Nutritional and biochemical insights into multiple pressure ulcer management: a case report
Alica Hokynková, Hana Paulová, Petr Šín, Marie Nováková, Petr Babula, Andrea Pokorná

TL;DR
This case report explores how nutritional and biochemical markers influenced the treatment of pressure ulcers in a paraplegic patient with a complex medical history.
Contribution
The study highlights the importance of monitoring 8-OHdG and nutritional parameters to guide surgical timing in complex pressure ulcer cases.
Findings
Decreased 8-OHdG and nutritional markers were observed at the start of treatment.
CRP levels were elevated initially but decreased as the patient improved.
Monitoring these parameters helped guide successful multistage surgical therapy.
Abstract
This case report presents a unique study focused on relationship between nutritional parameters, C-reactive protein (CRP), and the marker of oxidative stress 8-hydroxy-2′-deoxyguanosine (8-OHdG), in 61-year-old male paraplegic patient with multiple pressure ulcers. A multidisciplinary approach was essential for the timing of the successful reconstruction process. The patient had a history of paraplegia since 1999 due to a skiing accident with fractures of thoracic vertebrae (Th6–Th9), requiring spinal surgery. His medical background includes acute pancreatitis with biliary tract revisions, partial pancreatic resection, acute respiratory failure with tracheostomy, renal failure treated with hemodialysis, bronchopneumonia, pseudomembranous colitis, and hyperuricemia. The patient also underwent multiple surgical interventions, including treatment for ulnar nerve paresis, cholecystectomy,…
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Figure 1
Figure 2| CLINICAL DATA | ||||||
|---|---|---|---|---|---|---|
| Pressure ulcer location | H1 | H2 | H3 | H4 | H5 | H6 |
| Ischial left side | ||||||
| Category | IV | IV | IV | IV | IV | IV |
| Size (length, | 9x8cm | 9x6cm | 8x5cm | 7x3cm | 5x4cm | 6x4cm |
| Debridement | Day 0: YES | Day 0: YES | Day 0: YES | Day 0: YES | Day 0: YES | Day 0: YES |
| Reconstruction | NO | NO | Day 0: YES | Day 7: YES, | NO | Day 7: suture |
| Local complications | Wound colonization | Polymicrobial colonization |
| Polymicrobial colonization |
| |
| Trochanteric left side | ||||||
| Category | IV | IV | IV | Healed | Healed | Healed |
| Size (length, | 5x5cm | 3x wound dehiscence | 6x3cm | NA | NA | NA |
| Debridement | Day 0: YES | Day 0: YES | Day 0: YES | NA | NA | NA |
| Reconstruction | Day 14: YES | NO | Day 0: YES | NA | NA | NA |
| Local complications | Osteomyelitis, | Polymicrobial colonization |
| NA | NA | NA |
| Sacral | ||||||
| Category | IV | IV | IV | IV | IV | Healed |
| Size (length, | 6x5cm | 10x10cm | 8x5cm | 4x4cm | 4x4cm | NA |
| Debridement | Day 0: YES | Day 0: YES | Day 0: YES | Day 0: YES | Day 0: YES | NA |
| Reconstruction | NO | NO | NO | Day 7: YES | DAY 0: YES | NA |
| Local complications | Wound colonization | Polymicrobial colonization | NO | Polymicrobial colonization | Polymicrobial colonization | NA |
| Nutritional and biochemical parameters | |||||||
|---|---|---|---|---|---|---|---|
| Parameter | Day | H1 | H2 | H3 | H4 | H5 | H6 |
| Prealbumin (g/L) | |||||||
| Day 0 | 0.19 | 0.09 | 0.24 | 0.19 | 0.21 | 0.19 | |
| Day 7 | 0.15 | 0.07 | # | 0.18 | # | 0.17 | |
| Day X | 0.17a | ## | 0.16b | ## | ## | ## | |
| Albumin (g/L) | |||||||
| Day 0 | 29.6 | 20.8 | 23.3 | 26.7 | 28.6 | 29.4 | |
| Day 7 | 27.1 | 19.5 | # | 25.6 | # | 26.9 | |
| Day X | 25.3a | ## | 25.2b | ## | ## | ## | |
| Total protein (g/L) | |||||||
| Day 0 | 74.0 | 70.9 | 79.0 | 89.8 | 82.6 | 78.5 | |
| Day 7 | 70.2 | 67.9 | # | 86.6 | # | 87.9 | |
| Day X | 66.6a | ## | 90.8 b | ## | ## | ## | |
| CRP (mg/L) | |||||||
| Day 0 | 70.1 | 157.2 | 44.2 | 44.2 | 23.6 | 20.9 | |
| Day 7 | 88.8 | 156.1 | # | 52.0 | # | 29.9 | |
| Day X | 41.8a | ## | 91.0b | ## | ## | ## | |
| 8-OHdG (ng/mg crea) | |||||||
| Day 0 | 13.3 | 10.44 | 19.66 | 9.38 | 7.63 | 9.8 | |
| Day 7 | # | 8.04 | # | 12.63 | # | 9.41 | |
| Day X | 17.07a | ## | 6.67b | ## | ## | ## | |
| Daily calculation and nutritional therapy | |||||||
| Daily protein intake | 71g | 122g | 100g | 100g | Not calculated | Not calculated | |
| Daily caloric intake | 5020kcal | 2253kcal | 2340kcal | 2190kcal | Not calculated | Not calculated | |
| Nutritional therapy per os | Sipping (Cubitan 2x200ml, Nutridrink compact protein- 2x 200ml/24 h) | Sipping (Cubitan)- 2x200ml /24 h | Sipping (Cubitan)- 2x200ml /24 h | Sipping (Cubitan)- 2x200ml /24 h | Sipping (Diben drink 1.200ml/24 h, Cubitan 1x200ml/ 24 h) | Sipping (Cubitan)- 2x200ml /24 h | |
| Nutritional therapy enteral via nasojejunal tube | None | None | Nutrison Diason Energy HP 250ml/24 h | Diben 500ml/24 h | None | None | |
| Nutritional therapy parenteral via central venous catheter | None | None | All in One bags 910ml/24 h (940 kcal, 60g proteins) | None | None | None | |
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Taxonomy
TopicsPressure Ulcer Prevention and Management · Wound Healing and Treatments · Body Contouring and Surgery
Introduction
Extensive and multiple deep pressure ulcers (PUs) represent a serious medical and socio-economic problems, especially in immobile patients (1). Their healing is negatively influenced by numerous factors, such as comorbidities, duration and number of hard-to-heal wounds, their local status (e.g., category, size, biofilm, osteomyelitis), and patients’ compliance and motivation (2). The success of surgical interventions depends, among other things, on the actual health status of the patient, monitored by a number of laboratory parameters, including nutritional ones (2). Another factor affecting the course of surgical therapy and subsequent healing is oxidative stress (3). One of the important markers of oxidative stress is 8-hydroxy-2′-deoxyguanosine (8-OHdG), an indicator of oxidative DNA damage (4). Although DNA damage can be assessed by various approaches (e.g., comet assay (5)) the most used parameter is 8-OHdG. It is stable molecule, freely filterable into the urine, where it can be subsequently determined.
This case report presents the dynamics of selected nutritional, inflammatory, and biochemical parameters in relation to planned multistage surgical therapy in a paraplegic patient with multiple PUs over a period of 17 months.
Case description
A 61-year-old male paraplegic patient (at the time of the first admission) with three PUs of deep category located in the left-sided ischial and trochanteric and sacral regions (see Figure 1) was planned for multi-stage reconstructive surgical treatment. The patient has been paraplegic since 1999 due to a skiing accident, which resulted in the fractures of thoracic vertebrae (Th6–Th9) and subsequent spinal surgery. He has a complex medical history, including acute pancreatitis requiring biliary tract revisions and partial pancreatic resection, acute respiratory failure with tracheostomy, and renal failure treated with hemodialysis. Additional complications include left-sided bronchopneumonia, pseudomembranous colitis, and hyperuricemia. Surgical interventions include treatment for ulnar nerve paresis, cholecystectomy with biliary tract revisions, and multiple PUs surgeries over several years. This history highlights the patient’s extensive medical challenges and the need for multidisciplinary care. This case report describes the course of comprehensive therapy and management of three extensive and deep PUs during repeated hospitalizations (H1–H6) between February 2022 and July 2023, with a focus on selected biochemical and nutritional parameters.
(A) Localization and pressure ulcers status before treatment (left-sided trochanteric PU - Ls T PU, left-sided ischial PU – Ls I PU, sacral PU – S PU) and (B) Healed pressure ulcers areas after treatment (left-sided trochanteric area – Ls T A, left-sided ischial area – Ls I A, sacral area – S A).
The patient’s overall condition fluctuated over time, and his clinical status corresponded with the local wound symptomatology. During H1–H3, the patient suffered from infection and renal insufficiency. These infections included signs of local infection with polymicrobial colonization of the PUs, systemic infection with positive blood cultures during H1, and a urinary tract infection in H2. Logically, the wound extents were the largest during this period. Moreover, some extrinsic factors influenced the course of therapy, such as an intestinal infection (Clostridium difficile colitis) in H4. The improved patient’s status during the H5-H6 hospitalizations allowed for the finalization of reconstructive surgeries, which were always planned according to the actual clinical condition and local wound symptomatology. Clinical data of the patient and wound status during the six hospitalizations are summarized in Table 1.
The clinical status of the patient was characterized by nutritional and biochemical parameters measured from plasma and urine. The samples were collected at the same time points as surgical interventions (if performed) - debridement of PUs at the beginning of the particular hospitalization (Day 0) and further reconstruction (Day 7). Due to the actual clinical situation of the patient, some samples could not be collected at all or were collected on different days of hospitalization. The detailed timeline outlining the progression and key events of the case report is illustrated in Figure 2.
Timeline of the case. More extensive photo documentation and data are available and can be obtained from the main author upon reasonable request.
In total, 59 biological samples related to surgical therapy (debridement and reconstruction) were analyzed over a 17-month period. The basic nutritional parameters (prealbumin and albumin) and biochemical parameters (total protein and CRP) were assessed from plasma samples using routine commercial kits (Roche, Switzerland). The oxidative stress parameter 8-OHdG was determined from morning urine samples using a modified LC/MS/MS method (6). The urinary concentrations of 8-OHdG were expressed in ng/mg creatinine. The measured values of all parameters are summarized in Table 2.
Surgical therapy was initiated with the debridement of all PUs during H1. However, it was necessary to respond to the patient’s unsatisfactory condition (signs of malnutrition and infectious complications), which lasted from H1-H3. Therefore, the reconstruction of PUs had to be spread over a longer period of time. In H1, the extirpation of the osteomyelitic femoral head on the left side, along with partial resection of the sacral and ischial tuber bone tissue for the osteolytic process, was performed. A previous flap plasty (done several years ago) above the resected femoral head on the left side was elevated and transponed over the trochanteric PU to allow successful wound closure. The postoperative status was further complicated by the presence of Vancomycin-resistant Enterococcus faecium (VRE) in all three PUs. Additionally, the femoral head resecate was accompanied by a positive hemoculture of Proteus mirabilis. The patient’s nutritional status began to worsen, and CRP levels increased. Therefore, nutritional support (sipping and high protein diet), conservative local therapy to eradicate biofilm, and prolonged systemic antibiotic therapy were indicated.
During the second hospitalization, further surgical management of multiple PUs was planned. Debridement was performed in all affected areas; however, due to severe malnutrition, reconstructive surgery was contraindicated. A significant deterioration of nutritional status (decrease in prealbumin and albumin) occurred, leading to reopening (dehiscence) of the left trochanteric PU. CRP levels increased significantly, whereas 8-OHdG concentrations simultaneously decreased.
Between the second and third hospitalization, the patient was admitted to the Metabolic ICU for intensive nutritional support and stabilization of nutritional parameters. The patient received enteral nutrition via a nasojejunal tube, which was maintained for a total of 8 months. In parallel, parenteral nutrition using All-in-One bags was administered for 1 month to support metabolic stabilization and optimize nutritional parameters. This comprehensive nutritional intervention aimed to optimize the patient’s metabolic status and ensure an adequate supply of essential nutrients necessary for surgical treatment and recovery at the beginning of H3.
The flap plasty of recurrent trochanteric PU was performed. However, during H3, the patient’s general clinical condition worsened, as demonstrated by an increase in CRP and a decrease in prealbumin and 8-OHdG. Therefore, the next reconstructive surgical procedure was postponed for 2 months. In H4, the flap plasty of the sacral and left side ischial PUs was performed. Although the monitored parameters did not indicate any complications or worsening of health status at the beginning of H4, the patient’s condition deteriorated again. This situation was attributed to an infection with Clostridium difficile colitis, suspected to be a hospital acquired infection (7).
Repeated contamination of sutured wounds with stool led to complete dehiscence of the sutured wound above the left ischial area and the release of the rotation flap in the sacral region, known as floating flap plasty. Consequently, reoperation using tissue sealant was necessary. During periods H5-H6, the reconstruction of the remaining PUs was gradually completed.
To provide a detailed overview of the patient’s nutritional intake, daily caloric and protein intake during the H1–H6 period, along with the type of nutritional therapy used, is summarized in Table 2. These values reflect the dynamic changes in metabolic support provided throughout the hospitalization periods. The patient remained under continuous supervision by nutritional specialists from the first to the last hospitalization. Throughout the entire course of treatment, nutritional experts closely monitored the patient’s condition, adjusting the nutritional strategy as needed to ensure optimal metabolic support and recovery.
From the patient’s perspective, the prolonged treatment period and multiple hospitalizations posed significant physical and psychological challenges. The patient reported frustration due to wound recurrence, surgical complications, and prolonged recovery times. However, the gradual improvement of biochemical parameters and clinical condition reinforced trust in the multidisciplinary approach, and the patient expressed high satisfaction with the final surgical outcomes.
Discussion
In this paper, we provide a comprehensive insight into the dynamic interplay among nutritional status, oxidative stress, and inflammatory markers in the context of multistage surgical reconstruction of multiple PUs in a paraplegic patient. The systemic therapy of patients with multiple PUs must reflect health status in combination with biochemical parameters according to Evidence Based Medicine (8). The nutritional status, as reflected by albumin and prealbumin levels, is essential for the successful continuation of PU reconstruction (9). Although several nutritional biomarkers are known (10), we focused on two routinely used ones: albumin and prealbumin. Among them, prealbumin is more useful for assessing nutritional status due to its shorter half-life (2–3 days vs. 19 days for albumin), indicating that it reflects rapid changes in nutritional state (11). However, it must be considered that both proteins are synthesized in the liver, and their levels decrease not only in malnutrition but also in other situations (e.g., inflammation, severe liver diseases) (12).
During inflammatory processes, the synthesis of prealbumin and albumin is reduced, while the synthesis of acute phase proteins, such as CRP, which is also synthesized in the liver, is increased. Thus, in inflammation, it is desirable to assess prealbumin with respect to CRP changes. Nevertheless, in the perioperative process, when CRP increase is expected, prealbumin is a useful parameter not only for monitoring nutritional status but also for planning nutritional intervention. It has been recommended that an increase in prealbumin of more than 0.04 g/L per week is a sign of satisfactory nutritional support (13). In our patient, nutritional support resulted in a 0.17 g/L increase in prealbumin level over 3 weeks (see Table 2, H2-Day 7 and H3-Day 0), which is even higher than the recommended value. Due to successful nutritional support, the first reconstruction could be performed at the beginning of H3. Thus, according to the results obtained, prealbumin can be used for the timing of reconstruction, which is also consistent with prediction of successful surgical procedure outcomes (9, 14). Our findings reinforce the crucial importance of real-time biochemical monitoring in perioperative planning.
Another factor influencing the healing of PUs and the success of reconstructive procedures is the level of oxidative stress (15). However, not only reactive oxygen species (ROS) but also inflammation play an important role in the complex process of wound healing. ROS activate signaling pathways leading to the production of cytokines such as IL-6 and TNF-α, which subsequently modulate the inflammatory phase of healing (15, 16). A marker of inflammation is CRP, the level of which increases in response to cytokines (e.g., IL-6 and TNF-α). Although ROS and CRP are not directly related, they are linked through inflammatory pathways (17).
Among the biomarkers of oxidative stress, urinary 8-OHdG is important, since it reflects the level of DNA damage (4). However, it has not yet been studied in patients with PUs. Thus, this study is the first to describe the dynamics of its levels during long-term treatment of multiple PUs in a paraplegic patient. The novelty of our study lies in the integration of oxidative stress parameters, particularly 8-OHdG, as a biomarker for surgical readiness in PU patients. While previous research has focused primarily on nutritional markers such as albumin and prealbumin (9, 12, 14), our study provides new evidence linking oxidative stress with clinical outcomes in the setting of long-term complex PU treatment.
It is well known that 8-OHdG is a highly recognized parameter of oxidative stress, and high levels of 8-OHdG are a risk factor for a number of pathologies (18–21). For example, elevated levels of urinary 8-OHdG are detected in patients with carcinomas and in diabetic patients (22). Yet, in this case, we observed different results. During H1 - H3, an inverse course of 8-OHdG and CRP was observed. When CRP was elevated, a low level of 8-OHdG was measured. The association of 8-OHdG with CRP was observed in a paraplegic patient with a severe clinical condition, which precluded PU reconstruction. This was accompanied by decreased values of nutritional parameters (especially prealbumin). Decreased serum 8-OHdG values were reported in several studies focusing on various pathologies, e.g., breast cancer (23, 24), polycystic ovary syndrome (25), and colorectal cancer (26). It has been shown that the low expression of 8-OHdG is associated with poor prognosis of breast cancer (24) and colorectal cancer (26). In this study, we assume that the main reason for our findings is the patient’s overall exhaustion. Moreover, the novel relationship between oxidative stress, as represented by urinary 8-OHdG, and inflammatory markers (particularly CRP) provides new insights into the biochemical dynamics during severe clinical conditions. This inverse trend suggests a unique biochemical response influenced by the patient’s overall health and exhaustion. To our best knowledge, this has not been previously described in the context of PU treatment.
During subsequent hospitalizations, the nutritional status and insignificantly fluctuating CRP and 8-OHdG values allowed reconstructions to be performed as scheduled. The data demonstrate that progressive nutritional optimization, particularly with high-protein supplementation, played a crucial role in stabilizing the patient’s metabolic status and enabling surgical interventions. These findings further support the importance of individualized, dynamic nutritional strategies in PU treatment and surgical planning.
This long-lasting process led to healing of all PUs. The 12-month follow-up after the last hospitalization revealed satisfactory results. The dynamics of the monitored biochemical parameters in the context of treating multiple PUs proved to be crucial for the timing of surgical reconstruction and achieving satisfactory therapeutic outcomes (see Figure 1B). The case also underscores the importance of continuous patient engagement and psychological support throughout long-term reconstructive treatments. Repeated hospitalizations and surgeries can lead to psychological distress, affecting treatment adherence and overall recovery. A multidisciplinary approach, including psychological counseling, enhances patient motivation and trust in the treatment process. Providing structured psychological support can improve emotional well-being and thus contribute to better clinical outcomes.
In the routine operation of a clinical unit, the metabolic status of the patient, determined especially by nutritional (prealbumin, albumin) and inflammatory parameters (CRP), is monitored for the timing of surgical interventions. However, the state of the body in terms of oxidative stress level is also important for the success of surgical interventions and subsequent wound healing. In routine practice, this aspect has not yet been emphasized. This gap can be filled by urinary 8-OHdG, a non-invasive oxidative stress parameter reflecting DNA damage. It may serve as a valuable tool in perioperative planning, improving both patient stratification and surgical outcomes. Therefore, by monitoring urinary 8-OHdG over time, clinicians can gain an objective, dynamic understanding of a patient’s readiness for surgical intervention.
Finally, the integration of urinary 8-OHdG into clinical decision-making can enhance the assessment of metabolic stress and healing potential in patients with multiple PUs. When combined with standard nutritional and inflammatory markers, it offers a more complete picture of the patient’s status. This multidisciplinary approach supports better timing of surgical interventions and more individualized, evidence-based care for multiple PUs patients.
Next, to its contribution, this study has some limitations. Firstly, as this is a single-case study, the results may not be generalizable to a wider patient population. Secondly, although 8-OHdG was used as a highly recognized marker of oxidative stress, other oxidative and inflammatory biomarkers could provide a more comprehensive understanding of the healing process.
Conclusion
The preparation and timing of PU reconstruction require complex approach with an emphasis on a multidisciplinary strategy. It includes local conservative treatment, surgical interventions, systemic antibiotic therapy, evaluation of the patient’s condition using laboratory parameters, and nutritional and psychological support. A comprehensive approach, involving collaboration between pre-clinical and clinical experts, leads to successful long-term therapy results. Monitoring nutritional, inflammatory, and oxidative stress parameters (such as prealbumin, CRP, and 8-OHdG) is highly beneficial and desirable for the timing of surgical strategies and can advance research in this area.
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