Bronchoscopy and Associated Procedures Coding in ICD-10
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Follicular Lymphoma
Follicular Lymphoma What is follicular lymphoma? Let us explain it to you. www.anticancerfund.org www.esmo.org ESMO/ACF Patient Guide Series based on the ESMO Clinical Practice Guidelines FOLLICULAR LYMPHOMA: A GUIDE FOR PATIENTS PATIENT INFORMATION BASED ON ESMO CLINICAL PRACTICE GUIDELINES This guide for patients has been prepared by the Anticancer Fund as a service to patients, to help patients and their relatives better understand the nature of follicular lymphoma and appreciate the best treatment choices available according to the subtype of follicular lymphoma. We recommend that patients ask their doctors about what tests or types of treatments are needed for their type and stage of disease. The medical information described in this document is based on the clinical practice guidelines of the European Society for Medical Oncology (ESMO) for the management of newly diagnosed and relapsed follicular lymphoma. This guide for patients has been produced in collaboration with ESMO and is disseminated with the permission of ESMO. It has been written by a medical doctor and reviewed by two oncologists from ESMO including the lead author of the clinical practice guidelines for professionals, as well as two oncology nurses from the European Oncology Nursing Society (EONS). It has also been reviewed by patient representatives from ESMO’s Cancer Patient Working Group. More information about the Anticancer Fund: www.anticancerfund.org More information about the European Society for Medical Oncology: www.esmo.org For words marked with an asterisk, a definition is provided at the end of the document. Follicular Lymphoma: a guide for patients - Information based on ESMO Clinical Practice Guidelines – v.2014.1 Page 1 This document is provided by the Anticancer Fund with the permission of ESMO. -
2019 Client Experience Summit Learn. Share. Succeed. 3M HIS Nosology Teams
2019 Client Experience Summit Learn. Share. Succeed. Nosology Nuggets Michele Taylor RHIT, CCS Rauna Gale RHIA 2019 Client Experience Summit Learn. Share. Succeed. 3M HIS Nosology Teams Nosology CAC Nosology Support Nosology Development Team Development Team Teams • 18 team members • 28 team members • 35 team members • RHIA, RHIT, • RHIA, RHIT, CCS, • RHIA, RHIT, CCS, CCS, CPC, CPC, RN, CDIP CCDS CPC-H, CDIP, IR CIRCC High-Volume Nosology Topics - Agenda ➢ Sepsis Sequencing ➢ Rehabilitation ➢ Bronchoscopy PCS ➢ CHF grouping ➢ NCCI and Other Edits with CMS website tips and tricks ➢ Separate Procedure Designation ➢ Podiatry ➢ LINX Sepsis Sequencing Sepsis Sequencing • If the reason for admission is both sepsis or severe sepsis and a localized infection, such as pneumonia or cellulitis, a code(s) for the underlying systemic infection (A41.9) should be assigned first and the code for the localized infection should be assigned as a secondary diagnosis. • If sepsis or severe sepsis is documented as associated with a noninfectious condition, such as a burn or serious injury, and this condition meets the definition for principal diagnosis, the code for the noninfectious condition should be sequenced first, followed by the code for the resulting infection. • If the infection (sepsis) meets the definition of principal diagnosis, it should be sequenced before the non-infectious condition. When both the associated non- infectious condition and the infection meet the definition of principal diagnosis, either may be assigned as principal diagnosis. Source: ICD-10-CM Official Guidelines for Coding and Reporting FY 2019 Page 25-27 Scenario: Patient is admitted with left diabetic foot ulcer with cellulitis and gangrene. -
Diagnostic Direct Laryngoscopy, Bronchoscopy & Esophagoscopy
Post-Operative Instruction Sheet Diagnostic Direct Laryngoscopy, Bronchoscopy & Esophagoscopy Direct Laryngoscopy: Examination of the voice box or larynx (pronounced “lair-inks”) under general anesthesia. An instrument called a laryngoscope is carefully placed into the mouth and used to visualize the larynx and surrounding structures. Bronchoscopy: Examination of the windpipe below the voice box in the neck and chest under general anesthesia. A long narrow telescope is passed through the larynx and used to carefully inspect the structures of the trachea and bronchi. Esophagoscopy: Examination of the swallowing pipe in the neck and chest under general anesthesia. An instrument called an esophagoscope is passed into the esophagus (just behind the larynx and trachea) and used to visualize the mucus membranes and surrounding structures of the esophagus. Frequently a small biopsy is taken to evaluate for signs of esophageal inflammation (esophagitis). What to Expect: Diagnostic airway endoscopy procedures generally take about 45 minutes to complete. Usually the procedure is well-tolerated and the child is back-to-normal the next day. Mild throat or tongue discomfort may persist for a few days after the procedure and is usually well-controlled with over-the-counter acetaminophen (Tylenol) or ibuprofen (Motrin). Warning Signs: Contact the office immediately at (603) 650-4399 if any of the following develop: • Worsening harsh, high-pitched noisy-breathing (stridor) • Labored breathing with chest retractions or flaring of the nostrils • Bluish discoloration of the lips or fingernails (cyanosis) • Persistent fever above 102°F that does not respond to Tylenol or Motrin • Excessive coughing or respiratory distress during feeding • Coughing or throwing up bright red blood • Excessive drowsiness or unresponsiveness Diet: Resume baseline diet (no special postoperative diet restrictions). -
Tracheal Wash Vs BAL 2
TRACHEAL WASHES IN DOGS AND CATS: WHY, WHAT, WHEN, AND HOW Eleanor C. Hawkins, DVM, Dipl ACVIM (SAIM) Professor, Small Animal Internal Medicine North Carolina State University Raleigh, North Carolina, USA 1. Introduction: Tracheal Wash vs BAL 2. Focus on Tracheal Wash TRACHEAL WASH vs BAL 1 TRACHEAL WASH vs BAL • Exudate from airways and alveoli • Samples all alveoli dependent on to the trachea via mucociliary the bronchus where scope or clearance +/‐ cough. catheter is lodged. • Good representation for most • Primarily a deep lung sample: diffuse bronchial disease and small airways, alveoli, and aspiration or bronchopneumonia. sometimes the interstitium. TRACHEAL WASH vs BAL TRACHEAL WASH vs BAL 2 DEFINITIONS – Slippery slope • TW becomes BAL • Catheter into small airways • Relatively large volumes of fluid used • BAL becomes TW • Single bolus • Relatively small volume Regardless of method • Tracheal wash (TW) and bronchoalveolar lavage (BAL) result in sufficient material for: Cytology Cultures PCR Flow cytometry Special stains / markers Cell function testing • BAL: greater volume, more cells than TW TW and BAL Cytology • Similar benefits › Less invasive than getting tissue 3 TW and BAL Cytology • Similar limitations › No architecture › Cells must exfoliate • E.g. not pulmonary fibrosis • E.g. not sarcoma › Organisms must be present in large numbers › Secondary processes must not “hide” primary • Infection vs non‐infectious disease • Inflammation vs neoplasia TW and BAL • MOST USEFUL FOR • Ruling IN infectious disease • Ruling IN neoplasia -
A Clinical Prediction Rule for Pulmonary Complications After Thoracic Surgery for Primary Lung Cancer
A Clinical Prediction Rule for Pulmonary Complications After Thoracic Surgery for Primary Lung Cancer David Amar, MD,* Daisy Munoz, MD,* Weiji Shi, MS,† Hao Zhang, MD,* and Howard T. Thaler, PhD† BACKGROUND: There is controversy surrounding the value of the predicted postoperative diffusing capacity of lung for carbon monoxide (DLCOppo) in comparison to the forced expired volume in 1 s for prediction of pulmonary complications (PCs) after thoracic surgery. METHODS: Using a prospective database, we performed an analysis of 956 patients who had resection for lung cancer at a single institution. PC was defined as the occurrence of any of the following: atelectasis, pneumonia, pulmonary embolism, respiratory failure, and need for supplemental oxygen at hospital discharge. RESULTS: PCs occurred in 121 of 956 patients (12.7%). Preoperative chemotherapy (odds ratio 1.64, 95% confidence interval 1.06–2.55, P ϭ 0.02, point score 2) and a lower DLCOppo (odds ratio per each 5% decrement 1.13, 95% confidence interval 1.06–1.19, P Ͻ 0.0001, point score 1 per each 5% decrement of DLCOppo less than 100%) were independent risk factors for PCs. We defined 3 overall risk categories for PCs: low Յ10 points, 39 of 448 patients (9%); intermediate 11–13 points, 37 of 256 patients (14%); and high Ն14 points, 42 of 159 patients (26%). The median (range) length of hospital stay was significantly greater for patients who developed PCs than for those who did not: 12 (3–113) days vs 6 (2–39) days, P Ͻ 0.0001, respectively. Similarly, 30-day mortality was significantly more frequent for patients who developed PCs than for those who did not: 16 of 121 (13.2%) vs 6 of 835 (0.7%), P Ͻ 0.0001. -
December 2020 E-Tips Solid Tumor Rules
New Jersey State Cancer Registry December 2020 E-Tips Cancer Epidemiology Services http://www.nj.gov/health/ces (609) 633-0500 Solid Tumor Rules: December 2020 Update ICD-0-3.2 changes have also been added to applicable site modules. Most changes are minor: terminology, additional definitions, new notes and examples. In order to clarify histology coding instructions, new rules have been added and histology tables updated. These updates do not require review of already abstracted cases. The December 2020 rules replace the current rules and should be used now. SEER Strongly recommends reading the December 2020 Change Log to understand what changes were made. The updated Solid Tumor Rules may be accessed at: https://seer.cancer.gov/tools/solidtumor/ Reportability Changes for 2021 Radiation Coding Total Dose (1533) Starting 01/01/2021 the following terms are reportable: If doses across phases to a single point of region, code Sum of all phases. ** (see 2019 update below) Early or evolving melanoma in situ, or any other early or If doses are to multiple metastatic sites, code highest evolving melanoma, are reportable. dose site. If doses are to primary site and metastatic site, code dose All GIST tumors are reportable and classified as 8936/3 in from the primary site only. ICD-O-3.2. When you have two different sites, you cannot add the Nearly all thymomas are reportable; the exceptions are doses together to get the total dose. microscopic thymoma or thymoma benign (8580/0), micronodular thymoma with lymphoid stroma (8580/1), Radiation Tips and updates for 2019 and ectopic hamartomatous thymoma (8587/0). -
Interpretation of Bronchoalveolar Lavage Fluid Cytology
Interpretation of bronchoalveolar lavage fluid cytology Contents Editor Marjolein Drent, MD, PhD Maastricht, The Netherlands Preface e-mail : [email protected] Foreword Contributors Introduction Prof. Robert Baughman, MD, PhD Cincinnati, Ohio, USA e-mail : [email protected] [email protected] History Prof. Ulrich Costabel, MD, PhD Essen, Germany e-mail: [email protected] Bronchoalveolar lavage Jan A. Jacobs, MD, PhD Text with illustrations Maastricht, The Netherlands e-mail: [email protected] Interactive predicting model Rob J.S. Lamers, MD, PhD Predicting program Heerlen, The Netherlands Software to evaluate BALF analysis e-mail: [email protected] Computer program using BALF Variables: a new release Paul G.H. Mulder, MSc, PhD Rotterdam, The Netherlands e-mail: [email protected] Prof. Herbert Y. Reynolds, MD, PhD Hershey, Pennsylvania, USA Glossary of abbreviations e-mail: [email protected] Acknowledgements Prof. Sjoerd Sc. Wagenaar, MD, PhD Amsterdam, The Netherlands e-mail: [email protected] Interpretation of BALF cytology Preface Bronchoalveolar lavage (BAL) explores large areas of the alveolar compartment providing cells as well as non-cellular constituents from the lower respiratory tract. It opens a window to the lung. Alterations in BAL fluid and cells reflect pathological changes in the lung parenchyma. The BAL procedure was developed as a research tool. Meanwhile its usefulness, also for clinical applications, has been appreciated worldwide in diagnostic work-up of infectious and non-infectious interstitial lung diseases. Moreover, BAL has several advantages over biopsy procedures. It is a safe, easily performed, minimally invasive, and well tolerated procedure. In this respect, when the clinician decides that a BAL might be helpful to provide diagnostic material, it is mandatory to consider the provided information obtained from BAL fluid analysis carefully and to have reliable diagnostic criteria. -
The Shelf in Every Comprehensive Hyperbaric Facility. Michael H
BOOKS,SOFTWARE, AND OTHER MEDIA the shelf in every comprehensive hyperbaric new and to improve existing protocols. This test for readiness with rapid-shallow- facility. collection of protocols was developed by breathing index, exercise, evaluate progress, the University of California’s Respiratory and report information to clinicians) proto- Michael H Bennett MD FANZCA Care Services Department, and is published col with an addendum for synchronized Department of Diving and by Daedalus Enterprises. The CD-ROM intermittent mandatory ventilation with Hyperbaric Medicine contains the patient-driven-protocol manual pressure support (SIMV/PS); STEER for Prince of Wales Hospital in an Abode Acrobat PDF file, and 25 pa- cardiothoracic service postoperative (day 1) and tient-driven-protocol algorithms in Mi- open-heart surgery; and metered-dose- Faculty of Medicine crosoft Visio format, which allow the reader inhaler protocol for ventilated patients. The University of New South Wales to print high-quality color versions of the protocols in Part II follow the same format Sydney, Australia protocols. Macintosh users may have diffi- as those in Part I. Because of the depth of culty viewing the files; Visio is not avail- each protocol, there is considerably more The author has disclosed no conflicts of interest. able for Macintosh computers, so a third- explanation given in the overview sections. party program is needed to view them. On Part III contains 2 pediatric protocols: Respiratory Care Patient-Driven Proto- my computer I easily accessed and printed metered-dose-inhaler protocol, and a wean- cols, 3rd edition. University of California the PDF file. ing protocol. San Diego, Respiratory Services. -
About Mastectomy and Sentinel Lymph Node Biopsy
All About Mastectomy and Sentinel Lymph Node Biopsy One of the most important goals of Moffitt Cancer Center is to provide you with quality patient care through education, research and patient care. The following information has been developed to help you understand the mastectomy and sentinel lymph node biopsy procedures for which you have been scheduled. Members of your health care team will review this information with you and answer any questions that you may have. Definitions: Mastectomy – Removal of the entire breast but not the muscles underneath. Lymph Nodes - Small bean shaped glands found in the armpit. They remove waste and fluids from the arm and breast and help fight infection. They are also call lymph glands. Sentinel Lymph Node - The first place breast cancer may metastasize (or spread) is to lymph nodes in the axilla (underarm area) on the side of the body where the cancer is. The first lymph node(s) are referred to as the sentinel lymph node(s) or the “gate keepers”. These nodes are first biopsied to determine if the cancer has spread. If cancer cells are not found in the sentinel lymph node(s) that were removed, it will not be necessary to remove the remaining lymph nodes in the arm pit. Sentinel Lymph Node Mapping and Biopsy - This procedure is a two step process. Performing the sentinel lymph node biopsy requires a small incision in your axilla. In the first step, the doctor injects a radioactive substance and/ or blue dye in the area around the tumor. Lymphatic channels (like blood vessels) carry these materials to the sentinel lymph node. -
Consensus Guideline on the Management of the Axilla in Patients with Invasive/In-Situ Breast Cancer
- Official Statement - Consensus Guideline on the Management of the Axilla in Patients With Invasive/In-Situ Breast Cancer Purpose To outline the management of the axilla for patients with invasive and in-situ breast cancer. Associated ASBrS Guidelines or Quality Measures 1. Performance and Practice Guidelines for Sentinel Lymph Node Biopsy in Breast Cancer Patients – Revised November 25, 2014 2. Performance and Practice Guidelines for Axillary Lymph Node Dissection in Breast Cancer Patients – Approved November 25, 2014 3. Quality Measure: Sentinel Lymph Node Biopsy for Invasive Breast Cancer – Approved November 4, 2010 4. Prior Position Statement: Management of the Axilla in Patients With Invasive Breast Cancer – Approved August 31, 2011 Methods A literature review inclusive of recent randomized controlled trials evaluating the use of sentinel lymph node surgery and axillary lymph node dissection for invasive and in-situ breast cancer as well as the pathologic review of sentinel lymph nodes and indications for axillary radiation was performed. This is not a complete systematic review but rather, a comprehensive review of recent relevant literature. A focused review of non-randomized controlled trials was then performed to develop consensus guidance on management of the axilla in scenarios where randomized controlled trials data is lacking. The ASBrS Research Committee developed a consensus document, which was reviewed and approved by the ASBrS Board of Directors. Summary of Data Reviewed Recommendations Based on Randomized Controlled -
How Is Pulmonary Fibrosis Diagnosed?
How Is Pulmonary Fibrosis Diagnosed? Pulmonary fibrosis (PF) may be difficult to diagnose as the symptoms of PF are similar to other lung diseases. There are many different types of PF. If your doctor suspects you might have PF, it is important to see a specialist to confirm your diagnosis. This will help ensure you are treated for the exact disease you have. Health History and Exam Your doctor will perform a physical exam and listen to your lungs. • If your doctor hears a crackling sound when listening to your lungs, that is a sign you might have PF. • It is also important for your doctor to gather detailed information about your health. ⚪ This includes any family history of lung disease, any hazardous materials you may have been exposed to in your lifetime and any diseases you’ve been treated for in the past. Imaging Tests Tests like chest X-rays and CT scans can help your doctor look at your lungs to see if there is any scarring. • Many people with PF actually have normal chest X-rays in the early stages of the disease. • A high-resolution computed tomography scan, or HRCT scan, is an X-ray that provides sharper and more detailed pictures than a standard chest X-ray and is an important component of diagnosing PF. • Your doctor may also perform an echocardiogram (ECHO). ⚪ This test uses sound waves to look at your heart function. ⚪ Doctors use this test to detect pulmonary hypertension, a condition that can accompany PF, or abnormal heart function. Lung Function Tests There are several ways to test how well your lungs are working. -
Application of Preoperative Computed Tomographic Lymphography For
Wen et al. BMC Surg (2021) 21:187 https://doi.org/10.1186/s12893-021-01190-7 RESEARCH ARTICLE Open Access Application of preoperative computed tomographic lymphography for precise sentinel lymph node biopsy in breast cancer patients Shishuai Wen1,2,3†, Yiran Liang1†, Xiaoli Kong1, Baofeng Liu4, Tingting Ma1, Yeqing Zhou1, Liyu Jiang1, Xiaoyan Li1 and Qifeng Yang1,5,6* Abstract Background: In light of the extensive application of sentinel lymph node biopsy (SLNB) in clinically node-negative breast cancer patients and the recently investigated failure of SLNB after lumpectomy, it has become important to explore methods for preoperative mapping of sentinel lymph nodes (SLNs) and their lymphatics to direct precise SLNB and improve the identifcation rate of SLNs. Methods: Twenty-seven patients with suspected breast cancer based on the results of the clinical examination and imaging were enrolled in the study. Computed tomographic lymphography (CTLG) followed by CT three-dimensional reconstruction was performed to determine the localization of SLNs and lymphatics on the body surface preopera- tively. Intraoperatively combined staining with methylene blue and indocyanine green was used to evaluate the accuracy and feasibility of CTLG. Results: SLNs and lymphatics from the breast were identifed using CTLG in all patients, and preoperative SLNs and lymphatics localization on the body surface showed a signifcant role in the selection of operative incision and injec- tion points. The accuracy rate of SLN and lymphatic detection by CTLG was 92.6% compared with intraoperatively combined staining. Moreover, preoperative CTLG performed well in SLN number detection, and the accuracy rate was 95.2%. Conclusion: We evaluate the procedure and application of preoperative CTLG in the superfcial localization of SLNs and lymphatics, which may lead to a decreased incidence of cutting of the lymphatics of SLNs and consequently more rapid and accurate SLN detection.