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Family Practice Notebook Updates 2016

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2601. bisphosphonates in the treatment of Paget's disease

(2) Reference: (1) (2) Links: General Practice Notebook General Practice Notebook The information provided herein should not be used for diagnosis or treatment of any medical condition. A licensed medical practitioner should be consulted for diagnosis and treatment of any and all medical conditions. Copyright 2016 Oxbridge Solutions Ltd®. Any distribution or duplication of the information contained herein is strictly prohibited. Oxbridge Solutions Ltd® receives funding from advertising (...) bisphosphonates in the treatment of Paget's disease bisphosphonates in the treatment of Paget's disease - General Practice Notebook This site is intended for healthcare professionals General Practice Notebook | Medical search bisphosphonates in the treatment of Paget's disease bisphosphonates are the mainstay of treatment of Paget's disease lead to inhibition of bone resorption bind to calcium hydroxyapatite - leads to prevention of bone turnover cellular effects - inhibition of osteoclast

2010 GP Notebook

2602. attention deficit hyperactivity disorder

as first-line pharmacological treatment Reference: (1) Links: General Practice Notebook General Practice Notebook The information provided herein should not be used for diagnosis or treatment of any medical condition. A licensed medical practitioner should be consulted for diagnosis and treatment of any and all medical conditions. Copyright 2016 Oxbridge Solutions Ltd®. Any distribution or duplication of the information contained herein is strictly prohibited. Oxbridge Solutions Ltd® receives funding (...) attention deficit hyperactivity disorder attention deficit hyperactivity disorder - General Practice Notebook This site is intended for healthcare professionals General Practice Notebook | Medical search attention deficit hyperactivity disorder Attention deficit hyperactivity disorder (ADHD) is a heterogeneous behavioural syndrome characterised by the core symptoms of: hyperactivity impulsivity inattention while these symptoms tend to cluster together, some people are predominantly hyperactive

2010 GP Notebook

2603. social phobia

social phobia social phobia - General Practice Notebook This site is intended for healthcare professionals General Practice Notebook | Medical search social phobia Patients with social phobia (social anxiety disorder) have a fear of being scrutinized, ridiculed or humiliated by other people. In generalised social phobia the patient will avoid all contact with people outside the family circle. Other patients have phobia which are more focussed, for example, fears concerning: public speaking (...) Practice Notebook General Practice Notebook The information provided herein should not be used for diagnosis or treatment of any medical condition. A licensed medical practitioner should be consulted for diagnosis and treatment of any and all medical conditions. Copyright 2016 Oxbridge Solutions Ltd®. Any distribution or duplication of the information contained herein is strictly prohibited. Oxbridge Solutions Ltd® receives funding from advertising but maintains editorial independence. GPnotebook

2010 GP Notebook

2604. oral contraceptives and breast cancer

Bulletin (2006); 17(2):1-9. Links: General Practice Notebook General Practice Notebook The information provided herein should not be used for diagnosis or treatment of any medical condition. A licensed medical practitioner should be consulted for diagnosis and treatment of any and all medical conditions. Copyright 2016 Oxbridge Solutions Ltd®. Any distribution or duplication of the information contained herein is strictly prohibited. Oxbridge Solutions Ltd® receives funding from advertising (...) oral contraceptives and breast cancer oral contraceptives and breast cancer - General Practice Notebook This site is intended for healthcare professionals General Practice Notebook | Medical search oral contraceptives and breast cancer There is evidence (1,2) that women who currently use or have stopped using combined oral contraceptive pills have a slightly increased risk of breast cancer (odds ratio 1.24 for current users and 1.16 for women who stopped using the pill one to four years before

2010 GP Notebook

2605. Airways and Intubation

. 2007 Feb54(2):124-8. ; American Thoracic Society ; Tracheostomy practice in adults with acute respiratory failure. Crit Care Med. 2012 Oct40(10):2890-6. ; Rapid sequence induction and intubation: current controversy. Anesth Analg. 2010 May 1110(5):1318-25. doi: 10.1213/ANE.0b013e3181d5ae47. Epub 2010 Mar 17. ; Best evidence topic report. Cricoid pressure in emergency rapid sequence induction. Emerg Med J. 2005 Nov22(11):815-6. ; Family Practice Notebook ; The success of emergency endotracheal (...) Airways and Intubation Airways and Intubation. Oral intubation information. Patient | Patient TOPICS Try our Symptom Checker TREATMENT RESOURCES Try our Symptom Checker PROFESSIONAL Upgrade to Patient Pro / / Search Airways and Intubation Authored by , Reviewed by | Last edited 2 Nov 2016 | Certified by This article is for Medical Professionals Professional Reference articles are designed for health professionals to use. They are written by UK doctors and based on research evidence, UK

2008 Mentor

2606. records in general practice

records in general practice records in general practice - General Practice Notebook This site is intended for healthcare professionals General Practice Notebook | Medical search records in general practice General practice records consist of: consultation records plus: registration data reminders and recalls personal data repeat medication list past medical history summary family history health promotion data hospital and community team communications More and more records are being kept (...) Practice Notebook General Practice Notebook The information provided herein should not be used for diagnosis or treatment of any medical condition. A licensed medical practitioner should be consulted for diagnosis and treatment of any and all medical conditions. Copyright 2016 Oxbridge Solutions Ltd®. Any distribution or duplication of the information contained herein is strictly prohibited. Oxbridge Solutions Ltd® receives funding from advertising but maintains editorial independence. GPnotebook

2010 GP Notebook

2607. familial dysbetalipoproteinaemia

familial dysbetalipoproteinaemia familial dysbetalipoproteinaemia - General Practice Notebook This site is intended for healthcare professionals General Practice Notebook | Medical search familial dysbetalipoproteinaemia This condition is characterised by raised triglyceride and cholesterol levels due to abnormally high concentration of IDL and chylomicrons. It is inherited as an autosomal recessive trait. This is a type III hyperlipidaemia according to the WHO classification. This disease (...) of a type III hyperlipidaemia because of the mechanism of the hyperlipidaemia being related to excess VLDL particles (see linked item). First-line treatment is usually with a fibrate or fish oil Reference: Durrington, PN (1995). Hyperlipidaemia: diagnosis and management. 2nd edition. Butterworth-Heinemann Limited. Links: General Practice Notebook General Practice Notebook The information provided herein should not be used for diagnosis or treatment of any medical condition. A licensed medical

2010 GP Notebook

2608. familial combined hyperlipidaemia

familial combined hyperlipidaemia familial combined hyperlipidaemia - General Practice Notebook This site is intended for healthcare professionals General Practice Notebook | Medical search familial combined hyperlipidaemia This condition causes a variable increase in cholesterol (6.5-10 mmol/L) and triglycerides (2.3-12 mmol/L). It is the second commonest primary hyperlipidaemia (after polygenic hypercholesterolaemia). Patients presenting with this condition are: generally over 30 years of age (...) may be seen about 0.5 %-1% of the general population and in up to 15% of patients suffering myocardial infarctions who were less than 60 years old at the time of the myocardial infarction. Links: General Practice Notebook General Practice Notebook The information provided herein should not be used for diagnosis or treatment of any medical condition. A licensed medical practitioner should be consulted for diagnosis and treatment of any and all medical conditions. Copyright 2016 Oxbridge Solutions

2010 GP Notebook

2609. hypoparathyroidism (familial)

hypoparathyroidism (familial) hypoparathyroidism (familial) - General Practice Notebook This site is intended for healthcare professionals General Practice Notebook | Medical search hypoparathyroidism (familial) Idiopathic hypoparathyroidism is an uncommon condition characterised by the absence, fatty replacement or atrophy of the parathyroid glands. It may be familial or sporadic. Familial idiopathic hypoparathyroidism may be inherited as a sex linked recessive, autosomal recessive (...) General Practice Notebook The information provided herein should not be used for diagnosis or treatment of any medical condition. A licensed medical practitioner should be consulted for diagnosis and treatment of any and all medical conditions. Copyright 2016 Oxbridge Solutions Ltd®. Any distribution or duplication of the information contained herein is strictly prohibited. Oxbridge Solutions Ltd® receives funding from advertising but maintains editorial independence. GPnotebook stores small data

2010 GP Notebook

2610. familial idiopathic hypoparathyroidism

familial idiopathic hypoparathyroidism familial idiopathic hypoparathyroidism - General Practice Notebook This site is intended for healthcare professionals General Practice Notebook | Medical search familial idiopathic hypoparathyroidism Idiopathic hypoparathyroidism is an uncommon condition characterised by the absence, fatty replacement or atrophy of the parathyroid glands. It may be familial or sporadic. Familial idiopathic hypoparathyroidism may be inherited as a sex linked recessive (...) Practice Notebook General Practice Notebook The information provided herein should not be used for diagnosis or treatment of any medical condition. A licensed medical practitioner should be consulted for diagnosis and treatment of any and all medical conditions. Copyright 2016 Oxbridge Solutions Ltd®. Any distribution or duplication of the information contained herein is strictly prohibited. Oxbridge Solutions Ltd® receives funding from advertising but maintains editorial independence. GPnotebook

2010 GP Notebook

2611. familial breast cancer

oncoplastic or breast reconstructive skills Reference: Pulse (2005); 65(14):55-60. Evans DGR et al. (1994). Familial breast cancer. BMJ; 308:183-7 McPherson et al. (1994). BMJ;309: 1004 Links: General Practice Notebook General Practice Notebook The information provided herein should not be used for diagnosis or treatment of any medical condition. A licensed medical practitioner should be consulted for diagnosis and treatment of any and all medical conditions. Copyright 2016 Oxbridge Solutions Ltd®. Any (...) familial breast cancer familial breast cancer - General Practice Notebook This site is intended for healthcare professionals General Practice Notebook | Medical search familial breast cancer Up to 10% of breast cancer in western countries is due to genetic predisposition. Susceptibility to breast cancer appears to be inherited as an autosomal dominant with limited penetrance and may thus be inherited from either father or mother. About 5% of breast cancer is due to highly penetrant dominant

2010 GP Notebook

2612. familial lipoprotein lipase deficiency

familial lipoprotein lipase deficiency familial lipoprotein lipase deficiency - General Practice Notebook This site is intended for healthcare professionals General Practice Notebook | Medical search familial lipoprotein lipase deficiency Lipoprotein lipase deficiency is a rare condition and inherited as an autosomal recessive condition. It is characterised by the presence of chylomicrons in fasting plasma. Fasting tryglyceride levels are characteristically > 10 mmol/L. Characteristically (...) is characterized by a deficiency of apolipoprotein C-II, causing an accumulation of chylomicrons and very low density lipoproteins (VLDL) xanthomas and hepatosplenomegaly are less common in C-II anapolipoproteinemia than in lipoprotein lipase deficiency (1) Reference: Links: General Practice Notebook General Practice Notebook The information provided herein should not be used for diagnosis or treatment of any medical condition. A licensed medical practitioner should be consulted for diagnosis and treatment

2010 GP Notebook

2613. sarcoma (familial syndromes)

: neurofibromatosis familial retinoblastoma Li-Fraumeni syndrome Beckwith-Wiedemann syndrome basal cell naevus Gardner syndrome Links: General Practice Notebook General Practice Notebook The information provided herein should not be used for diagnosis or treatment of any medical condition. A licensed medical practitioner should be consulted for diagnosis and treatment of any and all medical conditions. Copyright 2016 Oxbridge Solutions Ltd®. Any distribution or duplication of the information contained herein (...) sarcoma (familial syndromes) sarcoma (familial syndromes) - General Practice Notebook This site is intended for healthcare professionals General Practice Notebook | Medical search sarcoma (familial syndromes) Soft tissue sarcomata are rare tumours accounting for less than 1% of adult tumours but up to 6% of childhood tumours. A genetic risk factor for sarcoma formation may be present in as many as one third of all patients with childhood sarcomata. Familial syndromes causing sarcomata include

2010 GP Notebook

2614. familial mediterranean fever

familial mediterranean fever familial mediterranean fever - General Practice Notebook This site is intended for healthcare professionals General Practice Notebook | Medical search familial mediterranean fever This is an inherited condition of unknown aetiology. It is characterized be episodes of fever, peritonitis and/or pleuritis. Amyloidosis, skin lesions and arthritis may be seen in these patients. This condition occurs most often in non-Ashkenazi Jews, Armenians and Arabs (...) . It is not restricted to these groups and may occur in, among others, people of Ashkenazi Jewish, Italian, and Anglo-saxon descent. Links: General Practice Notebook General Practice Notebook The information provided herein should not be used for diagnosis or treatment of any medical condition. A licensed medical practitioner should be consulted for diagnosis and treatment of any and all medical conditions. Copyright 2016 Oxbridge Solutions Ltd®. Any distribution or duplication of the information contained herein

2010 GP Notebook

2615. familial paroxysmal polyserositis

familial paroxysmal polyserositis familial paroxysmal polyserositis - General Practice Notebook This site is intended for healthcare professionals General Practice Notebook | Medical search familial paroxysmal polyserositis This is an inherited condition of unknown aetiology. It is characterized be episodes of fever, peritonitis and/or pleuritis. Amyloidosis, skin lesions and arthritis may be seen in these patients. This condition occurs most often in non-Ashkenazi Jews, Armenians and Arabs (...) . It is not restricted to these groups and may occur in, among others, people of Ashkenazi Jewish, Italian, and Anglo-saxon descent. Links: General Practice Notebook General Practice Notebook The information provided herein should not be used for diagnosis or treatment of any medical condition. A licensed medical practitioner should be consulted for diagnosis and treatment of any and all medical conditions. Copyright 2016 Oxbridge Solutions Ltd®. Any distribution or duplication of the information contained herein

2010 GP Notebook

2616. mediterranean fever(familial)

mediterranean fever(familial) mediterranean fever(familial) - General Practice Notebook This site is intended for healthcare professionals General Practice Notebook | Medical search mediterranean fever(familial) This is an inherited condition of unknown aetiology. It is characterized be episodes of fever, peritonitis and/or pleuritis. Amyloidosis, skin lesions and arthritis may be seen in these patients. This condition occurs most often in non-Ashkenazi Jews, Armenians and Arabs (...) . It is not restricted to these groups and may occur in, among others, people of Ashkenazi Jewish, Italian, and Anglo-saxon descent. Links: General Practice Notebook General Practice Notebook The information provided herein should not be used for diagnosis or treatment of any medical condition. A licensed medical practitioner should be consulted for diagnosis and treatment of any and all medical conditions. Copyright 2016 Oxbridge Solutions Ltd®. Any distribution or duplication of the information contained herein

2010 GP Notebook

2617. familial amaurotic idiocy

familial amaurotic idiocy familial amaurotic idiocy - General Practice Notebook This site is intended for healthcare professionals General Practice Notebook | Medical search familial amaurotic idiocy Tay-Sachs disease is a condition caused by an inborn error of metabolism where there is a deficiency in the enzyme hexosaminidase A, which splits the terminal N- acetylgalactosamine residue from GM2 ganglioside. The disease is particularly common in the Ashkenazi Jewish population, where it has (...) an incidence of 1 in 3 - 4000 births. It is a hundred times less frequent in other racial groups. Inheritance is autosomal recessive with the disrupted locus on chromosome 15. Links: General Practice Notebook General Practice Notebook The information provided herein should not be used for diagnosis or treatment of any medical condition. A licensed medical practitioner should be consulted for diagnosis and treatment of any and all medical conditions. Copyright 2016 Oxbridge Solutions Ltd®. Any distribution

2010 GP Notebook

2618. familial Creutzfeldt-Jacob disease

familial Creutzfeldt-Jacob disease familial Creutzfeldt-Jacob disease - General Practice Notebook This site is intended for healthcare professionals General Practice Notebook | Medical search familial Creutzfeldt-Jacob disease The familial forms of Creutzfeldt-Jacob (CJD) disease: have a wide spectrum of clinical features may vary in its clinical features between and within families have an autosomal dominant mode of inheritence account for 10% of cases of CJD In general: familial CJD presents (...) earlier, from 40 years on the clinical course is longer Links: General Practice Notebook General Practice Notebook The information provided herein should not be used for diagnosis or treatment of any medical condition. A licensed medical practitioner should be consulted for diagnosis and treatment of any and all medical conditions. Copyright 2016 Oxbridge Solutions Ltd®. Any distribution or duplication of the information contained herein is strictly prohibited. Oxbridge Solutions Ltd® receives funding

2010 GP Notebook

2619. family history

age and cause of death of family members position in family and number of siblings consanguinity (especially cousin marriages) Links: General Practice Notebook General Practice Notebook The information provided herein should not be used for diagnosis or treatment of any medical condition. A licensed medical practitioner should be consulted for diagnosis and treatment of any and all medical conditions. Copyright 2016 Oxbridge Solutions Ltd®. Any distribution or duplication of the information (...) family history family history - General Practice Notebook This site is intended for healthcare professionals General Practice Notebook | Medical search family history The most relevant family history is that of first-degree relatives, the parents, siblings and children. The health of more distant relatives and certainly that of the spouse, although not a blood relative, can also be important to a patient's well-being. Factors include: general and psychiatric health current age of family members

2010 GP Notebook

2620. familial triglyceridaemia

familial triglyceridaemia familial triglyceridaemia - General Practice Notebook This site is intended for healthcare professionals General Practice Notebook | Medical search familial triglyceridaemia Familial hypertriglycidaemia 2.3-10 mmol/L This condition has an autosomal dominant inheritance. This condition is characterised by increased VLDL only (high VLDL production, decreased lipoprotein lipase activity) [Fredrickson type IV]. This condition occurs in approximately 1% of general (...) Notebook General Practice Notebook The information provided herein should not be used for diagnosis or treatment of any medical condition. A licensed medical practitioner should be consulted for diagnosis and treatment of any and all medical conditions. Copyright 2016 Oxbridge Solutions Ltd®. Any distribution or duplication of the information contained herein is strictly prohibited. Oxbridge Solutions Ltd® receives funding from advertising but maintains editorial independence. GPnotebook stores small

2010 GP Notebook

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