MO Optometry Jurisprudence study materials
MO Optometry Jurisprudence study resources

MO Optometry Jurisprudence study plan

MO Optometry Jurisprudence · Give each week a clear focus.

8 weeks · About 6 hours per week

Week 1

Statutory framework: optometry practice act, definitions, scope of practice

  • Outline the structure of the Missouri optometry practice act, identifying the sections that define scope of practice, licensure, and board authority.

  • Define key statutory terms such as 'optometry,' 'practice of optometry,' and 'licensee' in your own words, citing the relevant section numbers.

  • List the allowed and prohibited acts under the scope of practice, including surgical and pharmaceutical limitations.

  • Compare the statutory scope with the board's rules to identify any additional restrictions or clarifications.

  • Create a one-page summary table of the statutory framework for quick reference.

Your checkpoint

A one-page summary table of the statutory framework with section references.

Week 2

Statutory framework: optometry practice act, definitions, scope of practice & Licensure: requirements, application, examination, reciprocity and endorsement

  • Explain the licensure pathways (examination, reciprocity, endorsement) and the specific requirements for each.

  • Describe the application process, including required documents, fees, and timelines, from the board's rules.

  • Identify the examination requirements, including passing scores and any required components.

  • Summarize reciprocity and endorsement provisions, noting any conditions or additional qualifications.

  • Outline the steps for licensure by examination versus by endorsement in a flowchart.

Your checkpoint

A flowchart comparing licensure by examination and by endorsement, with key requirements annotated.

Week 3

Missouri State Board of Optometry: composition, powers, duties, and procedures

  • Describe the composition of the Missouri State Board of Optometry, including member qualifications and appointment process.

  • List the board's powers and duties, such as rulemaking, licensing, and disciplinary authority.

  • Explain the board's procedures for meetings, hearings, and investigations, including notice and quorum requirements.

  • Identify the statutory basis for board actions and the limits of its authority.

  • Create a diagram of the board's organizational structure and decision-making process.

Your checkpoint

An organizational diagram of the board with a brief explanation of each role and procedure.

Week 4

License renewal, continuing education, and lapsed or inactive status

  • Detail the license renewal cycle, including deadlines, fees, and late penalties.

  • List the continuing education requirements, including hours, approved topics, and documentation.

  • Explain the procedures for inactive or lapsed licenses, including reactivation requirements.

  • Identify common pitfalls that lead to lapsed status and how to avoid them.

  • Develop a personal renewal checklist that incorporates CE tracking and deadlines.

Your checkpoint

A personal renewal and CE tracking checklist with deadlines and required documentation.

Week 5

Grounds for discipline, complaint handling, and disciplinary proceedings

  • Enumerate the statutory grounds for discipline, such as unprofessional conduct, incompetence, and violations.

  • Describe the complaint handling process from filing to resolution, including investigation and hearing procedures.

  • Outline the disciplinary proceedings, including due process rights, appeals, and sanctions.

  • Differentiate between minor violations and serious offenses, and the typical disciplinary actions for each.

  • Analyze a hypothetical complaint scenario and map it to the disciplinary process.

Your checkpoint

A case study analysis of a hypothetical complaint, mapping each step to the statutory process.

Week 6

Pharmaceutical agents: certification, prescribing authority, and limitations

  • Explain the certification process for pharmaceutical agents, including educational and examination requirements.

  • List the categories of pharmaceutical agents that optometrists may prescribe and any limitations.

  • Describe the prescribing authority, including dosage, duration, and recordkeeping requirements.

  • Identify the restrictions on prescribing, such as prohibited drugs and referral obligations.

  • Create a reference sheet of allowed and prohibited pharmaceutical agents with key limitations.

Your checkpoint

A reference sheet summarizing pharmaceutical certification requirements and prescribing limitations.

Week 7

Patient records, confidentiality, informed consent, and release of information & Advertising, fee splitting, referrals, and unprofessional conduct

  • Outline the requirements for patient records, including retention periods, content, and confidentiality.

  • Explain informed consent requirements and the release of information procedures, including HIPAA considerations.

  • Identify prohibited advertising practices, such as false or misleading claims.

  • Describe the rules on fee splitting and referrals, including permitted and prohibited arrangements.

  • Define unprofessional conduct and give examples relevant to advertising and fee arrangements.

Your checkpoint

A compliance checklist for patient records, informed consent, and advertising practices.

Week 8

Unlicensed practice, delegation, and supervision of ancillary personnel

  • Define unlicensed practice and identify activities that constitute it.

  • Explain the rules for delegation and supervision of ancillary personnel, including allowed tasks and supervision levels.

  • Describe the consequences of improper delegation or supervision.

  • Review all domains through practice questions, focusing on weak areas.

  • Develop a one-page quick-reference guide for unlicensed practice and delegation rules.

Your checkpoint

A one-page quick-reference guide on unlicensed practice and delegation, plus a self-assessment quiz score of at least 80%.

Milestones

Week 4: Score at least 80% on a 30-question cumulative quiz covering Domains 1–4, and complete the personal renewal checklist.

Week 6: Score at least 80% on a 20-question quiz covering Domain 6, and correctly identify all allowed and prohibited pharmaceutical agents on the reference sheet.

Week 8: Pass a 50-question comprehensive practice exam with a score of 75% or higher, and submit all deliverables for review.