People v. Maria T. , 371 Ill. App. 3d 318 ( 2007 )


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  •                                               THIRD DIVISION
    JANUARY 31, 2007
    No. 1-06-0170
    In re M.T., Alleged to be a Person       )    Appeal from the
    Subject to Involuntary Treatment With    )    Circuit Court of
    Psychotropic Medication                  )    Cook County.
    )
    (The People of the State of Illinois,    )
    )
    Petitioner-Appellee,     )    No. 06 COMH 130
    )
    v.                                       )
    )
    Maria T.,                                )    Honorable
    )    Nathaniel R. Howse,
    Respondent-Appellant).   )    Judge Presiding.
    JUSTICE GREIMAN delivered the opinion of the court:
    Respondent, Maria T., appeals from an order of the circuit
    court of Cook County authorizing her involuntary treatment with
    psychotropic medication.   She contends that the order should be
    reversed because the State failed to prove by clear and
    convincing evidence that the benefits of the medication
    outweighed the harm.
    The State, through Dr. Joanna Poniaquwicz of Lutheran
    General Hospital, petitioned the court on January 11, 2006, to
    begin the involuntary treatment of respondent with psychotropic
    medications pursuant to section 2-107.1 of the Mental Health and
    Developmental Disabilities Code (Code) (405 ILCS 5/2-107.1 (West
    2004)).   In the petition, Dr. Poniaquwicz stated that respondent
    suffered from paranoid schizophrenia, that she was currently
    psychotic and unable to function, and sought to medicate her with
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    Proloxin Decanoate (12.5- to 25-milligram injection every two
    weeks), and alternatively with Risperidone1 Consta (25- to
    50-milligram injection every two weeks), oral Proloxin tablets
    (up to 40 milligrams per day), and oral risperidone tablets (up
    to 8 milligrams per day).
    On January 13, 2006, Dr. Poniaquwicz responded to a routine
    bill of particulars, stating that respondent had been
    involuntarily admitted to Chicago Read Hospital in December 2004,
    received Proloxin Decanoate, and responded "well," as she was
    able to care for herself and be discharged from the hospital in
    March 2005.   However, because respondent became noncompliant with
    her medication, she was readmitted to Swedish Covenant Hospital
    in November 2005.
    On January 20, 2006, a hearing was held on the State's
    petition.   Nancy S., respondent's daughter, testified regarding
    the series of events leading to respondent's present
    hospitalization.    During the first two weeks of November 2005,
    respondent told her that she owned at least one other home, which
    she did not, and that when she went there to bathe herself, the
    police came and took her to Swedish Covenant Hospital.    She also
    told her that she was the Virgin Mary, that she was rich, and
    that banks owed her money.    On December 22, 2005, when Nancy took
    1
    "Risperidone" and "Risperdal" are used interchangeably
    throughout the record.
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    respondent to a grocery store, respondent was reluctant to
    purchase fruits, vegetables, and milk for fear of contamination.
    On January 5, 2006, respondent told Nancy that she had not been
    eating because her food was being poisoned, which statement
    respondent had made to her at least six times during December
    2005.   Nancy had also noticed that respondent had lost about 15
    pounds from October 2005 to the time of the hearing.
    On January 6, 2006, respondent was admitted to Lutheran
    General Hospital and continued to express that her food was being
    poisoned.   She also told Nancy to cover herself to prevent
    people from inserting objects into her orifices and that she had
    inserted tampons "in her behind."   In addition, respondent told
    Nancy that her home was "fine" and that she had been using the
    heat; however, when Nancy visited there five days later, she had
    to crawl through a broken window to enter the house because the
    entrance was barricaded, the refrigerator was unplugged and in
    the living room with a chain around it, the furnace was turned
    off, the oven was turned on and opened, and a waffle iron was
    turned on to heat the basement.   Respondent subsequently told
    Nancy, on January 8, 2006, that she could not eat the hospital
    food because it smelled "funny" and because voices had told her
    not to do so.
    Nancy further testified that respondent had been on long-
    term psychotropic medications in the past, most recently from
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    October 2004 through February 2005, when she was involuntarily
    admitted to Read Hospital.    At that time, respondent was
    prescribed Risperdal, among other things, and after receiving
    this medication, respondent was more rational, did not
    hallucinate as often, and talked more about everyday life.
    Although she experienced some side effects from the medication,
    they were able to be controlled.    When respondent was discharged,
    she was still "a little paranoid," but she was better able to
    care for herself and her home, i.e., she bought a wider variety
    of foods, gained weight, cleaned her house, and used space
    heaters.    Nancy acknowledged that she "probably" told Dr.
    Poniaquwicz that Risperdal had not done respondent "a lot of
    good" in the past.
    Dr. Poniaquwicz, an expert in the field of psychiatry and
    respondent's attending physician, testified that respondent was
    admitted to Lutheran General Hospital on January 6, 2006.     Dr.
    Poniaquwicz first examined respondent on January 7, 2006, and
    about six days a week thereafter.    Based on her inquiry into
    respondent's social history, including talking to Nancy,
    reviewing respondent's medical records, and discussing the case
    with her peers, she opined that respondent suffered from paranoid
    schizophrenia and had done so for 26 years.    Respondent was
    currently symptomatic and experiencing paranoid delusions, i.e.,
    her food was being poisoned and voices were telling her not to
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    eat.    She was also displaying disorganized behaviors, i.e., she
    attempted to tie a stocking around her neck and knelt on her bed
    with the covers over her head.    In addition, respondent was
    displaying isolating behaviors and talking to herself.     Based on
    respondent's condition, i.e., her inability to keep her house
    safe or eat properly, Dr. Poniaquwicz believed that respondent's
    ability to function had deteriorated.
    On January 9, 2006, Dr. Poniaquwicz observed respondent
    attempting to tie a stocking around her neck and concluded that
    respondent presented a threat to herself and that she lacked the
    capacity to make decisions regarding her treatment.    She
    therefore administered two separate, 10-milligram emergency doses
    of Proloxin to respondent.    Although respondent became calmer
    after receiving the medication, she complained that she was tired
    and that her tongue felt large after the second dose was
    administered on January 13, 2006.    Dr. Poniaquwicz explained that
    respondent had experienced a dystonic reaction to the medication,
    a side effect which caused her tongue muscle to tense up, so Dr.
    Poniaquwicz issued a "stat" order for Cogentin to relieve the
    side effect.    Because the Cogentin did not completely resolve the
    issue, Dr. Poniaquwicz subsequently ordered Benadryl, which
    completely resolved the problem.    Dr. Poniaquwicz then
    discontinued the administration of Proloxin for two reasons: the
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    side effects and her uncertainty regarding the amount of time she
    could administer the medication under the circumstances.
    Despite respondent's reaction, Dr. Poniaquwicz still sought
    permission to treat respondent with Proloxin Decanoate and,
    alternatively, with Risperdal Consta, oral tablets of Proloxin,
    and oral tablets of Risperdal, in the dosages indicated in the
    petition, for 90 days.   Dr. Poniaquwicz based her request on the
    fact that respondent had historically responded best to Proloxin,
    as she had taken it during her last inpatient hospitalization and
    in the 1990s during a hospitalization in Montana.   Moreover,
    Nancy had told her that when respondent had previously taken
    Proloxin for an extended period of time, her symptoms markedly
    diminished and that she was able to function independently and be
    discharged from the hospital.   With regard to the risperidone,
    Dr. Poniaquwicz testified that Nancy had informed her that
    respondent had responded well to the medication in the past and
    that she would have to further explore Nancy's statement that it
    had not done respondent "much good."
    Dr. Poniaquwicz acknowledged that the possible side effects
    of Proloxin, as well as the alternative medications listed in the
    petition, included tardive dyskinesia, extrapyramidal symptoms,
    dystonia, tremor, akinesia, neuroleptic malignant syndrome (NMS),
    and diabetes.   She further acknowledged that respondent's age and
    gender put her at an increased risk of developing tardive
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    dyskinesia, i.e., abnormal movements, and NMS, which was
    potentially, but rarely, fatal.   Nevertheless, Dr. Poniaquwicz
    opined that the anticipated benefits of administering the
    proposed psychotropic medications outweighed the possible harm
    because the side effects could be "remedied with appropriate
    medications," and she "hoped" and "believed" that the requested
    medications would enable respondent to function independently,
    eat regularly, and be discharged from the hospital.    She
    conversely believed that, if left untreated, respondent's
    symptoms would worsen, her condition would further deteriorate,
    and she would be unable to live independently.   Dr. Poniaquwicz
    further opined that a less restrictive treatment was
    inappropriate for respondent's condition.
    Dr. Poniaquwicz finally testified that due to respondent's
    most recent reaction to Proloxin, she would start her on a low
    dose, closely monitor whether she experienced any side effects,
    and if so, administer the "appropriate medications" to counter
    them.   She also stated that she would be available daily to
    monitor respondent's response to the medications, would ensure
    that the medications were safely and effectively administered
    though various tests requested in the petition, e.g.,
    electrocardiograms, metabolic profiles, and vital signs, and that
    a psychiatrist would be available to intervene on an emergency
    basis if respondent experienced adverse side effects.    At the
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    conclusion of the hearing, the circuit court found that the State
    had proved the factors necessary to grant the petition by clear
    and convincing evidence. The court specifically found:
    "[A]lthough there were some side
    effects, they were completely abated by the
    administration of counteracting drugs.      The
    alternative for this individual is her not
    [being] able to live a normal life in her
    home the way she wants to live it.    With the
    medication she can go back to living her
    life.    The physical harm can be abated by the
    counteracting drugs, and, therefore, the
    petition is granted."
    The court then entered an order allowing Dr. Poniaquwicz to
    administer Proloxin Decanoate (12.5- to 50-milligram injections
    every two weeks) to respondent for 90 days.      The order
    alternatively granted Dr. Poniaquwicz the authority to administer
    Risperidone Consta (25- to 50-milligram injections every two
    weeks), Proloxin tablets (up to 40 milligrams per day), and
    risperidone tablets (up to 8 milligrams per day).
    In this appeal from that order, respondent asserts that the
    State failed to prove by clear and convincing evidence that the
    benefits of the medication outweighed the harm.        She thus
    requests that the order of the circuit court be reversed.
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    Initially, we observe that this case is moot.    The order
    authorizing the administration of respondent's involuntary
    treatment was effective for no more than 90 days, and thus
    expired on April 20, 2006.    405 ILCS 5/2-107.1(a-5)(5) (West
    2004).   Nevertheless, review of this appeal is appropriate under
    the "public interest exception" to the mootness doctrine.    In re
    Mary Ann P., 
    202 Ill. 2d 393
    , 401-02 (2002).
    Authorized involuntary treatment, i.e., the forced
    administration of psychotropic medication, shall not be
    administered to an adult recipient unless the State proves seven
    specific factors, including that the benefits of the treatment
    outweigh the harm, by clear and convincing evidence.    405 ILCS
    5/2-107.1(a-5)(4) (West 2004); In re C.E., 
    161 Ill. 2d 200
    , 208,
    221 (1994).   Clear and convincing evidence is deemed to be more
    than a preponderance, but does not reach the degree of proof
    necessary to convict a person of a criminal offense.    In re John
    R., 
    339 Ill. App. 3d 778
    , 781 (2003).    On review, we give great
    deference to the circuit court's factual findings and will not
    reverse its decision merely because we may have reached a
    different conclusion; instead, reversal is warranted only if the
    circuit court's decision is manifestly erroneous, i.e., the error
    is clearly evident, plain, and undisputable.    In re Jeffers, 
    239 Ill. App. 3d 29
    , 35 (1992).    For the reasons that follow, we do
    not find this to be such a case.
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    The record before us discloses respondent's history and
    deteriorating condition, i.e., her 26-year diagnosis of paranoid
    schizophrenia, and her recent behaviors and delusions which
    prohibited her from safely and properly caring for herself.
    Based on these behaviors and respondent's inability to conduct a
    reasonably safe existence, Dr. Poniaquwicz determined that the
    benefits of administering psychotropic medications, primarily
    Proloxin, outweighed the harm of the side effects.    She
    anticipated that if treated with the proposed psychotropic
    medications, respondent would be able to function independently,
    eat regularly, and be discharged from the hospital.    She
    conversely believed that, if left untreated, respondent's
    symptoms would worsen, her condition would further deteriorate,
    and she would be unable to live independently.
    Dr. Poniaquwicz based her opinion, in part, on Nancy's
    report of respondent's positive response to Proloxin in the past.
    When respondent had previously taken this medication for an
    extended period of time, her symptoms markedly diminished, and
    she was able to function independently and be discharged from the
    hospital.   Nancy specifically told her that when respondent was
    treated at Read Hospital with Proloxin (and Risperdal) from
    October 2004 through February 2005, she was more rational, did
    not hallucinate as often, talked more about everyday life, and
    better cared for herself and her home upon discharge from the
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    hospital.    Nancy also reported that although respondent had
    experienced side effects from the medications, they were able to
    be controlled.
    The evidence further showed that despite respondent's
    dystonic reaction to the second 10-milligram dose of Proloxin on
    January 13, 2006, Dr. Poniaquwicz was able to relieve the side
    effects with Cogentin and Benadryl, and would be available daily
    to monitor respondent's response to the medications and to
    administer "appropriate medications" to counteract any side
    effects.    In addition, the circuit court approved Dr.
    Poniaquwicz's request for laboratory tests to ensure that the
    psychotropic medications were administered safely and
    effectively.    We thus conclude that the State provided clear and
    convincing evidence that the benefits of administering
    psychotropic medications to respondent outweighed the harm (405
    ILCS 5/2-107.1(a-5)(4)(D) (West 2004)), and that the court's
    order to that effect was not manifestly erroneous.
    In so finding, we reject respondent's arguments that the
    circuit court's order should be reversed because the "side-
    effect-relieving" medications were not requested in the petition
    or authorized by the court, and because such medications posed
    the risk of side effects.    A petitioner is not required to set
    forth the specific medications she seeks to administer.    In re
    Miller, 
    301 Ill. App. 3d 1060
    , 1071 (1998).    Moreover, while an
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    order "shall *** specify the medications and the anticipated
    range of dosages that have been authorized and may include a list
    of any alternative medications and range of dosages" (405 ILCS
    5/2-107.1(a-5)(6) (West 2004)), we have not found, and respondent
    has not provided, any case law where an order entered under
    section 2-107.1 was reversed because a medication used to quell
    the side effects of a psychotropic medication was not listed in
    the court's order.
    Rather, reviewing courts have reversed circuit court orders
    where the order, and the court's oral ruling, failed to specify
    the psychotropic medications and the range of dosages requested
    in the petition.     See, e.g., In re Gwendolyn N., 
    326 Ill. App. 3d 427
    , 430-31 (2001); In re Williams, 
    305 Ill. App. 3d 506
    , 511-512
    (1999); In re Len P., 
    302 Ill. App. 3d 281
    , 285 (1999).      Here,
    the circuit court heard the harm and benefits associated with all
    of the medications listed in the petition, and its order properly
    enumerated each of those medications and ranges of dosages.         In
    re Mary Ann 
    P., 202 Ill. 2d at 405
    .      In addition, the circuit
    court's ruling made it clear that the side effects of the
    psychotropic medications were to be relieved with "counteracting
    drugs."   Thus, we find no cause for reversal based on
    respondent's argument with regard to the auxiliary medications.
    We further find that reversal is not warranted where
    respondent failed to object to the omission of the counteracting
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    drugs when the court entered its order, and where the record
    shows that Dr. Poniaquwicz was intimately familiar with
    respondent's treating protocol.   Dr. Poniaquwicz treated
    respondent when she experienced side effects from Proloxin, acted
    as respondent's attending physician for weeks before the hearing,
    and intended to continue in that role when the requested
    medications were administered.
    Moreover, respondent has failed to argue or demonstrate that
    she was prejudiced by the omission of the counteracting
    medications from the order.   In re 
    Miller, 301 Ill. App. 3d at 1072
    .   Instead, she merely asserts that Dr. Poniaquwicz lacked
    the authorization to administer counteracting medications to her
    in the event that she experienced side effects from the
    psychotropic medications.   This argument is clearly refuted by
    the record.
    Finally, we refuse to consider respondent's argument, raised
    for the first time on appeal, that Cogentin and Benadryl may
    cause side effects.   In re 
    Jeffers, 239 Ill. App. 3d at 37
    .
    Accordingly, we affirm the order of the circuit court of
    Cook County.
    Affirmed.
    THEIS, P.J., and KARNEZIS, J., concur.
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Document Info

Docket Number: 1-06-0170 Rel

Citation Numbers: 371 Ill. App. 3d 318, 862 N.E.2d 1079, 308 Ill. Dec. 876, 2007 Ill. App. LEXIS 67, 2007 WL 268954

Judges: Greiman

Filed Date: 1/31/2007

Precedential Status: Precedential

Modified Date: 11/8/2024