<?xml version="1.0" encoding="UTF-8"?><response><lst name="responseHeader"><int name="status">0</int><int name="QTime">0</int><lst name="params"><str name="sort">da desc</str><str name="tr">export-xml.xsl</str><str name="q">*:*</str><str name="facet.limit">20</str><str name="qt">standard</str><str name="wt">xslt</str><str name="fq">db:"NGC"</str><str name="rows">10</str></lst></lst><result name="response" numFound="305" start="0"><doc><arr name="category"><str>Evaluation</str><str>Management</str><str>Risk Assessment</str><str>Screening</str><str>Technology Assessment</str><str>Treatment</str></arr><str name="db">NGC</str><str name="id">10014</str><arr name="outcome"><str>Overall survival</str><str>Disease-free survival</str><str>Quality of life</str><str>Toxicity</str><str>Cost-effectiveness</str></arr><arr name="practices"><str>Preoperative carcinoembryonic antigen (CEA) testing for staging and surgical treatment planning</str><str>Postoperative CEA testing to detect possible metastatic disease</str><str>CEA testing to monitor metastatic colorectal cancer during systemic therapy</str><str>CA 19-9 testing for monitoring response to therapy</str><str>CEA as a screening test for colorectal cancer</str><str>CEA testing to determine whether to treat patients with colorectal cancer with adjuvant therapy</str><str>Use of CA 19-9 for screening, diagnosis, staging, surveillance, or monitoring treatment of patients with colorectal cancer</str><str>Use of flow-cytometrically derived DNA ploidy (DNA index) or DNA flow cytometric proliferation analysis (%S phase) to determine prognosis of early stage colorectal cancer</str><str>Use of p53 expression or mutation for screening, diagnosis, staging, surveillance, or monitoring treatment of patients with colorectal cancer</str><str>Use of the rasoncogene for screening, diagnosis, staging, surveillance, or monitoring treatment of patients with colorectal cancer</str><str>Use of thymidine synthase (TS), dihydropyrimidine dehydrogenase (DPD), and thymidine phosphorylase (TP) tests for screening, prognosis, predicting response to therapy, or monitoring response to therapy of patients with colorectal cancer</str><str>Microsatellite instability (MSI) ascertained by polymerase chain reaction (PCR) to determine the prognosis of operable colorectal cancer or to predict the effectiveness of fluorouracil (FU) adjuvant chemotherapy</str><str>Assaying for loss of heterozygosity (LOH) on the long arm of chromosome 18 (18q) or deleted in colon cancer (DCC) protein determination by immunohistochemistry to determine the prognosis of operable colorectal cancer, or to predict response to therapy</str><str>Use of CA 19-9 as a screening test for pancreatic cancer</str><str>Use of CA 19-9 testing alone for determining operability or the results of operability in pancreatic cancer and for providing definitive evidence of disease recurrence</str></arr><arr name="speciality"><str>Colon and Rectal Surgery</str><str>Family Practice</str><str>Gastroenterology</str><str>Internal Medicine</str><str>Oncology</str><str>Radiation Oncology</str><str>Surgery</str></arr><arr name="target"><str>Patients with colorectal cancer or pancreatic cancer</str></arr><arr name="ti"><str>ASCO 2006 update of recommendations for the use of tumor markers in gastrointestinal cancer.</str></arr><arr name="ur"><str>http://www.guidelines.gov/summary/summary.aspx?ss=15&amp;doc_id=10014</str></arr></doc><doc><str name="db">NGC</str><str name="id">10015</str><arr name="intended"><str>Advanced Practice Nurses</str><str>Allied Health Personnel</str><str>Clinical Laboratory Personnel</str><str>Dietitians</str><str>Health Care Providers</str><str>Health Plans</str><str>Nurses</str><str>Patients</str><str>Physician Assistants</str><str>Physicians</str><str>Social Workers</str></arr><arr name="outcome"><str>Morbidity (including cardiovascular and cerebrovascular events) and mortality among end-stage renal disease patients on hemodialysis</str><str>Longevity</str><str>Indicators of hemodialysis adequacy</str><str>Frequency of intradialytic symptoms</str><str>Frequency of hospitalization</str><str>Intermediate outcomes (e.g. clearance and filtration measures)</str><str>Adverse events due to treatment</str><str>Quality of life</str></arr><arr name="practices"><str>Patient education about kidney failure and options for its treatment</str><str>Estimation of kidney function (glomerular filtration rate)</str><str>Optimal timing of initiation of dialysis</str><str>Monitoring of hemodialysis dose (including formal urea kinetic modeling)</str><str>Assessment of hemodialysis adequacy (including blood urea nitrogen [BUN])</str><str>Control of fluid volume and blood pressure</str><str>Preservation of residual kidney function (RKF) (e.g., use of angiotensin-converting enzyme inhibitors and/or angiotensin receptor blockers, avoidance of nephrotoxic insults)</str><str>Quality improvement programs</str></arr><arr name="speciality"><str>Family Practice</str><str>Internal Medicine</str><str>Nephrology</str><str>Pediatrics</str></arr><arr name="target"><str>Adult and pediatric patients on hemodialysis</str></arr><arr name="ti"><str>NKF-K/DOQI clinical practice guidelines for hemodialysis adequacy: update 2006.</str></arr><arr name="ur"><str>http://www.guidelines.gov/summary/summary.aspx?ss=15&amp;doc_id=10015</str></arr></doc><doc><arr name="category"><str>Management</str><str>Treatment</str></arr><str name="db">NGC</str><str name="id">10016</str><arr name="intended"><str>Advanced Practice Nurses</str><str>Allied Health Personnel</str><str>Clinical Laboratory Personnel</str><str>Health Care Providers</str><str>Health Plans</str><str>Nurses</str><str>Patients</str><str>Physician Assistants</str><str>Physicians</str><str>Social Workers</str></arr><arr name="outcome"><str>Morbidity (including cardiovascular and cerebrovascular events) and mortality among end-stage renal disease patients on hemodialysis</str><str>Survival</str><str>Indicators of peritoneal dialysis (PD) adequacy</str><str>Patient adherence to PD prescription</str><str>Hospitalization</str><str>Technique survival</str><str>Nutrition</str><str>Growth (pediatrics)</str><str>Cognitive function (pediatrics)</str><str>Blood pressure/hypertension</str><str>Left ventricular hypertrophy (LVH)</str><str>Quality of Life</str></arr><arr name="practices"><str>Patient education about kidney failure and options for its treatment</str><str>Estimation of kidney function by estimation of glomerular filtration rate (GFR)</str><str>Optimal timing of initiation of dialysis</str><str>Measures of peritoneal dialysis dose and total solute clearance</str><str>Preservation of residual kidney function, including use of angiotensin-converting enzyme (ACE) inhibitors and angiotensin receptor blockers (ARBs) and avoiding insults to residual kidney function (RKF)</str><str>Maintenance of euvolemia through monthly monitoring and therapies to optimize extracellular water, blood volume, and blood pressure</str><str>Establishment of quality improvement programs</str></arr><arr name="speciality"><str>Family Practice</str><str>Internal Medicine</str><str>Nephrology</str><str>Pediatrics</str></arr><arr name="target"><str>Adult and pediatric patients with end-stage renal disease who receive peritoneal dialysis (PD) treatment, primarily patients on continuous ambulatory PD (CAPD)</str></arr><arr name="ti"><str>NKF-KDOQI clinical practice guidelines for peritoneal dialysis adequacy: update 2006.</str></arr><arr name="ur"><str>http://www.guidelines.gov/summary/summary.aspx?ss=15&amp;doc_id=10016</str></arr></doc><doc><arr name="category"><str>Evaluation</str><str>Management</str><str>Treatment</str></arr><str name="db">NGC</str><str name="id">10017</str><arr name="intended"><str>Advanced Practice Nurses</str><str>Allied Health Personnel</str><str>Clinical Laboratory Personnel</str><str>Dietitians</str><str>Health Care Providers</str><str>Health Plans</str><str>Nurses</str><str>Patients</str><str>Physician Assistants</str><str>Physicians</str><str>Social Workers</str></arr><arr name="outcome"><str>Vascular access-related morbidity</str><str>Maturation and function of new arteriovenous fistula (AVF)</str><str>Change in approach to access placement</str><str>Infection rates</str><str>Infection clearing rates</str><str>Reinfection rates</str><str>Infection-free time</str><str>Access survival</str><str>Maintenance of access patency/function</str><str>Blood flow achieved</str><str>Sensitivity and specificity of tests for periodic monitoring of access</str><str>Re-establishment of patency/function in malfunctioning catheter</str><str>Hospitalization</str><str>Costs associated with the maintenance of access patency</str></arr><arr name="practices"><str>Patient education on modalities of kidney replacement therapy (KRT) and monitoring of accesses</str><str>Patient evaluation prior to placement of permanent hemodialysis (HD) access, including history and physical exam, duplex ultrasound, and central vein evaluation</str><str>Structured approach to selection of the type of hemodialysis access (fistula, graft, or peritoneal dialysis catheter)</str><str>Structured approach to selection of the location of hemodialysis access Fistula: wrist, elbow, or transposed brachial basilica vein Arteriovenous graft (AVG): forearm loop, upper arm, chest wall Catheters and port catheter systems: right internal jugular vein or secondary locations</str><str>Structured approach to selection of the location of hemodialysis access Fistula: wrist, elbow, or transposed brachial basilica vein</str><str>Arteriovenous graft (AVG): forearm loop, upper arm, chest wall</str><str>Catheters and port catheter systems: right internal jugular vein or secondary locations</str><str>Placement of functional permanent access prior to initiation of dialysis therapy</str><str>Use of aseptic technique and appropriate cannulation methods of fistulae and grafts</str><str>Optimal timing of fistula and graft cannulation</str><str>Monitoring of fistula maturation</str><str>Use of infection control measures for all HD catheters</str><str>An organized monitoring/surveillance approach to detect access dysfunction Physical examination Surveillance of grafts and fistulae Referral for evaluation (diagnostic) and treatment</str><str>An organized monitoring/surveillance approach to detect access dysfunction Physical examination</str><str>Surveillance of grafts and fistulae</str><str>Referral for evaluation (diagnostic) and treatment</str><str>Timely evaluation and treatment of fistula complications Assessment of persistent swelling, delays in maturation, inadequate blood flow, venous stenosis, thrombosis, aneurysm, ischemia, infection Treatment of stenosis with percutaneous angioplasty (PTA) or surgical revision Treatment of thrombosis with thrombectomy Referral of patients with an arteriovenous fistula (AVF) with ischemia to a vascular access surgeon Treatment of infections with antibiotics and, for extensive infection, resection of the infected graft material</str><str>Timely evaluation and treatment of fistula complications Assessment of persistent swelling, delays in maturation, inadequate blood flow, venous stenosis, thrombosis, aneurysm, ischemia, infection</str><str>Treatment of stenosis with percutaneous angioplasty (PTA) or surgical revision</str><str>Treatment of thrombosis with thrombectomy</str><str>Referral of patients with an arteriovenous fistula (AVF) with ischemia to a vascular access surgeon</str><str>Treatment of infections with antibiotics and, for extensive infection, resection of the infected graft material</str><str>Management and treatment of AVG complications Assessment of extremity edema, risks for graft rupture, severe degenerative changes, pseudoaneurysm, stenosis, thrombosis, infection Treatment of AVGs with severe degenerative changes or pseudoaneurysm with revision/repair Treatment of stenosis without thrombosis with angioplasty or surgical revision Treatment of thrombosis and associated stenosis with percutaneous thrombectomy with angioplasty or surgical thrombectomy with AVG revision Treatment of infection with antibiotics, and for extensive infection, resection of the infected graft material</str><str>Management and treatment of AVG complications Assessment of extremity edema, risks for graft rupture, severe degenerative changes, pseudoaneurysm, stenosis, thrombosis, infection</str><str>Treatment of AVGs with severe degenerative changes or pseudoaneurysm with revision/repair</str><str>Treatment of stenosis without thrombosis with angioplasty or surgical revision</str><str>Treatment of thrombosis and associated stenosis with percutaneous thrombectomy with angioplasty or surgical thrombectomy with AVG revision</str><str>Treatment of infection with antibiotics, and for extensive infection, resection of the infected graft material</str><str>Evaluation of dysfunctional catheters and ports to facilitate prevention and early treatment Treatment of dysfunctional catheters and ports with repositioning, thrombolytics, or catheter exchange with sheath disruption Treatment infected HD catheter or port with antibiotic(s)</str><str>Evaluation of dysfunctional catheters and ports to facilitate prevention and early treatment Treatment of dysfunctional catheters and ports with repositioning, thrombolytics, or catheter exchange with sheath disruption</str><str>Treatment infected HD catheter or port with antibiotic(s)</str><str>Use of continuous quality improvement (CQI) to monitor clinical outcome goals</str></arr><arr name="speciality"><str>Family Practice</str><str>Internal Medicine</str><str>Nephrology</str><str>Pediatrics</str></arr><arr name="target"><str>Adult and pediatric patients with end-stage renal disease who receive hemodialysis treatment</str></arr><arr name="ti"><str>NKF-KDOQI clinical practice guidelines for vascular access: update 2006.</str></arr><arr name="ur"><str>http://www.guidelines.gov/summary/summary.aspx?ss=15&amp;doc_id=10017</str></arr></doc><doc><arr name="category"><str>Evaluation</str><str>Management</str><str>Treatment</str></arr><str name="db">NGC</str><str name="id">10018</str><arr name="outcome"><str>Erectile function as measured by the International Index of Erectile Function (IIEF)</str><str>Intercourse satisfaction</str><str>Ability to have intercourse</str><str>Return to normal function</str><str>Adverse events</str></arr><arr name="practices"><str>Identification of comorbidities and psychosexual dysfunctions through sexual, medical, and psychosocial history</str><str>Laboratory tests</str><str>Focused physical examination</str><str>Prostate-specific antigen measurement</str><str>Rectal examination</str><str>Additional testing, such as testosterone level measurement, vascular and/or neurological assessment and monitoring of nocturnal erections</str><str>Educate patients regarding treatment options and associated risks and benefits</str><str>Manage risk factors for erectile dysfunction (e.g., lifestyle modifications to prevent or reverse erectile dysfunction [ED])</str><str>Consider comorbidities when managing patients with ED (e.g., provide appropriate management of patients with ED in the presence of cardiovascular disease)</str><str>Pharmacologic therapy Phosphodiesterase type 5 (PDE5) inhibitors (sildenafil, tadalafil, and vardenafil) Alprostadil intra-urethral suppositories Intracavernous injection with alprostadil, papaverine, or phentolamine or combinations</str><str>Pharmacologic therapy Phosphodiesterase type 5 (PDE5) inhibitors (sildenafil, tadalafil, and vardenafil)</str><str>Alprostadil intra-urethral suppositories</str><str>Intracavernous injection with alprostadil, papaverine, or phentolamine or combinations</str><str>Vacuum constriction devices</str><str>Surgery Penile prosthesis implantation with preoperative administration of antibiotics Vascular surgery (penile arterial reconstructive surgery)</str><str>Surgery Penile prosthesis implantation with preoperative administration of antibiotics</str><str>Vascular surgery (penile arterial reconstructive surgery)</str><str>Periodic follow-up of efficacy, side effects, and change in health status</str></arr><arr name="speciality"><str>Family Practice</str><str>Internal Medicine</str><str>Surgery</str><str>Urology</str></arr><arr name="target"><str>Men who have erectile dysfunction after a well-established period of normal erectile function, whose erectile dysfunction is primarily organic rather than psychological in nature, and who have no evidence of hypogonadism or hyperprolactinemia</str></arr><arr name="ti"><str>(1) The management of erectile dysfunction: an update. (2) 2006 addendum.</str></arr><arr name="ur"><str>http://www.guidelines.gov/summary/summary.aspx?ss=15&amp;doc_id=10018</str></arr></doc><doc><str name="db">NGC</str><str name="id">10019</str><arr name="intended"><str>Advanced Practice Nurses</str><str>Health Care Providers</str><str>Nurses</str><str>Physician Assistants</str><str>Physicians</str><str>Respiratory Care Practitioners</str><str>Social Workers</str></arr><arr name="objective"><str>To integrate environmental management of asthma into pediatric health care</str><str>To educate health care professionals on how to advise families about environmental interventions that can reduce or eliminate triggers for children who are already diagnosed with asthma</str><str>To guide primary care providers to consider environmental factors that may affect their patients' asthma. In some cases triggers may be more readily apparent than others</str></arr><arr name="outcome"><str>Asthma associated morbidity</str><str>Reduction or elimination of triggers for children who are already diagnosed with asthma</str></arr><arr name="practices"><str>Administration of environmental history Environmental History Form for Pediatric Asthma Patient</str><str>Administration of environmental history Environmental History Form for Pediatric Asthma Patient</str><str>Allergy testing if indicated</str><str>Referral to asthma specialist if indicated</str><str>Counseling of patient and patient's family on controlling exposures that trigger child's asthma: Dust mites Animal allergens Cockroach allergen Mold/mildew Tobacco smoke Air pollution</str><str>Counseling of patient and patient's family on controlling exposures that trigger child's asthma: Dust mites</str><str>Animal allergens</str><str>Cockroach allergen</str><str>Mold/mildew</str><str>Tobacco smoke</str><str>Air pollution</str><str>Follow-up visits</str></arr><arr name="speciality"><str>Allergy and Immunology</str><str>Emergency Medicine</str><str>Family Practice</str><str>Internal Medicine</str><str>Nursing</str><str>Pediatrics</str><str>Pulmonary Medicine</str></arr><arr name="target"><str>Children 0 to 18 years of age already diagnosed with asthma</str></arr><arr name="ti"><str>Environmental management of pediatric asthma. Guidelines for health care providers.</str></arr><arr name="ur"><str>http://www.guidelines.gov/summary/summary.aspx?ss=15&amp;doc_id=10019</str></arr></doc><doc><arr name="category"><str>Diagnosis</str><str>Evaluation</str><str>Management</str><str>Rehabilitation</str><str>Treatment</str></arr><str name="db">NGC</str><str name="id">10043</str><arr name="intended"><str>Allied Health Personnel</str><str>Dentists</str><str>Dietitians</str><str>Health Care Providers</str><str>Nurses</str><str>Physicians</str><str>Speech-Language Pathologists</str></arr><arr name="outcome"><str>Incidence of head and neck cancer</str><str>Recurrence rate</str><str>Survival rate</str><str>Quality of life</str></arr><arr name="practices"><str>Smoking and chewing tobacco cessation</str><str>Alcohol limitation</str><str>Alcohol counseling services</str><str>Dietary counseling</str><str>Prevention leaflet availability</str><str>Fine needle aspiration</str><str>Endoscopy</str><str>Chest x-ray</str><str>Computed tomography (CT) scan</str><str>Magnetic resonance imaging (MRI)</str><str>Fluorodeoxy glucose positron emission tomography (FDG-PET)</str><str>Tumor-node-metastasis (TNM) staging</str><str>Human papillomavirus (HPV) subtyping</str><str>Proliferation indices/molecular markers</str><str>Surgery Radical neck dissection Modified radical neck dissection Tumor resection Endoscopic laser excision Reconstructive surgery</str><str>Surgery Radical neck dissection</str><str>Modified radical neck dissection</str><str>Tumor resection</str><str>Endoscopic laser excision</str><str>Reconstructive surgery</str><str>External-beam radiotherapy Conventional fractionation Hypofractionation Hyperfractionation Accelerated fractionation Decreased total dose and very accelerated fractionation Modified fractionation and chemotherapy</str><str>External-beam radiotherapy Conventional fractionation</str><str>Hypofractionation</str><str>Hyperfractionation</str><str>Accelerated fractionation</str><str>Decreased total dose and very accelerated fractionation</str><str>Modified fractionation and chemotherapy</str><str>Brachytherapy</str><str>Prevention of radiation-induced side effects Benzydamine oral rinse to prevent mucositis Pilocarpine for xerostomia Amifostine for xerostomia (not recommended)</str><str>Prevention of radiation-induced side effects Benzydamine oral rinse to prevent mucositis</str><str>Pilocarpine for xerostomia</str><str>Amifostine for xerostomia (not recommended)</str><str>Adjuvant radiotherapy following surgery</str><str>Chemotherapy in combination with surgery (neoadjuvant and adjuvant chemotherapy are not recommended)</str><str>Radiotherapy and concurrent chemotherapy with cisplatin, cisplatin/5-fluorouracil (5FU), cisplatin/5FU/docetaxel</str><str>Radiotherapy and concurrent monoclonal antibody therapy with cetuximab</str><str>Salvage surgery</str><str>Re-irradiation</str><str>Brachytherapy</str><str>Chemotherapy with methotrexate, cisplatin, cisplatin/5FU, or cisplatin/5FU/cytarabine</str><str>Radiotherapy</str><str>Surgery</str><str>Oral and dental rehabilitation</str><str>Speech and language therapy</str><str>Nutrition support</str><str>Patient support</str><str>Follow-up</str></arr><arr name="speciality"><str>Dentistry</str><str>Family Practice</str><str>Internal Medicine</str><str>Nursing</str><str>Nutrition</str><str>Oncology</str><str>Otolaryngology</str><str>Physical Medicine and Rehabilitation</str><str>Plastic Surgery</str><str>Radiation Oncology</str><str>Speech-Language Pathology</str><str>Surgery</str></arr><arr name="target"><str>Patients at risk for or who have the following head and neck cancers: laryngeal cancer, hypopharyngeal cancer, oropharyngeal cancer, or oral cavity cancer</str></arr><arr name="ti"><str>Diagnosis and management of head and neck cancer. A national clinical guideline.</str></arr><arr name="ur"><str>http://www.guidelines.gov/summary/summary.aspx?ss=15&amp;doc_id=10043</str></arr></doc><doc><arr name="category"><str>Assessment of Therapeutic Effectiveness</str><str>Management</str></arr><str name="db">NGC</str><str name="id">10153</str><arr name="objective"><str>To provide guidelines for the therapeutic use of androgens in women</str><str>To outline the areas of future research</str></arr><arr name="outcome"><str>Accuracy (sensitivity, specificity) of existing methods of testosterone measurement</str><str>Response to androgen therapy in terms of bone mineral density, cognitive function, quality of life, sexual function, mood, cardiovascular function, body composition, and muscle strength and function in women with androgen deficiency</str><str>Safety profile of androgen therapy</str></arr><arr name="speciality"><str>Endocrinology</str></arr><arr name="target"><str>Women with androgen deficiency</str></arr><arr name="ti"><str>Androgen therapy in women: an Endocrine Society clinical practice guideline.</str></arr><arr name="ur"><str>http://www.guidelines.gov/summary/summary.aspx?ss=15&amp;doc_id=10153</str></arr></doc><doc><arr name="category"><str>Assessment of Therapeutic Effectiveness</str><str>Management</str><str>Treatment</str></arr><str name="db">NGC</str><str name="id">10158</str><arr name="objective"><str>To evaluate the optimal surgical management of ductal carcinoma in situ (DCIS) of the breast</str><str>To evaluate whether breast irradiation should be offered to women with DCIS, following breast-conserving surgery (defined as excision of the tumour with microscopically clear resection margins)</str><str>To evaluate whether there are patients who could be spared breast irradiation postâbreast-conserving surgery for DCIS</str><str>To evaluate the role of tamoxifen in the management of DCIS</str></arr><arr name="outcome"><str>Overall survival</str><str>Disease-free survival</str><str>Local recurrence</str><str>Breast conservation</str><str>Distant recurrence</str><str>Toxicity</str><str>Quality of life</str></arr><arr name="practices"><str>Total mastectomy</str><str>Breast-conserving surgery (lumpectomy)</str><str>Radiotherapy following breast-conserving surgery</str><str>Tamoxifen and radiotherapy versus radiotherapy alone</str></arr><arr name="speciality"><str>Oncology</str><str>Radiation Oncology</str><str>Surgery</str></arr><arr name="target"><str>Women with ductal carcinoma in situ (DCIS) of the breast</str></arr><arr name="ti"><str>Management of ductal carcinoma in situ of the breast: a clinical practice guideline.</str></arr><arr name="ur"><str>http://www.guidelines.gov/summary/summary.aspx?ss=15&amp;doc_id=10158</str></arr></doc><doc><str name="db">NGC</str><str name="id">10160</str><arr name="intended"><str>Advanced Practice Nurses</str><str>Nurses</str><str>Physicians</str></arr><arr name="objective"><str>To prevent catheter-related intraluminal thrombosis and local or systemic catheter-related infection, minimize the need to replace devices, and enhance quality of life among children and adults with cancer by assessing: Whether central venous access devices (CVAD) should be locked with heparin or saline</str><str>What volume and strength of solution should be used to lock CVADs</str><str>How frequently CVADs should be locked</str><str>What type of catheter should be used</str><str>To evaluate, in patients who require systemic therapy for cancer, the indicators (e.g., functional or quantitative neutropenia, age, diagnosis, therapy, immune status, or patient convenience) that have an impact on the decision to insert a central venous access device</str></arr><arr name="outcome"><str>Catheter-related thrombosis</str><str>Catheter-related infection</str><str>Rates of removal due to infection or occlusion</str><str>Quality of life</str></arr><arr name="speciality"><str>Oncology</str></arr><arr name="target"><str>Adult and pediatric patients requiring central venous access devices for cancer treatment</str></arr><arr name="ti"><str>Managing central venous access devices in cancer patients: a clinical practice guideline.</str></arr><arr name="ur"><str>http://www.guidelines.gov/summary/summary.aspx?ss=15&amp;doc_id=10160</str></arr></doc></result><lst name="facet_counts"><lst name="facet_queries"/><lst name="facet_fields"><lst name="tag"><int name="guideline">305</int></lst><lst name="mh_cluster"/><lst name="year"/></lst><lst name="facet_dates"/><lst name="facet_ranges"/></lst></response>