in patients with type 2
diabetes is approximately 15%. The 4-year mortality of microalbuminuric type 2 patients is
32% and 50% of proteinuric type 2 patients have died within 4 years. One in 250 pregnancies is complicated by diabetes. Perinatal mortality is 5 times higher in babies of diabetic
mothers. (- due to congenital malformations) Standard published in : Delivery published in :
2% of UK diabetic population is registered blind (2002). A diabetic has a 10-20 fold increased risk of blindness. 2% of type I diabetics have retinopathy at diagnosis and 8% by 5 years. 30 years after diagnosis 98% of type I diabetics have retinopathy with 30% of these having proliferative retinopathy. 14% of T1DM who become blind do so because of maculopathy. 20-40% of T2DM have retinopathy at diagnosis. Among T2DM, 85% of those on insulin and 60% of those not on insulin are expected to have retinopathy at 15 years. T2DM patients are 10 times more likely to have maculopathy than T1DM. Cataracts occur in 60% of diabetic 35-55 years age. 15% of patients undergoing cataract surgery can have diabetes In the DCCT, intensive glycaemic control in type I DM slowed the rate of progression of existing retinopathy by 54% and the risk of severe NON PDR or PDR was reduced by 47%. In the UKPDS intensive glycaemic control in T2DM patients reduced progression of retinopathy by 21% and produced a 29% reduction in the need for laser therapy. 50% of patients entering End stage renal disease have T2DM. 18% of patients entering ESRD and replacement programmes have diabetes. Nephropathy is the cause of 15% of all deaths in diabetics <50 years of age. The cumulative incidence of microalbuminuria in patients with type 2 diabetes at 10 years disease duration is approximately 20-25%. 20% of microalbuminuric type 2 patients who survive for 10 years develop proteinuria. The prevalence of proteinuria in patients with type 2 diabetes is approximately 15%. Treated proteinuric, hypertensive type 2 patients lose glomerular function at a rate of approximately 8 ml/min/year. Patients with microalbuminuria have a two to fourfold increase in cardiovascular morbidity and mortality. The 4-year mortality of microalbuminuric type 2 patients is 32% and 50% of proteinuric type 2 patients have died within 4 years. The cumulative incidence of microalbuminuria in patients with type 1 diabetes at 30 years disease duration is approximately 40%. 2/3rd of type 1 diabetics with proteinuria will subsequently develop renal failure. 85% of type I patients with nephropathy are hypertensive. Captopril in type 1 patients reduces progression of microalbuminuria to albuminuria by 68%. In the DCCT, intensive glycaemic control reduced progression to microalbuminuria by 30% and further progression to albuminuria by 54%. Nerve conduction studies show abnormalities in 80% of patients with diabetes. Erectile dysfunction affects 40% of men with diabetes. Sildenafil therapy is effective in 60% of diabetics.
Pancreatic Transplantation:
Diabetes affects 6% of the population of developed countries. A doubling in incidence is predicted with the projected total exceeding 300 million people within the next 25 years. The societal cost estimates for diabetes and inevitable sequelae are enormous consuming between nine percent and 15% of healthcare expenditure in developed countries. Early attempts at whole pancreas transplantation had a mortality rate exceeding 60 percent, and fewer than 3% grafts remained functional at one-year. There have been over 447 islet allografts performed worldwide, 394 in the past decade. Fewer than 10% patients have been able to remain free of insulin for sustained periods. Less than 20 percent of patients remained free of insulin beyond the first year when cyclosporine azathioprine and steroids were used. 50 percent of the infused islet mark was destroyed to autoimmune inflammatory pathways and apoptotic mechanisms. A total of 15 patients with type 1 diabetes have now being treated using the Edmonton protocol. sustained insulin independence has been achieved in 85 percent of these recipients.
Cardiovascular disease accounts for 75% of deaths in T2DM and 35% in T1DM. Overall 10% of patients have peripheral vascular disease. Diabetics with PVD have a 15 fold higher risk of a non traumatic amputation. Thromboembolic Cerebrovascular events Strokes account for 15% of death in T2DM. Lactic acidosis occurs in 0.024-0.15 cases/1000 patient years in Metformin treated patients. (Swedish study) Cardiovascular statistics: (General) 2% of US population have CCF
In patients older than 60 years, it was 3 per 1,000 person years. About 1 in 20 people aged 65 years or older have AF (4.7%). The authors calculated that of the 21,000 strokes annually in patients with AF, 3,000 are probably prevented by anticoagulation, but that another 3,000-5,000 could be prevented if there was wider use of anticoagulant therapy. Bandolier
Phaeochromocytoma: About 10 percent of the tumors are extraadrenal, but 95 percent are within the abdomen. Although any site containing paraganglionic tissue may be involved, the most common extraadrenal locations are the superior and inferior paraaortic areas (75 percent of extraadrenal tumors), the bladder (10 percent), the thorax (10 percent), and the head, neck, and pelvis (5 percent). In approximately 60% of cases the hypertension is sustained, and half of patients with sustained hypertension have distinct crises or paroxysms. The other 40% have blood pressure elevations only during an attack. The 5-year survival rate after surgery is usually over 95%, the recurrence rate is <10%. For malignant pheochromocytoma, the 5-year survival rate is <50%. Maternal mortality is 17% while fetal mortality is 30% if not treated urgently. The incidence of pheochromocytoma in some kindred with von Hippel-Lindau disease may be as high as 10 to 25%
Addisons disease: Incidence is 40-60 cases per 1,000,000 persons.
75% of orally administered thyroxine is absorbed. 90% of orally administered T3 is absorbed.
20% of elderly thyrotoxic patients do not have a goitre. Graves disease complicates 0.1% of pregnancies. Graves ophthalmopathy affects about 25-50% of graves patients. 1-5% of patients with graves disease have significant ophthalmopathy.
25% of women with lymphocytic thyroiditis postpartum have a recurrence in a subsequent pregnancy. Hypothyroidism develops in 25% and recurrent hyperthyroidism in 10% post subtotal thyroidectomy. 1% incidence of hypoparathyroidism or injury to laryngeal nerve. The overall incidence of thyroid nodules in the population is 4%. 12,000 new cases of thyroid cancer develop each year in the US. Less than 0.2% of thyroid cancers become clinically obvious every year. More than 87% of subjects with thyroid cancer have intrathyroidal or extra thyroidal spread at the time of surgery. In single nodules the incidence of thyroid carcinoma is 20%. In MNG the incidence of thyroid cancer is only 4.8%. 7% develop recurrent clinical cancer in the remaining thyroid lobe. 43% of metastases in thyroid cancer develop within 1 year of diagnosis, 23% develop between 1 and 5 years, and 9% beyond 10 years (Cancer1988: 61:1-6).
Sporadic PHPT in general population is
0.5- 10%. Male: female ratio for sporadic PHPT is 3:1. 50% of PHPT
patients are discovered incidentally- asymptomatic. Success rate of four gland exploration by an experienced endocrine surgeon for primary hyperparathyroidism is 95% (CE 59: 539-554 2003). A 50% decrease in Intraoperative PTH levels predict a cure in more than 95%. 27% of asymptomatic patients with PHPT show disease progression requiring surgical intervention over 10 years. (Silverberg et al 1999). In primary hyperparathyroidism, 85% present with a
single adenoma, 5% with multiple adenomata, 3-5% with a carcinoma, and 10% with
hyperplasia of multiple glands.
MEN1 and MEN 2 : M E N 1 mutation has been found in about 20 percent of reported FIHPT. 25% of MEN 1 mutations are nonsense, 45 percent are small deletions, 15 percent are small insertions, and less than 5% are donor splice mutations. No germ line mutation is found in 10-20 percent of index cases for familial MEN 1. Parathyroid hyperplasia or multiple adenomas occur in 90% of patients with MEN 1. Pituitary lesions occur in 50% of patients with MEN 1.75% of patients with MEN 1 have pancreatic tumours. 40% develop adrenal adenomas, and 20% have thyroid adenomas. After 8-12 years of successful total parathyroidectomy in men one,50% will have recurred. Anterior pituitary adenoma is the first clinical manifestation of MEN 1 in up to 25 percent of sporadic cases. its prevalence in MEN 1 varies from 10-60 percent. Adrenocortical lesions occur in 20-40 percent of MEN. Multiple facial angiofibromas occur in 40-80% of MEN 1. 50% of cases have five or more angiofibromas. MTC occurs in 90% of MEN 2A. Phaeochromocytoma occurs in 70% of MEN 2A . Hyperparathyroidism occurs in 20-30%. The RET oncogene is 100% predictive for development of medullary thyroid carcinoma in MEN 2A and 2B. 98% of subjects with MEN 2A carry a known RET mutation. Early thyroidectomy has lowered the mortality from hereditary MTC to less than 5%. MEN 2B: MCT and multiple gangliomas occur in 100%. Phaeochromocytoma occurs in 33%. Hyperparathyroidism in 5%. The likelihood of RET germline mutation in patients with apparently sporadic MTC is 1-7%. Hereditary etiology among apparently sporadic cases of pheochromocytoma is a far 5-15%. Familial Hypocalciuric hypercalcaemia represents 1-2% of cases of asymptomatic hypercalcaemia. Tumor associated local osteolysis accounts for hypercalcaemia in 20-40% of hypercalcaemia in malignant cases. Humoral hypercalcaemia accounts for 40-50% cases. Hypercalcaemia occurs in 10% of patients with sarcoidosis. Hypercalciuria occurs in 50% of sarcoidosis. Hypercalcaemia occurs in 25% of patients with thyrotoxicosis. Hypercalcaemia occurs in 5% of lithium treated patients.
Adrenal Radiology: As regards Phaeochromocytoma, positive and negative predictive values of CT were 69 and 98 percent. Both CT and MRI are quite sensitive (98 to 100 percent), but are only about 70 percent specific because of the higher prevalence of adrenal "incidentalomas. Multiple tumors are found in approximately 10 percent of patients, particularly those with extra adrenal tumors. Localisation of Phaeochromocytoma is right adrenal 25%; left adrenal 17%; bilateral adrenal 17%; intra-abdominal extra adrenal 32%. I123 MIBG imaging has revealed that upto 46% of patients with Phaeochromocytoma develop metastatic disease, and only 21% is detected at surgery. Following surgery, there is a 50% local recurrence and subsequent dissemination.
Thyroid Radiology : 13% of persons exposed to low dose therapeutic irradiation (6.5 to 3000 rad calculated dose to the thyroid) develop thyroid cancer. 40% of persons exposed to low dose therapeutic radiation who have a discrete thyroid nodule have thyroid cancer in the gland. In 60% the index nodule is the cancer and in 40% the cancer is elsewhere in the thyroid. 60% of pulmonary metastases from the thyroid, take up radioactive iodine. Dose of radioiodine should be increased by 25% in patients who have had anti thyroid drugs within the previous 10 days. The hypothyroidism post radioiodine in the first 6 months is transient in 25% of patients. The incidence of hypothyroidism is 10-20% after 1 year and increases at a rate of 2% and 4% every year. Pure cystic lesions are malignant in 7% of cases. Cystic lesions atleast 4 cm in diameter are more frequently malignant. Solid lesions are malignant in 21% of cases.
Parathyroid Radiology: CT or USG has a sensitivity of 50-75% in detecting parathyroid disease Reproductive: Ultrasound has a sensitivity of 91% for PCOS. Transvaginal ultrasound witll identify 90% of ovarian virilizing tumours.
PCOD 95% of women presenting with hirsutism have PCOD. Estimated prevalence of PCOS is 8% based on clinical criteria, and 22% based on ultrasonic diagnosis. Oligomenorrhea is seen in 70% of PCOS patients and hirsutism in 60%. 25% of women with PCOS have acne or alopecia. Obesity is seen in 35% and infertility in 30%. LH is raised in 50-70% of patients with PCOS. SHBG is low in 50% of PCOS patients. Hyperprolactinemia is present in 30%. 40% of PCOS have IGT and 10% have DM.
MEN 1 the prevalence of enteropancreatic islet tumours in men 1 individuals varies from 30-75 percent. one-third of sporadic and men one associated ZES cases eventually die from their malignancy. 16% of MEN 1 patients were free of disease immediately after gastrinomas surgery and at 5 years this had declined to 6%. The disease free rates in gastrinomas without MEN 1 is 45 percent and 40 percent respectively.
Audit commission report
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. This page was last updated on: 07/03/2007 |