Chapter 2 Setting Up an Endoscopy Facility
Introduction
The safe and efficient performance of gastrointestinal (GI) endoscopy has the following requirements:1
Many of the above-listed requirements for safe and efficient GI endoscopy depend on the careful development of endoscopy areas—specifically the setting up or planning and design of an endoscopy facility. This chapter describes that process, beginning with laying the groundwork, including the development of a business plan and review of regulatory issues; site selection; facility planning and design, including patient flow and space needs; equipment requirements; staffing needs; and scheduling considerations. Some additional issues, such as endoscope cleaning and storage, tissue specimen processing and handling, record keeping and documentation, and quality assurance and improvement, are discussed briefly but are covered in more detail in subsequent chapters of this book (see Chapters 4, 5, and 9).
Exploring Possibilities
Type of Facility
The decision regarding which type of facility to establish is affected by the practice environment (solo practitioner, small or large group, single-specialty or multispecialty group, independent or hospital-based) and local economics and politics. Regardless of the service location, high quality must be maintained. The American Society for Gastrointestinal Endoscopy (ASGE) has stated that the “standards for out-of-hospital endoscopic practice should be identical to those recognized guidelines followed in the hospital.”1 In an insurance-based environment, the hospital-based unit poses the fewest financial risks and demands for the endoscopist during the early phases of operation, and its use avoids alienating hospital administration by preserving hospital case volume. The hospital-based unit affords the endoscopist little control over operations, however, and offers him or her the lowest total financial return. Office endoscopy offers control and convenience with better financial return for the physician, but it poses some safety and liability concerns.8,9 A single-specialty endoscopic ambulatory surgery center (EASC) provides the best of control, efficiency, convenience, and reimbursement for the physician owners and is extremely popular with patients, referring physicians, and payers.10,11 At the time of this writing, a major ASC payment reform is being implemented by the Centers for Medicare and Medicaid Services (CMS), which is resulting in drastic cuts of facility payments for endoscopic services. How this reform will affect efforts to provide beneficial GI services to patients at a reasonable cost remains to be seen. More information about this payment reform is available elsewhere.12 Regardless of the type of facility being developed, formulating a business plan and understanding various regulatory issues are usually the first steps in the process.
Business Plan
The decision to set up an endoscopy facility should be made only after detailed data gathering and the formulation of a business plan (e.g., market analysis, financial pro forma, implementation time line).13–15 For a hospital-based unit or academic medical center, facility planners and accountants often perform these functions. For an office-based suite or an EASC, the tasks fall to the physician owners, aided by numerous consultants, contractors, or corporate partners. Even with skilled help, however, development of an accurate and reliable business plan and pro forma are highly dependent on physician estimates, insights, and work habits. Physician input into the business plan makes the difference between a perfunctory exercise and an accurate predictor of future performance. Endoscopy facilities represent small to medium-sized investments requiring substantial financial resources and staff. Procedure volume must be sufficient to produce adequate revenue to cover the costs of building and running the facility and to generate a profit on investment. Generally, three or four busy endoscopists performing 1200 to 1800 total procedures per year are required to offset the financial risk of the facility.16
Many factors influence the financial performance of an endoscopy facility, including initial investment, expected volumes of service, revenue per unit of service, fixed operating costs, and variable costs per unit of service. The initial investment includes the cost of construction, equipment, and working capital for the first few months of operation. Strategic planning is important to anticipate group growth and demand for services in the coming 5 to 10 years.13,15 The impact of managed care plans or other major health plans on the practice must also be anticipated. In addition, competition, new technology, population changes, and demographics might affect case volume for the practice and the endoscopy facility.
A pro forma is a calculation examining the financial feasibility of a project based on anticipated investment and operating costs and revenues. The purpose of the pro forma is to predict reliably cash flows and profitability for the project. Initial investment costs have been defined previously. Also incorporated in the pro forma are estimated total costs per case based on estimated fixed and variable costs and expected case volume. Fixed costs are costs that remain constant regardless of the number of procedures performed and include rent, interest, depreciation, taxes, insurance, amortization, and management fees. Variable costs, which account for the largest component of the average cost per case, include salaries and benefits, medical supplies, medications, equipment, maintenance and repair, administrative supplies, utilities, and accounting and legal fees. Break-even volumes can be determined by subtracting the variable expense per procedure from the average payment per procedure to indicate the contribution available to be used for overhead and profit. Dividing fixed costs by the contribution margin per procedure indicates the number of procedures needed to pay the fixed costs, also known as the break-even point. Additional service units above that level constitute profit. Vicari and Garry13 provided a simple example of a pro forma. The business plan and pro forma are mandatory in assessing the financial feasibility of the proposed endoscopy unit before construction. They further aid discussions in obtaining financing and help the architect design the unit for anticipated volumes.
Regulatory and Certification Issues
Before planning and designing the facility, one must understand the relevant regulatory and certification issues. As with the business plan, units developed in a hospital or academic medical center usually benefit from administrators and planners familiar with these complex issues. Physician owners of an office endoscopy suite or EASC must gain their own understanding. Various agencies provide myriad rules and regulations concerning endoscopy facilities.17–23 Legislation can come from federal, state, or local authorities. Regulations may come from federal agencies, state departments of health, and third-party accreditation organizations and private payers. Although these rules and regulations can seem excessive and needlessly costly, their intent is to ensure safe and successful outcomes for patients. Regulations and certification issues for endoscopy facilities can be divided into six main categories, as follows:17
Medicare Certification
Medicare certification is usually sought after obtaining state licensure and is required for any facility seeking reimbursement for Medicare and Medicaid work. Medicare regulations and requirements are usually more extensive than regulations of the state and address governance of the facility, transfer agreements with a nearby hospital, continuous quality improvement activities, Medicare architectural requirements, and medical records. Additional standards concern organization and staffing, administration of drugs, and procurement of laboratory and radiology services. Two other requirements warrant special attention as they relate to EASCs. First, the facility must be used exclusively for providing “surgical” services, a definition that includes GI endoscopies. This requirement mandates a separation from other health care activities, separate staffing, and maintenance of special medical and financial records. Finally, the facility must comply with state licensure laws,20 which is potentially difficult in some states because of restrictive CON requirements.
Payer Requirements
Individual health plans or insurers may have their own requirements, and these may vary significantly from payer to payer. Careful attention to local payer mix and any special requirements is necessary before designing and building an endoscopy facility to ensure qualification for payment. As outlined previously, the regulatory and certification issues for endoscopy facilities are “complex, detailed, and broad.”17 Any physician wishing to develop an endoscopy facility must understand these rules of regulation and certification. Appropriate legal counsel should be considered essential.
Facility Planning and Design
After forming a realistic business plan and acquiring an understanding of relevant regulatory and certification issues, attention turns to the planning and design of the facility. Although the remainder of this chapter includes some remarks about issues specifically related to hospital units, the main focus of the discussion is on the development of an outpatient endoscopy facility, details of which are equally applicable to hospital units. Objectives must be articulated to the design professionals to ensure that the facility meets the needs of patients, endoscopists, and staff. Some points to keep in mind are the following:24