Paul K. Maciejewski’s research while affiliated with Life Care Medical Center and other places

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Publications (213)


Chapter 8. Conclusion
  • Chapter

December 2024

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2 Reads

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Paul Maciejewski

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Prolonged grief disorder: detection, diagnosis, and approaches to intervention
  • Article
  • Full-text available

October 2024

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55 Reads

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1 Citation

World psychiatry: official journal of the World Psychiatric Association (WPA)

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Flowchart presenting inclusion and exclusion of cases for the present study from the Coping with Cancer II study dataset. Starting at the top box of the chart, a total of 470 individuals were screened as potentially eligible to participate in the CwC II study. Within the second box, we show screened cases that were ineligible due to cognitive impairment, non-advanced diagnosis and cognitive impairment, age, or an unspecified reason; refused participation upon approach to consent; and did not provide consent. The third box down in the flowchart shows the remaining cases that were eligible following the screening and consent process. The next box presents cases that were excluded due to current study criteria. Reasons for exclusion included as follows: no baseline data, missing all data from the McGill Quality of Life (QoL) questionnaire, missing partial data from the McGill QoL questionnaire, and missing data regarding aggressiveness of end-of-life care. The final box presents the total number of cases included in the current study
Associations between perceived interpersonal support and aggressiveness of care in the last month of life among patients with advanced cancer

September 2024

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21 Reads

Supportive Care in Cancer

Purpose To determine quality of life (QoL) domains in the months leading up to death associated with the receipt of aggressive care in the last month of life among patients with advanced cancer. Methods A multisite, prospective cohort study conducted from January 2010 to May 2015 of 59 patients with advanced cancer (distant metastases and/or progression of disease following at least first-line chemotherapy) and poor prognosis (≤ 6 months) followed through death. At baseline, a median of 4 months from death, the McGill Quality of Life Questionnaire measured overall QoL and four QoL domains (i.e., interpersonal support, physical well-being, psychological, and existential). Postmortem data were collected via medical chart review and nurse/caregiver report and combined to capture the aggressiveness of end-of-life (EoL) care in patients’ last month of life. Aggressive EoL care was defined as any receipt of care in an intensive care unit, being on a ventilator, or chemotherapy in the last month of life. Results Patients with higher interpersonal support domain scores (i.e., rating the world as more “caring and responsive” to their needs and their felt support as more complete) received significantly less aggressive care in their last month of life (odds ratio = 0.39, 95% confidence interval 0.20 to 0.75, p = 0.004). Conclusion Perceived interpersonal support is the only QoL domain assessed that was associated with aggressiveness of care in the last month of life for patients with advanced cancer. Prioritizing caring and responsive relationships for patients may decrease receipt of aggressive EoL care.




Citations (69)


... This review supports the notion that complicated grief is a condition characterized by intense yearning and significant distress (Maciejewski & Prigerson, 2023;Reed et al., 2022). While this review cannot establish that these characteristics clearly distinguish complicated grief from uncomplicated grief, descriptions from the primary studies do suggest that complicated grief is more profound than uncomplicated grief reactions. ...

Reference:

Experiences of Complicated Grief - A Synthesis of Qualitative Studies
Chapter 4. Defining and Diagnosing Prolonged Grief Disorder
  • Citing Chapter
  • December 2024

... F amily members of patients who die in intensive care units (ICU) may be at risk of experiencing prolonged grief symptoms, such as difficulty accepting the loss, bitterness, intense yearning, inability to trust others, emotional numbness, and the feeling of being trapped in grief. 1 While the formal diagnosis of prolonged grief disorder occurs several months after the loss, many family members exhibit symptoms of prolonged grief during their time in the ICU and shortly thereafter. 1,2 The transition from curative treatment to end-of-life care, aggressive medical interventions, difficulties with communication, unexpected death, or treatment withdrawal/withholding decisions can be distressing for families, who often have limited time to process the possible PROOF impact of an anticipated death. 3,4 When families face withdrawing life-sustaining treatment decisions, feelings of stress, doubt, and guilt can arise. ...

EMPOWER: A Multi-Site Pilot Trial to Reduce Distress in Surrogate Decision-Makers in the ICU
  • Citing Article
  • March 2024

Journal of Pain and Symptom Management

... Prior research on factors associated with aggressive EoL care in patients with cancer has examined primarily socio-demographic, clinical, and healthcare service factors. Factors associated with higher likelihood of aggressive EoL care include as follows: young age [6][7][8][9], male identity [6,9], race (e.g., Black patients linked to higher odds of aggressive acute care [9], white patients linked to higher odds of EoL systemic treatments [10]), more patient comorbidities [6], shorter time since cancer diagnosis [6], commercial insurance [10], and caregiver personality characteristic [11]. Factors associated with lower likelihood of aggressive EoL care include as follows: accurate prognostic understanding [2]; receipt [12] and duration [13] of palliative care; and access to psychological, social work, and/or spiritual care [14][15][16]. ...

Patient-Caregiver Dyads & End-of-Life Care: Caregiver Personality Disrupts Gender-Based Norms
  • Citing Article
  • January 2024

Journal of Pain and Symptom Management

... To mitigate these disparities, policymakers could intervene by improving health literacy, enhancing social support systems, increasing educational opportunities, and promoting family health in rural areas. For instance, previous research had implemented a communication intervention for diverse advanced cancer patient-caregiver dyads, and the results indicated that patients demonstrated an improvement in the completion of ACP [68]. Additionally, government initiatives could focus on improving economic conditions in rural regions to elevate residents' income levels, thereby fostering greater acceptance of ACP [69]. ...

A communication intervention to improve prognostic understanding and engagement in advance care planning among diverse advanced cancer patient-caregiver dyads: A pilot study
  • Citing Article
  • August 2023

Palliative and Supportive Care

... QoL domains such as patient perceived interpersonal support, physical well-being, psychological health, and existential beliefs are often targeted by interventions aiming to improve QoL near the EoL and the quality of EoL care (e.g., EoL discussions [2,[17][18][19], palliative care [20,21]). However, how these QoL domains relate to receipt of aggressive EoL care remains essentially unknown [22]. ...

Planning for Your Advance Care Needs (PLAN): A Communication Intervention to Improve Advance Care Planning among Latino Patients with Advanced Cancer

... This is consistent with the study of Funk-Lawler et al. (2020), who reported that nearly half of the patients were severely distressed, but there was no significant association between the total distress score and demographic and illness-related characteristics [25]. However, several studies found demographic correlations with distress levels, such as younger age, gender and type of cancer [19,26,27]. The patients in this study reported a wide range of distressing issues that were significantly influenced by practical, family issues, emotional, and physical factors. ...

Patient characteristics associated with psychosocial distress about end-of-life.
  • Citing Article
  • June 2023

Journal of Clinical Oncology

... Education about glioblastoma's progression, expected symptoms, and treatment effects can empower caregivers with the knowledge needed to assist patients while managing their own emotional health. Hospice and palliative care teams often provide holistic support, addressing the spiritual, psychological, and physical aspects of care, which can help both patients and families navigate the advanced stages of the disease with dignity and comfort [64,65]. ...

Advance care planning (ACP) to promote receipt of value-concordant care: Results vary according to patient priorities

... In the case of grief, Western cultural discourses, reflected through interpersonal interactions (i.e., talk), have historically constrained understandings of grief as a "normalized" response to the death of a person (Andipatin et al., 2019;Neimeyer et al., 2014). This discourse informs that there are boundaries distinguishing grief from bereavement, asserting that expressions of grief should be potent but transitory, and constrained to palatable emotions (e.g., concealment), dictated by gendered, racial-ethnic, and social expectations (Cacciatore & DeFrain, 2015;Falzarano et al., 2022;Moran, 2016). ...

Grief and Bereavement in the Latino/a Community: A Literature Synthesis and Directions for Future Research

... Three instruments were used in this research. The first was the Prolonged Grief Questionnaire (PG-13) created by Prigerson and Maciejewski,19 adapted and validated in Spanish in 2016 by Estevan. 20 The PG-13 consists of 13 items with Likert-type responses, and it can be used for both purposes assessing the intensity of grief in a continuous form on a dimensional scale and diagnosing prolonged grief disorder according to the five proposed criteria: grief (necessary prior to filling out the questionnaire in the first place), symptoms of intense separation anxiety (2 items), duration greater than 6 months (1 item), cognitive, emotional and behavioral symptoms (9 items), and functional impairment (1 item). ...

Prolonged grief disorder

The Lancet Psychiatry

... Tergas et al. performed multi-institutional study of 302 cancer patients across the United States evaluated the effect of immigrant status on end of life. The authors found that immigrants were more likely to die in hospital settings, less likely to die at their preferred location, and more likely to report poor quality of death [60]. It has been suggested that early palliative care consultation may neutralize some racial/ethnic differences in access to hospice and palliative care services [61]. ...

Association between immigrant status and advanced cancer patients' location and quality of death