Emergency Sections An agency may adopt a new or amended section or repeal an existing section on an emergency basis if it determines that such action is necessary for the public health, safety, or welfare of this state. The section may become effective immediately upon filing with the Texas Register, or on a stated date less than 20 days after filing, for no more than 120 days. The emergency action is renewable once for no more than 60 days. Symbology in amended emergency sections. New language added to an existing section is indicated by the use of bold text. [Brackets] indicate deletion of existing material within a section. TITLE 25. HEALTH SERVICES Part I. Texas Department of Health Subchapter 98. HIV and STD Control Subchapter C. Texas HIV Medication Program General Provisions 25 TAC sec.98.104, sec.98.105 The Texas Department of Health (department) adopts on an emergency basis amendments to existing sec.98.104 and sec.98.105, concerning the Texas HIV Medication Program. The sections implement the provisions of the "Communicable Disease Prevention and Control Act," Health and Safety Code, Chapter 85.063, Subchapter C, concerning the Texas HIV Medication Program. The program assists hospital districts, local health departments, public or nonprofit hospitals and clinics, nonprofit community organizations, and HIV infected individuals in the purchase of medications approved by the board that have been shown to be effective in reducing hospitalizations due to HIV related conditions. Generally, the sections cover eligibility for participation and medication coverage. The amendments expand coverage of the program to include atovaquone for eligible participants and adds language to make the two sections uniform. Atovaquone will be used as an oral treatment for acute mild to moderate Pneumocystis carinii Pneumonia (PCP)
    in patients who are intolerant to trimethoprim-sulfamethoxazole (SMZ-TMP) to reduce the hospitalization and decline of the general health of the HIV infected persons on this program. These amendments are being proposed for permanent adoption in this issue of the Texas Register. The amendments are adopted on an emergency basis in order to expeditiously provide medications to HIV infected individuals. It is imperative to address this serious and imminent health condition by providing approved medications as soon as possible. Also these amendments are proposed for permanent adoption in this issue of the Texas Register. 12> The amendments are adopted on an emergency basis under the Health and Safety Code, sec.85.063, which provides the Texas Board of Health with the authority to adopt rules concerning a Texas HIV Medication Program; and Health and Safety Code, s12.001, which provides the Texas Board of Health with the authority to adopt rules for the performance of every duty imposed by law on the Texas Board of Health, the Texas Department of Health, and the Commissioner of Health; and Texas Civil Statutes, Article 6252-13a, sec.5, which provide the Board with authority to adopt rules on an emergency basis. sec.98.104. Medication Coverage. The following medications will be provided to each eligible participant. (1)
      [(a)] Zidovudine capsules must be provided in increments of 100 not to exceed 400 capsules per month. Zidovudine syrup must be provided in eight ounce bottles. (2)
        [(b)] Pentamidine for inhalation solution must be provided in one 300 mg. vial per month. (3)
          [(c)] Sulfamethoxazole-trimethoprim (DS) tablets must be provided in increments of 100 tablets for a maximum of 200 per month. Sulfamethoxazole- trimethoprim suspension must be provided in bottles of 480 ml. (4)
            [(d)] Didanosine tablets must be provided in increments of 60 tablets not to exceed 120 tablets per month. (5)
              [(e)] Fluconazole must be provided in increments of 30 tablets not to exceed 120 tablets in three months. (6)
                [(f)] Erythropoietin is provided through the Texas HIV Medication Program for children younger than 18 years of age. Adults and children that meet the financial and drug specific criteria will be eligible to receive this drug under the Ortho Biotech program. (7)
                  [(g)] Immune Globulin Intravenous (Human) will be provided in 2.5 and 5 gm. vials. (8)
                    [(h)] Texas HIV Medication Program will reimburse the Tuberculosis Elimination Division for the following listed drugs used to treat atypical mycobacterial infections in individuals that are HIV infected: (A)
                      [(1)] Amikacin-1 g vial; (B)
                        [(2)] Capreomycin-1 g vial; (C)
                          [(3)] Ciprofloxacin-750 mg. tablets; (D)
                            [(4)] Cycloserine-250 mg. capsules; (E)
                              [(5)] Ethambutol-100 mg. tablets; (F)
                                [(6)] Ethambutol-400 mg. tablets; (G)
                                  [(7)] Ethionamide-250 mg. tablets; (H)
                                    [(8)] Isoniazid (INH) syrup; (I)
                                      [(9)] Isoniazid (INH)-100 mg. tablets; (J)
                                        [(10)] Isoniazid (INH)-300 mg. tablets; (K)
                                          [(11)] Kanamycin-1 g vial; (L)
                                            [(12)] Pyrazinamide-500 mg. tablets; (M)
                                              [(13)] Pyridoxine (Vit.B-6)-50 mg. tablets; (N)
                                                [(14)] Rifampin-300 mg./Isoniazid (INH) 150 mg. capsules; (O)
                                                  [(15)] Rifampin-300 mg. capsules; (P)
                                                    [(16)] Sodium P.A.S. tablets; and (Q)
                                                      [(17)] Streptomycin-5 g. (9)
                                                        [(i)] Acyclovir capsules must be provided in increments of 100, not to exceed 200 per month. Acyclovir suspension must be provided in 473 ml. bottles of 200 mg./ml., not to exceed two bottles per month. Acyclovir powder for injection must be provided in 500 mg. vials, not to exceed 2-10 ml. vials per month. (10)
                                                          [(j)] Zalcitabine tablets must be provided in increments of 100 not to exceed 100 tablets per month. (11)
                                                            [(k)] IV Pentamidine must be provided in 300 mg. vials not to exceed 14 vials per course of therapy (one vial per day for 14 days). (12)
                                                              [(l)] Interferon-Alpha must be provided in commercially available vials not to exceed 450 million units
                                                                [50 million unit vials not to exceed nine] per month. (13)
                                                                  [(m)] Amphotericin-B must be provided in 50 mg. vials not to exceed 40 per month. (14) Atovaquone must be provided in increments of 200 tablets not to exceed 200 tablets per 21-day treatment therapy following each diagnosis. sec.98.105. Drug specific eligibility criteria. A person is eligible for: (1)-(9) (No change.) (10) Interferon-Alpha for the treatment of disseminated Kaposi's sarcoma in HIV infected persons with T-cell counts over 500. The total amount to be expended on this drug is $122, 600. The requesting physician must complete a form to be returned to the program which will allow the program to evaluate the benefits of providing this medication; [and] (11) Amphotericin-B for the treatment of patients with progressive, and potentially fatal disseminated fungal infections. The total amount to be expended on this drug is $46,200. The requesting physician must complete a form to be returned to the program which will allow the program to evaluate the benefits of providing this medication; and
                                                                    [.] (12) Atovaquone for the oral treatment of acute mild to moderate Pneumocystis carinii Pneumonia (PCP) in patients who are intolerant to trimethoprim-sulfamethoxazole (TMP-SMX). Issued in Austin, Texas, on March 23, 1993. TRD-9320724 Robert A. MacLean, M.D. Deputy Commissioner Texas Department of Health Effective date: March 23, 1993 Expiration date: July 21, 1993 For further information, please call: (512) 458-7500