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Hydronephrosis
Hydronephrosis Natasha Brownrigg RN(EC), MN, NP-Pediatrics Assistant Clinical Professor, McMaster School of Nursing Nurse Practitioner, Pediatric Urology, McMaster Children’s Hospital, Hamilton, ON, Canada Dr. Jorge DeMaria Pediatric Urologist, McMaster Children’s Hospital Professor Department of Surgery/Urology, McMaster University, Hamilton, ON, Canada Dr. Luis H.P. Braga Pediatric Urologist, McMaster Children’s Hospital. Associate professor Department of Surgery/Urology, McMaster University, Hamilton, ON, Canada What is hydronephrosis? Hydro Nephrosis Hydronephrosis += Refers to water Refers to the kidney A build up of fluid or fluid (urine) in the kidney Hydronephrosis is the medical term for a build-up of urine in the kidney. As the urine builds up, it stretches or dilates the inside of the kidney, known as the collecting system. If an unborn baby has hydronephrosis, an ultrasound scan will show a build-up of urine in the kidney. This is called “antenatal hydronephrosis.” Hydronephrosis is found in as many as five out of 100 pregnancies. Hydronephrosis may also be found after birth. For example, if a baby has a urinary tract infection, an ultrasound of the baby’s kidneys and bladder may detect hydronephrosis. Key points to remember if your baby has hydronephrosis • Your baby can grow and develop normally with hydronephrosis. • Hydronephrosis may affect one kidney or both. • Hydronephrosis is a finding, not a disease. • Further tests are needed to find the cause of hydronephrosis. • If the cause is known, a pediatric urologist will discuss the possible treatment. Surgery is sometimes required to correct the cause of the hydronephrosis. Hydronephrosis is often transient and improves without any intervention. -
Urinary Incontinence: Impact on Long Term Care
Urinary Incontinence: Impact on Long Term Care Muhammad S. Choudhury, MD, FACS Professor and Chairman Department of Urology New York Medical College Director of Urology Westchester Medical Center 1 Urinary Incontinence: Overview • Definition • Scope • Anatomy and Physiology of Micturition • Types • Diagnosis • Management • Impact on Long Term Care 2 Urinary Incontinence: Definition • Involuntary leakage of urine which is personally and socially unacceptable to an individual. • It is a multifactorial syndrome caused by a combination of: • Genito urinary pathology. • Age related changes. • Comorbid conditions that impair normal micturition. • Loss of functional ability to toilet oneself. 3 Urinary Incontinence: Scope • Prevalence of Urinary incontinence increase with age. • Affects more women than men (2:1) up to age 80. • After age 80, both women and men are equally affected. • Urinary Incontinence affect 15% to 30% of the general population > 65 years. • > 50% of 1.5 million Long Term Care residents may be incontinent. • The cost to care for this group is >5 billion per year. • The total cost of care for Urinary Incontinence in the U.S. is estimated to be over $36 billion. Ehtman et al., 2012. 4 Urinary Incontinence: Impact on Quality of Life • Loss of self esteem. • Avoidance of social activity and interaction. • Decreased ability to maintain independent life style. • Increased dependence on care givers. • One of the most common reason for long term care placement. Grindley et al. Age Aging. 1998; 22: 82-89/Harris T. Aging in the eighties. NCHS # 121 1985. Noelker L. Gerontologist 1987; 27: 194-200. 5 Health related consequences of Urinary Incontinence • Increased propensity for fall/fracture. -
Percutaneous Nephrostomy and Sclerotherapy with 96% Ethanol for the Treatment of Simple Renal Cysts: Pilot Study Mustafa Kadıhasanoğlu1, Mete Kilciler2, Özcan Atahan3
İstanbul Med J 2016; 17: 20-3 Original Article DOI: 10.5152/imj.2016.20981 Percutaneous Nephrostomy and Sclerotherapy with 96% Ethanol for the Treatment of Simple Renal Cysts: Pilot Study Mustafa Kadıhasanoğlu1, Mete Kilciler2, Özcan Atahan3 Introduction: The objectives of this study was to evaluate the safety and efficacy of aspiration with percutaneous nephrostomy tube and sclerotherapy with 96% ethanol for simple renal cyst. Methods: Between 2011-2014, 34 patients with symptomatic renal cysts were included in the study. Mean age was 52.3±4.6 years (range, 39-72 years). The Abstract patients had only flank pain. Procedure was performed with ultrasound guidance and under fluoroscopic control. After puncture with 18 G angiography needle, guide-wire was advanced to the collecting system. An 14Fr nephrostomy catheter was then advanced over the guide wire. After taking cystography 96% ethyl alcohol was injected into the cyst and drained amount 10%. We continued daily to inject same amount of alcohol postoperatively until the drainage was less than 50 mL. 6th months and yearly follow-up were performed with ultrasound.. Results: Percutaneous access was achieved in all patients. Cysts were unilateral, single and with a mean diameter 9.1±3.2 cm (range, 7-16 cm). Median drained volume was 212 mL (200-1600 mL) and median the injected ethanol volume was 54 mL (20- 160 mL). Radiological improvement at the end of the 6th month was amount 94.1% and 91.1% at the end of the 1st year while 83.3% of patients had symptomatic decline. There was no major complication after the procedure. -
CMS Manual System Human Services (DHHS) Pub
Department of Health & CMS Manual System Human Services (DHHS) Pub. 100-07 State Operations Centers for Medicare & Provider Certification Medicaid Services (CMS) Transmittal 8 Date: JUNE 28, 2005 NOTE: Transmittal 7, of the State Operations Manual, Pub. 100-07 dated June 27, 2005, has been rescinded and replaced with Transmittal 8, dated June 28, 2005. The word “wound” was misspelled in the Interpretive Guidance section. All other material in this instruction remains the same. SUBJECT: Revision of Appendix PP – Section 483.25(d) – Urinary Incontinence, Tags F315 and F316 I. SUMMARY OF CHANGES: Current Guidance to Surveyors is entirely replaced by the attached revision. The two tags are being combined as one, which will become F315. Tag F316 will be deleted. The regulatory text for both tags will be combined, followed by this revised guidance. NEW/REVISED MATERIAL - EFFECTIVE DATE*: June 28, 2005 IMPLEMENTATION DATE: June 28, 2005 Disclaimer for manual changes only: The revision date and transmittal number apply to the red italicized material only. Any other material was previously published and remains unchanged. However, if this revision contains a table of contents, you will receive the new/revised information only, and not the entire table of contents. II. CHANGES IN MANUAL INSTRUCTIONS: (N/A if manual not updated.) (R = REVISED, N = NEW, D = DELETED) – (Only One Per Row.) R/N/D CHAPTER/SECTION/SUBSECTION/TITLE R Appendix PP/Tag F315/Guidance to Surveyors – Urinary Incontinence D Appendix PP/Tag F316/Urinary Incontinence III. FUNDING: Medicare contractors shall implement these instructions within their current operating budgets. IV. ATTACHMENTS: Business Requirements x Manual Instruction Confidential Requirements One-Time Notification Recurring Update Notification *Unless otherwise specified, the effective date is the date of service. -
ICD-10 Coding Clinic Corner: Accountability Act of 1996 (HIPAA) Is 413.65(A)(2): Diabetes and Osteomyelitis
Issue No. 6 Volume No. 2 September 2015 New and Revised Place of Service TABLE of CONTENTS Codes for OutpatientNote Hospital from Tony New and Revised Place of Joette P. Derricks, MPA, CMPE, CHC, CPC, CSSGB Service Codes for Outpatient Joh Vice President of Regulatory Affairs & Research Hospital ..................................... 1 MiraMed Global Services ERCP with Exchange of a Common Bile Duct Stent .......... 3 Any health insurer subject to the policy. Contractor editing shall Laparoscopic Procedure: An uniform electronic claim transaction treat POS 19 and POS 22 in the Education .................................. 5 and code set standards under the same way. The definition of a Health Insurance Portability and “campus” is found in Title 42 CFR ICD-10 Coding Clinic Corner: Accountability Act of 1996 (HIPAA) is 413.65(a)(2): Diabetes and Osteomyelitis ..... 7 required to make changes to the Campus means the physical Place of Service (POS) code from the Stars of MiraMed ...................... 8 area immediately adjacent to POS code set maintained by the the provider’s main buildings, Are You a Good Auditor? ......... 9 Centers for Medicare and Medicaid other areas and structures that Services (CMS) effective January 1, Coding Case Scenario ............. 11 are not strictly contiguous to 2016. the main buildings but are The POS code set provides setting located within 250 yards of the If you have an article information necessary to main buildings, and any other appropriately pay Medicare and areas determined on an or idea to share for The Medicaid claims. Other payers may individual case basis, by the Code , please submit to: or may not use the POS codes in the CMS regional office, to be part Dr. -
Rare Case of Female Behçet's Disease with Urological Involvement
CASE REPORTS Ref: Ro J Rheumatol. 2019;28(2) DOI: 10.37897/RJR.2019.2.6 RARE CASE OF female Behçet’s disease WITH UROLOGICAL INVOLVEMENT Claudia Cobilinschi1,2, Catalin Belinski3, Daniela Opris-Belinski1,2 1„Carol Davila“ University of Medicine and Pharmacy, Bucharest, Romania 2„St. Maria“ Clinical Hospital, Bucharest, Romania 3„Prof. Dr. Dimitrie Gerota“ Emergency Hospital, Bucharest, Romania Abstract Behçet’s disease is a systemic vasculitis with several well-defined organ manifestations, including various mu- cocutaneous features. Among them, the urinary tract involvement is rarely cited, most data focusing on bladder dysfunction due to neuroBehçet. This article presents a rare case of a young female patient with urological complaints that was diagnosed with right ureteral ulceration, later confirmed as vasculitis at the histopathological examination. Urological intervention together with adequate immunosuppression let to the healing of the ulcer- ative lesion. The unusual vasculitic lesion site indicates the complexity of Behçet’s disease that requires careful investigation and treatment. Keywords: Behçet’s disease, ureteral ulceration, ureteral stent, immunosuppressant INTRODUCTION The onset of the disease was in 2013 when the patient presented to her general practitioner (GP) for Behçet’s disease (BD) is a variable size vasculitis repeated febrile episodes that were essentially ves- that can affect both arteries and veins characterized peral, occurring in the afternoon followed by odyno- by recurrent episodes of orogenital ulcers, eye and phagia and painful aphthae on her oral mucosa. Due skin involvement, neurologic manifestations accom- to her prominent ENT symptoms, her GP referred panied by a positive patergy test (1). The genetic the patient to a specialist who prescribed multiple background is best described by HLA B51 positivity antibiotic schemes because of the high suspicion of which associates with a more extensive clinical ex- streptococcal infection. -
Acute Phosphate Nephropathy Alexander K
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Elsevier - Publisher Connector http://www.kidney-international.org the renal consult & 2009 International Society of Nephrology Acute phosphate nephropathy Alexander K. Rocuts1, Sushrut S. Waikar1, Mariam P. Alexander1,2, Helmut G. Rennke2 and Ajay K. Singh1 1Renal Division, Department of Medicine, Brigham and Women’s Hospital, Harvard Medical School, Boston, Massachusetts, USA and 2Department of Pathology, Brigham and Women’s Hospital, Harvard Medical School, Boston, Massachusetts, USA minute. The rest of the examination was unremarkable. CASE PRESENTATION HerlaboratorydataissummarizedinTable1. A 60-year-old white Latino female with a clinical diagnosis A postoperative kidney ultrasound showed no of diabetes mellitus (diagnosed in 1993) and hypertension hydronephrosis. was referred to the chronic kidney disease clinic at The etiology of the acute kidney injury was unclear. Brigham and Women’s Hospital for the evaluation of acute Progressive diabetic nephropathy exacerbated by other kidney injury; serum creatinine had increased from a contributory factors, such as exposure to lisinopril, baseline of 0.9 to 1.5 mg/dl in a 11-week period. She was acetylsalicylic acid, or naproxen, was regarded as the most asymptomatic at the time of presentation. Her past plausible explanation. Despite discontinuation of these medical history included a total abdominal hysterectomy medications, kidney function did not improve; it worsened with bilateral salpingo oophorectomy and upper in a 4-week period after presentation. Hence, a kidney vaginectomy for high-grade squamous intraepithelial biopsy was performed. lesion of the cervix, 11 weeks prior to presentation. Three weeks prior to presentation (8 weeks after surgery) and within a week of each other, she was evaluated for two consecutive episodes of acute onset of chest pain with pulmonary edema in the setting of severe hypertension. -
Ended Megaureter in a 23-Year-Old Woman Causing Chronic Pain
341 Central European Journal of Urology CASE REPORT URINARY TRACT INFECTIONS The remnant of a congenital, blind- ended megaureter in a 23-year-old woman causing chronic pain and urinary infections Tomislav Pejcic1, Biljana Markovic2, Zoran Dzamic1, Milan Radovanovic1, Jovan Hadzi-Djokic3 1Clinical Center of Serbia, Urological Clinic, Belgrade, Serbia 2Clinical Center of Serbia, Institute of Radiology, Belgrade, Serbia 3Serbian Academy of Sciences and Arts, Belgrade, Serbia Article history Multicystic dysplastic kidney (MCDK) is a congenital anomaly as the result of abnormal interaction be- Received: March 31, 2103 tween the ureteric bud and metanephric mesenchyme. Unilateral MCDK can be associated with other Accepted: May 19, 2013 anomalies of the genitourinary tract. Relatively rare associated anomaly is the presence of ipsilateral Correspondence refluxing blind megaureter. Tomislav Pejcic The patient reported herein is a 23–years–old woman with involuted MCDK and ipsilateral blind mega- 129/9, Bulevar Zorana ureter causing chronic urinary infection and chronic abdominal pain. Preoperative and intraoperative Djindjica 11070 Belgrade, Serbia examination failed to detect the communication between megaureter and the urinary bladder. phone: +38 111 212 1616 [email protected] Key Words: multicystic dysplastic kidney ‹› refluxing blind megaureter INTRODUCTION CASE REPORT Multicystic dysplastic kidney (MCDK) is a congeni- A 23–year–old woman from a small village was sent tal anomaly that is the result of abnormal interac- to the urologist from the gynecologist, due to solitary tion between the ureteric bud and metanephric right kidney, cystic mass on the left side of the uri- mesenchyme, early ureteral obstruction, or ureteral nary bladder and the presence of chronic pain and atresia. -
Guidelines for Management of Acute Renal Failure (Acute Kidney Injury)
Guidelines for management of Acute Renal Failure (Acute Kidney Injury) Children’s Kidney Centre University Hospital of Wales Cardiff CF14 4XW DISCLAIMER: These guidelines were produced in good faith by the author(s) reviewing available evidence/opinion. They were designed for use by paediatric nephrologists at the University Hospital of Wales, Cardiff for children under their care. They are neither policies nor protocols but are intended to serve only as guidelines. They are not intended to replace clinical judgment or dictate care of individual patients. Responsibility and decision-making (including checking drug doses) for a specific patient lie with the physician and staff caring for that particular patient. Version 1, S. Hegde/Feb 2009 Guidelines on management of Acute Renal Failure (Acute Kidney Injury) Definition of ARF (now referred to as AKI) • Acute renal failure is a sudden decline in glomerular filtration rate (usually marked by rise in serum creatinine & urea) which is potentially reversible with or without oliguria. • Oliguria defined as urine output <300ml/m²/day or < 0.5 ml/kg/h (<1 ml/kg/h in neonates). • Acute on chronic renal failure suggested by poor growth, history of polyuria and polydipsia, and evidence of renal osteodystrophy However, immediately after a kidney injury, serum creatinine & urea levels may be normal, and the only sign of a kidney injury may be decreased urine production. A rise in the creatinine level can result from medications (e.g., cimetidine, trimethoprim) that inhibit the kidney’s tubular secretion. A rise in the serum urea level can occur without renal injury, such as in GI or mucosal bleeding, steroid use, or protein loading. -
Increase Thirst and Urination (Polydyspsia and Polyuria)
Increase Thirst and Urination (Polydyspsia and Polyuria) 803-808-7387 www.gracepets.com What are the causes of increased thirst and urination? These clinical signs are non-specific and can be caused by many different diseases or conditions. Usually it is the production of excess, dilute urine that results in a compensatory increase in water consumption, but occasionally the condition is one of increased water intake resulting in the production of large volumes of dilute urine. The following is not a complete listing of the diseases that may result in increased thirst and urination. However it outlines the most common causes: Conditions related to the urinary and reproductive systems including kidney failure, infections of the kidneys or bladder, and infections of the uterus. Endocrine or hormone related conditions including hyperadrenocorticism and hypoadrenocorticism, hyperthyroidism, diabetes mellitus and diabetes insipidus. Liver disease, certain drugs, fever, pain and certain electrolyte imbalances may also result in increased thirst and urination. Rarely, a behavioral problem is at the root of increased drinking behavior. This list is huge! How can we possibly determine what the cause is in my pet? Certain diseases are more common in certain species (dogs versus cats) so this may narrow down the range of possibilities. In addition, the specific history of the pet, including a list of all medications and supplements that your pet has recently received, is helpful. This information, along with a physical examination, will often narrow the list further. A panel of screening tests will also exclude a large number of these conditions and may even provide a definitive diagnosis. -
Renal Agenesis, Renal Tubular Dysgenesis, and Polycystic Renal Diseases
Developmental & Structural Anomalies of the Genitourinary Tract DR. Alao MA Bowen University Teach Hosp Ogbomoso Picture test Introduction • Congenital Anomalies of the Kidney & Urinary Tract (CAKUT) Objectives • To review the embryogenesis of UGS and dysmorphogenesis of CAKUT • To describe the common CAKUT in children • To emphasize the role of imaging in the diagnosis of CAKUT Introduction •CAKUT refers to gross structural anomalies of the kidneys and or urinary tract present at birth. •Malformation of the renal parenchyma resulting in failure of normal nephron development as seen in renal dysplasia, renal agenesis, renal tubular dysgenesis, and polycystic renal diseases. Introduction •Abnormalities of embryonic migration of the kidneys as seen in renal ectopy (eg, pelvic kidney) and fusion anomalies, such as horseshoe kidney. •Abnormalities of the developing urinary collecting system as seen in duplicate collecting systems, posterior urethral valves, and ureteropelvic junction obstruction. Introduction •Prevalence is about 3-6 per 1000 births •CAKUT is one of the commonest anomalies found in human. •It constitute approximately 20 to 30 percent of all anomalies identified in the prenatal period •The presence of CAKUT in a child raises the chances of finding congenital anomalies of other organ-systems Why the interest in CAKUT? •Worldwide, CAKUT plays a causative role in 30 to 50 percent of cases of end-stage renal disease (ESRD), •The presence of CAKUT, especially ones affecting the bladder and lower tract adversely affects outcome of kidney graft after transplantation Why the interest in CAKUT? •They significantly predispose the children to UTI and urinary calculi •They may be the underlying basis for urinary incontinence Genes & Environment Interact to cause CAKUT? • Tens of different genes with role in nephrogenesis have been identified. -
Acute Onset Flank Pain-Suspicion of Stone Disease (Urolithiasis)
Date of origin: 1995 Last review date: 2015 American College of Radiology ® ACR Appropriateness Criteria Clinical Condition: Acute Onset Flank Pain—Suspicion of Stone Disease (Urolithiasis) Variant 1: Suspicion of stone disease. Radiologic Procedure Rating Comments RRL* CT abdomen and pelvis without IV 8 Reduced-dose techniques are preferred. contrast ☢☢☢ This procedure is indicated if CT without contrast does not explain pain or reveals CT abdomen and pelvis without and with 6 an abnormality that should be further IV contrast ☢☢☢☢ assessed with contrast (eg, stone versus phleboliths). US color Doppler kidneys and bladder 6 O retroperitoneal Radiography intravenous urography 4 ☢☢☢ MRI abdomen and pelvis without IV 4 MR urography. O contrast MRI abdomen and pelvis without and with 4 MR urography. O IV contrast This procedure can be performed with US X-ray abdomen and pelvis (KUB) 3 as an alternative to NCCT. ☢☢ CT abdomen and pelvis with IV contrast 2 ☢☢☢ *Relative Rating Scale: 1,2,3 Usually not appropriate; 4,5,6 May be appropriate; 7,8,9 Usually appropriate Radiation Level Variant 2: Recurrent symptoms of stone disease. Radiologic Procedure Rating Comments RRL* CT abdomen and pelvis without IV 7 Reduced-dose techniques are preferred. contrast ☢☢☢ This procedure is indicated in an emergent setting for acute management to evaluate for hydronephrosis. For planning and US color Doppler kidneys and bladder 7 intervention, US is generally not adequate O retroperitoneal and CT is complementary as CT more accurately characterizes stone size and location. This procedure is indicated if CT without contrast does not explain pain or reveals CT abdomen and pelvis without and with 6 an abnormality that should be further IV contrast ☢☢☢☢ assessed with contrast (eg, stone versus phleboliths).