Dial-In Instructions Conference Name: Modifiers -52, -73, and -74: Ensure proper coding at the point of care Scheduled Conference Date: Thursday, February 2, 2006 Scheduled Conference Time: 1:00 p.m.–2:30 p.m. (Eastern), 12:00 p.m.–1:30 p.m. (Central), 11:00 a.m.– 12:30 p.m. (Mountain), 10:00 a.m.–11:30 a.m (Pacific) Scheduled Conference Duration: 90 Minutes PLEASE NOTE: If the audioconference occurs April through October, the time reflects daylight savings. If your area does NOT observe daylight savings, times will be one hour earlier. Your registration entitles you to ONE telephone connection to the audioconference. Invite as many people as you wish to listen to the audioconference on your speakerphone. Permission is given to make copies of the written materials for anyone else who is listening. In order to avoid delays in connecting to the conference, we recommend that you dial into the audioconference 15 minutes prior to the start time. Dial-In Instructions: 1. Dial 877/407-2989 and follow the voice prompts. 2. You will be greeted by an operator 3. Give the operator your pass code 020206 and the last name of the person who registered for the audioconference. 4. The operator will then verify the name of your facility. 5. You will then be placed into the conference. Technical Difficulties 1. If you experience any difficulties with the dial-in process, please call the conference center reservation line at 877/407-7177. 2. If you should need technical assistance during the audio portion of the program, please press the star (*) key followed by the 0 key on your touch-tone phone and an operator will assist you. If you are disconnected during the conference, dial 877/407-2989. Q&A Session 1. To enter the questioning queue during the Q&A session, callers need to push the star (*) key followed by the 1 key on their touch-tone phones. Note: For most programs, this portion generally falls after the first hour of presentation. 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Please follow the instructions provided in the CE Documentation. 200 Hoods Lane PO Box 1168 Marblehead MA 01945 TEL 781 639 1872 FAX 781 639 7857 URL www.hcpro.com Program Evaluation Dear Audioconference Participant, Thank you for attending the HCPro audioconference today. We hope that you find the information provided valuable. In our effort to ensure that our customers have a positive experience when taking part in our audioconferences we are requesting your feedback. We would also like to request that you forward the link to others in your facility that attended the audioconference. We realize that your time is valuable, so we’ve limited the evaluation to a few brief questions. Please click on the link below. h t t p : / / w w w. z o o m e r a n g . c o m / s u r v e y. z g i ? p = W E B 2 2 4 X H N M T F Q 4 The information provided from the evaluation is crucial towards our goal of delivering the best possible products and services. To insure that your completed form receives our attention, please return to us within six days from the date of this audioconference. We appreciate your time and suggestions. We hope that you will continue to rely on HCPro audioconferences as an important resource for pertinent and timely information. Sincerely, Frank Morello Director of Multimedia HCPro, Inc. presents . . . Modifiers -52, -73, and -74: Ensure proper coding at the point of care A 90-minute interactive audioconference Thursday, February 2, 2006 1:00 p.m.–2:30 p.m. (Eastern) 12:00 p.m.–1:30 p.m. (Central) 11:00 a.m.–12:30 p.m. (Mountain) 10:00 a.m.–11:30 a.m. (Pacific) In our materials we strive to provide our audience with useful, timely information. The live audioconference will follow the enclosed agenda. Occasionally our speakers will refer to the materials enclosed. We have noticed that other non-HCPro audioconference materials follow the speaker’s presentation bullet-by-bullet, page-by-page. Because our presentations are less rigid and rely more on speaker interaction, we do not include each speaker’s entire presentation. The materials contain helpful forms, crosswalks, policies, charts, and graphs. We hope that you find this information useful in the future. HCPro is not affiliated in any way with the Joint Commission on Accreditation of Healthcare Organizations, which owns the JCAHO trademark. ii Modifiers -52, -73, and -74: Ensure proper coding at the point of care The “Modifiers -52, -73, and -74: Ensure proper coding at the point of care” audioconference materials package is published by HCPro, 200 Hoods Lane, P.O. Box 1168, Marblehead, MA 01945. Copyright 2006, HCPro, Inc. Attendance at the audioconference is restricted to employees, consultants, and members of the medical staff of the Licensee. The audioconference materials are intended solely for use in conjunction with the associated HCPro audioconference. Licensee may make copies of these materials for your internal use by attendees of the audioconference only. All such copies must bear this legend. Dissemination of any information in these materials or the audioconference to any party other than the Licensee or its employees is strictly prohibited. Advice given is general, and attendees and readers of the materials should consult professional counsel for specific legal, ethical, or clinical questions. HCPro is not affiliated in any way with the Joint Commission on Accreditation of Healthcare Organizations, which owns the JCAHO trademark. For more information, contact HCPro, Inc. 200 Hoods Lane P.O. Box 1168 Marblehead, MA 01945 Phone: 800/650-6787 Fax: 781/639-0179 E-mail: [email protected] Web site: www.hcpro.com Modifiers -52, -73, and -74: Ensure proper coding at the point of care iii 200 Hoods Lane P.O. Box 1168 Marblehead, MA 01945 Tel: 800/650-6787 Fax: 800/639-8511 Dear colleague, Thank you for participating in our “Modifiers -52, -73, and -74: Ensure proper coding at the point of care” audioconference with Lolita M. Jones, RHIA, CCS, and Susan Garrison, CPC, CHC, CPC-H, CCS-P, CPAR, moderated by Lisa Eramo. We are excited about the opportunity to interact with you directly and encourage you to take advantage of the opportunity to ask our experts your questions during the audioconference. If you would like to submit a question before the audioconference, please send it to [email protected] and provide the program date in the subject line. We cannot guarantee your question will be answered during the program, but we will do our best to take a good cross-section of questions. If at any time you have comments, suggestions, or ideas about how we might improve our audioconferences, or if you have any questions about the audioconference itself, please do not hesitate to contact me. And if you would like any additional information about other products and services, please contact our Customer Service Department at 800/650-6787. Along with these audioconference materials, we have enclosed a fax evaluation. We value your opinion. After the audioconference, please take a minute to complete the evaluation to let us know what you think. Thanks again for working with us. Best regards, Wendy Walsh Audioconference associate Fax: 781/639-7857 E-mail: [email protected] iv Modifiers -52, -73, and -74: Ensure proper coding at the point of care Contents Agenda . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .vi Speaker profiles . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .vii Exhibit A . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 Presentation by Lolita M. Jones, RHIA, CCS, and Susan Garrison, CPC, CHC, CPC-H, CCS-P, CPAR Exhibit B . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 41 Collection of Articles from Briefings on APCs Source: Brian Murphy, HCPro. Resources . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .48 Modifiers -52, -73, and -74: Ensure proper coding at the point of care v Agenda I. Previous/former guidelines for reporting the modifiers II. Current official guidelines—the changes and what they mean III. OPPS 2006 issues—what to expect IV. Review of GI endoscopy A. Guidelines B. Operational issues C. Case studies V. Interventional radiology A. Guidelines B. Operational issues C. Case studies VI. Summary A. Data mining B. Reporting Live Q&A vi Modifiers -52, -73, and -74: Ensure proper coding at the point of care Speaker profiles Lolita M. Jones, RHIA, CCS Lolita M. Jones, RHIA, CCS, is the principal of Lolita M. Jones Consulting Services and vice president of educational programs for Medical Marketing Resources, Inc., in Fort Washington, MD. She is the author of two editions of HCPro’s The Modifier Clinic: A Guide to Hospital Outpatient Challenges and has authored a column about appropriate modifier use for the monthly newsletter Briefings on APCs for the past five years. She has over 15 years of experience in publishing, training, and auditing for the hospital outpatient and freestanding ambulatory surgery center markets. Susan Garrison, CPC, CHC, CPC-H, CCS-P, CPAR Susan Garrison, CPC, CHC, CPC-H, CCS-P, CPAR, is vice president of healthcare consulting services at Magnus Confidential. She has more than 25 years of experience in healthcare management, including in the areas of documentation, coding, billing, and reimbursement for both outpatient hospital and physician services. She was previously responsible for 3M Consulting’s Outpatient Coding Validation and Education Services. She has conducted hundreds of engagements at hospitals across the country to improve hospital and physician compliance and reimbursement. Modifiers -52, -73, and -74: Ensure proper coding at the point of care vii Exhibit A Presentation by Lolita M. Jones, RHIA, CCS, and Susan Garrison, CPC, CHC, CPC-H, CCS-P, CPAR EXHIBIT A Modifiers -52, -73, and -74: Ensure proper coding at the point of care Audioconference February 2, 2006 Lolita M. Jones, RHIA, CCS Lolita M. Jones Consulting Service Susan Garrison, CPC, CHC, CPC-H, CCS-P, CPAR Vice President of Healthcare Consulting Services Magnus Confidential, Inc. 2 Modifiers -52, -73, and -74: Ensure proper coding at the point of care EXHIBIT A Previous Guidelines for Reporting the Discontinued Modifiers Prior to February 22, 2005: Modifier -52 is used in those situations in which modifier -73 or modifier -74 would have been appropriate, but since the use of anesthesia was not an inherent part of performing the procedure, modifier -52 is used to show that the procedure was discontinued. Per the April 7, 2000, Federal Register: use Modifier -52 (reduced services) to indicate that a procedure did not require anesthesia, but the procedure was terminated after the patient had been prepared for the procedure, received sedation and was taken to the room where the procedure was to be performed. Use the code that explains the extent of the procedure. If no code exists for what was performed, report the intended code with modifier -52. Examples: if a barium swallow is not complete because the patient can’t handle the barium, assign CPT code 74270-52. If only one view of a chest x-ray is performed, do not report 7102052 (for x-ray, two views—reduced service), report 71010 (x-ray chest, single view) Source: Medicare Program Memorandum Intermediaries, Transmittal No. A-99-41, September 1999, www.hcfa.gov/pubforms/transmit/A994160.htm. Modifiers -52, -73, and -74: Ensure proper coding at the point of care 3 EXHIBIT A Current Official Guidelines: The changes and what they mean Even though all modifiers are tricky, modifiers 52, 73, and 74 are particularly onerous simply because the rules have been unclear and changing. 52 = Reduced/discontinued procedure w/o anesthesia 73 = Terminated procedure before necessary anesthesia 74 = Terminated procedure after necessary anesthesia Fortunately, last year with Transmittal 442, Medicare clarified pieces of the puzzle for us. Let’s begin there. You may download this transmittal from: http://www.cms.hhs.gov/Transmittals/downloads/R442CP.pdf The following outlines the major instructions from this transmittal. • • • • • “These modifiers (52, 73, 74) are used to report procedures that are discontinued by the physician due to unforeseen circumstances. Modifier -52 is used to indicate partial reduction or discontinuation of radiology procedures and other services that do not require anesthesia.” “For surgeries and certain diagnostic procedures requiring anesthesia (including colonoscopies), the hospital may receive 50 percent of the OPPS payment amount for cases in which the procedure is discontinued after the beneficiary was prepared for the procedure and taken to the room where the procedure was to be performed.” “If the procedure is discontinued after the beneficiary has received anesthesia or after the procedure was started (e.g., scope inserted, intubation started, incision made) the hospital may receive the full OPPS payment amount for the discontinued procedure.” “For purposes of billing for services furnished in the hospital outpatient department, anesthesia is defined to include: o local, o regional block(s), o moderate sedation/analgesia (“conscious sedation”), o deep sedation/analgesia, and o general anesthesia. Modifier -73 is used by the facility to indicate that a surgical or diagnostic procedure requiring anesthesia was terminated due to extenuating circumstances or to circumstances that threatened the well being of the patient after the patient had been prepared for the procedure (including procedural pre-medication when provided), and been taken to the room where the procedure was to be performed, but prior to administration of anesthesia. For purposes of billing for services furnished in the hospital outpatient department, anesthesia is defined to include local, regional block(s), moderate sedation/analgesia (“conscious sedation”), 4 Modifiers -52, -73, and -74: Ensure proper coding at the point of care EXHIBIT A deep sedation/analgesia, or general anesthesia. This modifier code was created so that the costs incurred by the hospital to prepare the patient for the procedure and the resources expended in the procedure room and recovery room (if needed) could be recognized for payment even though the procedure was discontinued. Modifier -74 is used by the facility to indicate that a surgical or diagnostic procedure requiring anesthesia was terminated after the induction of anesthesia or after the procedure was started (e.g., incision made, intubation started, scope inserted) due to extenuating circumstances or circumstances that threatened the well being of the patient. Termination Where Multiple Procedures Planned 1. 2. 3. 4. When one or more of the procedures planned is completed, the completed procedures are reported as usual. The other(s) that were planned, and not started, are not reported. When none of the procedures that were planned are completed, and the patient has been prepared and taken to the procedure room, the first procedure that was planned, but not completed is reported with modifier -73. If the first procedure has been started (scope inserted, intubation started, incision made, etc.) and/or the patient has received anesthesia, modifier -74 is used. The other procedures are not reported. If the first procedure is terminated prior to the induction of anesthesia and before the patient is wheeled into the procedure room, the procedure should not be reported. The patient has to be taken to the room where the procedure is to be performed in order to report modifier -73 or -74.” Modifiers -52, -73, and -74: Ensure proper coding at the point of care 5 EXHIBIT A OPPS 2006 Issues: What payment changes to expect Since implementation of the OPPS in 2000, CMS has required hospitals to report modifiers -52, 73, and -74 to indicate procedures that were terminated before their completion. Before 2006, hospitals were paid 50 percent of the APC payment for services with modifier -73 appended and 100 percent for procedures with modifier -52 or -74 reported, The pre-2006 OPPS policy required providers to use modifier -52 to indicate that a service that did not require anesthesia was partially reduced or discontinued at the physician's discretion. The physician may discontinue or cancel a procedure that is not completed in its entirety due to a number of circumstances, such as adverse patient reaction or medical judgment that completion of the full study is unnecessary. The modifier is reported most often to identify interrupted or reduced radiological and imaging procedures, and CMS’ pre-2006 policy was to make full payment for procedures with a -52 modifier. Compared to surgical procedures that require anesthesia, a number of general and procedurespecific supplies, and reserved procedure rooms that must be cleaned and prepared prior to performance of each specific procedure, the costs to the hospital outpatient department for the rooms and supplies typically associated with procedures not requiring anesthesia are much more limited. For example, the scheduling maintained for radiological services not requiring anesthesia generally exhibits greater flexibility than that for surgical procedures, and the procedure rooms are used for many unscheduled services that are fit in, when possible, between those that are scheduled. Consequently, CMS believes that the loss of revenue that may result from a surgical procedure being discontinued prior to its initiation in the procedure room is usually more substantial than that lost as the result of a discontinued service not requiring anesthesia, such as a radiology procedure. 6 Modifiers -52, -73, and -74: Ensure proper coding at the point of care EXHIBIT A CMS has examined their data and given careful consideration to the public comments and the APC Panel's discussion and recommendations regarding OPPS payment policies for interrupted procedures. Given the nature of the procedures that were likely reported appropriately with the 52 modifier in CY 2004, CMS continues to believe that there are considerable savings associated with their incomplete performance. CMS thinks that in the hospital outpatient setting, there are generally many opportunities to utilize the rooms and equipment that would otherwise be left unused as a result of discontinued procedures. CMS also believes that, although there may be occasional instances in which a discontinued procedure appropriately reported with the -52 modifier consumes more resources than one that is completed without interruption, those are unusual events and the vast majority of discontinued cases are significantly less costly than completed procedures. Therefore, CMS finalized their proposed policy to apply a 50 percent reduction to the APC payments for interrupted procedures reported with the -52 modifier in CY 2006 (effective January 1, 2006). CMS will provide billing guidance for CY 2006 regarding modifiers -52, -73, and -74 to offer hospitals additional instructions regarding the appropriate use of the three modifiers in the OPPS. CMS’ goal is to assure that hospitals understand and report these modifiers correctly so that they receive appropriate payments for the services they provide. Modifiers -52, -73, and -74: Ensure proper coding at the point of care 7 EXHIBIT A Review of GI Endoscopy GUIDELINES Esophagoscopy is limited to study of the esophagus. When the endoscope passes the diaphragm, the procedure is esophagogastroscopy. When the pyloric channel is traversed, it becomes an esophagogastroduodenoscopy. The collection of specimens is now included in the parent code for all GI endoscopic procedures and these are also all separate procedures. Proctosigmoidoscopy is the examination of the rectum and sigmoid colon. Sigmoidoscopy is the examination of the entire rectum, sigmoid colon and may include examination of a portion of the descending colon. Colonoscopy is the examination of the entire colon, from the rectum to the cecum, and may include the examination of the terminal ileum. If the same therapeutic endoscopy is repeated (e.g. polyp removal) in the s same area described by the CPT narrative, only one CPT code is reported with one unit of service. 8 Modifiers -52, -73, and -74: Ensure proper coding at the point of care EXHIBIT A When endoscopic esophageal dilation is performed, the appropriate endoscopic esophageal dilation code is to be reported. Do not code 43450-43458 (dilation of esophagus) in addition (even if an unsuccessful attempt prior to endoscopic dilation). Only the most extensive endoscopic procedure is reported for a session. For example if a sigmoidoscopy is completed and the physician performs a colonoscopy during the same session only the colonoscopy, is coded. Modifiers -52, -73, and -74: Ensure proper coding at the point of care 9 EXHIBIT A OPERATIONAL ISSUES Some considerations for Operational Issues for GI Services: 1. Sometimes hospitals have GI codes built into the CDM and sometimes HIM codes these cases. So, step 1 is understanding who is responsible for driving the coding. Who makes the decision for which modifier? (charge entry, HIM, billing, built into CDM, other?) 2. What is that individual’s level of training around coding? Little-to-none 10 Trained Thoroughly 3. What is the process of entering the modifier – how clean is it? Is it reviewed prior to dropping the bill? After dropping the bill? During random audits? 4. What follow-up monitoring is provided to ensure the modifier is used when necessary and not used when inappropriate? Modifiers -52, -73, and -74: Ensure proper coding at the point of care EXHIBIT A CASE STUDIES Quick exercise: 1. Patient has a planned colonoscopy with conscious sedation. When vitals are taken preprocedure, patient decides against procedure. 52___ 73___ 74___ None___ 2. Patient has a planned colonoscopy with conscious sedation. Due to poor prep, the scope does not advance beyond the sigmoid region. 52___ 73___ 74___ None___ 3. CPT 82270 is for Occult Blood; feces, 1-3 determinations. If only one is performed, do I need a modifier? 52___ 73___ 74___ None___ 4. Nerve conduction studies were performed, but no measurable values were able to be obtained? 52___ 73___ 74___ None___ Modifiers -52, -73, and -74: Ensure proper coding at the point of care 11 EXHIBIT A CASE 1 (paraphrased from CPT Assistant): An upper gastrointestinal endoscopy was intended to be performed. Although attempted, the physician could not complete the entire procedure due to obstruction at the distal esophagus. Rationale: In this instance, for non-Medicare reporting, CPT code 43235 (EGD) with the modifier 52 appended indicates that the intended procedure was reduced. However, CMS does not allow the use of the modifier 52 when the endoscopic procedure is "incomplete," and there is a code to describe the actual service performed. CMS requires the reporting of a code describing only the anatomy examined at that endoscopic procedure. Therefore, if a code is available that fully describes the hospital outpatient procedure performed, this code choice supersedes the reporting of a code describing the intended procedure. Example (CMS requirement): An upper gastrointestinal endoscopy was intended to be performed. Although attempted, the physician could not complete the entire procedure due to obstruction at the distal esophagus. Rationale: In this instance, for Medicare reporting, CPT code 43200, Esophagoscopy describes the procedure performed. 12 Modifiers -52, -73, and -74: Ensure proper coding at the point of care EXHIBIT A CASE 2 (paraphrased from CPT Assistant): A 70-year-old male patient is brought to the OR for repair of a recurrent inguinal hernia. Surgical prep has occurred, but prior to the administration of general anesthesia, the patient complains of radiating chest pain and the cardiac monitor reflecting S-T segment changes. Due to the possibility of an evolving cardiac event, the procedure is cancelled. Rationale: Under these circumstances, the intended service that was prepared for, but cancelled, can be reported with its usual procedure code and modifier '73' appended (CPT 49520-73). Modifiers -52, -73, and -74: Ensure proper coding at the point of care 13 EXHIBIT A CASE 3 (paraphrased from CPT Assistant): The plan is for a laparoscopic cholecystectomy on a 66-year-old female patient. After anesthesia is administered, the anesthesiologist detects ventricular fibrillation on the cardiac monitor. Ventilation continues while defibrillator pads and paddles are brought into the surgical field. Upon the second defibrillation effort, the arrhythmia abates, but ventricular irritability is present. The procedure is cancelled pending further cardiac stabilization. Rationale: Under these circumstances, the procedure started but was terminated. This can be reported with its usual procedure code number with the modifier '74' appended (CPT 47562-74). 14 Modifiers -52, -73, and -74: Ensure proper coding at the point of care EXHIBIT A CASE 4 COLONOSCOPY REPORT PROCEDURE: Colonoscopy with hot biopsy destruction of sessile 3 mm mid sigmoid colon polyp and multiple cold biopsies taken randomly throughout the colon. PREOPERATIVE DIAGNOSIS: Fecal incontinence. Diarrhea. Constipation. BOWEL PREPARATION: The bowel preparation with GoLytely was good. ANESTHETIC: Demerol 50 mg and Versed 3 mg both given intravenously. PROCEDURE DESCRIPTION: The digital examination revealed no masses. The pediatric variable flexion Olympus colonoscope was introduced into the rectum and attempted advancement to the cecum. However, due to poor prep, we were only able to reach the sigmoid colon. The scope was then carefully extubated. The mucosa looked normal. Random biopsies were taken from the sigmoid colon and rectum. There was a 3 mm sessile polyp in the mid sigmoid colon which was destroyed by hot biopsy. IMPRESSION: Sigmoid colon polyp destroyed by hot biopsy. RECOMMENDATION: I have asked the patient to call my office in a week to get the results of the pathology. Cold biopsies taken because of history of diarrhea. 52___ 73___ 74___ Other___ None___ Modifiers -52, -73, and -74: Ensure proper coding at the point of care 15 EXHIBIT A CASE 5 Preoperative Diagnosis: Failed PEG tube. Postoperative Diagnosis: Same. Procedure: Endoscopically guided replacement of gastrostomy tube with removal of previous failed PEG Procedure: The patient was brought to the endoscopy suite, placed on the endoscopy table in the left lateral decubitus position. After adequate IV sedation the flexible end viewing gastroscope was introduced under direct visualization into the stomach which was insufflated. A polypectomy snare was placed about the rubber bolster which was visualized at the failed gastrostomy tube and snaring it and grasping it in this fashion. Outside the abdominal wall, the tube was cut, residual stump of the tube with the rubber bolster was brought up next to the scope and the scope and it removed in total. As we removed the tube, the patient’s blood pressure began to fall and we decided to stop the procedure and stabilize the patient. The patient, once able, will be brought back into the OR for the tube placement. Next day, a Foley type gastrostomy tube was placed through the existing gastrostomy tract with a 20 cc balloon of saline used to fill it and the balloon then snugged to the anterior wall of the stomach. The patient tolerated the procedure well without difficulty and after brief period of for reaction was taken to the floor to be evaluated and transferred to the nursing home when alert and stable. 52___ 73___ 74___ Other___ 16 None___ Modifiers -52, -73, and -74: Ensure proper coding at the point of care EXHIBIT A CASE 6 Postop Dx: Gangrenous cholecystitis Procedure: Laparoscopic converted to open cholecystectomy After explaining the risks and benefits of the procedure to the patient, including but not limited to bleeding, infection, conversion to open operation, all questions were answered and informed consent was obtained. The patient was brought to the operating room after voiding in the holding area. He was placed in the supine position and under general anesthesia. A nasogastric tube, thigh high TED hose, and Thromboguards were placed. He had received IV antibiotics preoperatively. The abdomen was prepped and draped in a sterile fashion. An infraumbilical incision was made using a scalpel and taken down through subcutaneous tissues. The fascia was grasped using kocher clamps and divided transversely. A hasson cannula was inserted intraperitoneally and secured using 0 vicryl ties. The camera was placed intraperitoneally and a pneumoperitoneum using CO2 insufflation. After sufficient abdominal distention, a transverse subxiphoid incision was made using scalpel and taken down through subcutaneous tissues. A 10mm disposable trocar was inserted under direct visualization without difficulty. Two right upper quadrant 5mm incisions and nondisposable trocars were inserted under visualization without difficulty. The gallbladder was tense with fluid and it was unable to be grasped. It was decompressed using a needle which aspirated green foul smelling bile. This allowed the gallbladder to be grasped and then was retracted cephalad over the liver. There were numerous omental adhesions to the anterior surface that appeared to be fairly acute in nature. These were taken down bluntly. The gallbladder was entered during this blunt dissection. It was grasped at this point but all subsequent fluid was aspirated clean. Further dissection failed to identify sufficiently the gallbladder neck. Because of the amount of inflammation and the obvious gangrene of the gallbladder, conversion to an open cholecystectomy was necessary. The anterior fascia was divided and the rectus muscle was divided. The posterior fascia was divided after placing a finger intraperitoneally through a previous port. The iron intern retractor was placed. Blood and irrigant fluid was aspirated until the field was clear. The gallbladder was taken down retrograde using electrocautery. After taking the anterior most peritoneal attachments, the remainder of the gallbladder lifted easily off the liver bed. The liver was retracted cephalad. The cystic artery was identified and encircled. It was doubly clipped then transected. Further dissection with a Kitner and right angle was identified with cystic duct coming the common duct. It was ligated just distal to the junction. The cystic duct was then transected and the gallbladder removed. The operative field was then copiously irrigated using saline then aspirated dry. Hemostasis was checked and achieved. There was a small amount of ooze from the liver bed over which was placed a piece of surgicel. The operative field was drained using a 19 French Blake drain brought out through a separate stab incision and secured to the skin using 2-0 silk suture. The fascia of the subxiphoid and infraumbilical sites was reapproximated using 0 vicryl suture in figure of eight stitches. The posterior fascia of the right upper quadrant incision was then reapproximated using Modifiers -52, -73, and -74: Ensure proper coding at the point of care 17 EXHIBIT A #1 vicryl suture in interrupted figure of eight stitches. This layer was copiously irrigated using saline then infiltrated using .25% marcaine for postop analgesia. The anterior layer was then reapproximated using #1 double stranded PDS suture in a running stitch started at either end and tied in the middle. This subcutaneous tissues were copiously irrigated using saline and skin of all incisions closed using surgical clips. The wound was then cleaned, dried, then sterile dressing applied. The patient tolerated the procedure well and there were no immediate complications. Sponge, needle and instrument counts were correct x2. Specimens: Gallbladder 52___ 73___ 74___ Other___ 18 None___ Modifiers -52, -73, and -74: Ensure proper coding at the point of care EXHIBIT A Interventional Radiology—Discontinued procedures GUIDELINES Modifier -52 Effective 2/22/05: Use modifier -52 to indicate partial reduction or discontinuation of radiology procedures and other services that do not require anesthesia. For purposes of billing for services furnished in the hospital outpatient department, anesthesia is defined to include local, regional block(s), moderate sedation/analgesia (“conscious sedation”), deep sedation/analgesia, and general anesthesia. Although the new CMS policy states that modifier -52 should be used for the discontinuation of radiology procedures that do not require anesthesia, there are interventional radiology procedures that may in fact involve the use of anesthesia. When discontinued, these interventional radiology procedures that require anesthesia, would be reported using the modifier -73 or -74 as appropriate. Modifiers -52, -73, and -74: Ensure proper coding at the point of care 19 EXHIBIT A Multiple Procedures Scheduled - One or More Discontinued: Report completed procedures as usual when one or more of the planned procedures are completed. Do not report the other(s) that were planned, and not started. If the first procedure has been started (scope inserted, intubation started, incision made, etc.) and/or the patient has received anesthesia, use modifier -74. The other procedures are not reported. Do not report the procedure if the first procedure is terminated prior to the induction of anesthesia and before the patient is wheeled into the procedure room. The patient has to be taken to the room where the procedure is to be performed in order to report modifier -73 or 74. Source: Medicare Program Memorandum Intermediaries, Transmittal No. A-99September 1999, www.hcfa.gov/pubforms/transmit/A994160.htm . 20 41, Modifiers -52, -73, and -74: Ensure proper coding at the point of care EXHIBIT A OPERATIONAL ISSUES If it is your hospital’s policy to enter into the radiology information system the reason or “reason code” for a reduced/discontinued procedure, you should do one of the following: • Develop a policy and procedure that requires the radiology staff to print the radiology information system computer screen that contains the text regarding the reason or “reason code” whenever there is a reduced/discontinued procedure. • Develop and carry out internal policies and procedures that specify the level of documentation needed for reduced/discontinued procedures. This is particularly important for departments such as radiology and interventional radiology, where the physicians traditionally have not written or dictated a note when a procedure is reduced/discontinued (after the patient is taken to the room where the procedure is scheduled to be performed). Modifiers -52, -73, and -74: Ensure proper coding at the point of care 21 EXHIBIT A CASE STUDIES CASE 1 CARDIAC CATH 92980-52-RC,93510,93545,93556 INDICATIONS FOR PROCEDURE: Mr. Smith is a 75 year old gentleman with history of pulmonary hypertension, coronary artery disease underwent catheterization in the fall of 2004. At that time he had a high grade greater than 95% ostial right coronary artery lesion with calcification. There was a moderate 50% ostial left main lesion. The LAD and circumflex had noncritical disease. He had prior to this, a positive nuclear study with inferior wall reversible schema. His ejection fraction was at the low limits of normal. He has had crescendo angina pectoris and was a very poor operative candidate. Therefore, PTCA of the ostial right coronary artery was recommended for symptomatic therapy. Indeed this would be a difficult case with the ostial and accentric opening of the vessel and his history of renal insufficiency. Risks and benefits were understood, potential complications were understood prior to the procedure and discussed with the family. He does have renal insufficiency and dye conservation would clearly play into discussions in the cath lab. PROCEDURE PERFORMED: Left heart catheterization with coronary arteriography, attempted PTCA of the right coronary artery. SITE: Right femoral artery. CATHETERS USED: 8 French AR-1, 0.014 BMW wire, 0.014 choice BT wire. ANESTHESIA: 1% Lidocaine. DESCRIPTION OF OPERATIVE TECHNIQUE: Please refer to cath course flow sheet on chart. TOTAL FLUOROSCOPY TIME: 55.3 minutes. This was prolonged due to marked difficulty in crossing the lesion, the ostial lesion and attempts at dye conservation. TOTAL CONTRAST: 150 mL of Omnipaque. RESULTS: HEMODYNAMICS: Central aortic pressure was 124/ 63. SELECTIVE CORONARY ARTERIOGRAPHY REVEALED THE FOLLOWING: 22 Modifiers -52, -73, and -74: Ensure proper coding at the point of care EXHIBIT A The right coronary artery is a moderate size dominant vessel which has a calcified, 98% proximal lesion. There was a posterior takeoff of this vessel. There was an AV nodal artery that arose from the proximal portion of the right coronary artery out of the calcified ostium. ATTEMPTED PTCA/STENT: The 98% lesion was not able to be crossed with the BMW wire. This was stressed with the soft portion of a Choice PT wire on two occasions. Both occasions unable to advance the transition of the wire into the proximal portion of the vessel. The proximal portion of the vessel had an acute angle at the takeoff as well as a lateral angle out of place. There was significant tortuosity in the proximal portion of this vessel along with the highgrade calcified lesion. There was lack of guide support due to the ostial nature of this lesion and at this point 150 mL of contrast was used and the procedure was aborted. There was no change in the vessel. The patient tolerated the procedure well without complications. COMPLICATIONS: None. CONCLUSION: Unsuccessful attempted PTCA of the right coronary artery. RECOMMENDATIONS: 1. Continue medical therapy. 2. Follow renal function. 3. Possibly reconsider surgical evaluation if refractory symptoms. Thank you for referring this interesting patient. Modifiers -52, -73, and -74: Ensure proper coding at the point of care 23 EXHIBIT A CASE 2 CARDIAC CATH 35471-52,93510,93545,93556,75724,G0275 INDICATIONS FOR PROCEDURE: Mr. is a 73-year old gentleman with history of hypertensive cerebrovascular disease, risk factors for coronary artery disease, hypertension with lability and chronic renal insufficiency, a creatinine in the range of 2.9. He had a renal angiogram which showed right renal artery stenosis with 95% stenosis at the origin of the right renal artery. A left pelvic kidney with an arterial supply off a branch of the inferior mesenteric artery without evidence of significant stenosis. Cardiac catheterization is therefore recommended for diagnosis, prognosis and in consideration for revascularization. Renal PTCA/ stent if anatomy is found compelling. PROCEDURE PERFORMED: 1. Left heart catheterization. 2. Coronary arteriography. 3. Selective renal angiogram. 4. Inferior mesenteric angiogram. 5. Abdominal aortogram. SITE: Right femoral artery. CATHETERS USED: 8 French pigtail, JL -4, JR-4, 6 French internal mammary artery catheter. ANESTHESIA: 1% lidocaine. DESCRIPTION OF OPERATION TECHNIQUE: Please refer to cathcor flow sheet on chart. TOTAL FLUOROSCOPY TIME: 25.4 minutes. Arterial time was 48 minutes. TOTAL CONTRAST: 117 cc of Omnipaque. RESULTS: HEMODYNAMICS: Central aortic pressure was 156/77 with a mean of 107. Renal angiogram of the right renal artery, the right kidney had a dual supple. The upper vessel had a 10% ostial irregularity. The lower supple had a subtotal occlusion at its origin. This was in an area of aneurysmal dilatation of the central aorta. The left renal artery arose from the interior mesenteric artery and was visualized by MRA. Abdominal angiogram confirmed above with moderate diffusely aortic disease. Selective coronary arteriography revealed the following. The left main coronary artery was had a 20% distal lesion with an area of ulceration. The left anterior descending artery had a 50% mid lesion. There was diffuse disease in the distal vessel. Diagonal #1 had a 30-50% 24 Modifiers -52, -73, and -74: Ensure proper coding at the point of care EXHIBIT A proximal lesion. The circumflex had a 50-70% proximal lesion and gave rise to a moderate size obtuse marginal branch. The right coronary artery had a 50-60% mid lesion with a dominant vessel which gave rise to a posterior descending and posterolateral branch which was free of significant disease. COMPLICATIONS: None. SUMMARY: 1. Moderate left main coronary artery disease. 2. Three-vessel coronary artery disease. 3. Preserved Left ventricular function by echocardiogram. 4. Right renal artery stenosis. 5. Chronic renal insufficiency. 6. Attempted percutaneous transluminal coronary angioplasty of the right renal artery was aborted due to 1. ______ contrast reaching 17 cc. At this time the origin of the vessel was difficult to engage at this time we will hydrate and follow renal function closely post catheterization. Would consider readmission for attempt at percutaneous transluminal angioplasty/ stent of the right renal artery when the renal fraction tests stabilize in approximately 4-5 weeks. 7. Continue medical therapy risk factor reduction, aspirin and Plavix long term. Thank you for referring this interesting patient. Modifiers -52, -73, and -74: Ensure proper coding at the point of care 25 EXHIBIT A CASE 3 OPERATIVE REPORT 64470-RT, 64472-RT, 64472-RT, 76005 PREOPERATIVE DIAGNOSIS: Thoracic facet artheropathy POSTOPERATIVE DIAGNOSIS: OPERATION: Same. Right T3 through T6 thoracic facet median branch nerve block with fluoroscopic localization. ANESTHESIA: IV sedation. BRIEF CLINICAL HISTORY: The patient returns for the planned diagnostic facet nerve block. He reports greater symptoms on the right mastoid. We discussed initially performing bilateral injections for the diagnostic value. DISPOSITION: I explained the risks, benefits, and expectations and a written consent was obtained. OPERATIVE PROCEDURE: The patient was brought to the operating room and placed in the prone position. Anesthesia and monitoring were applied. An adequate scout view of the thoracic spine was observed. The thoracic region was prepped and draped in the usual sterile fashion., 1% preservative free lidocaine was used for local throughout using a 22-gauge spinal needle for the procedure. The area of pain in the thoracic region was localized with fluoroscopy from T3 through T6. On the right side, the needle was advanced with a 3 cc syringe of lidocaine attached. It is placed in the medial aspect of the T3, where the median branch lies. It was then advanced to T4, T5 and T6. At each level, 1.5 cc of 0.5% bupivacaine was injected using 20 mg of Depo-Medrol in toto. Then, the plan was to perform similar treatment on left side, however, the patient had a degree of emesis and began coughing. He also moved in such a way that it could not hold this position. Therefore, the procedure on the left was aborted. The patient was placed on a stretcher and brought to recovery room awake, alert and in good condition. After a period of observation with stable vital signs, tolerating PO, ambulating without assistance, and avoiding without difficulty, the patient was discharged. If this brings temporary benefits, then we will establish the diagnosis. We will discuss results during his next visit. 26 Modifiers -52, -73, and -74: Ensure proper coding at the point of care EXHIBIT A CASE 4 INJECTION REPORT 62290-74 PROCEDURE: Attempted three-level lumbar discogram. However, the procedure was aborted due to the patient begin vomiting once anesthesia was initiated. Therefore, anesthesia was discontinued. Airway was protected and O2 was given, as the patient’s O2 sats went down to the 80s upon clearing of the airway and giving him oxygen, his sats came back up to 98. At that time, his vital signs were stable, and he was transferred to the recovery room. The patient will reschedule this lumbar discogram for a later date. Modifiers -52, -73, and -74: Ensure proper coding at the point of care 27 EXHIBIT A CASE 5 OPERATIVE REPORT 21660 or 61793-74 PREOPERATIVE DIAGNOSIS: Multiple brain metastases. POST OPERATIVE DIAGNOSIS: Multiple brain metastases. PROCEDURE: Aborted/attempted gamma knife radiosurgery for multiple brain metastases. INDICATIONS: This is the case of a 47-year-old lady on whom I had performed surgery secondary to a very large and highly symptomatic left frontal metastasis. At the time of her surgery, the patient was found to have three other metastases. Keeping in mind that this was all she had, we decided to present her at the gamma knife conference. At that time, she was approved for further treatment. For that reason, she was brought to the gamma knife suite. DETAILS OF THE PROCEDURE: The patient came to the gamma knife suite where she underwent the placement of the Leksell stereotatic frame without complications. This was done via the standard four-point fixation using local anesthetic. The patient tolerated the procedure well and it was performed without problems. However, upon performing her MRI we found out that the patient had blossomed into many other metastases. Upon discussing this with Dr. Thad, our radiation oncologist, it was decided that it would not be in the patient’s best interest to proceed with gamma knife radiosurgery and then implied radiating will be the way to go. For that reason, no gamma knife radiosurgery was given. This was discussed with her husband. The frame was removed without complications and the patient discharged home. I have asked them to please come see me in a month with followup MRI after they complete the whole brain radiation to which the patient had preliminarily agreed. 28 Modifiers -52, -73, and -74: Ensure proper coding at the point of care EXHIBIT A CASE 6 MRI 70553 MRI OF THE BRAIN WITHOUT ANDWITH IV CONTRAST, GAMMA PROTOCOL-OPD CLINICAL HISTORY: Metastatical adenocarcinoma to the brain in a 47 year old woman COMPARISON: Outside examination from ___________ dated 9/16/05 TECHNIQUE: The study is reviewed in multiplanar spin-echo sequences including sagittal contrast-enhanced T1 and gradient echo axial contrast-enhanced, thin-section images FINDINGS: Using standard gamma protocols, there are eight lesions identified within the brain including a large mass in the right brainstem extending from superior through inferior pons, a mass between the lateral ventricles and their mid-body, and a mass at or adjacent to the wall of third ventricle on the left. All contrast-enhancing neoplastic lesions are incorporated on gradient echo contrast-enhanced axial sequences, extending roughly from image 33 through image 163 and are separately detailed in conference with the Gamma Radiotherapy Personnel. IMPRESSION: Gamma protocol MR of the brain for localization of metastatic lesions. Modifiers -52, -73, and -74: Ensure proper coding at the point of care 29 EXHIBIT A CASE 7 OPERATIVE REPORT 62268-74, 76003 Anesthesia: Total intravenous anesthesia/local infiltration. Procedure: 1. Attempted facet injection with drainage of synovial cyst, right L4-L5. 2. Fluoroscopic needle placement/guidance, right L4-L5 facet. Diagnoses: 1. Evidence of synovial cyst, right L4-L5, causing pressure and pain following the right L4 and L5 distribution. 2. Acute/chronic abdominal pain with history of severe abdominal adhesions, states post lysis of adhesions times eight. 3. Chronic back and lower extremity pain in association with evidence of diffusion degenerative disc disease. 4. Evidence of pancreatitis with secondary history of diffuse abdominal pain and scar formation, improved sinus implantation of a drug delivery system, March 1999. 5. Depressive disorder associated with panic attacks and an anxiety response. 6. Status post basilar skull fracture, 2001. 7. Status post implantation of a drug delivery system in March 1995, revised in July 2004. INDICATIONS: The patient has been seen previously when drainage of the synovial cyst was completed by in the Radiology Department, under CT guidance. Recently the patient has had a re-exacerbation of her discomfort and we planned today to drain the cyst and replace this fluid with a steroid. We discussed the risks versus the benefits as the details of the procedure. The patient understood and wished to proceed. PROCEDURE: The patient was seen preoperatively where informed consent was given. She was then taken to the fluoroscopy room and placed in the prone position. Throughout the procedure, the patient as monitored with the use of a Dinamap and a pulse oximeter and was given oxygen by nasal cannula. The area over the right L4-L5 level was noted and marked as such. With the use of fluoroscopic guidance, the widest aperture of the facet joint to the right of the midline and in an oblique positioning of the fluoroscopic beam at approximately 30 to 45 degrees. It was noted that there was significant evidence of sclerosis of the facet joint. This area was marked as such, utilizing fluoroscopic guidance. The area over the right flank was prepped and draped in the usual sterile fashion, using Betadine solution. At this juncture, in order to make the patient as comfortable as possible in a rather awkward, uncomfortable prone position, I felt it medically necessary to sedate the patient. The patient was substantially sedated with incremental doses of 100 milligrams of propofol. After appropriate sedation, a total of 3 ml of 1.5% lidocaine with epinephrine solution was injection subcutaneously into the deep subcutaneous tissue of the target site. After appropriate analgesia and sedation, a #22 gauge 5 inch Chiba needle utilized in an attempt to enter the 30 Modifiers -52, -73, and -74: Ensure proper coding at the point of care EXHIBIT A facet joint, in multiple locations, and multiple angles. We were unable to penetrate the facet joint and the procedure was then abandoned. The needles were removed and a sterile dressing was placed over the angle site. The patient was awakened from her light anesthesia and returned to the Recovery Room in satisfactory condition. She tolerated the procedure well without complications. PLAN: We will be seeing the patient in the near future in our office. We will write the patient a prescription for lyrica today, utilizing 75 mg one tablet every twelve hours for the first week and two tablets every twelve hours for the second week. Modifiers -52, -73, and -74: Ensure proper coding at the point of care 31 EXHIBIT A CASE 8 OPERATIVE REPORT 33208-74 (Can’t use 33225-74 because this is an add-on code) INDICATIONS FOR PROCEDURE: Mrs. is a middle-aged lady with an ischemic cardiomyopathy bypass grafting and a pacemaker that I placed over on the right side a number of years ago because of sick sinus syndrome. She now is being paced with left bundle branch block and left ventricular dysynchrony and class III stable systolic congestive heart failure. She had initially undergone an attempt at upgrade to biventricular device from the right subclavian vein which is the site of her earlier lead implant but unfortunately the right subclavian vein could not be cannulated. She comes back for a whole new system on the left side. PROCEDURE PERFORMD: 1. Attempted placement of a left ventricular lead 2. Attempted placement of a dual chamber pacemaker 3. Coronary sinus venogram DESCRIPTION OF OPERATIVE TECHNIQUE: The patient was brought to the electrophysiology laboratory in the fasting resting state. She underwent infusion of vancomycin. The left chest was prepped and draped sterilely. 1% lidocaine was used as local anesthetic. A 2-inch incision was made in the left pectoral region and carried down to pectoralis fascia using electrocautery. The pocket was made over the pectoralis fascia using blunt and shard dissection. The left axillary vein was cannulated via two separate needle sticks using an 18 gauge thin-wall needle and the J-wired advanced to the level of the inferior vena cava. Over one of the J-wires a 7-French sheath was placed, double wired and then advanced over one of the wires. Via this sheath, a Medtronic model #5076 lead was advanced, prolapsed across the tricuspid valve and advanced to the high right ventricular septum where it was affixed under fluoroscopic guidance. Over the separate needle stick wire, a 10.5 French sheath was introduced into the axillary vein. Next a Medtronic Attain multipurpose catheter was then advanced over an 0.025 J-wire. Initial attempts to cannulate the coronary sinus were unsuccessful with the multipurpose Attain sheath and an 0.025 J-wire. I then switched to a multipurpose inner guide catheter which was a 6= French coronary catheter and with this I still could not cannulate the vein using a wire. I then switched to an AL-2 , AL-3 and a right Judkins #4 coronary catheters and even with these end dye I could not cannulate the vein. I then switched back to a multipurpose coronary catheter and with a multipurpose guide sheath going very posteriorly I was able to inject dye imaging the interatrial septum and finally I was able to locate the os of the coronary sinus that was quite posterior and more superior than I had 32 Modifiers -52, -73, and -74: Ensure proper coding at the point of care EXHIBIT A originally thought. With dye injection immediately after the os, there was a very acute takeoff posterior vein and also a very acute takeoff coronary sinus proper. I then tried for the next hour to cannulate this vein using a multitude of inner guide catheters including the previously mentioned coronary 6-French catheters, a Medtronic navigator electrophysiology steerable radiofrequency ablation catheter and also a Medtronic steerable inner lumen catheter. I also switched out and tried a straight Attain coronary guide sheath with a variety of the aforementioned inner guide catheters. The case time was approaching three hours and we were over eighty minutes of fluoroscopy and I decided that I was going to be unable to cannulate the coronary sinus. At that point the case was aborted with the J-wires, sheaths and previously placed 5076 lead being removed. Hemostasis was obtained, the pocket irrigated with vancomycin irrigation solution, and then the pocket was closed in three layers using a 2-0 interrupted, 3-0 running and a 4-0 mattress Dexon suture. Steri-Strips and a dry sterile dressing were applied. CONCLUSION: I conclude abnormal coronary sinus anatomy precluding successful cannulation of the coronary sinus for placement of lead. RECOMMENDATIONS: I am going to go ahead to refer the patient to Dr. Armani for an epicardial LV lead. I have fully explained this to the family. Modifiers -52, -73, and -74: Ensure proper coding at the point of care 33 EXHIBIT A CASE 9 INJECTION REPORT 0062T-74 Today’s Procedure (under light MAC sedation) 1. Attempted again bilateral extrapedicular intradiscal electrothermal annuloplasty at L4-5. From both sides again, despite introducer needle being perfectly placed in center portion of the disc by AP and lateral views, a thermal catheter could not be threaded around adequately to the posterior annulus or safely within the posterior annular wall to obtain the desired positioning across the mid posterior disc annulus. We had tried this before on 10/26/05. The decision was made to retry it today before moving onto a surgical decision. Knowing that on 10/26/05 we had not been able to accomplish the catheter threading with multiple attempts, I limited the number of tries from each side today in order to assess whether we could thread the catheter again and we could not. 2. Postprocedure intradiscal corticosteroid and antibiotic injection. I did not give any local anesthetic. On the 10/26/05 procedure, I did not give local anesthetic and corticosteroid, and the patient actually did have at least 20 to 30% pain relief for two weeks and actually used half of her pain medicine compared to usual baseline and was able to go out shopping, etc. Diagnoses and Indications: 1. Lumbar discogenic pain 2. internal disc disruption and annular tears at L4-5 with positive discogram Allergies and Anticoagulants: The patient is allergic to penicillin; therefore, she received Cleocin today for her discitis prophylaxis and intradiscal postprocedure injection. Pregnancy: Negative. Procedure Note: The patient was again cleared medically an by anesthesia for the light MAC sedation. Consent was obtained and the procedure was discussed. In the fluoroscopy suite again, the patient was sterilely prepped and draped and padded in the usual fashion in the prone position. Fluoroscopy was utilized to identify the target position counting from the last rib as T12 down to the last number segment which is considered L5. There is a partial pseudoarthrosis of the right L5 transverse process to the sacral ala. The L4-5 disc space was identified. I initially approached from the right using the L5 superior articular facet process as the guide towards the L4-5 central disc space making the end plates of L4 and L5 parallel for the approach to the disc. The same technique was done on the left when we came from that side. On each side separately, surface marks were made. Superficial local anesthetic was given. A 3.5 inch, 25-gauge spinal needle was advanced down to the SAP of the particular side being approached with local anesthetic being given there and then all along the deep and intermediate muscle needle tract. Then under fluoroscopic imaging, the introducer needle was threaded down to the lateral margin of the SAP and then skiving just past it into the posterolateral annulus of the L4-5 disc. It was kept close to the SAP lateral margin in order to avoid the course of the traversing nerve root superolateral to this. With the posterior annulus engaged, the needle was 34 Modifiers -52, -73, and -74: Ensure proper coding at the point of care EXHIBIT A threaded through the introducer needle monitoring from AP and lateral views. Despite multiple attempts on the right, the catheter could not be threaded around to the posterior annular wall. It did make it to the left posterolateral corner, but I could not get it to turn that corner or stay within the disc space as far as my judgement is concerned to make it to the posterior part of the L4-L5 annulus centrally. After several attempts, this catheter was removed as was the introducer needle. The exact same set of steps was done on the left side with the same fluoroscopic guides and the local anesthetic infusions. A new catheter was used on the left and could not be threaded from that side either. With some concern for kinking of the catheter because of running into obstruction likely due to internal disc disruption, the catheter was removed without a problem as was the introducer needle. Before removing the introducer needle however, I used a combination of Decadron and Cleocin infused into the intradiscal space. 1 mL of Decadron (10 mg/mL) combined with 2 mL (150 mg/mL) of Cleocin was combined. 1.75 mL of this combination was infused in the intranuclear position. The further 1.25mL remaining was infused into the annulus and then out along the deep needle tract. The rest of the needle tract intermediate and superficial muscles were infused with 4 mL of 0.05% PF Marcaine without epinephrine for assistance in pain block. The patient tolerated the procedure well and was aroused from her light sedation and transferred herself back onto the cart. She will be brought to the recovery room. Once cleared there by Anesthesia, she will be discharged to Same Day, and once stable there will be discharged home. I will have the patient follow in the office. We will likely have to discuss with Dr. Stapler moving on to a decision about surgery options, whether fusion or disc replacement given the inability despite two bilateral attempts to avoid surgery and try to do a percutaneous decompression and annular pain fiber cauterization. Modifiers -52, -73, and -74: Ensure proper coding at the point of care 35 EXHIBIT A Summary DATA MINING AND REPORTING How do hospitals struggle? • Lack of automated edits in nonsurgery coding areas • Lack of consistency in modifier application • Documentation does not support modifier use • Feedback not provided to generating department • Misunderstanding of modifiers STEP 1 – Ask yourself: • What is the problem? o Modifier used—not needed o Modifier omitted—needed • How do you know? • What/who caused the problem? • How to correct? o TrainingProcess o improvementInterface o improvement • Train (documentation, charging, billing, coding)? • Feedback to generating department STEP 2 – Data mining and reporting: • Keep it simple and easy to understand • Make it specific (claim, service) • Get a reporting tool to provide consistent data for analysis. o Reports could be: report on remittance data from your FI top 10 cancelled scenarios in that department top procedures where the modifiers were used o Compare the same report(s) each time to avoid confusion and delay STEP 3 - Make effective—not fast—changes: 36 • You won’t resolve all problems immediately • Focus on priorities (risk/$) and drive expedient improvement here • Basics: Modifiers -52, -73, and -74: Ensure proper coding at the point of care EXHIBIT A o o o o o o • Generate reports Determine what departments are generating cancelled procedures Determine which codes are tied to those procedures Errors should be taken back to generating department to be resolved correctly and for education - Problems should be addressed at source Departments should be held accountable to bring problems to resolution Monitor reports to ensure that problems are fixed Investigate: o Inadequate chargemaster maintenance procedures o Insufficient training and regulatory updates o Lack of quality control audits o Data entry issues o Incomplete or incorrect documentation by care giver o Revenue code/CPT mismatches o Inappropriate use of modifiers o Lack of coding references o Incomplete coding policies o Interface issues STEP 4 – Solutions • Chargemaster review • Chargemaster update and maintenance procedures • Ancillary department education • Modifier implementation • Delineation of services that should be coded in the chargemaster versus in HIM • Charging forms/screens update • Coding education • Periodic audits • Process assessment • Chart audit/training • Ongoing communication • Staffing analysis • Charge protocol inadequacies • Good and consistent reporting is vital • A/R management needs strength! • 1-stop coordination is helpful Modifiers -52, -73, and -74: Ensure proper coding at the point of care 37 EXHIBIT A USA Hospital Center Medicare OP with CPT Modifier -52, -73 or -74 and CPT Range 10000-99999 Period: 01/01/05-10/31/05 38 Acct No 5645535 5646289 5647859 5648115 5649050 5650206 5650413 5650931 CPT 7609252 7609252 7609252 7609252 7609252 7609252 7609252 7609252 5651154 5652967 5653116 5655207 5655215 5656540 5657144 5657354 5657942 5658118 5661633 5664784 5666352 5667987 5668379 91110 7609252 7609252 7609252 7609252 7609252 7609252 7609252 7609252 7609252 7609252 7609252 7609252 7609252 7609252 5669792 5671090 5673248 5674353 5676221 5676500 5677506 5678191 5682783 5684130 5686091 5686118 5686489 5690034 5691428 5693326 5695425 5695870 50590 7609252 7609252 7609252 7609252 7609252 7609252 7609252 7609252 7609252 7609252 7609252 7609252 7609252 7609252 7609252 7609252 7609252 CPT Desc MAMMOGRAM, SCREENING MAMMOGRAM, SCREENING MAMMOGRAM, SCREENING MAMMOGRAM, SCREENING MAMMOGRAM, SCREENING MAMMOGRAM, SCREENING MAMMOGRAM, SCREENING MAMMOGRAM, SCREENING GI TRACT CAPSULE ENDOSCOPY MAMMOGRAM, SCREENING MAMMOGRAM, SCREENING MAMMOGRAM, SCREENING MAMMOGRAM, SCREENING MAMMOGRAM, SCREENING MAMMOGRAM, SCREENING MAMMOGRAM, SCREENING MAMMOGRAM, SCREENING MAMMOGRAM, SCREENING MAMMOGRAM, SCREENING MAMMOGRAM, SCREENING MAMMOGRAM, SCREENING MAMMOGRAM, SCREENING MAMMOGRAM, SCREENING FRAGMENTING OF KIDNEY STONE MAMMOGRAM, SCREENING MAMMOGRAM, SCREENING MAMMOGRAM, SCREENING MAMMOGRAM, SCREENING MAMMOGRAM, SCREENING MAMMOGRAM, SCREENING MAMMOGRAM, SCREENING MAMMOGRAM, SCREENING MAMMOGRAM, SCREENING MAMMOGRAM, SCREENING MAMMOGRAM, SCREENING MAMMOGRAM, SCREENING MAMMOGRAM, SCREENING MAMMOGRAM, SCREENING MAMMOGRAM, SCREENING MAMMOGRAM, SCREENING MAMMOGRAM, SCREENING Discharge Date 1/4/2005 1/8/2005 1/7/2005 1/11/2005 1/12/2005 1/14/2005 1/14/2005 1/13/2005 1/14/2005 5/5/2005 1/18/2005 1/24/2005 1/24/2005 1/25/2005 1/27/2005 1/28/2005 1/31/2005 1/28/2005 2/7/2005 2/11/2005 2/15/2005 2/17/2005 2/18/2005 2/22/2005 2/23/2005 3/1/2005 3/1/2005 3/7/2005 4/13/2005 3/7/2005 3/9/2005 3/17/2005 3/21/2005 3/24/2005 3/23/2005 5/10/2005 3/30/2005 5/19/2005 4/7/2005 5/23/2005 4/11/2005 Modifiers -52, -73, and -74: Ensure proper coding at the point of care EXHIBIT A 5696958 5697571 5699216 5700183 5701310 5702645 5704576 5706406 5709112 5709639 5715699 5715912 5716037 5716055 5717283 5718772 5719467 5720395 5720535 5721162 5722458 5724504 5725146 5725288 5725621 5725941 5728670 5729623 5730642 5730918 5734704 5738125 5738287 5738482 5741282 5741410 5742655 5755599 5756462 5762717 5763004 5763066 5766422 5766991 5767101 5768297 45378 7609252 7609252 7609252 7609252 7609252 7609252 7609252 7609252 7609252 7609252 7609252 7609252 7609252 7609252 7609252 7609252 45378 7609252 7609252 7609252 7609252 45378 7609252 7609252 7609252 7609252 45378 7609252 7609252 7609252 7609252 7609252 7609252 7609252 7609252 7609252 7609252 7609252 7609252 45330 7609252 7609252 7609252 7609252 7609252 5780232 5802309 92961 43235 DIAGNOSTIC COLONOSCOPY MAMMOGRAM, SCREENING MAMMOGRAM, SCREENING MAMMOGRAM, SCREENING MAMMOGRAM, SCREENING MAMMOGRAM, SCREENING MAMMOGRAM, SCREENING MAMMOGRAM, SCREENING MAMMOGRAM, SCREENING MAMMOGRAM, SCREENING MAMMOGRAM, SCREENING MAMMOGRAM, SCREENING MAMMOGRAM, SCREENING MAMMOGRAM, SCREENING MAMMOGRAM, SCREENING MAMMOGRAM, SCREENING MAMMOGRAM, SCREENING DIAGNOSTIC COLONOSCOPY MAMMOGRAM, SCREENING MAMMOGRAM, SCREENING MAMMOGRAM, SCREENING MAMMOGRAM, SCREENING DIAGNOSTIC COLONOSCOPY MAMMOGRAM, SCREENING MAMMOGRAM, SCREENING MAMMOGRAM, SCREENING MAMMOGRAM, SCREENING DIAGNOSTIC COLONOSCOPY MAMMOGRAM, SCREENING MAMMOGRAM, SCREENING MAMMOGRAM, SCREENING MAMMOGRAM, SCREENING MAMMOGRAM, SCREENING MAMMOGRAM, SCREENING MAMMOGRAM, SCREENING MAMMOGRAM, SCREENING MAMMOGRAM, SCREENING MAMMOGRAM, SCREENING MAMMOGRAM, SCREENING MAMMOGRAM, SCREENING DIAGNOSTIC SIGMOIDOSCOPY MAMMOGRAM, SCREENING MAMMOGRAM, SCREENING MAMMOGRAM, SCREENING MAMMOGRAM, SCREENING MAMMOGRAM, SCREENING CARDIOVERSION, ELECTRIC, INT UPPR GI ENDOSCOPY, DIAGNOSIS Modifiers -52, -73, and -74: Ensure proper coding at the point of care 4/15/2005 4/14/2005 4/15/2005 5/4/2005 4/25/2005 4/22/2005 4/27/2005 4/28/2005 6/24/2005 5/6/2005 5/18/2005 5/16/2005 5/17/2005 5/17/2005 5/19/2005 5/24/2005 7/21/2005 6/1/2005 5/27/2005 5/25/2005 5/27/2005 6/3/2005 6/6/2005 6/28/2005 7/27/2005 7/28/2005 8/4/2005 6/14/2005 7/29/2005 8/9/2005 6/24/2005 6/27/2005 7/1/2005 7/1/2005 7/7/2005 7/6/2005 7/6/2005 8/5/2005 8/3/2005 8/12/2005 8/16/2005 8/16/2005 8/25/2005 8/24/2005 8/25/2005 8/26/2005 9/14/2005 10/24/2005 39 EXHIBIT A Snapshot Comparison Chart of the Modifiers Pre-2006 As of 2006 40 Modifier -52 Modifier -73 Modifier -74 No discount 50% No discount 50% 50% No discount Modifiers -52, -73, and -74: Ensure proper coding at the point of care Exhibit B EXHIBIT B Modifiers negate need for C codes with device-dependent procedures from Briefings on APCs In this month’s Modifier Clinic, Lolita Jones, RHIA, CCS, of Lolita M. Jones Consulting in Fort Washington, MD, discusses how modifiers negate the need for reporting a C code with a devicedependent procedure. Per the OPPS 2005 final rule published in the November 15, 2004, Federal Register, for services provided on or after January 1, 2005, CMS requires hospitals to report device category HCPCS C codes on claims when providers use these devices in conjunction with procedures billed and paid for under OPPS. To ensure hospital compliance with these device coding requirements, CMS provides updated lists of these codes on the agency’s Web site at www.cms.hhs.gov/providers/hopps/default.asp. The current version is the October 2005 device code edits, which you can find near the bottom of the Web page. For example, per the October 2005 device code edits, if you report CPT code 63650 (Percutaneous implantation of neurostimulator electrode array, epidural), you must also report device code C1778 (Lead, neurostimulator [implantable]). Modifiers negate need However, modifiers -73 (Discontinued service/procedure prior to anesthesia) and -74 (Discontinued service/procedure after anesthesia) allow providers to bypass these new edits, since these modifiers signify an interrupted procedure. “CMS recognizes that in those cases, the procedure might have been interrupted before the device was implanted,” Jones says. Below is a case study that includes a physician’s notes about a procedure for which a coder reports a device-related CPT code with a modifier indicating a discontinued procedure. Case study: Discontinued device-dependent procedure Preoperative diagnosis: 1. Lipoprotein lipase (LPL) syndrome with radiculopathy; significant epidural fibrosis and septi Postoperative diagnosis: 1. LPL syndrome with radiculopathy; 2. Significant epidural fibrosis and septi Procedure: Attempted spinal cord stimulator lead placement at T12-L1 to T9 and at L5-S1 to T9 and to T12 Anesthesia: Local with IV sedation Complications: None Narrative of procedure: The patient was in the operating room status post epidurogram for neural mapping at T12-L1 and L5-S1 (epidurogram report is on file). At T12-L1 level with the needle in place, a Pisces-Quad™ electrode was placed through the needle and guided up 42 Modifiers -52, -73, and -74: Ensure proper coding at the point of care EXHIBIT B just to the right of midline at T9. When using multiple configurations with programming, the patient could not feel any stimulation. The electrode was then pulled back and reguided in the midline to the superior aspect of T9 and again the patient could not feel any sensation. The catheter was then pulled back and guided up to the T8 right of midline. The patient could not feel any sensation. The catheter was pulled back again and guided to a more lateral position at the T9 level and duplicated the exact configuration that was seen on the trial. The patient again could not feel any sensation. The electrode was then trolled down all the way to L2 and the patient could not feel any sensation. At this point I elected to remove the needle and place it in again, this time at the L5-S1 level. Again, using numerous configurations and multiple advancements and positions, I could not cause any sensation in the patient’s right lower extremity or hip. After spending approximately 50 minutes attempting to manipulate the catheter and electrode to various positions and programming, I could not get the patient to feel any sensation. Therefore, I elected to abort the remainder of the procedure. No incision was made. The needles were removed. The patient was discharged to the recovery room where I talked to him, his wife, and family. Coding-modifier rationale The correct code to report for this case study is 63650-74. The physician attempted this patient’s procedure after administering a local anesthetic with conscious sedation to the patient, therefore, modifier -74 is appropriate. The intended procedure was the percutaneous implantation of an electrode, therefore code 63650 is appropriate. The device code edit for code 63650—used by the Medicare fiscal intermediary—does not require coders to report device code C1778 if the procedure is appended with modifier -74 (Discontinued outpatient procedure after anesthesia administration). “However, the hospital will not be penalized if [it] reports C1778, since the electrode was in fact utilized in this unsuccessful attempt to stimulate the patient,” Jones says. Modifiers -52, -73, and -74: Ensure proper coding at the point of care 43 EXHIBIT B New reporting guidelines for modifiers -52, -73, and -74 CMS now considers conscious sedation part of anesthesia from Briefings on APCs CMS released on January 21, 2005 a major update that both clarifies and changes the reporting of modifiers -52, -73, and -74. Most significantly, CMS now considers conscious sedation a part of anesthesia and requires the reporting of these modifiers to reflect this new definition. The changes took effect February 22, 2005. Go to www.cms.hhs.gov/manuals/pm_trans/R442CP.pdf to read CMS Transmittal 442, “Use of modifiers -52, -73, and -74 for reduced or discontinued services.” “This is a major change,” says Lolita Jones, RHIA, CCS, of Lolita M. Jones Consulting in Fort Washington, MD. “For the past four and a half years, a CMS guideline has prohibited hospitals from reporting modifiers -73 and -74 for discontinued procedures involving conscious sedation.” The old guideline derived from a question and answer CMS posted on its OPPS claims processing Web site in September 2000. In the guidance on reporting modifier -52 with a colonoscopy, CMS’ answer limited the definition of anesthesia to local, regional block, or general. Anesthesia gets new definition Effective February 22, 2005, the definition of anesthesia changed. In Transmittal 442, CMS states that for purposes of billing for services furnished in the hospital outpatient department, anesthesia includes • local • regional block(s) • moderate sedation/analgesia (“conscious sedation”) • deep sedation/analgesia • general anesthesia This manual revision also clarifies that providers cannot use modifiers -73 and -74 in the reporting of discontinued radiology procedures that do not require anesthesia. Modifier -52 indicates partial reduction or discontinuation of radiology procedures and other services that do not require anesthesia. Instead, facilities should use modifier -73 to indicate that a surgical or diagnostic procedure requiring anesthesia was terminated due to extenuating circumstances or those that threatened the well-being of the patient after preparation for the procedure (including procedural premedication when provided) and transfer to the site of the procedure, but prior to administration of anesthesia. “This modifier was created so that the costs incurred by the hospital to prepare the patient for the procedure and the resources expended in the procedure room and recovery room (if needed) could be recognized for payment even though the procedure was discontinued,” Jones says. Use modifier -74 to indicate that a surgical or diagnostic procedure requiring anesthesia was terminated after the induction of anesthesia or after start of the procedure (e.g., incision made, intubation started, scope inserted) due to extenuating circumstances or circumstances that threatened the well-being of the patient. 44 Modifiers -52, -73, and -74: Ensure proper coding at the point of care EXHIBIT B “This modifier was created so that the costs incurred by the hospital to initiate the procedure—preparation of the patient, procedure room, recovery room—could be recognized for payment, even though the procedure was discontinued prior to completion,” she says. Case scenarios With the above information as guidance, read the following two case studies to understand how the new guidance operates in real-life scenarios. Case study 1 Discontinued outpatient hospital/ASC procedure after anesthesia. Colorectal cancer screening; colonoscopy on high-risk individual. Operative report Procedure: Colonoscopy Indications: Family history of colon cancer Instrument: Olympus video colonoscope CF 100L Pre-medication: Versed 4 mg, Demerol 75 mg Description of procedure: A 75-year-old patient presents for a colonoscopy. He understands the nature of the procedure, the risks and consequences, and alternative procedures, and consents to the procedure. The patient receives educational materials, information on the risks of the procedure, and answers to frequently asked questions. The patient is placed in the left lateral decubitus position. The rectal exam reveals normal sphincter tone and no masses. A colonoscope is introduced into the rectum and advanced to the distal sigmoid colon. Further advancement is impossible due to the marked fixation and severe angulation of the rectosigmoid colon. On withdrawal, no masses or polyps are noted and the mucosa is normal throughout. Retroflexion in the rectal vault is unremarkable. The patient tolerates the procedure without difficulty. Final impression: Normal colonoscopy, only to the distal sigmoid colon. Plan: Strong recommendation for a barium enema. Coding: G0105-74 (Colorectal screening, high risk individual). Use G0105 because this is a colonoscopy screening exam. No signs or symptoms necessitate this exam performed on a highrisk patient due to a family history of colon cancer. Case study 2 Discontinued outpatient hospital/ASC procedure without anesthesia. Colonoscopy through stoma; diagnostic, with or without collection of specimen(s) by brushing or washing (separate procedure). Operative report Preoperative diagnosis: History of colon cancer with recent constipation Postoperative diagnosis: Inability to intubate the stoma site, questionable stricture at the colostomy site Modifiers -52, -73, and -74: Ensure proper coding at the point of care 45 EXHIBIT B Procedure performed: Attempted colonoscopy through colostomy site Anesthesia: None Instrument: Olympus video colonoscopy tried first, then Olympus video upper endoscope of smaller caliber Complications: None Description of procedure: Patient is placed in the supine position and the colostomy bag is removed. The colostomy site is identified and lubricated. The instrument is inserted into the ostomy and insufflated. Physician makes several attempts to intubate the colon through the colostomy site but is unsuccessful. Final impression: Questionable stricture of the ostomy site. Plan: Barium enema via colostomy to delineate the anatomy. Follow up based on the findings of the barium enema. Disposition: Patient is discharged without recovery because she did not receive any conscious sedation. The physician will see her again two weeks after the barium enema for further management. Coding: 44388-52. Use code 44388 (Colonoscopy), and per Medicare Transmittal 442, use modifier -52 for services that do not require anesthesia. Additional clarifications in Transmittal 442 • Bilateral modifier -50. Per the Transmittal, you may report bilateral procedure modifier -50 with diagnostic and radiology procedures, as well as with surgical procedures. Use it to report bilateral procedures performed at the same operative session as a single line item. Do not use modifiers -RT and -LT when modifier -50 applies. Report a bilateral procedure on a single line of the claim using modifier -50. Modifier -50 applies to any bilateral procedure performed on both sides at the same session. • Termination of multiple planned procedures. When you complete one or more planned procedures, report them as usual. Do not report other planned but not started procedure(s). When you complete none of the planned procedures, but have prepared the patient and taken him or her the procedure room, append the first procedure that was planned (but not completed) with modifier -73. If you begin the first procedure (e.g., scope inserted, intubation started, incision made, etc.) and/or give the patient anesthesia, use modifier -74. Do not report the other procedures. If you terminate the first procedure prior to the induction of anesthesia and before the transfer of the patient into the procedure room, do not report the procedure. The patient must be moved to the room where the procedure is to be performed for you to report modifier -73 or -74. Outstanding issues raised by Transmittal 442 Transmittal 442 does not clearly address some issues pertaining to reporting modifiers -52, -73, and -74. Industry experts say CMS will likely clarify them in a future transmittal. 46 Modifiers -52, -73, and -74: Ensure proper coding at the point of care EXHIBIT B In the meantime, Lolita M. Jones, RHIA, CCS, of Lolita M. Jones Consulting in Fort Washington, MD tells providers to contact Dana Burley ([email protected]), the listed Transmittal contact at CMS for further assistance. Per Transmittal 442, “discontinued radiology procedures that do not require anesthesia can not be reported using modifiers -73 and -74.” However, CMS doesn’t state whether providers can report discontinued interventional radiology procedures with modifiers -73 and -74. “Interventional radiology procedures have both a radiological and surgical/procedural component,” Jones says. For example, when a patient undergoes a percutaneous transluminal angioplasty, radiological imaging for the placement of the balloon is used to perform the procedure, which is the balloon dilation/angioplasty of the vessel. Also, per Transmittal 442, “modifier -52 indicates partial reduction or discontinuation of radiology procedures and other services that do not require anesthesia.” Training manual OPPS guidelines used by CMS contractors in 2000 said, “Do not use modifier -52 if there is a code that classifies the extent of the procedure that was performed. “ “However, in the Transmittal 442, CMS doesn’t state whether it is still appropriate to code to the extent of the procedure performed,” Jones says. Modifiers -52, -73, and -74: Ensure proper coding at the point of care 47 Resources "Modifier -52, -73, and -74" audioconference attendees SAVE $50! Briefings on APCs The editorial team at Briefings on APCs is already on staff with your peers across the country. Why not join this winning team? Who’s going to keep your APC staff on track with the 2006 OPPS rule and quarterly changes? Are you billing drug administration according to CMS’ guidelines? 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