How often should a treatment and services plan be assessed?
An individual's treatment and services plan must be assessed continually and modified as necessary to ensure that it meets his or her changing needs. A patient may require varying combinations of services and treatment components during the course of treatment and recovery.
How long should a patient stay in treatment?
Remaining in treatment for an adequate period of time is critical. The appropriate duration for an individual depends on the type and degree of the patient’s problems and needs.
How often should a treatment and rehabilitation plan be updated?
Treatment Plan Updates Due Treatment and rehabilitation plans shall be reviewed and updated at least every 30 days. For those projects whose client treatment regime is less than 30 days, the treatment and rehabilitation plan, review and update shall occur at least every 15 days.
Is there a single treatment that is appropriate for everyone?
No single treatment is appropriate for everyone. Treatment varies depending on the type of drug and the characteristics of the patients.
What is the definition of a suicidal ideation Pmkee?
what is the definition of a suicidal ideation? a thought or plan. which of the following component is NOT part of the personal financial management program? financial assistance.
When operating electrical equipment the term one hand rule is best defined by which of the following?
When operating electrical equipment, the term "one-hand rule" is best defined by which of the following phrases? Always energize or turn on electrical equipment with one hand free.
What device on a ribbon indicates additional awards received for participation?
A service star is a miniature metal device worn by members of the seven uniformed services of the United States on medals and ribbons issued by the uniformed services to denote additional awards or periods of service.
Which of the following conditions is the most likely cause of suicide or attempted?
Depression is the most common condition associated with suicide, and it is often undiagnosed or untreated. Conditions like depression, anxiety, and substance problems, especially when unaddressed, increase risk for suicide.
Who is responsible for establishing policy and ensuring FAP meets command sailor and family members needs?
b. NAVPERSCOMb. NAVPERSCOM (PERS-61) is responsible for establishing policy and ensuring that the program meets command, Sailor, and family member needs.
When in uniform under what situation is a cell phone permitted to be worn on a belt?
(b) Only one communication device is authorized for wear and can only be worn on the belt of Working and Service Uniforms aft of the elbow.
What does Bronze Star on Vietnam Service Medal mean?
The Bronze Star is awarded for meritorious service or acts of valor while serving in combat operations.
How many lines is a NAM?
Non-combat citations are limited to 7 ½ lines. A citation consists of three parts: 1.
What does a gold star on a military ribbon mean?
Gold stars are worn with medals and ribbons issued by the Navy, Marine Corps, Coast Guard, Public Health Service, and National Oceanographic and Atmospheric Administration, and United States Air Force to indicate the second and subsequent awards of a particular medal.
What are the steps to take if someone is suicidal?
Here's what you can do.Encourage the person to call a suicide hotline number. ... Encourage the person to seek treatment. ... Offer to help the person take steps to get assistance and support. ... Encourage the person to communicate with you. ... Be respectful and acknowledge the person's feelings. ... Don't be patronizing or judgmental.More items...
What are some signs symptoms of someone who is experiencing suicidal thoughts tendencies?
Suicide Warning SignsSevere sadness or moodiness. Long-lasting sadness, mood swings, and unexpected rage.Hopelessness. ... Sleep problems.Sudden calmness. ... Withdrawal. ... Changes in personality or appearance. ... Dangerous or self-harmful behavior. ... Recent trauma or life crisis.More items...•
What are the three steps in the intervention process for faculty and staff?
Enact a three-step intervention to help a person at risk for suicide: Question – question to determine if the person is at risk for suicide. Persuade – persuade the person at risk to seek help. Refer – refer to treatment.
What is a covered entity's notice of privacy practices?
A covered entity is required to provide the individual with adequate notice of its privacy practices, including the uses or disclosures the covered entity may make of the individual’s information and the individual’s rights with respect to that information.
What is the right to request privacy protection?
Individuals have the right to request restrictions on how a covered entity will use and disclose protected health information about them for treatment, payment, and health care operations. A covered entity is not required to agree to an individual’s request for a restriction, ...
What is the minimum necessary requirement for a covered entity?
A covered entity must develop policies and procedures that reasonably limit its disclosures of, and requests for, protected health information for payment and health care operations to the minimum necessary . A covered entity also is required to develop role-based access policies and procedures that limit which members of its workforce may have access to protected health information for treatment, payment, and health care operations, based on those who need access to the information to do their jobs. However, covered entities are not required to apply the minimum necessary standard to disclosures to or requests by a health care provider for treatment purposes.
What is consent in healthcare?
A covered entity that chooses to have a consent process has complete discretion under the Privacy Rule to design a process that works best for its business and consumers. A “consent” document is not a valid permission to use or disclose protected health information for a purpose that requires an “authorization” under the Privacy Rule (see 45 CFR 164.508), or where other requirements or conditions exist under the Rule for the use or disclosure of protected health information. Right to Request Privacy Protection.
What is the HIPAA Privacy Rule?
The HIPAA Privacy Rule establishes a foundation of Federal protection for personal health information, carefully balanced to avoid creating unnecessary barriers to the delivery of quality health care. As such, the Rule generally prohibits a covered entity from using or disclosing protected health information unless authorized by patients, except where this prohibition would result in unnecessary interference with access to quality health care or with certain other important public benefits or national priorities. Ready access to treatment and efficient payment for health care, both of which require use and disclosure of protected health information, are essential to the effective operation of the health care system. In addition, certain health care operations—such as administrative, financial, legal, and quality improvement activities—conducted by or for health care providers and health plans, are essential to support treatment and payment. Many individuals expect that their health information will be used and disclosed as necessary to treat them, bill for treatment, and, to some extent, operate the covered entity’s health care business. To avoid interfering with an individual’s access to quality health care or the efficient payment for such health care, the Privacy Rule permits a covered entity to use and disclose protected health information, with certain limits and protections, for treatment, payment, and health care operations activities.
What are some examples of payment activities?
In addition to the general definition, the Privacy Rule provides examples of common payment activities which include, but are not limited to: Determining eligibility or coverage under a plan and adjudicating claims; Risk adjustments; Billing and collection activities; Reviewing health care services for medical necessity, coverage, ...
What is the importance of access to treatment and efficient payment for health care?
Ready access to treatment and efficient payment for health care, both of which require use and disclosure of protected health information, are essential to the effective operation of the health care system. In addition, certain health care operations—such as administrative, financial, legal, and quality improvement activities—conducted by or ...
What is the purpose of the Surface Water Treatment Rules?
The purpose of the Surface Water Treatment Rules (SWTRs) is to reduce illnesses caused by pathogens in drinking water. The disease-causing pathogens include Legionella , Giardia lamblia, and Cryptosporidium.
What is surface water treatment?
EPA has developed the Surface Water Treatment Rules (SWTRs) to improve your drinking water quality. The regulations provide protection from disease-causing pathogens, such as Giardia lamblia, Legionella, and Cryptosporidium. The regulations also protect against contaminants that can form during drinking water treatment.
What is the purpose of the microbial protection provision?
Provides provisions to ensure that systems maintain microbial protection as they take steps to reduce the formation of disinfection byproducts
Does watershed protection require filtration?
Requires that watershed protection programs address Cryptosporidium for system that are not required to provide filtration
What is the HHS requirement for consent?
The HHS regulations require that “An investigator shall seek such consent only under circumstances that provide the prospective subject or the representative sufficient opportunity to consider whether or not to participate and that minimize the possibility of coercion or undue influence ” ( 45 CFR 46.116 ).
How far in advance can a subject consent to a study?
The HHS regulations at 45 CFR part 46 do not specify how far in advance of study entry a subject can provide consent. The amount of time required by a subject to make a decision would presumably depend on the nature of the study, taking into account, among other factors, the degree of risk, potential benefits, alternatives, and desire to consult with family members or others. However, if a prolonged period of time elapses from the date of consent to the date of entry into the study even if there have been no changes in the study design or no new significant findings affecting the study it might be prudent to review the information contained in the consent form with the subject prior to initiating any research procedures with the subject.
What is the requirement for informed consent in research?
When informed consent is required, it must be sought prospectively, and documented to the extent required under HHS regulations at 45 CFR 46.117. [Food and Drug Administration (FDA) regulations at 21 CFR part 50 may also apply if the research involves a clinical investigation regulated by FDA.]
How effective is informed consent?
Informed consent is legally effective if it is both obtained from the subject or the subject’s legally authorized representative and documented in a manner that is consistent with the HHS protection of human subjects regulations and with applicable laws of the jurisdiction in which the research is conducted. In general terms, the regulations stipulate that an investigator should seek consent only under circumstances that provide the prospective subject or the legally authorized representative sufficient opportunity to consider whether to participate and that minimize the possibility of coercion or undue influence. The information provided should be in language that is understandable to the subject or the representative. No informed consent, whether oral or written, may include any exculpatory language.
What is consent form?
The consent form is intended, in part, to provide information for the potential subject’s current and future reference and to document the interaction between the subject and the investigator. However, even if a signed consent form is required, it alone does not constitute an adequate consent process.
What is the term for an overt or implicit threat of harm that is intentionally presented by one person to another in order?
Coercion occurs when an overt or implicit threat of harm is intentionally presented by one person to another in order to obtain compliance. For example, an investigator might tell a prospective subject that he or she will lose access to needed health services if he or she does not participate in the research.
What is informed consent?
The informed consent process is an ongoing exchange of information between the investigator and the subject and could include, for example, use of question and answer sessions, community meetings, and videotape presentations.
